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Carbon dioxide ion dissociations after inner shell excitation and ionization: The origin of site-specific effects
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
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2014 (Engelska)Ingår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 140, nr 18, s. 184305-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Multi-coincidence experiments with detection of both electrons and ions from decay of core-excited and core-ionized states of CO2 confirm that O-2(+) is formed specifically in Auger decay from the C1s-pi* and O1s-pi* resonances. Molecular rearrangement occurs by bending in the resonant states, and O-2(+) is produced by both single and double Auger decay. It is suggested that electron capture by C+ after partial dissociation in the doubly ionized core of excited CO2+, formed by shake-up in spectator resonant Auger decay, accounts for high kinetic energy and high internal energy in some C + O-2(+) fragments.

Ort, förlag, år, upplaga, sidor
2014. Vol. 140, nr 18, s. 184305-
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Den kondenserade materiens fysik
Identifikatorer
URN: urn:nbn:se:uu:diva-228478DOI: 10.1063/1.4872218ISI: 000336782700069OAI: oai:DiVA.org:uu-228478DiVA, id: diva2:734227
Tillgänglig från: 2014-07-15 Skapad: 2014-07-15 Senast uppdaterad: 2017-12-05Bibliografiskt granskad
Ingår i avhandling
1. Single-photon multiple ionisation of atoms and molecules investigated by coincidence spectroscopy: Site-specific effects in acetaldehyde and carbon dioxide
Öppna denna publikation i ny flik eller fönster >>Single-photon multiple ionisation of atoms and molecules investigated by coincidence spectroscopy: Site-specific effects in acetaldehyde and carbon dioxide
2016 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

In this thesis, multiple ionisation processes of free atoms and molecules upon single photon absorption are studied by means of a versatile multi-electron-ion coincidence spectroscopy method based on a magnetic bottle, primarily in combination with synchrotron radiation. The latter offered the possibility to access not only valence but also core levels, revealing processes, which promote the target systems into different charge states.

One study focuses on double and triple ionisation processes of acetaldehyde (ethanal) in the valence region as well as single and double Auger decay of initial 1s core vacancies. The latter are investigated site-selectively for the two chemically different carbon atoms of acetaldehyde, scrutinising theoretical predictions specifically made for that system.

A related study concentrates on core-valence double ionisation spectra of acetaldehyde, which have been investigated in the light of a previously established empirical model, and which have been used as test cases for analysing this kind of spectra by means of quantum chemical electronic structure methods of increasing sophistication.

A third study investigates site-specific fragmentation upon 1s photoionisation of acetaldehyde using a magnetic bottle augmented with an in-line ion time-of-flight mass spectrometer. Experimental evidence is presented that bond rupture occurs with highest probability in the vicinity of the initial charge localisation and possible mechanisms are discussed. A site-specificity parameter P is introduced to show that differences in fragmentation behavior between initial ionisations at chemically different carbon atoms probably persist even for identical internal energy contents in the nascent dications.

In another study where both electrons and ions from Auger decay of core-excited and core-ionised states of CO2 are detected in coincidence, it is confirmed that O2+ is formed specifically in Auger decay from the C1s → π* and O1s → π* resonances, suggesting a decisive role of the π* orbital in the molecular rearrangement. Also, the molecular rearrangement is found to occur by bending in the resonant states, and O2+ is produced by both single and double Auger decay.

A new version of the multi-electron-ion coincidence method, where the ion time-of-flight spectrometer is mounted perpendicularly to the electron flight tube, which affects less the electron resolution and which allows for position sensitive detection of the ions, is employed in combination with tunable soft X-rays to reveal the branching ratios to final Xen+ states with 2 < n < 9 from pure 4d-1, 4p-1, 4s-1, 3d-1 and 3p-1 Xe+ hole states. The coincident electron spectra give information on the Auger cascade pathways.

Ort, förlag, år, upplaga, sidor
Uppsala: Acta Universitatis Upsaliensis, 2016. s. 84
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1410
Nyckelord
acetaldehyde, carbon dioxide, xenon, electron correlation, double ionisation, triple ionisation, core-valence ionisation, site-specific Auger decay, multiple Auger decay, branching ratios, site-specific photodissociation, molecular rearrangement, time-of-flight multi-electron-ion coincidence spectroscopy, synchrotron radiation
Nationell ämneskategori
Atom- och molekylfysik och optik
Forskningsämne
Fysik med inriktning mot atom- molekyl- och kondenserande materiens fysik
Identifikatorer
urn:nbn:se:uu:diva-301128 (URN)978-91-554-9665-4 (ISBN)
Disputation
2016-09-30, Polhemssalen, Ångstömlaboratoriet, Lägerhyddsvägen 1, Uppsala, 13:15 (Engelska)
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Byte av lokal vid disputation till Polhemssalen.

Tillgänglig från: 2016-09-09 Skapad: 2016-08-18 Senast uppdaterad: 2016-09-27

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