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  • 1.
    Almeida, Roseley
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Univ Fed Bahia, Inst Fis, Campus Univ Ondina, Salvador, BA, Brazil.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Almeida, Jailton
    Univ Fed Bahia, Inst Fis, Campus Univ Ondina, BR-40210340 Salvador, BA, Brazil..
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, Stockholm, Sweden.
    Theoretical Evidence behind Bifunctional Catalytic Activity in Pristine and Functionalized Al2C Monolayers2018Ingår i: ChemPhysChem, ISSN 1439-4235, E-ISSN 1439-7641, Vol. 19, nr 1, s. 148-152Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    First principles electronic structure calculations based on the density functional theory (DFT) framework are performed to investigate hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) on two-dimensional Al2C monolayers. In addition to the pristine Al2C monolayer, monolayers doped with Nitrogen (N), Phosphorous (P), Boron (B), and Sulphur (S) are also investigated. After determining the individual adsorption energy of hydrogen and oxygen on the different functionalized Al2C monolayers, the adsorption free energies are predicted for each of the functionalized monolayers in order to assess their suitability for HER or OER. The density of states and optical absorption spectra calculations along with the work function of the functionalized Al2C monolayers enable us to gain a profound understanding of the electronic structure for the individual system and their relation to the water splitting mechanism.

  • 2.
    Araujo, Rafael B.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Panigrahi, Puspamitra
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Hindustan Univ, Ctr Clean Energy & Nanoconvergence, Madras, Tamil Nadu, India.
    Yang, Li
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Sjödin, Martin
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Strömme, Maria
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Araujo, C. Moyses
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat, Appl Mat Phys, S-10044 Stockholm, Sweden.; Royal Inst Technol KTH, Dept Engn, S-10044 Stockholm, Sweden.
    Assessing Electrochemical Properties of Polypyridine and Polythiophene for Prospective Application in Sustainable Organic Batteries2017Ingår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, nr 4, s. 3307-3314Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Conducting polymers are being considered promising candidates for sustainable organic batteries mainly due to their fast electron transport properties and high recyclability. In this work, key properties of polythiophene and polypyridine have been assessed through a combined theoretical and experimental study focusing on such applications. A theoretical protocol has been developed to calculate redox potentials in solution within the framework of the density functional theory and using continuous solvation models. Here, the evolution of the electrochemical properties of solvated oligomers as a function of the length of the chain is analyzed and then the polymer properties are estimated via linear regressions using ordinary least square. The predicted values were verified against our electrochemical experiments. This protocol can now be employed to screen a large database of compounds in order to identify organic electrodes with superior properties.

  • 3.
    Araujo, Rafael B.
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Panigrahi, Puspamitra
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Hindustan Univ, Ctr Clean Energy & Nanoconvergence, Chennai, Tamil Nadu, India.
    Yang, Li
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Strömme, Maria
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Sjödin, Martin
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Araujo, C. Moyses
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden.
    Designing strategies to tune reduction potential of organic molecules for sustainable high capacity batteries application2017Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, nr 9, s. 4430-4454Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Organic compounds evolve as a promising alternative to the currently used inorganic materials in rechargeable batteries due to their low-cost, environmentally friendliness and flexibility. One of the strategies to reach acceptable energy densities and to deal with the high solubility of known organic compounds is to combine small redox active molecules, acting as capacity carrying centres, with conducting polymers. Following this strategy, it is important to achieve redox matching between the chosen molecule and the polymer backbone. Here, a synergetic approach combining theory and experiment has been employed to investigate this strategy. The framework of density functional theory connected with the reaction field method has been applied to predict the formal potential of 137 molecules and identify promising candidates for the referent application. The effects of including different ring types, e.g. fused rings or bonded rings, heteroatoms, [small pi] bonds, as well as carboxyl groups on the formal potential, has been rationalized. Finally, we have identified a number of molecules with acceptable theoretical capacities that show redox matching with thiophene-based conducting polymers which, hence, are suggested as pendent groups for the development of conducting redox polymer based electrode materials.

  • 4.
    Araujo, Rafael Barros Neves de
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden..
    Divulging the Hidden Capacity and Sodiation Kinetics of NaxC6Cl4O2: A High Voltage Organic Cathode for Sodium Rechargeable Batteries2017Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 121, nr 26, s. 14027-14036Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In the current emerging sustainable organic battery field, quinones are seen as one of the prime candidates for application in rechargeable battery electrodes. Recently, C6Cl4O2, a modified quinone, has been proposed as a high voltage organic cathode. However, the sodium insertion mechanism behind the cell reaction remained unclear due to the nescience of the right crystal structure. Here, the framework of the density functional theory (DFT) together with an evolutionary algorithm was employed to elucidate the crystal structures of the compounds NaxC6Cl4O2 (x = 0.5, 1.0, 1.5 and 2). Along with the usefulness of PBE functional to reflect the experimental potential, also the importance of the hybrid functional to divulge the hidden theoretical capacity is evaluated. We showed that the experimentally observed lower specific capacity is a result of the great stabilization of the intermediate phase Na1.5C6Cl4O2. The calculated activation barriers for the ionic hops are 0.68, 0.40, and 0.31 eV, respectively, for NaC6Cl4O2, Na1.5C6Cl4O2, and Na2C6Cl4O2. These results indicate that the kinetic process must not be a limiting factor upon Na insertion. Finally, the correct prediction of the specific capacity has confirmed that the theoretical strategy used, employing evolutionary simulations together with the hybrid functional framework, can rightly model the thermodynamic process in organic electrode compounds.

  • 5.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Materials Modelling for Energy Harvesting: From Conversion to Application through Storage2019Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
    Abstract [en]

    In this Ph.D. thesis, ab initio density functional theory along with molecular dynamics and global optimization methods are used to unveil and understand the structures and properties of energy relevant materials. In this connection, the following applications are considered: i. electrocatalyst for solar fuel production through water splitting, ii. hybrid perovskite solar cell for generation of electrical energy and iii. Battery materials to store the electrical energy. The water splitting mechanism in terms of hydrogen evolution and oxygen evolution reactions (HER and OER) on the catalytic surfaces has been envisaged based on the free energy diagram, named reaction coordinate, of the reaction intermediates. The Ti-functionalized two-dimensional (2D) borophene monolayer has been emerged as a promising material for HER and OER mechanisms as compared to the pristine borophene sheet. Further investigation in the series of this noble metal free monolayer catalyst is 2D Al2C monolayer both in form of pristine and functionalized with nitrogen (N), phosphorous (P), boron (B), and sulphur (S). It has been observed that only B substituted Al2C shows very close to thermoneutral, that could be the most promising candidate for HER on functionalized Al2C monolayer. The adsorption of O* intermediate is stronger in S-substituted Al2C, whereas it is less strongly adsorbed on N-substituted Al2C. The subsequent consideration is being the case of n-type doping (W) along with Ti codoped in BiVO4 to enhance the efficiency of BiVO4 photoanode for water splitting. The determined adsorption energy and corresponding Gibbs free energies depict that the Ti site is energetically more favorable for water splitting. Moreover, the Ti site possesses a lower overpotential in the W–Ti codoped sample as compared to the mono-W doped sample. We have also explored the effect of mixed cation and mixed anion substitution in the hybrid perovskite in terms of structural stability, electronic properties and optical response of hybrid perovskite crystal structures. It has been found that the insertion of bromine (Br) into the system could modulate the stability of the Guanidinium lead iodide (GAPbI3) hybrid perovskite.  Moreover, the band gap of the mixed hybrid perovskite is increased with the inclusion of smaller Br anion while replacing partially the larger iodine (I) anion. Finally the electrochemical storage mechanism for Sodium (Na) and lithium (Li) ion insertion has been envisaged in inorganic electrode (eldfellite, NaFe(SO4)2) as well as in more sustainable organic electrode (di-lithium terephthalate, Li2TP). The full desodiation capability of the eldfellite enhances the capacity while the activation energies (higher than 1 eV) for the Na+ ion diffusion for the charged state lower the ionic insertion rate. The key factor as the variation of Li-O coordination in the terephthalate, for the disproportionation redox reaction in Li2TP is also identified.

    Delarbeten
    1. Scrupulous Probing of Bifunctional Catalytic Activity of Borophene Monolayer: Mapping Reaction Coordinate with Charge Transfer
    Öppna denna publikation i ny flik eller fönster >>Scrupulous Probing of Bifunctional Catalytic Activity of Borophene Monolayer: Mapping Reaction Coordinate with Charge Transfer
    2018 (Engelska)Ingår i: ACS Applied Energy Materials, ISSN 2574-0962, Vol. 1, nr 8, s. 3571-3576Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    We have envisaged the hydrogen evolution and oxygen evolution reactions (HER and OER) on two-dimensional (2D) noble metal free borophene monolayer based on first-principles electronic structure calculations. We have investigated the effect of Ti functionalization on borophene monolayer from the perspective of HER and OER activities enhancement. We have probed the activities based on the reaction coordinate, which is conceptually related to the adsorption free energies of the intermediates of HER and OER, as well as from the vibrational frequency analysis with the corresponding charge transfer mechanism between the surface and the adsorbate. Ti-functionalized borophene has emerged as a promising material for HER and OER mechanisms. We believe that our probing method, based on reaction coordinate coupled with vibrational analysis that has been validated by the charge transfer mechanism, would certainly become as a robust prediction route for HER and OER mechanisms in coming days.

    Keywords: borophene; hydrogen evolution reaction; oxygen evolution reaction; reaction coordinate; vibrational frequency

    Nyckelord
    borophene; hydrogen evolution reaction; oxygen evolution reaction; reaction coordinate; vibrational frequency
    Nationell ämneskategori
    Den kondenserade materiens fysik
    Identifikatorer
    urn:nbn:se:uu:diva-369691 (URN)10.1021/acsaem.8b00813 (DOI)000458706400007 ()
    Forskningsfinansiär
    Carl Tryggers stiftelse för vetenskaplig forskning StandUpVetenskapsrådet
    Tillgänglig från: 2018-12-16 Skapad: 2018-12-16 Senast uppdaterad: 2019-03-07Bibliografiskt granskad
    2. Theoretical Evidence behind Bifunctional Catalytic Activity in Pristine and Functionalized Al2C Monolayers
    Öppna denna publikation i ny flik eller fönster >>Theoretical Evidence behind Bifunctional Catalytic Activity in Pristine and Functionalized Al2C Monolayers
    Visa övriga...
    2018 (Engelska)Ingår i: ChemPhysChem, ISSN 1439-4235, E-ISSN 1439-7641, Vol. 19, nr 1, s. 148-152Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    First principles electronic structure calculations based on the density functional theory (DFT) framework are performed to investigate hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) on two-dimensional Al2C monolayers. In addition to the pristine Al2C monolayer, monolayers doped with Nitrogen (N), Phosphorous (P), Boron (B), and Sulphur (S) are also investigated. After determining the individual adsorption energy of hydrogen and oxygen on the different functionalized Al2C monolayers, the adsorption free energies are predicted for each of the functionalized monolayers in order to assess their suitability for HER or OER. The density of states and optical absorption spectra calculations along with the work function of the functionalized Al2C monolayers enable us to gain a profound understanding of the electronic structure for the individual system and their relation to the water splitting mechanism.

    Nyckelord
    adsorption free energy, Al2C monolayer, bifunctional catalysis, density functional calculations, doping
    Nationell ämneskategori
    Fysik
    Identifikatorer
    urn:nbn:se:uu:diva-341495 (URN)10.1002/cphc.201700768 (DOI)000419338600020 ()28925531 (PubMedID)
    Anmärkning

    De 2 första författarna delar förstaförfattarskapet.

    Tillgänglig från: 2018-02-19 Skapad: 2018-02-19 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    3. Simultaneous enhancement in charge separation and onset potential for water oxidation in a BiVO4 photoanode by W-Ti codoping
    Öppna denna publikation i ny flik eller fönster >>Simultaneous enhancement in charge separation and onset potential for water oxidation in a BiVO4 photoanode by W-Ti codoping
    Visa övriga...
    2018 (Engelska)Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 6, nr 35, s. 16965-16974Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Efficient charge separation of photo-generated electrons and holes is critical to achieve high solar to hydrogen conversion efficiency in photoelectrochemical (PEC) water splitting. N-type doping is generally used to improve the conductivity by increasing the majority carrier density and enhance the charge separation in the photoanode. However, minority carrier transport is also very important in the process of charge separation, especially in materials that possess inadequate minority carrier mobility. Herein, we take a BiVO4 PEC water splitting cell as an example to demonstrate how to analyze the limiting factor and to formulate the corresponding solutions to improve the hole mobility. The benefits and problems caused by n-type doping (W-doping here) of BiVO4 are analyzed. Codoping with Ti further enhances the charge separation by improving the hole transport and leads to a cathodic shift of the photocurrent onset potential. A high charge separation efficiency (79% at 1.23 V-RHE) in a compact BiVO4 photoanode has been achieved without any nanostructure formation. Theoretical results show that W-Ti codoping has decreased the hole polaron hopping activation energy by 11.5% compared with mono-W doping, and this has resulted in a hole mobility increase by 29%. The calculated adsorption energy and reaction Gibbs free energies indicate that the Ti site is energetically more favorable for water splitting. Moreover, the Ti site possesses a lower overpotential in the W-Ti codoped sample compared with the mono-W doped sample. The current study indicates that in order to improve the solar energy conversion efficiency, there should be a balanced charge transport of both majority and minority charge carriers. This can be achieved by simply choosing appropriate codoping elements.

    Ort, förlag, år, upplaga, sidor
    ROYAL SOC CHEMISTRY, 2018
    Nationell ämneskategori
    Fysikalisk kemi Materialkemi
    Identifikatorer
    urn:nbn:se:uu:diva-366730 (URN)10.1039/c8ta05491f (DOI)000445218000025 ()
    Forskningsfinansiär
    VetenskapsrådetEnergimyndigheten
    Tillgänglig från: 2018-12-11 Skapad: 2018-12-11 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    4. Bromination-induced stability enhancement with a multivalley optical response signature in guanidinium [C(NH2)(3)](+)-based hybrid perovskite solar cells
    Öppna denna publikation i ny flik eller fönster >>Bromination-induced stability enhancement with a multivalley optical response signature in guanidinium [C(NH2)(3)](+)-based hybrid perovskite solar cells
    2017 (Engelska)Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, nr 35, s. 18561-18568Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Guanidinium lead iodide (GAPbI(3)) has been synthesized experimentally, but stability remains an issue, which can be modulated by the insertion of bromine (Br) into the system. We have performed a systematic theoretical investigation to see how bromination can tune the stability of GAPbI(3). The optical properties were also determined, and we have found formation enthalpy-based stability in the perovskite systems, which are active in the visible and IR region even after bromine insertion and additionally more active in the IR range with the transition from GAPbI(3) to GAPbBr(3). The spin orbit coupling effect is considered throughout the band structure calculations. The ensemble of the primary and secondary gaps in the half and fully brominated hybrid perovskites leads to the phenomenon of a multipeak response in the optical spectra, which can be subsequently attributed as multivalley optical response behaviour. This multivalley optical behaviour enables the brominated guanidinium-based hybrid perovskites to exhibit broad light harvesting abilities, and this can be perceived as an idea for natural multi-junction solar cells.

    Ort, förlag, år, upplaga, sidor
    ROYAL SOC CHEMISTRY, 2017
    Nationell ämneskategori
    Den kondenserade materiens fysik
    Identifikatorer
    urn:nbn:se:uu:diva-336031 (URN)10.1039/c7ta03114a (DOI)000410597200026 ()
    Forskningsfinansiär
    Carl Tryggers stiftelse för vetenskaplig forskning VetenskapsrådetEnergimyndighetenStandUp
    Tillgänglig från: 2017-12-13 Skapad: 2017-12-13 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    5. Rashba Triggered Electronic and Optical Properties in De Novo Designed Mixed Halide Hybrid Perovskites
    Öppna denna publikation i ny flik eller fönster >>Rashba Triggered Electronic and Optical Properties in De Novo Designed Mixed Halide Hybrid Perovskites
    (Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
    Nationell ämneskategori
    Den kondenserade materiens fysik
    Identifikatorer
    urn:nbn:se:uu:diva-369693 (URN)
    Tillgänglig från: 2018-12-16 Skapad: 2018-12-16 Senast uppdaterad: 2018-12-19
    6. Cesium bismuth iodide, CsxBiyIz, solar cell compounds from systematic molar ratio variation
    Öppna denna publikation i ny flik eller fönster >>Cesium bismuth iodide, CsxBiyIz, solar cell compounds from systematic molar ratio variation
    Visa övriga...
    (Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
    Nationell ämneskategori
    Den kondenserade materiens fysik
    Identifikatorer
    urn:nbn:se:uu:diva-369694 (URN)
    Tillgänglig från: 2018-12-16 Skapad: 2018-12-16 Senast uppdaterad: 2018-12-19
    7. Unveiling the thermodynamic and kinetic properties of NaxFe(SO4)2 (x = 0–2): toward a high-capacity and low-cost cathode material
    Öppna denna publikation i ny flik eller fönster >>Unveiling the thermodynamic and kinetic properties of NaxFe(SO4)2 (x = 0–2): toward a high-capacity and low-cost cathode material
    2016 (Engelska)Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 4, s. 17960-17969Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    The mineral eldfellite, NaFe(SO4)2, was recently proposed as an inexpensive candidate for the next generation of cathode application in Na-based batteries. Employing the density functional theory framework, we have investigated the phase stability, electrochemical properties and ionic diffusion of this eldfellite cathode material. We showed that the crystal structure undergoes a volume shrinkage of ≈8% upon full removal of Na ions with no imaginary frequencies at the Γ point of phonon dispersion. This evokes the stability of the host structure. According to this result, we proposed structural changes to get higher specific energy by inserting two Na ions per redox-active metal. Our calculations indicate NaV(SO4)2 as the best candidate with the capability of reversibly inserting two Na ions per redox center and producing an excellent specific energy. The main bottleneck for the application of eldfellite as a cathode is the high activation energies for the Na+ ion hop, which can reach values even higher than 1 eV for the charged state. This effect produces a low ionic insertion rate.

    Nationell ämneskategori
    Fysik Den kondenserade materiens fysik
    Identifikatorer
    urn:nbn:se:uu:diva-311345 (URN)10.1039/C6TA05330K (DOI)000388505400007 ()
    Forskningsfinansiär
    VetenskapsrådetEnergimyndighetenStandUp
    Tillgänglig från: 2016-12-23 Skapad: 2016-12-23 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    8. Designing strategies to tune reduction potential of organic molecules for sustainable high capacity batteries application
    Öppna denna publikation i ny flik eller fönster >>Designing strategies to tune reduction potential of organic molecules for sustainable high capacity batteries application
    Visa övriga...
    2017 (Engelska)Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, nr 9, s. 4430-4454Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Organic compounds evolve as a promising alternative to the currently used inorganic materials in rechargeable batteries due to their low-cost, environmentally friendliness and flexibility. One of the strategies to reach acceptable energy densities and to deal with the high solubility of known organic compounds is to combine small redox active molecules, acting as capacity carrying centres, with conducting polymers. Following this strategy, it is important to achieve redox matching between the chosen molecule and the polymer backbone. Here, a synergetic approach combining theory and experiment has been employed to investigate this strategy. The framework of density functional theory connected with the reaction field method has been applied to predict the formal potential of 137 molecules and identify promising candidates for the referent application. The effects of including different ring types, e.g. fused rings or bonded rings, heteroatoms, [small pi] bonds, as well as carboxyl groups on the formal potential, has been rationalized. Finally, we have identified a number of molecules with acceptable theoretical capacities that show redox matching with thiophene-based conducting polymers which, hence, are suggested as pendent groups for the development of conducting redox polymer based electrode materials.

    Nationell ämneskategori
    Nanoteknik
    Forskningsämne
    Teknisk fysik med inriktning mot nanoteknologi och funktionella material
    Identifikatorer
    urn:nbn:se:uu:diva-314502 (URN)10.1039/C6TA09760J (DOI)000395926100022 ()
    Forskningsfinansiär
    Stiftelsen för strategisk forskning (SSF)EnergimyndighetenStandUpVetenskapsrådet
    Tillgänglig från: 2017-02-02 Skapad: 2017-02-02 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    9. Assessing Electrochemical Properties of Polypyridine and Polythiophene for Prospective Application in Sustainable Organic Batteries
    Öppna denna publikation i ny flik eller fönster >>Assessing Electrochemical Properties of Polypyridine and Polythiophene for Prospective Application in Sustainable Organic Batteries
    Visa övriga...
    2017 (Engelska)Ingår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, nr 4, s. 3307-3314Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    Conducting polymers are being considered promising candidates for sustainable organic batteries mainly due to their fast electron transport properties and high recyclability. In this work, key properties of polythiophene and polypyridine have been assessed through a combined theoretical and experimental study focusing on such applications. A theoretical protocol has been developed to calculate redox potentials in solution within the framework of the density functional theory and using continuous solvation models. Here, the evolution of the electrochemical properties of solvated oligomers as a function of the length of the chain is analyzed and then the polymer properties are estimated via linear regressions using ordinary least square. The predicted values were verified against our electrochemical experiments. This protocol can now be employed to screen a large database of compounds in order to identify organic electrodes with superior properties.

    Nationell ämneskategori
    Nanoteknik
    Forskningsämne
    Teknisk fysik med inriktning mot nanoteknologi och funktionella material
    Identifikatorer
    urn:nbn:se:uu:diva-311276 (URN)10.1039/C6CP07435A (DOI)000394940400071 ()28091636 (PubMedID)
    Forskningsfinansiär
    Stiftelsen för strategisk forskning (SSF)EnergimyndighetenStandUpVetenskapsrådet
    Tillgänglig från: 2016-12-22 Skapad: 2016-12-22 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    10. Divulging the Hidden Capacity and Sodiation Kinetics of NaxC6Cl4O2: A High Voltage Organic Cathode for Sodium Rechargeable Batteries
    Öppna denna publikation i ny flik eller fönster >>Divulging the Hidden Capacity and Sodiation Kinetics of NaxC6Cl4O2: A High Voltage Organic Cathode for Sodium Rechargeable Batteries
    2017 (Engelska)Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 121, nr 26, s. 14027-14036Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    In the current emerging sustainable organic battery field, quinones are seen as one of the prime candidates for application in rechargeable battery electrodes. Recently, C6Cl4O2, a modified quinone, has been proposed as a high voltage organic cathode. However, the sodium insertion mechanism behind the cell reaction remained unclear due to the nescience of the right crystal structure. Here, the framework of the density functional theory (DFT) together with an evolutionary algorithm was employed to elucidate the crystal structures of the compounds NaxC6Cl4O2 (x = 0.5, 1.0, 1.5 and 2). Along with the usefulness of PBE functional to reflect the experimental potential, also the importance of the hybrid functional to divulge the hidden theoretical capacity is evaluated. We showed that the experimentally observed lower specific capacity is a result of the great stabilization of the intermediate phase Na1.5C6Cl4O2. The calculated activation barriers for the ionic hops are 0.68, 0.40, and 0.31 eV, respectively, for NaC6Cl4O2, Na1.5C6Cl4O2, and Na2C6Cl4O2. These results indicate that the kinetic process must not be a limiting factor upon Na insertion. Finally, the correct prediction of the specific capacity has confirmed that the theoretical strategy used, employing evolutionary simulations together with the hybrid functional framework, can rightly model the thermodynamic process in organic electrode compounds.

    Nationell ämneskategori
    Materialteknik Fysik
    Identifikatorer
    urn:nbn:se:uu:diva-329995 (URN)10.1021/acs.jpcc.7b03621 (DOI)000405252800007 ()
    Forskningsfinansiär
    EnergimyndighetenVetenskapsrådetStandUp
    Anmärkning

    Divulging the Hidden Capacity and Sodiation Kinetics of NaxC6Cl4O2: A High Voltage Organic Cathode for Sodium Rechargeable Batteries

    Tillgänglig från: 2017-10-13 Skapad: 2017-10-13 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
    11. Identifying the tuning key of disproportionation redox reaction in terephthalate: A Li-based anode for sustainable organic batteries
    Öppna denna publikation i ny flik eller fönster >>Identifying the tuning key of disproportionation redox reaction in terephthalate: A Li-based anode for sustainable organic batteries
    2018 (Engelska)Ingår i: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 47, s. 301-308Artikel i tidskrift (Refereegranskat) Published
    Abstract [en]

    The ever-increasing consumption of energy storage devices has pushed the scientific community to realize strategies toward organic electrodes with superior properties. This is owed to advantages such as economic viability and eco-friendliness. In this context, the family of conjugated dicarboxylates has emerged as an interesting candidate for the application as negative electrodes in advanced Li-ion batteries due to the revealed thermal stability, rate capability, high capacity and high cyclability. This work aims to rationalize the effects of small molecular modifications on the electrochemical properties of the terephthalate anode by means of first principles calculations. The crystal structure prediction of the investigated host compounds dilithium terephthalate (Li2TP) and diethyl terephthalate (Et2Li0TP) together with their crystal modification upon battery cycling enable us to calculate the potential profile of these materials. Distinct underlying mechanisms of the redox reactions were obtained where Li2TP comes with a disproportionation reaction while Et2Li0TP displays sequential redox reactions. This effect proved to be strongly correlated to the Li coordination number evolution upon the Li insertion into the host structures. Finally, the calculations of sublimation enthalpy inferred that polymerization techniques could easily be employed in Et2Li0TP as compared to Li2TP. Similar results are observed with methyl, propyl, and vinyl capped groups. That could be a strategy to enhance the properties of this compound placing it into the gallery of the new anode materials for state of art Li-batteries.

    Nyckelord
    Li-ion organic battery, Lithium terephthalate, Disproportionation, Redox potential
    Nationell ämneskategori
    Fysikalisk kemi Materialkemi Teknik och teknologier
    Identifikatorer
    urn:nbn:se:uu:diva-354095 (URN)10.1016/j.nanoen.2018.02.038 (DOI)000430057000031 ()
    Forskningsfinansiär
    Vetenskapsrådet, 2016-06014
    Tillgänglig från: 2018-06-19 Skapad: 2018-06-19 Senast uppdaterad: 2018-12-19Bibliografiskt granskad
  • 6.
    Banerjee, Amitava
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Araujo, Rafael B.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden.
    Unveiling the thermodynamic and kinetic properties of NaxFe(SO4)2 (x = 0–2): toward a high-capacity and low-cost cathode material2016Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 4, s. 17960-17969Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The mineral eldfellite, NaFe(SO4)2, was recently proposed as an inexpensive candidate for the next generation of cathode application in Na-based batteries. Employing the density functional theory framework, we have investigated the phase stability, electrochemical properties and ionic diffusion of this eldfellite cathode material. We showed that the crystal structure undergoes a volume shrinkage of ≈8% upon full removal of Na ions with no imaginary frequencies at the Γ point of phonon dispersion. This evokes the stability of the host structure. According to this result, we proposed structural changes to get higher specific energy by inserting two Na ions per redox-active metal. Our calculations indicate NaV(SO4)2 as the best candidate with the capability of reversibly inserting two Na ions per redox center and producing an excellent specific energy. The main bottleneck for the application of eldfellite as a cathode is the high activation energies for the Na+ ion hop, which can reach values even higher than 1 eV for the charged state. This effect produces a low ionic insertion rate.

  • 7.
    Banerjee, Amitava
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Araujo, Rafael Barros
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Sjödin, Martin
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Appl Mat Phys, Dept Mat, S-10044 Stockholm, Sweden;Royal Inst Technol KTH, Appl Mat Phys, Dept Engn, S-10044 Stockholm, Sweden.
    Identifying the tuning key of disproportionation redox reaction in terephthalate: A Li-based anode for sustainable organic batteries2018Ingår i: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 47, s. 301-308Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The ever-increasing consumption of energy storage devices has pushed the scientific community to realize strategies toward organic electrodes with superior properties. This is owed to advantages such as economic viability and eco-friendliness. In this context, the family of conjugated dicarboxylates has emerged as an interesting candidate for the application as negative electrodes in advanced Li-ion batteries due to the revealed thermal stability, rate capability, high capacity and high cyclability. This work aims to rationalize the effects of small molecular modifications on the electrochemical properties of the terephthalate anode by means of first principles calculations. The crystal structure prediction of the investigated host compounds dilithium terephthalate (Li2TP) and diethyl terephthalate (Et2Li0TP) together with their crystal modification upon battery cycling enable us to calculate the potential profile of these materials. Distinct underlying mechanisms of the redox reactions were obtained where Li2TP comes with a disproportionation reaction while Et2Li0TP displays sequential redox reactions. This effect proved to be strongly correlated to the Li coordination number evolution upon the Li insertion into the host structures. Finally, the calculations of sublimation enthalpy inferred that polymerization techniques could easily be employed in Et2Li0TP as compared to Li2TP. Similar results are observed with methyl, propyl, and vinyl capped groups. That could be a strategy to enhance the properties of this compound placing it into the gallery of the new anode materials for state of art Li-batteries.

  • 8.
    Banerjee, Amitava
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden..
    Bromination-induced stability enhancement with a multivalley optical response signature in guanidinium [C(NH2)(3)](+)-based hybrid perovskite solar cells2017Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, nr 35, s. 18561-18568Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Guanidinium lead iodide (GAPbI(3)) has been synthesized experimentally, but stability remains an issue, which can be modulated by the insertion of bromine (Br) into the system. We have performed a systematic theoretical investigation to see how bromination can tune the stability of GAPbI(3). The optical properties were also determined, and we have found formation enthalpy-based stability in the perovskite systems, which are active in the visible and IR region even after bromine insertion and additionally more active in the IR range with the transition from GAPbI(3) to GAPbBr(3). The spin orbit coupling effect is considered throughout the band structure calculations. The ensemble of the primary and secondary gaps in the half and fully brominated hybrid perovskites leads to the phenomenon of a multipeak response in the optical spectra, which can be subsequently attributed as multivalley optical response behaviour. This multivalley optical behaviour enables the brominated guanidinium-based hybrid perovskites to exhibit broad light harvesting abilities, and this can be perceived as an idea for natural multi-junction solar cells.

  • 9.
    Banerjee, Amitava
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Teoretisk fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Rashba Triggered Electronic and Optical Properties in De Novo Designed Mixed Halide Hybrid PerovskitesManuskript (preprint) (Övrigt vetenskapligt)
  • 10.
    Banerjee, Amitava
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Jena, Naresh K.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Scrupulous Probing of Bifunctional Catalytic Activity of Borophene Monolayer: Mapping Reaction Coordinate with Charge Transfer2018Ingår i: ACS Applied Energy Materials, ISSN 2574-0962, Vol. 1, nr 8, s. 3571-3576Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    We have envisaged the hydrogen evolution and oxygen evolution reactions (HER and OER) on two-dimensional (2D) noble metal free borophene monolayer based on first-principles electronic structure calculations. We have investigated the effect of Ti functionalization on borophene monolayer from the perspective of HER and OER activities enhancement. We have probed the activities based on the reaction coordinate, which is conceptually related to the adsorption free energies of the intermediates of HER and OER, as well as from the vibrational frequency analysis with the corresponding charge transfer mechanism between the surface and the adsorbate. Ti-functionalized borophene has emerged as a promising material for HER and OER mechanisms. We believe that our probing method, based on reaction coordinate coupled with vibrational analysis that has been validated by the charge transfer mechanism, would certainly become as a robust prediction route for HER and OER mechanisms in coming days.

    Keywords: borophene; hydrogen evolution reaction; oxygen evolution reaction; reaction coordinate; vibrational frequency

  • 11.
    Chakraborty, Sudip
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Watcharatharapong, Teeraphat
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Araujo, Rafael Barros
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, Stockholm, Sweden.
    Current computational trends in polyanionic cathode materials for Li and Na batteries2018Ingår i: Journal of Physics: Condensed Matter, ISSN 0953-8984, E-ISSN 1361-648X, Vol. 30, nr 28, artikel-id 283003Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    A long-standing effort has been devoted for the development of high energy density cathodes both for Li-and Na-ion batteries (LIBs and SIBs). The scientific communities in battery research primarily divide the Li- and Na-ion cathode materials into two categories: layered oxides and polyanionic compounds. Researchers are trying to improve the energy density of such materials through materials screening by mixing the transition metals or changing the concentration of Li or Na in the polyanionic compounds. Due to the fact that there is more stability in the polyanionic frameworks, batteries based on these materials mostly provide a prolonged cycling life as compared to the layered oxide materials. Nevertheless, the bottleneck for such compounds is the weight penalty from polyanionic groups that results into the lower capacity. The anion engineering could be considered as an essential way out to design such polyanionic compounds to resolve this issue and to fetch improved cathode performance. In this topical review we present a systematic overview of the polyanionic cathode materials used for LIBs and SIBs. We will also present the computational methodologies that have become significantly relevant for battery research. We will make an attempt to provide the theoretical insight with a current development in sulfate (SO4), silicate (SiO4) and phosphate (PO4) based cathode materials for LIBs and SIBs. We will end this topical review with the future outlook, that will consist of the next generation organic electrode materials, mainly based on conjugated carbonyl compounds.

  • 12.
    Djouambi, Nadia
    et al.
    Univ Badji Mokhtar Annaba, Lab Mat Avances, BP 12, El Hadjar 23000, Annaba, Algeria.
    Bougheloum, Chafika
    Univ Badji Mokhtar Annaba, Lab Mat Avances, BP 12, El Hadjar 23000, Annaba, Algeria.
    Messalhi, Abdelrani
    Univ Badji Mokhtar Annaba, Lab Mat Avances, BP 12, El Hadjar 23000, Annaba, Algeria.
    Bououdina, Mohamed
    Univ Bahrain, Coll Sci, Dept Phys, POB 32038, Zallaq, Bahrain.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden.
    New Concept on Photocatalytic Degradation of Thiophene Derivatives: Experimental and DFT Studies2018Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 122, nr 27, s. 15646-15651Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In this study, the photocatalytic degradation of seven sulfur compounds (2-methylthiophene, 3-methylthiophene, 2-phenylthiophene, 3-phenylthiophene, 2,5-diphenylthiophene, 2-(2-thienyl) pyridine, and 2-(3-thienyl) pyridine in semiaqueous medium are compared to thiophene. The apparent-reaction-rate constant (k) is found to decrease in the following order: 2,5-diphenylthiophene > 2-(2-thienyl) pyridine > 2-penhylthiophene methylthiophene > 3-penhylthiophene > 2-methylthiophene > 2-(3-thienyl) pyridine > 3-thiophene. From the data obtained by UV light absorption (lambda(max)) measurements and electronic structure calculations (frontier orbitals energy, global hardness, and global softness), the kinetic parameters of the reaction have been determined. Among the studied compounds, thiophene with a high lambda(max) and low calculated LUMO-HOMO gap energy has showed higher activity under UV irradiation. Interestingly, a lower activity is observed with low lambda(max) and high LUMO-HOMO gap energy. This demonstrates, for the first time, that the reactivity depends essentially on the thermodynamic stability of the sulfur compound rather than on the nature or the position of the substituent on the ring.

  • 13.
    Johansson, Malin B
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Philippe, Bertrand
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Strukturkemi. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Phuyal, Dibya
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Cameau, Mathis
    Zhu, Huimin
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Teoretisk fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Boschloo, Gerrit
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Johansson, Erik M. J.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Cesium bismuth iodide, CsxBiyIz, solar cell compounds from systematic molar ratio variationManuskript (preprint) (Övrigt vetenskapligt)
  • 14.
    Johansson, Malin B
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Philippe, Bertrand
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Phuyal, Dibya
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Mukherjee, Soham
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Cameau, Mathis
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Zhu, Huimin
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Ahuja, Rajeev
    Uppsala Univ, Dept Phys & Astron, Mat Theory Div, Condensed Matter TRoyal Inst Technol, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden.
    Boschloo, Gerrit
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Rensmo, Håkan
    Johansson, Erik
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi.
    Cesium Bismuth Iodide Solar Cells from Systematic Molar Ratio Variation of CsI and BiI32019Ingår i: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 58, nr 18, s. 12040-12052Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Metal halide compounds with photovoltaic properties prepared from solution have received increased attention for utilization in solar cells. In this work, low-toxicity cesium bismuth iodides are synthesized from solution, and their photovoltaic and, optical properties as well as electronic and crystal structures are investigated. The X-ray diffraction patterns reveal that a CsI/BiI3 precursor ratio of 1.5:1 can convert pure rhombohedral BiI3 to pure hexagonal Cs3Bi2I9, but any ratio intermediate of this stoichiometry and pure BiI3 yields a mixture containing the two crystalline phases Cs3Bi2I9 and BiI3, with their relative fraction depending on the CsI/BiI3 ratio. Solar cells from the series of compounds are characterized, showing the highest efficiency for the compounds with a mixture of the two structures. The energies of the valence band edge were estimated using hard and soft X-ray photoelectron spectroscopy for more bulk and surface electronic properties, respectively. On the basis of these measurements, together with UV-vis-near-IR spectrophotometry, measuring the band gap, and Kelvin probe measurements for estimating the work function, an approximate energy diagram has been compiled clarifying the relationship between the positions of the valence and conduction band edges and the Fermi level.

  • 15.
    Klaa, Kaltoum
    et al.
    Badji Mokhtar Univ, Dept Phys, LNCTS Lab, Annaba, Algeria;Badji Mokhtar Univ, Dept Phys, LEREC Lab, Annaba, Algeria.
    Labidi, Salima
    Badji Mokhtar Univ, Dept Phys, LNCTS Lab, Annaba, Algeria.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Labidi, Malika
    Badji Mokhtar Univ, Dept Phys, LNCTS Lab, Annaba, Algeria.
    Amara, Abdelaziz
    Badji Mokhtar Univ, Dept Phys, LEREC Lab, Annaba, Algeria.
    Bououdina, Mohamed
    Univ Bahrain, Coll Sci, Dept Phys, POB Box 32038, Zallaq, Bahrain.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat, S-10044 Stockholm, Sweden.
    Composition dependent tuning of electronic and magnetic properties in transition metal substituted Rock-salt MgO2019Ingår i: Journal of Magnetism and Magnetic Materials, ISSN 0304-8853, E-ISSN 1873-4766, Vol. 475, s. 44-53Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Full potential linearized augmented plane wave (FP-LAPW) method based on the density functional theory (DFT) is used to investigate the structural, electronic and magnetic properties of Fe and Ni (3d transition metal) substituted Rock-salt wide band gap insulator Mg1-xMxO (M = Fe, Ni). We have performed spin polarized calculations throughout this work with generalized gradient approximation (GGA) type exchange correlation functional. Additionally, the electronic structures and density of states are computed using modified Becke-Johnson (mBJ) potential based approximation with the inclusion of coulomb energy (U = 7 eV). Based on the Vegard's law and structural optimization, the lattice parameter and bulk modulus are found to be in good agreement with experimental values. Moreover, the analysis of electronic band structures reveals an insulating character for Ni substituted MgO while semiconducting and half-metallic character for Fe substituted case. It has been found that the p-d super-exchange interaction provides a ferromagnetic character due to the 3d transition metal impurities and oxygen atom. The observed p-d hybridization at the top of the valence band edge in this investigations could be useful for magneto-optic and spintronic applications.

  • 16.
    Lai, Qiwen
    et al.
    Univ New S Wales, Sch Chem Engn, MERLin Grp, Sydney, NSW 2052, Australia..
    Paskevicius, Mark
    Aarhus Univ, Dept Chem, DK-8000 Aarhus, Denmark.;Aarhus Univ, iNANO, DK-8000 Aarhus, Denmark.;Curtin Univ, Dept Phys Astron & Med Radiat Sci, Bentley, WA 6102, Australia..
    Sheppard, Drew A.
    Curtin Univ, Dept Phys Astron & Med Radiat Sci, Bentley, WA 6102, Australia..
    Buckley, Craig E.
    Curtin Univ, Dept Phys Astron & Med Radiat Sci, Bentley, WA 6102, Australia..
    Thornton, Aaron W.
    CSIRO, Clayton, Vic 3169, Australia..
    Hill, Matthew R.
    CSIRO, Clayton, Vic 3169, Australia..
    Gu, Qinfen
    Australian Synchrotron, Clayton, Vic 3168, Australia..
    Mao, Jianfeng
    Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia..
    Huang, Zhenguo
    Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia..
    Liu, Hua Kun
    Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia..
    Guo, Zaiping
    Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia..
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Aguey-Zinsou, Kondo-Francois
    Univ New S Wales, Sch Chem Engn, MERLin Grp, Sydney, NSW 2052, Australia..
    Hydrogen Storage Materials for Mobile and Stationary Applications: Current State of the Art2015Ingår i: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 8, nr 17, s. 2789-2825Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    One of the limitations to the widespread use of hydrogen as an energy carrier is its storage in a safe and compact form. Herein, recent developments in effective high-capacity hydrogen storage materials are reviewed, with a special emphasis on light compounds, including those based on organic porous structures, boron, nitrogen, and aluminum. These elements and their related compounds hold the promise of high, reversible, and practical hydrogen storage capacity for mobile applications, including vehicles and portable power equipment, but also for the large scale and distributed storage of energy for stationary applications. Current understanding of the fundamental principles that govern the interaction of hydrogen with these light compounds is summarized, as well as basic strategies to meet practical targets of hydrogen uptake and release. The limitation of these strategies and current understanding is also discussed and new directions proposed.

  • 17.
    Minakshi, Manickam
    et al.
    Murdoch Univ, Engn & Informat Technol, Murdoch, WA 6150, Australia;Helmholtz Inst Ulm Electrochem Energy Storage HIU, D-89081 Ulm, Germany.
    Mitchell, David R. G.
    Univ Wollongong, Australian Inst Innovat Mat, Electron Microscopy Ctr, Innovat Campus, North Wollongong, NSW 2500, Australia.
    Baur, Christian
    Helmholtz Inst Ulm Electrochem Energy Storage HIU, D-89081 Ulm, Germany.
    Chable, Johann
    Helmholtz Inst Ulm Electrochem Energy Storage HIU, D-89081 Ulm, Germany.
    Barlow, Anders J.
    La Trobe Univ, Ctr Mat & Surface Sci, Bundoora, Vic 3086, Australia.
    Fichtner, Maximilian
    Helmholtz Inst Ulm Electrochem Energy Storage HIU, D-89081 Ulm, Germany.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Royal Inst Technol KTH, Dept Mat & Engn, Appl Mat Phys, S-10044 Stockholm, Sweden.
    Phase evolution in calcium molybdate nanoparticles as a function of synthesis temperature and its electrochemical effect on energy storage2019Ingår i: NANOSCALE ADVANCES, ISSN 2516-0230, Vol. 1, nr 2, s. 565-580Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The design of a suitable electrode is an essential and fundamental research challenge in the field of electrochemical energy storage because the electronic structures and morphologies determine the surface redox reactions. Calcium molybdate (CaMoO4) was synthesized by a combustion route at 300 degrees C and 500 degrees C. We describe new findings on the behaviour of CaMoO4 and evaluate the influence of crystallinity on energy storage performance. A wide range of characterization techniques was used to obtain detailed information about the physical and morphological characteristics of CaMoO4. The characterization results enable the phase evolution as a function of the electrode synthesis temperature to be understood. The crystallinity of the materials was found to increase with increasing temperature but with no second phases observed. Molecular dynamics simulation of electronic structures correlated well with the experimental findings. These results show that to enable faster energy storage and release for a given surface area, amorphous CaMoO4 is required, while larger energy storage can be obtained by using crystalline CaMoO4. CaMoO4 has been evaluated as a cathode material in classical lithium-ion batteries recently. However, determining the surface properties in a sodium-ion system experimentally, combined with computational modelling to understand the results has not been reported. The superior electrochemical properties of crystalline CaMoO4 are attributed to its morphology providing enhanced Na+ ion diffusivity and electron transport. However, the presence of carbon in amorphous CaMoO4 resulted in excellent rate capability, suitable for supercapacitor applications.

  • 18.
    Mir, Showkat H.
    et al.
    Cent Univ Gujarat, Ctr Nano Sci, Gandhinagar 382030, India..
    Jha, Prakash C.
    Cent Univ Gujarat, Sch Chem Sci, Gandhinagar 382030, India..
    Islam, Muhammed Shafiqul
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banarjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Luo, Wei
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Dabhi, Shweta D.
    Maharaja Krishnakumarsinhji Bhavnagar Univ, Dept Phys, Bhavnagar 364001, Gujarat, India..
    Jha, Prafulla K.
    Maharaja Sayajirao Univ Baroda, Dept Phys, Fac Sci, Vadodara 390002, India..
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Static and Dynamical Properties of heavy actinide Monopnictides of Lutetium2016Ingår i: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 6, artikel-id 29309Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In this work, density functional theory within the framework of generalized gradient approximation has been used to investigate the structural, elastic, mechanical, and phonon properties of lutetium monopnictides in rock-salt crystal structure. The spin orbit coupling and Hubbard-U corrections are included to correctly predict the essential properties of these compounds. The elastic constants, Young's modulus E, Poisson's ratio v, shear modulus G, anisotropy factor A and Pugh's ratio are computed. We found that all lutetium monopnictides are anisotropic and show brittle character. From the wave velocities along [100], [110] and [111] directions, melting temperature of lutetium monopnictides are predicted. Dynamical stability of these monopnictides has been studied by density functional perturbation theory.

  • 19.
    Philippe, Bertrand
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Jacobsson, T. Jesper
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Fysikalisk kemi. École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
    Correa-Baena, Juan-Pablo
    École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland; Massachusetts Institute of Technology, Cambridge, USA .
    Jena, Naresh K.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Cappel, Ute B.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Hagfeldt, Anders
    École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
    Odelius, Michael
    Stockholm University, Stockholm, Sweden.
    Rensmo, Håkan
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.
    Valence Level Character in a Mixed Perovskite Material and Determination of the Valence Band Maximum from Photoelectron Spectroscopy: Variation with Photon Energy2017Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 121, nr 48, s. 26655-26666Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A better understanding of the electronic structure of perovskite materials used in photovoltaic devices is essential for their development and optimization. In this investigation, synchrotron based photoelectron spectroscopy (PES) was used to experimentally delineate the character and energy position of the valence band structures of a mixed perovskite. The valence band was measured using PES with photon energies ranging from UPS (21.2 eV) to hard X-rays (up to 4,000 eV) and by taking the variation of the photoionization cross-sections into account, we could experimentally determine the inorganic and organic contributions. The experiments were compared to theoretical calculations to further distinguish the role of the different anions in the electronic structure. The investigation also includes a thorough study of the valence band maximum (VBM) and its position in relation to the Fermi level, which is crucial for the design and optimization of complete solar cells and their functional properties.

  • 20.
    Wärnå, John
    et al.
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Geovetenskapliga sektionen, Institutionen för geovetenskaper, Berggrundsgeologi. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Fysiska institutionen, Kondenserade materiens teori (Fysik IV). Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Fysiska institutionen, Fysik IV. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Fysiska institutionen, Fysik II. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och materialvetenskap, Materialteori. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Teoretisk fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Fysiska institutionen, Teoretisk magnetism. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Nanoteknologi och funktionella material. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Fysiska institutionen, Fysik III.
    Reaction Coordinate Mapping of Hydrogen Evolution Mechanism on Mg3N2MonolayerManuskript (preprint) (Övrigt vetenskapligt)
  • 21.
    Zhao, Xin
    et al.
    Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore.
    Hu, Jun
    Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore;Northwest Univ, Sch Chem Engn, Xian 710069, Shaanxi, Peoples R China.
    Wu, Bo
    Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637371, Singapore.
    Banerjee, Amitava
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Chakraborty, Sudip
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Feng, Jianyong
    Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore.
    Zhao, Zongyan
    Kunming Univ Sci & Technol, Fac Mat Sci & Engn, Kunming 650093, Yunnan, Peoples R China.
    Chen, Shi
    Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637371, Singapore.
    Ahuja, Rajeev
    Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Materialteori.
    Sum, Tze Chien
    Nanyang Technol Univ, Sch Phys & Math Sci, Singapore 637371, Singapore.
    Chen, Zhong
    Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore.
    Simultaneous enhancement in charge separation and onset potential for water oxidation in a BiVO4 photoanode by W-Ti codoping2018Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 6, nr 35, s. 16965-16974Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Efficient charge separation of photo-generated electrons and holes is critical to achieve high solar to hydrogen conversion efficiency in photoelectrochemical (PEC) water splitting. N-type doping is generally used to improve the conductivity by increasing the majority carrier density and enhance the charge separation in the photoanode. However, minority carrier transport is also very important in the process of charge separation, especially in materials that possess inadequate minority carrier mobility. Herein, we take a BiVO4 PEC water splitting cell as an example to demonstrate how to analyze the limiting factor and to formulate the corresponding solutions to improve the hole mobility. The benefits and problems caused by n-type doping (W-doping here) of BiVO4 are analyzed. Codoping with Ti further enhances the charge separation by improving the hole transport and leads to a cathodic shift of the photocurrent onset potential. A high charge separation efficiency (79% at 1.23 V-RHE) in a compact BiVO4 photoanode has been achieved without any nanostructure formation. Theoretical results show that W-Ti codoping has decreased the hole polaron hopping activation energy by 11.5% compared with mono-W doping, and this has resulted in a hole mobility increase by 29%. The calculated adsorption energy and reaction Gibbs free energies indicate that the Ti site is energetically more favorable for water splitting. Moreover, the Ti site possesses a lower overpotential in the W-Ti codoped sample compared with the mono-W doped sample. The current study indicates that in order to improve the solar energy conversion efficiency, there should be a balanced charge transport of both majority and minority charge carriers. This can be achieved by simply choosing appropriate codoping elements.

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