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Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique
During the last several decades TiO(2) photocatalytic oxidation using the molecular oxygen in air has emerged as a promising method for the degradation of recalcitrant organic pollutants and selective transformations of valuable organic chemicals. Despite extensive studies, the mechanisms of these p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271656/ https://www.ncbi.nlm.nih.gov/pubmed/25310153 http://dx.doi.org/10.3390/molecules191016291 |
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author | Pang, Xibin Chen, Chuncheng Ji, Hongwei Che, Yanke Ma, Wanhong Zhao, Jincai |
author_facet | Pang, Xibin Chen, Chuncheng Ji, Hongwei Che, Yanke Ma, Wanhong Zhao, Jincai |
author_sort | Pang, Xibin |
collection | PubMed |
description | During the last several decades TiO(2) photocatalytic oxidation using the molecular oxygen in air has emerged as a promising method for the degradation of recalcitrant organic pollutants and selective transformations of valuable organic chemicals. Despite extensive studies, the mechanisms of these photocatalytic reactions are still poorly understood due to their complexity. In this review, we will highlight how the oxygen-18 isotope labeling technique can be a powerful tool to elucidate complicated photocatalytic mechanisms taking place on the TiO(2) surface. To this end, the application of the oxygen-18 isotopic-labeling method to three representative photocatalytic reactions is discussed: (1) the photocatalytic hydroxylation of aromatics; (2) oxidative cleavage of aryl rings on the TiO(2) surface; and (3) photocatalytic decarboxylation of saturated carboxylic acids. The results show that the oxygen atoms of molecular oxygen can incorporate into the corresponding products in aqueous solution in all three of these reactions, but the detailed incorporation pathways are completely different in each case. For the hydroxylation process, the O atom in O(2) is shown to be incorporated through activation of O(2) by conduction band electrons. In the cleavage of aryl rings, O atoms are inserted into the aryl ring through the site-dependent coordination of reactants on the TiO(2) surface. A new pathway for the decarboxylation of saturated carboxylic acids with pyruvic acid as an intermediate is identified, and the O(2) is incorporated into the products through the further oxidation of pyruvic acid by active species from the activation of O(2) by conduction band electrons. |
format | Online Article Text |
id | pubmed-6271656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62716562018-12-27 Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique Pang, Xibin Chen, Chuncheng Ji, Hongwei Che, Yanke Ma, Wanhong Zhao, Jincai Molecules Review During the last several decades TiO(2) photocatalytic oxidation using the molecular oxygen in air has emerged as a promising method for the degradation of recalcitrant organic pollutants and selective transformations of valuable organic chemicals. Despite extensive studies, the mechanisms of these photocatalytic reactions are still poorly understood due to their complexity. In this review, we will highlight how the oxygen-18 isotope labeling technique can be a powerful tool to elucidate complicated photocatalytic mechanisms taking place on the TiO(2) surface. To this end, the application of the oxygen-18 isotopic-labeling method to three representative photocatalytic reactions is discussed: (1) the photocatalytic hydroxylation of aromatics; (2) oxidative cleavage of aryl rings on the TiO(2) surface; and (3) photocatalytic decarboxylation of saturated carboxylic acids. The results show that the oxygen atoms of molecular oxygen can incorporate into the corresponding products in aqueous solution in all three of these reactions, but the detailed incorporation pathways are completely different in each case. For the hydroxylation process, the O atom in O(2) is shown to be incorporated through activation of O(2) by conduction band electrons. In the cleavage of aryl rings, O atoms are inserted into the aryl ring through the site-dependent coordination of reactants on the TiO(2) surface. A new pathway for the decarboxylation of saturated carboxylic acids with pyruvic acid as an intermediate is identified, and the O(2) is incorporated into the products through the further oxidation of pyruvic acid by active species from the activation of O(2) by conduction band electrons. MDPI 2014-10-10 /pmc/articles/PMC6271656/ /pubmed/25310153 http://dx.doi.org/10.3390/molecules191016291 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pang, Xibin Chen, Chuncheng Ji, Hongwei Che, Yanke Ma, Wanhong Zhao, Jincai Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title | Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title_full | Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title_fullStr | Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title_full_unstemmed | Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title_short | Unraveling the Photocatalytic Mechanisms on TiO(2) Surfaces Using the Oxygen-18 Isotopic Label Technique |
title_sort | unraveling the photocatalytic mechanisms on tio(2) surfaces using the oxygen-18 isotopic label technique |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271656/ https://www.ncbi.nlm.nih.gov/pubmed/25310153 http://dx.doi.org/10.3390/molecules191016291 |
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