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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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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
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author Zhang, Yu
Payne, Daniel T.
Pang, Chi L.
Fielding, Helen H.
Thornton, Geoff
author_facet Zhang, Yu
Payne, Daniel T.
Pang, Chi L.
Fielding, Helen H.
Thornton, Geoff
author_sort Zhang, Yu
collection PubMed
description [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.
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spelling pubmed-46036132015-10-22 Non-Band-Gap Photoexcitation of Hydroxylated TiO(2) Zhang, Yu Payne, Daniel T. Pang, Chi L. Fielding, Helen H. Thornton, Geoff J Phys Chem Lett [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. American Chemical Society 2015-08-12 2015-09-03 /pmc/articles/PMC4603613/ /pubmed/26267712 http://dx.doi.org/10.1021/acs.jpclett.5b01508 Text en Copyright © 2015 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Zhang, Yu
Payne, Daniel T.
Pang, Chi L.
Fielding, Helen H.
Thornton, Geoff
Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title_full Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title_fullStr Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title_full_unstemmed Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title_short Non-Band-Gap Photoexcitation of Hydroxylated TiO(2)
title_sort non-band-gap photoexcitation of hydroxylated tio(2)
url 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
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