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Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)

[Image: see text] The photochemistry of TiO(2) has been studied intensively since it was discovered that TiO(2) can act as a photocatalyst. Nevertheless, it has proven difficult to establish the detailed charge-transfer processes involved, partly because the excited states involved are difficult to...

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Detalles Bibliográficos
Autores principales: Zhang, Yu, Payne, Daniel T., Pang, Chi L., Fielding, Helen H., Thornton, Geoff
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603613/
https://www.ncbi.nlm.nih.gov/pubmed/26267712
http://dx.doi.org/10.1021/acs.jpclett.5b01508
Descripción
Sumario:[Image: see text] The photochemistry of TiO(2) has been studied intensively since it was discovered that TiO(2) can act as a photocatalyst. Nevertheless, it has proven difficult to establish the detailed charge-transfer processes involved, partly because the excited states involved are difficult to study. Here we present evidence of the existence of hydroxyl-induced excited states in the conduction band region. Using two-photon photoemission, we show that stepwise photoexcitation from filled band gap states lying 0.8 eV below the Fermi level of rutile TiO(2)(110) excites hydroxyl-induced states 2.73 eV above the Fermi level that has an onset energy of ∼3.1 eV. The onset is shifted to lower energy by the coadsorption of molecular water, which suggests a means of tuning the energy of the excited state.