Femtosecond X-ray absorption study of electron localization in photoexcited anatase TiO2

Transition metal oxides are among the most promising solar materials, whose properties rely on the generation, transport and trapping of charge carriers (electrons and holes). Identifying the latter’s dynamics at room temperature requires tools that combine elemental and structural sensitivity, with...

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Veröffentlicht in:Scientific reports 2015-10, Vol.5 (1), p.14834-14834, Article 14834
Hauptverfasser: Santomauro, F. G., Lübcke, A., Rittmann, J., Baldini, E., Ferrer, A., Silatani, M., Zimmermann, P., Grübel, S., Johnson, J. A., Mariager, S. O., Beaud, P., Grolimund, D., Borca, C., Ingold, G., Johnson, S.L., Chergui, M.
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Sprache:eng
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Zusammenfassung:Transition metal oxides are among the most promising solar materials, whose properties rely on the generation, transport and trapping of charge carriers (electrons and holes). Identifying the latter’s dynamics at room temperature requires tools that combine elemental and structural sensitivity, with the atomic scale resolution of time (femtoseconds, fs). Here, we use fs Ti K-edge X-ray absorption spectroscopy (XAS) upon 3.49 eV (355 nm) excitation of aqueous colloidal anatase titanium dioxide nanoparticles to probe the trapping dynamics of photogenerated electrons. We find that their localization at Titanium atoms occurs in
ISSN:2045-2322
2045-2322
DOI:10.1038/srep14834