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Femtosecond time-resolved X-ray absorption spectroscopy of anatase TiO(2) nanoparticles using XFEL

The charge-carrier dynamics of anatase TiO(2) nanoparticles in an aqueous solution were studied by femtosecond time-resolved X-ray absorption spectroscopy using an X-ray free electron laser in combination with a synchronized ultraviolet femtosecond laser (268 nm). Using an arrival time monitor for t...

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Detalles Bibliográficos
Autores principales: Obara, Yuki, Ito, Hironori, Ito, Terumasa, Kurahashi, Naoya, Thürmer, Stephan, Tanaka, Hiroki, Katayama, Tetsuo, Togashi, Tadashi, Owada, Shigeki, Yamamoto, Yo-ichi, Karashima, Shutaro, Nishitani, Junichi, Yabashi, Makina, Suzuki, Toshinori, Misawa, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Crystallographic Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493491/
https://www.ncbi.nlm.nih.gov/pubmed/28713842
http://dx.doi.org/10.1063/1.4989862
Descripción
Sumario:The charge-carrier dynamics of anatase TiO(2) nanoparticles in an aqueous solution were studied by femtosecond time-resolved X-ray absorption spectroscopy using an X-ray free electron laser in combination with a synchronized ultraviolet femtosecond laser (268 nm). Using an arrival time monitor for the X-ray pulses, we obtained a temporal resolution of 170 fs. The transient X-ray absorption spectra revealed an ultrafast Ti K-edge shift and a subsequent growth of a pre-edge structure. The edge shift occurred in ca. 100 fs and is ascribed to reduction of Ti by localization of generated conduction band electrons into shallow traps of self-trapped polarons or deep traps at penta-coordinate Ti sites. Growth of the pre-edge feature and reduction of the above-edge peak intensity occur with similar time constants of 300–400 fs, which we assign to the structural distortion dynamics near the surface.