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  • 1.
    Agåker, Marcus
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Andersson, Joakim
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Englund, Carl-Johan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Rausch, J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rubensson, Jan-Erik
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Nordgren, Joseph
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Spectroscopy in the vacuum-ultraviolet2011Inngår i: Nature Photonics, ISSN 1749-4885, Vol. 5, nr 5, s. 248-248Artikkel i tidsskrift (Fagfellevurdert)
  • 2. Ahmadi, Sareh
    et al.
    Shariati, M. Nina
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Yu, Shun
    Göthelid, Mats
    Molecular layers of ZnPc and FePc on Au(111) surface: Charge transfer and chemical interaction2012Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 137, nr 8, s. 084705-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have studied zinc phthalocyanine (ZnPc) and iron phthalocyanine (FePc) thick films and monolayers on Au(111) using photoelectron spectroscopy and x-ray absorption spectroscopy. Both molecules are adsorbed flat on the surface at monolayer. ZnPc keeps this orientation in all investigated coverages, whereas FePc molecules stand up in the thick film. The stronger inter-molecular interaction of FePc molecules leads to change of orientation, as well as higher conductivity in FePc layer in comparison with ZnPc, which is reflected in thickness-dependent differences in core-level shifts. Work function changes indicate that both molecules donate charge to Au; through the pi-system. However, the Fe3d derived lowest unoccupied molecular orbital receives charge from the substrate when forming an interface state at the Fermi level. Thus, the central atom plays an important role in mediating the charge, but the charge transfer as a whole is a balance between the two different charge transfer channels; pi-system and the central atom.

  • 3.
    Andersson, Gabriella
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialfysik.
    Andersson, Staffan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Fysikundervisningens didaktik.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Linder, Cedric
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Fysikundervisningens didaktik.
    Aktiverande problemlösningsövningar i grupp.2010Inngår i: Att undervisa med vetenskaplig förankring – i praktiken!: Universitetspedagogisk utvecklingskonferens 8 oktober 2009 / [ed] Britt-Inger Johansson, Uppsala: Universitetstryckeriet , 2010, s. 103-113Kapittel i bok, del av antologi (Annet vitenskapelig)
  • 4.
    Andersson, Tomas
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Free Metal Clusters Studied by Photoelectron Spectroscopy2012Doktoravhandling, med artikler (Annet vitenskapelig)
    Abstract [en]

    Clusters are aggregates of a finite number of atoms or molecules. In the present work, free clusters out of metallic parent materials have been created and studied by synchrotron radiation-based photoelectron spectroscopy. The clusters have been formed and studied in a beam and the electronic structure of the clusters has been investigated. Conclusions have been drawn about the spatial distribution of atoms of different elements in bi-component clusters, about the development of metallicity in small clusters, and about the excitation of plasmons.

    Bi-component alloy clusters of sodium and potassium and of copper and silver have been produced. The site-sensitivity of the photoelectron spectroscopy technique has allowed us to probe the geometric distribution of the atoms of the constituent elements by comparing the responses from the bulk and surface of the clusters. In both cases, we have found evidence for a surface-segregated structure, with the element with the largest atoms and lowest cohesive energy (potassium and silver, correspondingly) dominating the surface and with a mixed bulk.

    Small clusters of tin and lead have been probed to investigate the development of metallicity. The difference in screening efficiency between metals and non-metals has been utilized to determine in what size range an aggregate of atoms of these metallic parent materials stops to be metallic. For tin this has been found to occur below ~40 atoms while for lead it happened somewhere below 20-30 atoms.

    The excitation of bulk and surface plasmons has been studied in clusters of sodium, potassium, magnesium and aluminium, with radii in the nanometer range. The excitation energies have been found to be close to those of the corresponding macroscopic solids. We have also observed spectral features corresponding to multi-quantum plasmon excitation in clusters of Na and K. Such features have in macroscopic solids been interpreted as due to harmonic plasmon excitation. Our observations of features corresponding to the excitation of one bulk and one surface plasmon however suggest the presence of sequential excitation in clusters.

    Delarbeid
    1. Single-component surface in binary self-assembled NaK nanoalloy clusters
    Åpne denne publikasjonen i ny fane eller vindu >>Single-component surface in binary self-assembled NaK nanoalloy clusters
    Vise andre…
    2009 (engelsk)Inngår i: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 80, nr 3, s. 033405-Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    Free metallic nanoalloy clusters created in a self-assembling process out of sodium and potassium mixed vapor have been studied by synchrotron-based photoelectron spectroscopy. The clusters are shown to consist of an alloy core surrounded by a surface layer containing only K in a range of conditions from K-rich to Na-rich nanoalloys. The size of the clusters as well as the fraction of the elements has been estimated from the spectra using our results on pure clusters. The mechanism behind the observed structure is discussed in terms of the total cohesive-energy minimization.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-128322 (URN)10.1103/PhysRevB.80.033405 (DOI)000268617800026 ()
    Tilgjengelig fra: 2010-07-22 Laget: 2010-07-20 Sist oppdatert: 2017-12-12bibliografisk kontrollert
    2. Size-dependent transformation of energy structure in free tin clusters studied by photoelectron spectroscopy
    Åpne denne publikasjonen i ny fane eller vindu >>Size-dependent transformation of energy structure in free tin clusters studied by photoelectron spectroscopy
    Vise andre…
    2010 (engelsk)Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 81, nr 2, s. 023203-Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    Free nanoscale tin clusters in the average size range of a few tens up to similar to 500 atoms are studied by means of valence and core-level photoelectron spectroscopy. A self-consistent picture arises from comparison of the work functions derived from the 4d core-level spectra, the experimental ionization energies extracted from the 5p valence spectra, and the expectations from the metallic sphere model for the clusters. The present studies demonstrate that the 4d core-level energy changes are a sensitive probe of the metal-to-semiconductor transition in the size range under investigation.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-137127 (URN)10.1103/PhysRevA.81.023203 (DOI)000275072500115 ()
    Tilgjengelig fra: 2010-12-15 Laget: 2010-12-15 Sist oppdatert: 2017-12-11bibliografisk kontrollert
    3. Plasmon single- and multi-quantum excitation in free metal clusters as seen by photoelectron spectroscopy
    Åpne denne publikasjonen i ny fane eller vindu >>Plasmon single- and multi-quantum excitation in free metal clusters as seen by photoelectron spectroscopy
    Vise andre…
    2011 (engelsk)Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 134, nr 9, s. 094511-Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    Plasmons are investigated in free nanoscale Na, Mg, and K metal clusters using synchrotron radiation-based x-ray photoelectron spectroscopy. The core levels for which the response from bulk and surface atoms can be resolved are probed over an extended binding energy range to include the plasmon loss features. In all species the features due to fundamental plasmons are identified, and in Na and K also those due to either the first order plasmon overtones or sequential plasmon excitation are observed. These features are discussed in view of earlier results for planar macroscopic samples and free clusters of the same materials.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-157480 (URN)10.1063/1.3563751 (DOI)000288085300048 ()
    Tilgjengelig fra: 2011-08-22 Laget: 2011-08-22 Sist oppdatert: 2017-12-08bibliografisk kontrollert
    4. The electronic structure of free aluminum clusters: Metallicity and plasmons
    Åpne denne publikasjonen i ny fane eller vindu >>The electronic structure of free aluminum clusters: Metallicity and plasmons
    Vise andre…
    2012 (engelsk)Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 136, nr 20, s. 204504-Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    The electronic structure of free aluminum clusters with similar to 3-4 nm radius has been investigated using synchrotron radiation-based photoelectron and Auger electron spectroscopy. A beam of free clusters has been produced using a gas-aggregation source. The 2p core level and the valence band have been probed. Photoelectron energy-loss features corresponding to both bulk and surface plasmon excitation following photoionization of the 2p level have been observed, and the excitation energies have been derived. In contrast to some expectations, the loss features have been detected at energies very close to those of the macroscopic solid. The results are discussed from the point of view of metallic properties in nanoparticles with a finite number of constituent atoms.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-178867 (URN)10.1063/1.4718362 (DOI)000304818400036 ()
    Tilgjengelig fra: 2012-08-06 Laget: 2012-08-02 Sist oppdatert: 2017-12-07bibliografisk kontrollert
    5. Valence-band narrowing and metallic-screening disappearance in the metal-to-insulator transition in small Pb clusters—as seen by photoelectron spectroscopy
    Åpne denne publikasjonen i ny fane eller vindu >>Valence-band narrowing and metallic-screening disappearance in the metal-to-insulator transition in small Pb clusters—as seen by photoelectron spectroscopy
    Vise andre…
    (engelsk)Manuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    A metal-to-insulator transition in small Pb clusters within the size range from a few tens of atoms up to ~100 atoms is investigated using synchrotron-based photoelectron spectroscopy. The electronic structure is seen to differ increasingly from that of the solid when the cluster size decreases. With the cluster size decrease the valence band narrows gradually -down to 25% of that of the solid-state at the smallest size of few tens of atoms. Simultaneously the Fermi-edge energy increases. The Pb 5d core level binding energy also increases and the spectral features broaden and change the shape. The changes observed for the valence and for the 5d energies and shapes are consistent with the picture of the loss of metallicity in Pb below the critical size of 20-30 atoms/cluster.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-183029 (URN)
    Tilgjengelig fra: 2012-10-26 Laget: 2012-10-21 Sist oppdatert: 2012-10-26
    6. Core-shell structure disclosed in self-assembled Cu-Ag nanoalloy particles—explanation for enhanced catalytic activity?
    Åpne denne publikasjonen i ny fane eller vindu >>Core-shell structure disclosed in self-assembled Cu-Ag nanoalloy particles—explanation for enhanced catalytic activity?
    Vise andre…
    (engelsk)Manuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    Core-shell segregation of copper and silver in self-assembled, free nanoparticles is established by means of electron spectroscopy using different photon energies. The nanoparticles are formed from metal-atom mixed vapor created by sputtering of a bimetallic sample. Even at dominating copper concentration in the primary vapor the surface of the nanoparticles is composed of only silver. These conclusions are based on the analysis of the photon-energy-dependent changes of the Cu 3d and Ag 4d photoelectron spectra. The role of such segregation is discussed in connection to the suggested enhanced catalytic properties of Cu-Ag nanoparticles.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-183030 (URN)
    Tilgjengelig fra: 2012-10-26 Laget: 2012-10-21 Sist oppdatert: 2012-10-26
  • 5.
    Andersson, Tomas
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Zhang, Chaofan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rosso, Aldana
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Bradeanu, Ioana
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Legendre, Sebastien
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Canton, S. E.
    Tchaplyguine, M.
    Ohrwall, G.
    Sorensen, S. L.
    Svensson, Svante
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Mårtensson, Nils
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Plasmon single- and multi-quantum excitation in free metal clusters as seen by photoelectron spectroscopy2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 134, nr 9, s. 094511-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Plasmons are investigated in free nanoscale Na, Mg, and K metal clusters using synchrotron radiation-based x-ray photoelectron spectroscopy. The core levels for which the response from bulk and surface atoms can be resolved are probed over an extended binding energy range to include the plasmon loss features. In all species the features due to fundamental plasmons are identified, and in Na and K also those due to either the first order plasmon overtones or sequential plasmon excitation are observed. These features are discussed in view of earlier results for planar macroscopic samples and free clusters of the same materials.

  • 6.
    Andersson, Tomas
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Zhang, Chaofan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Tchaplyguine, Maxim
    Svensson, Svante
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Mårtensson, Nils
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    The electronic structure of free aluminum clusters: Metallicity and plasmons2012Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 136, nr 20, s. 204504-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The electronic structure of free aluminum clusters with similar to 3-4 nm radius has been investigated using synchrotron radiation-based photoelectron and Auger electron spectroscopy. A beam of free clusters has been produced using a gas-aggregation source. The 2p core level and the valence band have been probed. Photoelectron energy-loss features corresponding to both bulk and surface plasmon excitation following photoionization of the 2p level have been observed, and the excitation energies have been derived. In contrast to some expectations, the loss features have been detected at energies very close to those of the macroscopic solid. The results are discussed from the point of view of metallic properties in nanoparticles with a finite number of constituent atoms.

  • 7. Arion, Tiberiu
    et al.
    Puettner, Ralph
    Lupulescu, Cosmin
    Ovsyannikov, Ruslan
    Förstel, Marko
    Öhrwall, Gunnar
    Lindblad, Andreas
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Ueda, Kiyoshi
    Svensson, Svante
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Bradshaw, Alex M.
    Eberhardt, Wolfgang
    Hergenhahn, Uwe
    New insight into the Auger decay process in O-2: The coincidence perspective2012Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 185, nr 8-9, s. 234-243Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Photoelectron-Auger electron coincidence spectroscopy is a powerful tool for the investigation of Auger decay processes with different core-ionized intermediate states. In this paper we describe an investigation into the Auger decay of the O-2 molecule, with the purpose of bringing new insight into the dynamics of the core hole decay mechanism. Using a novel experimental approach to measuring such coincidence spectra we report the highest resolution Auger spectrum of O-2 recorded hitherto. In our approach, we have combined the advantages of these coincidence spectra with the high resolution and excellent signal-to-noise ratios of non-coincident Auger spectra and a state-of-the-art fit analysis. In this way we have derived information about the potential energy curves of the final states W-3 Delta(u), B-3 Pi(g), and B' (3)Sigma(-)(u) and concluded that the corresponding Auger transitions are formed to a large part by strongly overlapping vibrational progressions. The present findings are compared to earlier results reported in the literature confirming some theoretical predictions.

  • 8. Berner, G.
    et al.
    Glawion, S.
    Walde, J.
    Pfaff, F.
    Hollmark, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Duda, Laurent
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Paetel, S.
    Richter, C.
    Mannhart, J.
    Sing, M.
    Claessen, R.
    LaAlO3/SrTiO3 oxide heterostructures studied by resonant inelastic x-ray scattering2010Inngår i: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 82, nr 24, s. 241405-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report the application of resonant inelastic X-ray scattering to explore the nature of the single conducting interface in the oxide heterostructure LaAlO/sub 3//SrTiO/sub 3/. From the Ti 3d crystal-field excitations measured at the Ti L/sub 3/ resonance we not only derive information on the local geometry at the interface but are also able to follow the evolution of the sheet carrier density with the thickness of the LaAlO/sub 3/ overlayer. These findings confirm after calibration to previous hard X-ray photoelectron spectroscopy measurements that the charge density from spectroscopy exceeds the one derived from Hall-effect measurements, indicating the coexistence of itinerant /i and/ localized Ti 3d electrons at the interface. On the other hand, we observe a saturation of the charge-carrier concentration above a LaAlO/sub 3/ thickness of 6 unit cells at ~1*10/sup 14/ cm/sup -2/, well below the canonical value for ideal electronic reconstruction.

  • 9. Berrah, Nora
    et al.
    Fang, Li
    Murphy, Brendan
    Osipov, Timur
    Ueda, Kiyoshi
    Kukk, Edwin
    Feifel, Raimund
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    van der Meulen, Peter
    Salen, Peter
    Schmidt, Henning T.
    Thomas, Richard D.
    Larsson, Mats
    Richter, Robert
    Prince, Kevin C.
    Bozek, John D.
    Bostedt, Christoph
    Wada, Shin-ichi
    Piancastelli, Maria N.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Tashiro, Motomichi
    Ehara, Masahiro
    Double-core-hole spectroscopy for chemical analysis with an intense X-ray femtosecond laser2011Inngår i: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 108, nr 41, s. 16912-16915Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Theory predicts that double-core-hole (DCH) spectroscopy can provide a new powerful means of differentiating between similar chemical systems with a sensitivity not hitherto possible. Although DCH ionization on a single site in molecules was recently measured with double-and single-photon absorption, double-core holes with single vacancies on two different sites, allowing unambiguous chemical analysis, have remained elusive. Here we report that direct observation of double-core holes with single vacancies on two different sites produced via sequential two-photon absorption, using short, intense X-ray pulses from the Linac Coherent Light Source free-electron laser and compare it with theoretical modeling. The observation of DCH states, which exhibit a unique signature, and agreement with theory proves the feasibility of the method. Our findings exploit the ultrashort pulse duration of the free-electron laser to eject two core electrons on a time scale comparable to that of Auger decay and demonstrate possible future X-ray control of physical inner-shell processes.

  • 10. Bomme, C.
    et al.
    Guillemin, R.
    Marin, T.
    Journel, L.
    Marchenko, T.
    Trcera, N.
    Kushawaha, R. K.
    Piancastelli, M. N.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Simon, M.
    Stener, M.
    Decleva, P.
    Molecular-frame photoelectron angular distribution imaging studies of OCS S1s photoionization2012Inngår i: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 45, nr 19, s. 194005-Artikkel i tidsskrift (Fagfellevurdert)
  • 11.
    Bose, Partha Pratim
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för biokemi och organisk kemi.
    Chatterjee, Urmimala
    Xie, Ling
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi.
    Johansson, Jan
    Göthelid, Emmanuelle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Arvidsson, Per I.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för biokemi och organisk kemi.
    Effects of Congo Red on A beta(1-40) Fibril Formation Process and Morphology2010Inngår i: ACS CHEMICAL NEUROSCIENCE, ISSN 1948-7193, Vol. 1, nr 4, s. 315-324Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Alzheimer's disease (AD), an age-related neurodegenerative disorder, is the most common form of dementia, and the seventh-leading cause of death in the United States. Current treatments offer only symptomatic relief; thus, there is a great need for new treatments with disease-modifying potential. One pathological hallmark of AD is so-called senile plaques, mainly made up of beta-sheet-rich assemblies of 40- or 42-residue amyloid beta-peptides (A beta). Hence, inhibition of A beta aggregation is actively explored as an option to prevent or treat AD. Congo red (CR) has been widely used as a model antiamyloid agent to prevent A beta aggregation. Herein, we report detailed morphological studies on the effect of CR as an antiamyloid agent, by circular dichroism spectroscopy, photo-induced cross-linking reactions, and atomic force microscopy. We also demonstrate the effect of CR on a preaggregated sample of A beta(1-40). Our result suggests that A beta(1-40) follows a different path for aggregation in the presence of CR.

  • 12. Boudet, S.
    et al.
    Bidermane, Ieva
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Lacaze, E.
    Gallas, B.
    Bouvet, M.
    Brunet, J.
    Pauly, A.
    Borensztein, Y.
    Witkowski, N.
    Growth mode and self-organization of LuPc2 on Si(001)-2 x 1 vicinal surfaces: An optical investigation2012Inngår i: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 86, nr 11, s. 115413-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report an investigation of the initial growth and of the self-organization of lutetium biphthalocyanine LuPc2 on Si(001)-2 x 1 vicinal surfaces. Using surface-sensitive optical spectroscopies, namely, surface-difference-reflectance spectroscopy (SDRS) and reflectance-anisotropy spectroscopy (RAS), together with local-probe microscopies, we are able to propose a scenario for the growth mode up to about 20 nm. We demonstrate that the growth mode initially proceeds through the formation of a wetting layer, followed by the formation of clusters whose sizes increase while keeping a constant shape in which the molecules are inclined. Moreover, the LuPc2 molecules are self-organized along the step edges, and we are able to estimate that about 30% to 100% of the molecules are aligned when considering that the molecules are tilted by 45 degrees to 63 degrees with respect to the surface normal.

  • 13. Bowen, K. P.
    et al.
    Stolte, W. C.
    Lago, A. F.
    Daacutevalos, J. Z.
    Piancastelli, M. N.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Lindle, D. W.
    Partial-ion-yield studies of SOCl 2 following x-ray absorption around the S and Cl K edges2012Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 137, nr 20, s. 204313-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We present a series of photoabsorption and partial-ion-yield experiments on thionyl chloride, SOCl2, at both the sulfur and chlorine K edges. The photoabsorption results exhibit better resolution than previously published data, leading to alternate spectral assignments for some of the features, particularly in the Rydberg-series region. Based on measured fragmentation patterns, we suggest the LUMO, of a' character, is delocalized over the entire molecular skeleton. Unusual behavior of the S2+ fragment hints at a relatively localized bond rupture (the S-O bond below the S K edge and the S-Cl bonds below the Cl K edge) following excitation to some of the higher lying intermediate states. 

  • 14.
    Brena, Barbara
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Puglia, Carla
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    de Simone, Monica
    Coreno, Marcello
    Tarafder, Kartick
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Feyer, Vitaly
    Banerjee, Rudra
    Gothelid, Emmanuelle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Sanyal, Biplab
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Oppeneer, Peter M.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Eriksson, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Valence-band electronic structure of iron phthalocyanine: An experimental and theoretical photoelectron spectroscopy study2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 134, nr 7, s. 074312-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The electronic structure of iron phthalocyanine (FePc) in the valence region was examined within a joint theoretical-experimental collaboration. Particular emphasis was placed on the determination of the energy position of the Fe 3d levels in proximity of the highest occupied molecular orbital (HOMO). Photoelectron spectroscopy (PES) measurements were performed on FePc in gas phase at several photon energies in the interval between 21 and 150 eV. Significant variations of the relative intensities were observed, indicating a different elemental and atomic orbital composition of the highest lying spectral features. The electronic structure of a single FePc molecule was first computed by quantum chemical calculations by means of density functional theory (DFT). The hybrid Becke 3-parameter, Lee, Yang and Parr (B3LYP) functional and the semilocal 1996 functional of Perdew, Burke and Ernzerhof (PBE) of the generalized gradient approximation (GGA-) type, exchange-correlation functionals were used. The DFT/B3LYP calculations find that the HOMO is a doubly occupied pi-type orbital formed by the carbon 2p electrons, and the HOMO-1 is a mixing of carbon 2p and iron 3d electrons. In contrast, the DFT/PBE calculations find an iron 3d contribution in the HOMO. The experimental photoelectron spectra of the valence band taken at different energies were simulated by means of the Gelius model, taking into account the atomic subshell photoionization cross sections. Moreover, calculations of the electronic structure of FePc using the GGA+U method were performed, where the strong correlations of the Fe 3d electronic states were incorporated through the Hubbard model. Through a comparison with our quantum chemical calculations we find that the best agreement with the experimental results is obtained for a U-eff value of 5 eV.

  • 15. Burmeister, Florian
    et al.
    Coutinho, L. H.
    Marinho, R. R. T.
    Homem, M. G. P.
    de Morais, M. A. A.
    Mocellin, A.
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Sorensen, S. L.
    Fonseca, P. T.
    Lindgren, A.
    Naves de Brito, A.
    Description and performance of an electron-ion coincidence TOF spectrometer used at the Brazilian synchrotron facility LNLS2010Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 180, nr 1-3, s. 6-13Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This paper reports the characteristics and performance of a Time-of-Flight Mass Spectrometer (TOF-MS) for coincidence measurements between electrons and ions that has been developed jointly in Sweden and Brazil. The spectrometer, used for studies of inner-shell photoexcitation of molecules in the gas-phase, has been optimized by implementing ion and electron lenses to allow the use of relatively small diameter detectors. Simulations were performed to understand the lens performance and they show that ions (electrons) could be collected without angular discrimination with a maximum kinetic energy up to ten (two) times higher than without the lens actions. A rotary vacuum chamber allows the spectrometer axis to be positioned at different angles relative to the polarization vector of the excitation beam. An important characteristic of the apparatus is that the acquisition setup allows a multi-hit capability with 1 ns resolution. Hereby, Photoelectron-Photoion-Photoion Coincidence (PEPIPICO) measurements can be performed on molecules containing two or more atoms of equal mass. A method to obtain experimental detection efficiencies of a single ion and one of one, two or three electrons has been developed. A systematic study of the interaction region has been performed to determine the shape of the photon and gas beams. Measurements on molecular nitrogen demonstrate the spectrometer's ability to resolve fragments with the same charge to mass ratio arriving within only a few ns. Simulations and experimental results of fragmentation of two singly charged cation nitrogen atoms agree, confirming that the spectrometer performance is well understood. (C) 2010 Elsevier B.V. All rights reserved.

  • 16.
    Cappel, Ute B.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Smeigh, Amanda L.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fotokemi och molekylärvetenskap, Kemisk fysik.
    Plogmaker, Stefan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Johansson, Erik M. J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Hammarström, Leif
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fotokemi och molekylärvetenskap, Kemisk fysik.
    Hagfeldt, Anders
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Boschloo, Gerrit
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Characterization of the Interface Properties and Processes in Solid State Dye-Sensitized Solar Cells Employing a Perylene Sensitizer2011Inngår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 115, nr 10, s. 4345-4358Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We recently reported on a perylene sensitizer, ID176, which performs much better in solid state dye-sensitized solar cells than in those using liquid electrolytes with iodide/tri-iodide as the redox couple (J. Phys. Chem. C2009, 113, 14595-14597). Here, we present a characterization of the sensitizer and of the TiO2/dye interface by UV-visible absorption and fluorescence spectroscopy, spectroelectrochemistry, photoelectron spectroscopy, electroabsorption spectroscopy, photoinduced absorption spectroscopy, and femtosecond transient absorption measurements. We report that the absorption spectrum of the sensitizer is red-shifted by addition of lithium ions to the surface due to a downward shift of the excited state level of the sensitizer, which is of the same order of magnitude as the downward shift of the titanium dioxide conduction band edge. Results from photoelectron spectroscopy and electrochemistry suggest that the excited state is largely located below the conduction band edge of TiO2 but that there are states in the band gap of TiO2 which might be available for photoinduced electron injection. The sensitizer was able to efficiently inject into TiO2, when a lithium salt was present on the surface, while injection was much less effective in the absence of lithium ions or in the presence of solvent. In the presence of the hole conductor 2,2-,7,7-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9-spirobifluorene (spiro-MeOTAD) and LiTFSI, charge separation was monitored by the emergence of a Stark shift of the dye in transient absorption spectra, and both injection and regeneration appear to be completed within 1 ps. Regeneration by spiro-MeOTAD is therefore several orders of magnitude faster than regeneration by iodide, and ID176 can even be photoreduced by spiro-MeOTAD.

  • 17. Carniato, S.
    et al.
    Journel, L.
    Guillemin, R.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Stolte, W. C.
    Lindle, D. W.
    Simon, M.
    A new method to derive electronegativity from resonant inelastic x-ray scattering2012Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 137, nr 14, s. 144303-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Electronegativity is a well-known property of atoms and substituent groups. Because there is no direct way to measure it, establishing a useful scale for electronegativity often entails correlating it to another chemical parameter; a wide variety of methods have been proposed over the past 80 years to do just that. This work reports a new approach that connects electronegativity to a spectroscopic parameter derived from resonant inelastic x-ray scattering. The new method is demonstrated using a series of chlorine-containing compounds, focusing on the Cl 2p(-1)LUMO(1) electronic states reached after Cl 1s -> LUMO core excitation and subsequent KL radiative decay. Based on an electron-density analysis of the LUMOs, the relative weights of the Cl 2p(z) atomic orbital contributing to the Cl 2p(3/2) molecular spin-orbit components are shown to yield a linear electronegativity scale consistent with previous approaches.

  • 18. Ceolin, D.
    et al.
    Travnikova, O.
    Bao, Z.
    Guimaraes, F. F.
    da Costa, M. S.
    Velkov, Y.
    Sisourat, N.
    Carniato, S.
    Simon, M.
    Piancastelli, M. N.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Site-selective resonant Auger spectroscopy of iso-dichloroethylene at the carbon K-edge2012Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 185, nr 8-9, s. 252-258Artikkel i tidsskrift (Fagfellevurdert)
  • 19.
    Ceolin, Denis
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Travnikova, Oksana
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Bao, Zhuo
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Guimaraes, F. F.
    da Costa, M. S.
    Velkov, Y.
    Sisourat, N.
    Carniato, S.
    Simon, M.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Site-selective resonant Auger spectroscopy of iso-dichloroethylene at the carbon K-edge2012Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 185, nr 8-9, s. 252-258Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This study focuses on the two C1s-to-LUMO (lowest unoccupied molecular orbital) excitations of the iso-dichloroethylene (H2C=CCl2) and the subsequent Auger decay. We investigate the effect of the two different carbon core excitations on the population of the cation produced after electronic relaxation. The resonant Auger spectra are interpreted by comparison to the valence shells photoionization spectrum and with the help of theoretical calculations. Several consequences of the core-hole localization on the electronic decay are observed. In particular, the resonant excitation of the C1s(CH2) to the LUMO leads to a large intensity increase in the region of the first satellite state, whereas no dramatic changes are observed for the C1s(CCl2) excitation.

  • 20.
    Ceolin, Denis
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Travnikova, Oksana
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Bao, Zhuo
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Kivimaeki, A.
    Carniato, S.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Effect of the Cl2p core orbital excitation on the nuclear dynamics of the three dichloroethylene isomers2011Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 184, nr 1-2, s. 24-28Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In this article, we present the X-ray absorption spectra of the three isomers of dichloroethylene C2H2Cl2 in the vicinity of the chlorine L-2 and L-3 edges. These isomers were excited along the first Cl2p to lowest unoccupied molecular orbital transition and an analysis of the corresponding resonant Auger spectra shows that the C-Cl bond can break before the electronic decay. An investigation of a possible Auger Doppler-like effect is also presented.

  • 21. Choudhury, D.
    et al.
    Mandal, P.
    Mathieu, Roland
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik.
    Hazarika, A.
    Rajan, S.
    Sundaresan, A.
    Waghmare, U. V.
    Knut, Ronny
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Nordblad, Per
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik.
    Sarma, Dipankar Das
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Near-Room-Temperature Colossal Magnetodielectricity and Multiglass Properties in Partially Disordered La2NiMnO62012Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 108, nr 12, s. 127201-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report magnetic, dielectric, and magnetodielectric responses of the pure monoclinic bulk phase of partially disordered La2NiMnO6, exhibiting a spectrum of unusual properties and establish that this compound is an intrinsically multiglass system with a large magnetodielectric coupling (8%-20%) over a wide range of temperatures (150-300 K). Specifically, our results establish a unique way to obtain colossal magnetodielectricity, independent of any striction effects, by engineering the asymmetric hopping contribution to the dielectric constant via the tuning of the relative-spin orientations between neighboring magnetic ions in a transition-metal oxide system. We discuss the role of antisite (Ni-Mn) disorder in emergence of these unusual properties.

  • 22.
    Choudhury, Debraj
    et al.
    Solid State and Structural Chemistry Unit, and Department of Physics, at Indian Institute of Science, Bangalore, Indien.
    Mukherjee, S
    Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore, Indien.
    Mandal, P
    Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, Indien.
    Sundaresan, A
    Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, Indien.
    Waghamare, U V
    Theoretical Science Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, Indien.
    Bhattacharjee, Satadeep
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Mathieu, Roland
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik.
    Lazor, Peter
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Geovetenskapliga sektionen, Institutionen för geovetenskaper, Berggrundsgeologi.
    Eriksson, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Sanyal, Biplab
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Nordblad, Per
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik.
    Sharma, Ajay
    Department of Physics, Indian Institute of Science, Bangalore, Indien.
    Bhat, S V
    Department of Physics, Indian Institute of Science, Bangalore, Indien.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Sarma, Dipankar Das
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Tuning of dielectric properties and magnetism of SrTiO3 by site-specific doping of Mn2011Inngår i: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 84, nr 12, s. 125124-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Combining experiments with first-principles calculations, we show that site-specific doping of Mn into SrTiO(3) has a decisive influence on the dielectric properties of these doped systems. We find that phonon contributions to the dielectric constant invariably decrease sharply on doping at any site. However, a sizable, random dipolar contribution only for Mn at the Sr site arises from a strong off-centric displacement of Mn in spite of Mn being in a non-d(0) state; this leads to a large dielectric constant at higher temperatures and gives rise to a relaxor ferroelectric behavior at lower temperatures. We also investigate magnetic properties in detail and critically reevaluate the possibility of a true multiglass state in such systems.

  • 23.
    Chow, Winnie W. Y.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Herwik, Stanislav
    Ruther, Patrick
    Göthelid, Emmanuelle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Oscarsson, Sven
    Bio-polymer coatings on neural probe surfaces: Influence of the initial sample composition2012Inngår i: Applied Surface Science, ISSN 0169-4332, E-ISSN 1873-5584, Vol. 258, nr 20, s. 7864-7871Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This paper presents the results of the study of hyaluronic acid (HyA) coating on two structural materials, silicon oxide (dielectric) surface and platinum (Pt) surface used for fabrication of probes developed for neurological investigations in the framework of the EU-project NeuroProbes. The silicon-based neural probes consist of multiple Pt electrodes on the probe shafts for neural recording applications. HyA coatings were proposed to apply on the probe surfaces to enhance the biocompatibility [1]. This study aims at understanding the influence of the initial composition of the probe surface on the structure and morphology of HyA coating. HyA was chemically functionalized by SS-pyridin using (N-Succinimidyl 3-[2-pyridyldithio]-propionate) (SPDP) and was immobilized on the surfaces via a covalent bond. The dielectric and Pt surfaces were derivatized by use of (3-mercaptopropyl) methyldimethoxysilane (MPMDMS). The silanol groups in MPMDMS bind to the dielectric surface, leaving the thiol groups at the uppermost surface and the thiol groups then bind covalently to the functionalized HyA. On the Pt surface, it is the thiol group which binds on the Pt surface. The coated surfaces were characterized by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). A well-defined HyA layer was observed on both dielectric and Pt surfaces. The coating of two molecular weights (340 kDa and 1.3 MDa) of HyA was examined. The influence of the silanized layer on the HyA coating was also investigated. 

  • 24.
    Céolin, D.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Forsell, J-O
    Wannberg, B.
    Legendre, S.
    Palaudoux, J.
    Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Farmaceutiska fakulteten, Institutionen för farmaci.
    Öhrwall, Gunnar
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Svensson, Svante
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    A rotatable electron spectrometer for multicoincidence experiments2010Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 81, nr 6, s. 063112-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have developed a rotatable hemispherical spectrometer with good energy and angular resolution, which can be positioned with the lens axis arbitrarily within a solid angle of 1 pi. The collection angle of the emitted electrons with respect to the polarization axis of the light is set by means of a three-axes goniometer, operating under vacuum. An important requirement for this setup was the possibility to perform coincidences between the electron analyzed by the spectrometer and one or several other particles, such as ions, electrons, or photons. The lens system and the hemispheres have been designed to accommodate such experimental demands, regarding parameters such as the resolving power, the acceptance angle, or the width of the kinetic energy window which can be recorded for a given pass energy. We have chosen to detect the impact position of the electron at the focal plane of the hemispherical analyzer with a delay line detector and a time-to-digital converter as acquisition card rather than using a conventional charge-coupled device camera.

  • 25.
    Eland, John H. D.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Andric, L.
    Linusson, P.
    Hedin, Lage
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Plogmaker, Stefan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Palaudoux, J.
    Penent, F.
    Lablanquie, P.
    Feifel, Raimund
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Triple ionization of CO(2) by valence and inner shell photoionization2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 135, nr 13, s. 134309-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Spectra of triply ionized CO(2) have been obtained from photoionization of the molecule using soft x-ray synchrotron light and an efficient multi-electron coincidence technique. Although all states of the CO(2)(+++) trication are unstable, the ionization energy for formation of molecular ions at a geometry similar to that of the neutral molecule is determined as 74 +/- 0.5 eV.

  • 26.
    Eland, John H. D.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Fink, R. F.
    Linusson, P.
    Hedin, L.
    Plogmaker, S.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Feifel, R.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Single and multiple photoionisation of H(2)S by 40-250 eV photons2011Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 13, nr 41, s. 18428-18435Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Multi-electron coincidence measurements on photoionisation of H(2)S have been carried out at photon energies from 40 to 250 eV. They quantify molecular field effects on the Auger process in detail and are in good agreement with the existing theory. Spectra of core-valence double ionisation of H(2)S are presented and partially analysed. Auger decays from the core-valence states produce triply charged product spectra with unexplained and surprising intensity distributions. Triple ionisation by the double Auger process from 2p hole states shows little effect of the molecular field splitting, but includes a substantial contribution from cascade processes, some involving dissociation in intermediate states. The onset of triple ionisation at the molecular geometry is determined as 61 +/- 0.5 eV.

  • 27. Eriksson, Kristofer
    et al.
    Johansson, LarsErik
    Göthelid, Emmanuelle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Nyholm, Leif
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Oorganisk kemi.
    Oscarsson, Sven
    Manufacturing of anisotropic particles by site specific oxidation of thiols2012Inngår i: Journal of Materials Chemistry, ISSN 0959-9428, E-ISSN 1364-5501, Vol. 22, nr 16, s. 7681-7683Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A novel method for the manufacturing of functional anisotropic particles based on an inexpensive and straightforward electrochemical approach is presented. The method enables large-scale manufacturing of anisotropic particles as well as fabrication of multifunctional beads which may be used in the design of barcodes for multiplex diagnostics.

  • 28.
    Eriksson, Kristofer L. E.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Chow, Winnie W. Y.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Puglia, Carla
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Bäckvall, Jan-Erling
    Göthelid, Emmanuelle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Oscarsson, Sven
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Performance of a Biomimetic Oxidation Catalyst Immobilized on Silicon Wafers: Comparison with Its Gold Congener2010Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 26, nr 21, s. 16349-16354Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    With the aim of extending the usefulness of an existing biomimetic catalytic system, cobalt porphyrin catalytic units with thiol linkers were heterogenized via chemical grafting to silicon wafers and utilized for the catalytic oxidation of hydroquinone to p-benzoquinone. Atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) were used to analyze the morphology and composition of the heterogeneous catalyst. The results of the catalytic oxidation of hydroquinone obtained with porphyrins grafted on silicon were compared with those obtained earlier with the same catalyst in homogeneous phase and immobilized on gold. It was found that the catalysis could run over 400 h, without showing any sign of deactivation. The measured catalytic activity is at least 10 times higher than that measured under homogeneous conditions, but also 10 times lower than that observed with the catalytic unit immobilized on gold. The reasons of this discrepancy are discussed in term of substrate influence and overlayer organization. The silicon-immobilized catalyst has potential as an advanced functional material with applications in oxidative heterogeneous catalysis of organic reactions, as it combines long-term relatively high activity with low cost.

  • 29. Eriksson, Kristofer
    et al.
    Palmgren, Pål
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Nyholm, Leif
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Oorganisk kemi.
    Oscarsson, Sven
    Electrochemical Synthesis of Gold and Protein Gradients on Particle Surfaces2012Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 28, nr 28, s. 10318-10323Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A straightforward, versatile approach to the production of protein gradients on planar and spherical particle surfaces is described. The method is based on the spatially controlled oxidation of thiolated surfaces by Au(III) ions generated via the electrochemical oxidation of a gold electrode in a phosphate-buffered saline solution (10 mM PBS, pH 7.2, 150 mM NaCl). Because the gold electrode is in direct contact with the thiolated surfaces, the released Au(III) ions, which are present as Au(III) chloride complexes, give rise to the formation of a surface gradient of Au(I)-thiolate complexes depending on the local redox potential given by the local Au(III) concentration. As is shown on the basis of the use of X-ray photoelectron spectroscopy and fluorescently labeled proteins, the Au(I)-thiolate complexes can subsequently be functionalized with thiolated proteins, yielding surface density protein gradients on micrometer-sized nonconducting polymer beads as well as linear Au(I)-thiolate gradients on planar silicon surfaces.

  • 30. Eyrich, C.
    et al.
    Huttema, W.
    Arora, M.
    Montoya, E.
    Rashidi, F.
    Burrowes, C.
    Kardasz, B.
    Girt, E.
    Heinrich, B.
    Mryasov, O. N.
    From, M.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Exchange stiffness in thin film Co alloys2012Inngår i: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 111, nr 7, s. 07C919-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The exchange stiffness (A(ex)) is one of the key parameters controlling magnetization reversal in magnetic materials. We used a method based on the spin spiral formation in two ferromagnetic films antiferromagnetically coupled across a non-magnetic spacer layer and Brillouin scattering to measure A(ex) for a series of Co1-delta X delta (X=Cr, Ni, Ru, Pd, Pt) thin film alloys. The results show that A(ex) of Co alloys does not necessarily scale with M-s; A(ex) approximately decreases at the rate of 1.1%, 1.5%, 2.1%, 3.5%, and 5.6%, while M-s decreases at the rate of 1.1%, 0.5%, 1.1%, 3.7%, and 2.5% per addition of 1 at% of Pt, Ni, Pd, Cr, and Ru, respectively.

  • 31. Fang, L.
    et al.
    Osipov, T.
    Murphy, B.
    Juranic, P.
    Berrah, N.
    Kukk, E.
    Ueda, K.
    Feifel, R.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    van der Meulen, P.
    Salen, P.
    Schmidt, H.
    Thomas, R.
    Larsson, M.
    Richter, R.
    Prince, K. C.
    Bozek, J. D.
    Bostedt, C.
    Wada, S.
    Piancastelli, M.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Tashiro, M.
    Ehara, M.
    Tarantelli, F.
    Multiple Ionization and Double Core-hole Production in Molecules using the LCLS X-ray FEL2012Inngår i: Journal of Physics, Conference Series, ISSN 1742-6588, E-ISSN 1742-6596, Vol. 388, nr 3, s. 032028-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We used the world's first hard x-ray FEL to investigate the response of molecular systems to the ultra-intense, femtosecond x-ray radiation. We report sequential multiphoton ionization, frustrated absorption and double core hole production mechanisms.

  • 32.
    Feifel, Raimund
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Core-level spectroscopy and dynamics of free molecules2011Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 183, nr 1-3, s. 10-28Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A review of recent results on spectroscopy and dynamics of free molecules is presented. The experimental research reported here is mainly concerned with processes of core excitation and decay of isolated molecules, primarily investigated by resonant Auger spectroscopy. Several examples are shown concerning the interplay of the timescales of electron decay with nuclear motion involving dissociation processes, the occurrence of interference phenomena and recoil. The capability of such studies to reveal subtle details of the light-matter interaction, of the electronic structure and of the evolution of the short-lived states thus created is enlightened.

  • 33. Foerstel, Marko
    et al.
    Mucke, Melanie
    Arion, Tiberiu
    Lischke, Toralf
    Barth, Silko
    Ulrich, Volker
    Öhrwall, Gunnar
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Hergenhahn, Uwe
    Bradshaw, Alex M.
    Observation of electronic energy bands in argon clusters2010Inngår i: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 82, nr 12, s. 125450-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The 3p valence region of argon clusters has been investigated with photoemission near the photoionization threshold. A strong feature between 14.6 and 15.3 eV binding energy shows a photon-energy dependence indicative of electronic-energy band dispersion. A similar feature at approximately the same binding energy and with a similar dispersion occurs in photoemission spectra of both the ordered and disordered solids. The effect is already fully developed for scaling-law mean cluster sizes < N > of approximately 200 atoms, thus showing an early onset of bulklike electronic properties.

  • 34.
    Fredin, Kristofer
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Johansson, Erik M. J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Hahlin, Maria
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Schölin, Rebecka
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Plogmaker, Stefan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Gabrielsson, Erik
    Sun, Licheng
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Solid state dye-sensitized solar cells prepared by infiltrating a molten hole conductor into a mesoporous film at a temperature below 150 degrees C2011Inngår i: Synthetic metals, ISSN 0379-6779, E-ISSN 1879-3290, Vol. 161, nr 21-22, s. 2280-2283Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Infiltration of a molten hole conductor in a mesoporous film at an elevated temperature exhibits good wetting performance and the procedure is therefore suitable as part of the preparation method for solid state dye-sensitized solar cells. Herein, we present a system prepared by infiltrating 4-(diethylamino)benzaldehyde-1,1)-diphenyl-hydrazone in its molten form at a temperature below 150 degrees C. The system displays a maximum photon-to-current conversion efficiency of about 35%, a value corresponding to an increase of about 5 times in comparison with a previously published system prepared by infiltrating a molten hole-conductor at a temperature exceeding 250 degrees C. By means of comparing charge transport and recombination with the results measured for a liquid analogue, we conclude that whereas the transport rates are similar, recombination is significantly more rapid in the solid-state device.

  • 35. Förstel, Marko
    et al.
    Mucke, Melanie
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Anon, Tiberiu
    Lischke, Toralf
    Barth, Silko
    Ulrich, Volker
    Öhrwall, Gunnar
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Hergenhahn, Uwe
    Bradshaw, Alex M.
    Energy band dispersion in photoemission spectra of argon clusters2011Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 184, nr 3-6, s. 107-112Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Using photoemission we have investigated free argon clusters from a supersonic nozzle expansion in the photon energy range from threshold up to 28 eV. Measurements were performed both at high resolution with a hemispherical electrostatic energy analyser and at lower resolution with a magnetic bottle device. The latter experiments were performed for various mean cluster sizes. In addition to the approximate to 15eV broad 3p-derived valence band seen in previous work, there is a sharper feature at approximate to 15eV binding energy. Surprisingly for non-oriented clusters, this peak shifts smoothly in binding energy over the narrow photon energy range 15.5-17.7 eV, indicating energy band dispersion. The onset of this bulk band-like behaviour could be determined from the cluster size dependence.

  • 36. Girt, Erol
    et al.
    Huttema, W.
    Mryasov, O. N.
    Montoya, E.
    Kardasz, B.
    Eyrich, C.
    Heinrich, B.
    Dobin, A. Yu.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    A method for measuring exchange stiffness in ferromagnetic films2011Inngår i: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 109, nr 7, s. 07B765-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    An exchange stiffness, A(ex), in ferromagnetic films is obtained by fitting the M(H) dependence of two ferromagnetic layers antiferromagnetically coupled across a nonmagnetic spacer layer with a simple micromagnetic model. In epitaxial and textured structures this method allows measuring A(ex) between the crystallographic planes perpendicular to the growth direction of ferromagnetic films. Our results show that A(ex) between [0001] planes in textured Co grains is 1.54 +/- 0.12 x 10(-11) J/m.

  • 37.
    Granroth, Sari
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Olovsson, Weine
    Holmström, Erik
    Knut, Ronny
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Gorgoi, Mihaela
    Svensson, Svante
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Karis, Olof
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Understanding interface properties from high kinetic energy photoelectron spectroscopy and first principles theory2011Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 183, nr 1-3, s. 80-93Artikkel, forskningsoversikt (Fagfellevurdert)
    Abstract [en]

    Advances in instrumentation regarding 3rd generation synchrotron light sources and electron spectrometers has enabled the field of high kinetic energy photoelectron spectroscopy (HIKE) (also often denoted hard X-ray photoelectron spectroscopy (HX-PES or HAXPES)). Over the last years, the amount of investigations that relies on the HIKE method has increased dramatically and can arguably be said to have given a rebirth of the interest in photoelectron spectroscopy in many areas. It is in particular the much increased mean free path at higher kinetic energies in combination with the elemental selectivity of the core level spectroscopies in general that has lead to this fact, as it makes it possible to investigate the electronic structure of materials with a substantially reduced surface sensitivity. In this review we demonstrate how HIKE can be used to investigate the interface properties in multilayer systems. Relative intensities of the core level photoelectron peaks and their chemical shifts derived from binding energy changes are found to give precise information on physico-chemical properties and quality of the buried layers. Interface roughening, including kinetic properties such as the rate of alloying, and temperature effects on the processes can be analyzed quantitatively. We will also provide an outline of the theoretical framework that is used to support the interpretation of data. We provide examples from our own investigations of multilayer systems which comprises both systems of more model character and a multilayer system very close to real applications in devices that are considered to be viable alternative to the present read head technology. The experimental data presented in this review is exclusively recorded at the BESSY-II synchrotron at the Helmholtz-Zentrum Berlin fur-Materialien und Energie. This HIKE facility is placed at the bending magnet beamline KMC-1, which makes it different from several other facilities which relies on undulators as the source. We will therefore also briefly describe some of the salient design features of this facility.

  • 38. Guillemin, R.
    et al.
    Sheinerman, S.
    Bomme, C.
    Journel, L.
    Marin, T.
    Marchenko, T.
    Kushawaha, R. K.
    Trcera, N.
    Piancastelli, M. N.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Simon, M.
    Ultrafast Dynamics in Postcollision Interaction after Multiple Auger Decays in Argon 1s Photoionization2012Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 109, nr 1, s. 013001-Artikkel i tidsskrift (Fagfellevurdert)
  • 39. Guillemin, Renaud
    et al.
    Stolte, Wayne C.
    Journel, Loic
    Carniato, Stephane
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Lindle, Dennis W.
    Simon, Marc
    Angular and dynamical properties in resonant inelastic x-ray scattering: Case study of chlorine-containing molecules2012Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 86, nr 1, artikkel-id 013407Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Polarization-dependent resonant inelastic x-ray scattering (RIXS) has been shown to be a probe of molecular-field effects on the electronic structure of isolated molecules. In this experimental analysis we explain the linear dichroism observed in Cl 2p polarized RIXS following Cl 1s excitation of a series of chlorofluoromethanes (CF3Cl, CF2Cl2, CFCl3, and CCl4) as due to molecular-field effects, including singlet-triplet exchange. We present an approach to extract directly the 2p inner-shell electronic state populations from the experimental measurements. Using the angular properties of the measured KV emission we also are able to determine the value of the polarization anisotropy parameter beta(p) for each resolved component of the KV emission spectra.

  • 40. Guillemin, Renaud
    et al.
    Stolte, Wayne C.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Lindle, Dennis W.
    Jahn-Teller coupling and fragmentation after core-shell excitation in CF4 investigated by partial-ion-yield spectroscopy2010Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 82, nr 4, s. 043427-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We investigate fragmentation processes induced by core-level photoexcitation in CF4 at both the carbon and fluorine K edges by means of partial-ion-yield spectroscopy. The molecule CF4 is a textbook example of systems in which Jahn-Teller coupling strongly manifests itself in the photoabsorption spectrum. Spectral features related to Jahn-Teller and quasi-Jahn-Teller splitting are observed, and important differences in the fragmentation pathways are revealed depending on the symmetries of the core-excited states. We interpret these experimental observations on the grounds of symmetry lowering from the T-d to the C-3v point group as well as preferential orientation with respect to the polarization vector of the incident radiation.

  • 41. Guillemin, Renaud
    et al.
    Stolte, Wayne C.
    Piancastelli, Maria Novella
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Lindle, Dennis W.
    Photofragmentation of BF3 on B and F K-shell excitation by partial ion yield spectroscopy2010Inngår i: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 43, nr 21, s. 215205-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The fragmentation of core-excited BF3 has been studied by means of partial cation and anion yield measurements around the B and F K edges. All detectable ionic fragments are reported, and differences among the fragments are discussed. The observations confirm earlier findings on the dynamics of molecular fragmentation studied by partial ion yields, notably on the influence of Rydberg excitations on fragmentation, the behaviour of anion production near threshold, and the importance of intramolecular rearrangement in the formation of F-2(+) ions.

  • 42. Guo, J. -H
    et al.
    Kastanov, S.
    Söderström, Johan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Glans, P. -A
    West, M.
    Learmonth, T.
    Chiou, J. -W
    Luo, Yi
    Nordgren, Joseph
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Mjukröntgenfysik.
    Smith, K.
    Pong, W. -F
    Cheng, H.
    Griffiss, J. M.
    Electronic structure study of the bases in DNA duplexes by in situ photon-in/photon-out soft X-ray spectroscopy2010Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 181, nr 2-3, s. 197-201Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Understanding protein functionality is of fundamental importance in biochemistry. Soft X-ray transitions, where the core-level vacancies are filled by the valence-orbital electrons, give direct information about the chemical bonding. Soft X-ray absorption and emission study of poly(dG) -poly(dC) in aqueous solutions can elucidate the relation between the structure and functionality of proteins. We report the N K-edge soft X-ray absorption (XAS) and resonant soft X-ray emission spectroscopy (XES) to characterize the electronic structure near the Fermi level of DNA duplexes to specify the charge migration mechanism. Since N atoms are included in only bases in DNA duplexes, the XES spectra excited from N Is to unoccupied states purely extract the electronic orbital features of the bases in DNA. The fact that N atoms in different bonding environments form well-defined structure has been determined. The experimental findings provide the evidence for the charge-hopping and/or charge-transfer effects in understanding of electric conduction in DNA duplexes when electrons pass through the pi* states of DNA bases. (C) 2010 Elsevier B.V. All rights reserved.

  • 43.
    Hahlin, Maria
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Electronic and Molecular Surface Structures of Dye-Sensitized TiO2 Interfaces2010Doktoravhandling, med artikler (Annet vitenskapelig)
    Abstract [en]

    The dye-sensitized solar cell is a promising solar cell technology. In these systems the key process for light to electricity conversion is molecular in nature and is initiated in dye molecules adsorbed at a semiconducting surface. This thesis focuses on the electronic and molecular surface structure of the dye/TiO2 interface, and the experimental results were obtained from surface sensitive X-ray based electron spectroscopic methods.

    Two families of dyes, triarylamine based organic dyes and ruthenium based inorganic dyes, were investigated. The effect of dye structural modications on the interfacial properties was studied, such as the surface concentrations, dye molecular surface orientation, molecular interactions, and energy level matching. Also, the impact of additional parameters such as the incorporation of coadsorbents and the solvents used for dye sensitization were studied and complementary photoelectrochemical characterization was used to demonstrate functional properties corresponding to changes in the molecular layers.

    The experiments provided information on how specic structural modications change the frontier electronic structure. The results also showed that the adsorption of the organic dye leads to submolecular electronic changes, and that the dye surface orientations in general favor effcient energy conversion. Moreover, effects of solvents and coadsorbents, on both energy level matching between the dye and the TiO2 substrate and the surfacemolecular structure were quantied.

    Delarbeid
    1. Electronic and molecular structures of organic dye/TiO2 interfaces for solar cell applications: a core level photoelectron spectroscopy study
    Åpne denne publikasjonen i ny fane eller vindu >>Electronic and molecular structures of organic dye/TiO2 interfaces for solar cell applications: a core level photoelectron spectroscopy study
    Vise andre…
    2010 (engelsk)Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 12, nr 7, s. 1507-1517Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    The electronic and molecular properties of three organic dye molecules with the general structure donor-linker-anchor have been investigated using core level photoelectron spectroscopy (PES). The molecules contain a diphenylaniline donor unit, a thiophene linker unit, and cyanoacrylic acid or rhodanine-3-acetic acid anchor units. They have been investigated both in the form of a multilayer and adsorbed onto nanoporous TiO2 and the experimental results were also compared with DFT calculations. The changes at the dye-sensitized TiO2 surface due to the modification of either the donor unit or the anchor unit was investigated and the results showed important differences in coverage as well as in electronic and molecular surface properties. By measuring the core level binding energies, the sub-molecular properties were characterized and the result showed that the adsorption to the TiO2 influences the energy levels of the sub-molecular units differently.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-128836 (URN)10.1039/b913548k (DOI)000274243200010 ()
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2017-12-12bibliografisk kontrollert
    2. Mapping the frontier electronic structures of triphenylamine based organic dyes at TiO2 interfaces
    Åpne denne publikasjonen i ny fane eller vindu >>Mapping the frontier electronic structures of triphenylamine based organic dyes at TiO2 interfaces
    Vise andre…
    2011 (engelsk)Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 13, nr 8, s. 3534-3546Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    The frontier electronic structure of a series of organic dye molecules containing a triphenylamine moiety, a thiophene moiety and a cyanoacrylic acid moiety have been investigated by photoelectron spectroscopy (PES), X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy (XES) and resonant photoelectron spectroscopy (RPES). The experimental results were compared to electronic structure calculations on the molecules which are used to confirm and enrich the assignment of the spectra. The approach allows us to experimentally measure and interpret the basic valence energy level structure in the dye, including the highest occupied energy level and how it depends on the interaction between the different units. Based on N1s X-ray absorption and emission spectra we also obtain insight into the structure of the excited states, the molecular orbital composition and dynamics. Together the results provide an experimentally determined energy level map useful in the design of these types of materials. Included is also results indicating femtosecond charge redistribution at the dye/TiO2 interface.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-128840 (URN)10.1039/c0cp01491e (DOI)000287041700060 ()21173950 (PubMedID)
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2017-12-12bibliografisk kontrollert
    3. Rhodanine dyes for dye-sensitized solar cells: spectroscopy, energy levels and photovoltaic performance
    Åpne denne publikasjonen i ny fane eller vindu >>Rhodanine dyes for dye-sensitized solar cells: spectroscopy, energy levels and photovoltaic performance
    Vise andre…
    2009 (engelsk)Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 11, nr 1, s. 133-141Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    Three new sensitizers for photoelectrochemical solar cells were synthesized consisting of a triphenylamine donor, a rhodanine-3-acetic acid acceptor and a polyene connection. The conjugation length was systematically increased, which resulted in two effects: first, it led to a red-shift of the optical absorption of the dyes, resulting in an improved spectral overlap with the solar spectrum.Secondly, the oxidation potential decreased systematically. The excited state levels were, however, calculated to be nearly stationary. The experimental trends were in excellent agreement with density functional theory (DFT) computations. The photovoltaic performance of this set of dyes as sensitizers in mesoporous TiOredox couple. The dye with the best absorption characteristics showed the poorest solar cell efficiency, due to losses by recombination of electrons in TiOthe electrolyte led to a strongly reduced photocurrent for all dyes due to a reduced electron injection efficiency, caused by a 0.15 V negative shift of the TiO 2 solar cells was investigated using electrolytes containing the iodide/triiodide2 with triiodide. Addition of 4-tert butylpyridine to2 conduction band potential.

    HSV kategori
    Forskningsprogram
    Oorganisk kemi
    Identifikatorer
    urn:nbn:se:uu:diva-120847 (URN)10.1039/b812154k (DOI)000263278900011 ()
    Tilgjengelig fra: 2010-03-16 Laget: 2010-03-16 Sist oppdatert: 2017-12-12bibliografisk kontrollert
    4. Surface Molecular Quantification and Photoelectrochemical Characterization of Mixed Organic Dye and Coadsorbent Layers on TiO2 for Dye-Sensitized Solar Cells
    Åpne denne publikasjonen i ny fane eller vindu >>Surface Molecular Quantification and Photoelectrochemical Characterization of Mixed Organic Dye and Coadsorbent Layers on TiO2 for Dye-Sensitized Solar Cells
    Vise andre…
    2010 (engelsk)Inngår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 114, nr 27, s. 11903-11910Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    Different molecular layers on TiO2 were prepared by using the p-dimethylaniline triphenylamine based organic dye, D29, together with the coadsorbents decylphosphonic acid (DPA), dineohexyl bis(3,3-dimethylbutyl)phosphinic acid (DINHOP), and chenodeoxycholic acid (CDCA). The surface molecular structure of dye and coadsorbent layers on TiO2 was investigated by photoelectron spectroscopy (PES). A focus was to determine the surface molecular concentrations using characteristic photoelectron core levels. Dye-sensitized solar cells (DSCs) were prepared from the same substrate and were further characterized by photoelectrochemical methods. Together the investigation gives information on the arrangement of the mixed molecular layer and a first insight to the extent to which the coadsorbents exchange with dye molecules on the TiO2 surface for the examined conditions.

    HSV kategori
    Identifikatorer
    urn:nbn:se:uu:diva-128835 (URN)10.1021/jp102381x (DOI)000279507900031 ()
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2017-12-12bibliografisk kontrollert
    5. Surface compostions of dye/TiO2 interfaces formed from ethanol, acetonitrile, and dichloromethane based solutions
    Åpne denne publikasjonen i ny fane eller vindu >>Surface compostions of dye/TiO2 interfaces formed from ethanol, acetonitrile, and dichloromethane based solutions
    Vise andre…
    (engelsk)Manuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The molecular and electronic surface structure of three TiO2 surfaces sensitized with 3-(5-(4-(diphenyl amino) styryl) thiophen-2-yl)-2-cyanoacrylic acid (D5) using different solvents (acetonitrile, dicloromethane, and ethanol) was investigated by photoelectron spectroscopy. The results showed solvent dependence in surface coverage, dye surface structure and energy level matching. Corresponding basic results on photocurrent conversion and UV-vis absorption is also included. Together the results indicated surface aggregation when using dichloromethane as a solvent.

    Identifikatorer
    urn:nbn:se:uu:diva-128839 (URN)
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2011-04-06
    6. Electronic and molecular surface structure of Ru(tcterpy)(NCS)(3) and Ru(dcbpy)(2)(NCS)(2) adsorbed from solution onto nanostructured TiO2: A photoelectron spectroscopy study
    Åpne denne publikasjonen i ny fane eller vindu >>Electronic and molecular surface structure of Ru(tcterpy)(NCS)(3) and Ru(dcbpy)(2)(NCS)(2) adsorbed from solution onto nanostructured TiO2: A photoelectron spectroscopy study
    2005 (engelsk)Inngår i: Journal of Physical Chemistry B, ISSN 1520-6106, E-ISSN 1520-5207, Vol. 109, nr 47, s. 22256-22263Artikkel i tidsskrift (Fagfellevurdert) Published
    Abstract [en]

    The element specificity of photoelectron spectroscopy (PES) has been used to compare the electronic and molecular structure of the dyes Ru(tcterpy)(NCS)(3) (BD) and Ru(dcbpY)(2)(NCS)(2) adsorbed from solution onto nanostructured TiO2. Ru(dcbpy)(2)(NCS)(2) was investigated in its acid (N3) and in its 2-fold deprotonated form (N719) having tetrabutylammonium (TBA(+)) as counterions. A comparison of the O1s spectra for the dyes indicates that the interactions through the carboxylate groups with the TiO2 surface are very similar for the dyes. However, we observe that some of the dye molecules also interact through the NCS groups when adsorbed at the TiO2 surface. Comparing the N719 and the N3 molecule, the fraction of NCS groups interacting through the sulfur atoms is smaller for N719 than for N3. We also note that the counterion TBA(+) is coadsorbed with the N719 and BD molecules although the amount was smaller than expected from the molecular formulas. Comparing the valence levels for the dyes adsorbed on TiO2, the position of the highest occupied electronic energy level is similar for N3 and N719, while that for BD is lower by 0.25 eV relative to that of the other complexes.

    Identifikatorer
    urn:nbn:se:uu:diva-128834 (URN)10.1021/jp0525282 (DOI)000233684500027 ()
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2017-12-12
    7.
    Posten ble ikke funnet. Det kan skyldes at posten ikke lenger er tilgjengelig eller det er feil id i adressefeltet.
    8. The Influence of Water on the Electronic and Molecular Surface Structures of Ru-dyes at Nanostructured TiO2
    Åpne denne publikasjonen i ny fane eller vindu >>The Influence of Water on the Electronic and Molecular Surface Structures of Ru-dyes at Nanostructured TiO2
    Vise andre…
    (engelsk)Inngår i: Artikkel i tidsskrift (Annet vitenskapelig) Submitted
    Abstract [en]

    The influence of water on the surface electronic and molecular properties of three Ru-dyes adsorbed at nanostructured TiO2 was investigated using photoelectron spectroscopy (PES). The dyes investigated were the Ru(dcbpy)2 (NCS)2 in its acid (N3) and in its 2-fold deprotonated form (N719) as well as a similar dye (Z-907) containing the hydrophobic ligand 4,4-dinonyl-2,2-bipyridine. Trends in surface structures depending on water exposure were followed for the three dyes. The results showed that the hydrophobic chains of the Z-907 dye effectively inhibit surface reorganization while large changes in surface electronic and molecular structure was observed for the N3 and N719 molecular layers. Specifically, large effects involving the thiocyanate ligands were detected and the S2p and N1s core level spectra indicate that the changes involve mixing of only two dominating surface configurations. Moreover, the PES results also showed water induced changes in the energy level matching between the dye and the TiO2, and water induced desorption of the TBA+ counter ion. Basic photoelectrochemical trends depending on water exposure to dye sensitized solar cell systems were also verified.

    Identifikatorer
    urn:nbn:se:uu:diva-128841 (URN)
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26 Sist oppdatert: 2016-04-20bibliografisk kontrollert
    9. A Photoelectron Spectroscopy Study of Z-907 Co-adsorbed with DPA on Nanostructured TiO2 Surfaces
    Åpne denne publikasjonen i ny fane eller vindu >>A Photoelectron Spectroscopy Study of Z-907 Co-adsorbed with DPA on Nanostructured TiO2 Surfaces
    Vise andre…
    (engelsk)Manuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The surface electronic and molecular properties of mixed dye/coadsorbent sensitized TiO2 surfaces was investigated using photoelectron spectroscopy (PES). The sensitization of the TiO2 was performed using the ruthenium based dye cis-disothiocyanato-(2,2-bipyridyl-4,4-dicarboxylic acid)-(2,2-bipyridyl-4,4-dinonyl) ruthenium(II) (Z-907) together with different concentrations of the coadsorbent decylphosphonic acid (DPA). The investigation showed large variations in surface concentration of Z-907 and DPA depending on the dye/coadsorbent ratio in solution, but that the relative amounts at the surface and in solution substantially differ. Generally the DPA coadsorbents exchange with dye Z-907 molecule and trends in the surface concentration show that each dye molecule is replaced by six coadsorbent molecules. The co-adsorption of DPA induced changes in the S2p spectra, indicating changes in the dye surface interaction. Still, investigation of the frontier electronic structure in the dye sensitized TiO2 surfaces show that co-adsorbtion of DPA do not alter the energy level matching between the dye and the TiO2.

    Identifikatorer
    urn:nbn:se:uu:diva-128842 (URN)
    Tilgjengelig fra: 2010-07-26 Laget: 2010-07-26
  • 44.
    Hahlin, Maria
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Johansson, Erik M J
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Plogmaker, Stefan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Siegbahn, Hans
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    A Photoelectron Spectroscopy Study of Z-907 Co-adsorbed with DPA on Nanostructured TiO2 SurfacesManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The surface electronic and molecular properties of mixed dye/coadsorbent sensitized TiO2 surfaces was investigated using photoelectron spectroscopy (PES). The sensitization of the TiO2 was performed using the ruthenium based dye cis-disothiocyanato-(2,2-bipyridyl-4,4-dicarboxylic acid)-(2,2-bipyridyl-4,4-dinonyl) ruthenium(II) (Z-907) together with different concentrations of the coadsorbent decylphosphonic acid (DPA). The investigation showed large variations in surface concentration of Z-907 and DPA depending on the dye/coadsorbent ratio in solution, but that the relative amounts at the surface and in solution substantially differ. Generally the DPA coadsorbents exchange with dye Z-907 molecule and trends in the surface concentration show that each dye molecule is replaced by six coadsorbent molecules. The co-adsorption of DPA induced changes in the S2p spectra, indicating changes in the dye surface interaction. Still, investigation of the frontier electronic structure in the dye sensitized TiO2 surfaces show that co-adsorbtion of DPA do not alter the energy level matching between the dye and the TiO2.

  • 45.
    Hahlin, Maria
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för materialkemi, Strukturkemi.
    Johansson, Erik M. J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Schölin, Rebecka
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Siegbahn, Hans
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Influence of Water on the Electronic: and Molecular Surface Structures of Ru-Dyes at Nanostructured TiO22011Inngår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 115, nr 24, s. 11996-12004Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The influence of water on the surface electronic and molecular properties of three Ru-dyes adsorbed at nanostructured TiO2 was investigated using photoelectron spectroscopy (PES). The dyes investigated were the Ru(dcbpy)(2)(NCS)(2) in its acid (N3) and in its 2-fold deprotonated form (N719) as well as a similar dye (Z-907) containing the hydrophobic ligand 4,4'-dinonyl-2,2'-bipyridine. Trends in surface structures depending on water exposure were followed for the three dyes. The results showed that the hydrophobic chains of the Z-907 dye effectively inhibit surface reorganization while large changes in surface electronic and molecular structure were observed for the N3 and N719 molecular layers. Specifically, large effects involving the thiocyanate ligands were detected, and the S2p and N Is core level spectra indicate that the changes involve mixing of only two dominating surface configurations. Moreover, the PES results also showed water-induced changes in the energy level matching between the dye and the TiO2, and water induced desorption of the TBA(+) counterion. Basic photoelectrochemical trends depending on water exposure to dye-sensitized solar cell systems were also verified.

  • 46.
    Hahlin, Maria
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Johansson, Erik M J
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Schölin, Rebecka
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Siegbahn, Hans
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    The Influence of Water on the Electronic and Molecular Surface Structures of Ru-dyes at Nanostructured TiO2Inngår i: Artikkel i tidsskrift (Annet vitenskapelig)
    Abstract [en]

    The influence of water on the surface electronic and molecular properties of three Ru-dyes adsorbed at nanostructured TiO2 was investigated using photoelectron spectroscopy (PES). The dyes investigated were the Ru(dcbpy)2 (NCS)2 in its acid (N3) and in its 2-fold deprotonated form (N719) as well as a similar dye (Z-907) containing the hydrophobic ligand 4,4-dinonyl-2,2-bipyridine. Trends in surface structures depending on water exposure were followed for the three dyes. The results showed that the hydrophobic chains of the Z-907 dye effectively inhibit surface reorganization while large changes in surface electronic and molecular structure was observed for the N3 and N719 molecular layers. Specifically, large effects involving the thiocyanate ligands were detected and the S2p and N1s core level spectra indicate that the changes involve mixing of only two dominating surface configurations. Moreover, the PES results also showed water induced changes in the energy level matching between the dye and the TiO2, and water induced desorption of the TBA+ counter ion. Basic photoelectrochemical trends depending on water exposure to dye sensitized solar cell systems were also verified.

  • 47.
    Hahlin, Maria
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Marinado, Tannia
    Quintana, Maria
    Johansson, Erik M J
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Siegbahn, Hans
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Hagfeldt, Anders
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Surface compostions of dye/TiO2 interfaces formed from ethanol, acetonitrile, and dichloromethane based solutionsManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The molecular and electronic surface structure of three TiO2 surfaces sensitized with 3-(5-(4-(diphenyl amino) styryl) thiophen-2-yl)-2-cyanoacrylic acid (D5) using different solvents (acetonitrile, dicloromethane, and ethanol) was investigated by photoelectron spectroscopy. The results showed solvent dependence in surface coverage, dye surface structure and energy level matching. Corresponding basic results on photocurrent conversion and UV-vis absorption is also included. Together the results indicated surface aggregation when using dichloromethane as a solvent.

  • 48.
    Hahlin, Maria
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för materialkemi, Strukturkemi.
    Odelius, Michael
    Magnuson, Martin
    Johansson, Erik M. J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
    Plogmaker, Stefan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Hagberg, Daniel
    Sun, Licheng
    Siegbahn, Hans
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Mapping the frontier electronic structures of triphenylamine based organic dyes at TiO2 interfaces2011Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 13, nr 8, s. 3534-3546Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The frontier electronic structure of a series of organic dye molecules containing a triphenylamine moiety, a thiophene moiety and a cyanoacrylic acid moiety have been investigated by photoelectron spectroscopy (PES), X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy (XES) and resonant photoelectron spectroscopy (RPES). The experimental results were compared to electronic structure calculations on the molecules which are used to confirm and enrich the assignment of the spectra. The approach allows us to experimentally measure and interpret the basic valence energy level structure in the dye, including the highest occupied energy level and how it depends on the interaction between the different units. Based on N1s X-ray absorption and emission spectra we also obtain insight into the structure of the excited states, the molecular orbital composition and dynamics. Together the results provide an experimentally determined energy level map useful in the design of these types of materials. Included is also results indicating femtosecond charge redistribution at the dye/TiO2 interface.

  • 49. Harnes, J.
    et al.
    Abu-samha, M.
    Bergersen, Henrik
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Winkler, M.
    Lindblad, Andreas
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Saethre, L. J.
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Borve, K. J.
    The structure of mixed methanol/chloroform clusters from core-level photoelectron spectroscopy and modeling2011Inngår i: New Journal of Chemistry, ISSN 1144-0546, E-ISSN 1369-9261, Vol. 35, nr 11, s. 2564-2572Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Mixed neutral molecular clusters have been produced by co-expansion of chloroform and methanol and characterized by carbon 1s photoelectron spectroscopy and theoretical modeling. The produced clusters are in the range 50-150 molecules and the clusters are not homogeneously mixed: chloroform is enriched in the bulk and methanol is found on or close to the surface. This is based on evidence from photoelectron depth profiling and molecular dynamics simulations of mixed clusters. The simulations suggest that methanol forms cyclic or linear oligomers in the surface layers of the mixed clusters. From thermodynamic models, the enrichment of methanol on the cluster surface can be rationalized from the difference in surface tension between the two pure components, which is connected to the qualitative differences in the respective bonding patterns.

  • 50. Huttula, Marko
    et al.
    Mikkelae, Mikko-Heikki
    Tchaplyguine, Maxim
    Björneholm, Olle
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
    Size-varied photoelectron spectroscopy of metal clusters using the Exchange Metal Cluster Source2010Inngår i: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, E-ISSN 1873-2526, Vol. 181, nr 2-3, s. 145-149Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The recently developed Exchange Metal Cluster Source (EXMEC) is described. The source is designed for electron-spectroscopic studies of neutral metal clusters. Preliminary results on the rubidium and tin clusters using synchrotron radiation excited photoelectron spectroscopy show the capability for cluster production in the size regime of few tens to few hundred of atoms per cluster. A wide range of metal evaporation temperatures is covered applying resistive and induction heating methods. (C) 2010 Elsevier B.V. All rights reserved.

123 1 - 50 of 142
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