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Water-Induced Reversal of the TiO(2)(011)-(2 × 1) Surface Reconstruction: Observed with in Situ Surface X-ray Diffraction
[Image: see text] The (011) termination of rutile TiO(2) is reported to be particularly effective for photocatalysis. Here, the structure of the interface formed between this substrate and water is revealed using surface X-ray diffraction. While the TiO(2)(011) surface exhibits a (2 × 1) reconstruct...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559052/ https://www.ncbi.nlm.nih.gov/pubmed/31205578 http://dx.doi.org/10.1021/acs.jpcc.9b04383 |
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author | Hussain, Hadeel Ahmed, Mahmoud H. M. Torrelles, Xavier Grinter, David C. Cabailh, Gregory Bikondoa, Oier Nicklin, Christopher Aschauer, Ulrich Lindsay, Robert Thornton, Geoff |
author_facet | Hussain, Hadeel Ahmed, Mahmoud H. M. Torrelles, Xavier Grinter, David C. Cabailh, Gregory Bikondoa, Oier Nicklin, Christopher Aschauer, Ulrich Lindsay, Robert Thornton, Geoff |
author_sort | Hussain, Hadeel |
collection | PubMed |
description | [Image: see text] The (011) termination of rutile TiO(2) is reported to be particularly effective for photocatalysis. Here, the structure of the interface formed between this substrate and water is revealed using surface X-ray diffraction. While the TiO(2)(011) surface exhibits a (2 × 1) reconstruction in ultra-high vacuum (UHV), this is lifted in the presence of a multilayer of water at room temperature. This change is driven by the formation of Ti–OH at the interface, which has a bond distance of 1.93 ± 0.02 Å. The experimental solution is in good agreement with density functional theory and first-principles molecular dynamics calculations. These results point to the important differences that can arise between the structure of oxide surfaces in UHV and technical environments and will ultimately lead to an atomistic understanding of the photocatalytic process of water splitting on TiO(2) surfaces. |
format | Online Article Text |
id | pubmed-6559052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65590522019-06-12 Water-Induced Reversal of the TiO(2)(011)-(2 × 1) Surface Reconstruction: Observed with in Situ Surface X-ray Diffraction Hussain, Hadeel Ahmed, Mahmoud H. M. Torrelles, Xavier Grinter, David C. Cabailh, Gregory Bikondoa, Oier Nicklin, Christopher Aschauer, Ulrich Lindsay, Robert Thornton, Geoff J Phys Chem C Nanomater Interfaces [Image: see text] The (011) termination of rutile TiO(2) is reported to be particularly effective for photocatalysis. Here, the structure of the interface formed between this substrate and water is revealed using surface X-ray diffraction. While the TiO(2)(011) surface exhibits a (2 × 1) reconstruction in ultra-high vacuum (UHV), this is lifted in the presence of a multilayer of water at room temperature. This change is driven by the formation of Ti–OH at the interface, which has a bond distance of 1.93 ± 0.02 Å. The experimental solution is in good agreement with density functional theory and first-principles molecular dynamics calculations. These results point to the important differences that can arise between the structure of oxide surfaces in UHV and technical environments and will ultimately lead to an atomistic understanding of the photocatalytic process of water splitting on TiO(2) surfaces. American Chemical Society 2019-05-13 2019-06-06 /pmc/articles/PMC6559052/ /pubmed/31205578 http://dx.doi.org/10.1021/acs.jpcc.9b04383 Text en Copyright © 2019 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 | Hussain, Hadeel Ahmed, Mahmoud H. M. Torrelles, Xavier Grinter, David C. Cabailh, Gregory Bikondoa, Oier Nicklin, Christopher Aschauer, Ulrich Lindsay, Robert Thornton, Geoff Water-Induced Reversal of the TiO(2)(011)-(2 × 1) Surface Reconstruction: Observed with in Situ Surface X-ray Diffraction |
title | Water-Induced Reversal of the TiO(2)(011)-(2
× 1) Surface Reconstruction: Observed with in Situ Surface X-ray
Diffraction |
title_full | Water-Induced Reversal of the TiO(2)(011)-(2
× 1) Surface Reconstruction: Observed with in Situ Surface X-ray
Diffraction |
title_fullStr | Water-Induced Reversal of the TiO(2)(011)-(2
× 1) Surface Reconstruction: Observed with in Situ Surface X-ray
Diffraction |
title_full_unstemmed | Water-Induced Reversal of the TiO(2)(011)-(2
× 1) Surface Reconstruction: Observed with in Situ Surface X-ray
Diffraction |
title_short | Water-Induced Reversal of the TiO(2)(011)-(2
× 1) Surface Reconstruction: Observed with in Situ Surface X-ray
Diffraction |
title_sort | water-induced reversal of the tio(2)(011)-(2
× 1) surface reconstruction: observed with in situ surface x-ray
diffraction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559052/ https://www.ncbi.nlm.nih.gov/pubmed/31205578 http://dx.doi.org/10.1021/acs.jpcc.9b04383 |
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