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dc.contributor.authorVon Eschwege, Karel G.
dc.contributor.authorConradie, Jeanet
dc.date.accessioned2022-11-18T12:30:31Z
dc.date.available2022-11-18T12:30:31Z
dc.date.issued2022-01-30
dc.description.abstractRuthenium had up to date been pivotal in electro- and photocatalytic applications involving reduction of CO<sub>2</sub> and H<sub>2</sub>O, and dye-sensitized solar cells. Commercial applications would seek use of earth-abundant metals instead. Towards this goal, it is key to review the synthesis, electrochemical and spectroscopical properties of associated metal-to-ligand charge transfer complexes of row-4 (Mn, Fe & Co) and column-8 (Fe, Ru & Os). The present report is limited to data obtained under exactly similar conditions, providing scientifically valid correlations. Only tris-coordinated bipyridyl and phenanthroline complex derivatives are considered, being representative of catalysts and dyes traditionally used in the above-mentioned fields. The accuracy of theoretical DFT techniques to simulate complex properties is highlighted.en_US
dc.identifier.citationVon Eschwege KG, Conradie J. Review of DFT-simulated and experimental electrochemistry properties of the polypyridyl Row-1 Mn, Fe & Co, and Group-8 Fe, Ru and Os MLCT complexes. Electrochemistry communications. 2022;136en_US
dc.identifier.cristinIDFRIDAID 2047362
dc.identifier.doi10.1016/j.elecom.2022.107225
dc.identifier.issn1388-2481
dc.identifier.issn1873-1902
dc.identifier.urihttps://hdl.handle.net/10037/27422
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalElectrochemistry communications
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)en_US
dc.titleReview of DFT-simulated and experimental electrochemistry properties of the polypyridyl Row-1 Mn, Fe & Co, and Group-8 Fe, Ru and Os MLCT complexesen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)