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Facile Vacuum Annealing-Induced Modification of TiO(2) with an Enhanced Photocatalytic Performance
[Image: see text] In this work, the photocatalytic performance enhancement of hydrothermally prepared TiO(2) was achieved by facile vacuum annealing treatment. Calcination of TiO(2) powder in air (CA-TiO(2)) maintained its white color, while gray powder was obtained when the annealing was performed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529652/ https://www.ncbi.nlm.nih.gov/pubmed/34693132 http://dx.doi.org/10.1021/acsomega.1c03762 |
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author | Cui, Zhenpeng Zhao, Min Que, Xueyan Wang, Jingjing Xu, Yang Ghazzal, Mohamed Nawfal Colbeau-Justin, Christophe Pan, Duoqiang Wu, Wangsuo |
author_facet | Cui, Zhenpeng Zhao, Min Que, Xueyan Wang, Jingjing Xu, Yang Ghazzal, Mohamed Nawfal Colbeau-Justin, Christophe Pan, Duoqiang Wu, Wangsuo |
author_sort | Cui, Zhenpeng |
collection | PubMed |
description | [Image: see text] In this work, the photocatalytic performance enhancement of hydrothermally prepared TiO(2) was achieved by facile vacuum annealing treatment. Calcination of TiO(2) powder in air (CA-TiO(2)) maintained its white color, while gray powder was obtained when the annealing was performed under vacuum (CV-TiO(2)). Fourier transform infrared, total organic carbon, X-ray photoelectron spectroscopy, and electron paramagnetic resonance analyses proved that vacuum annealing transformed ethanol adsorbed on the surface of TiO(2) into carbon-related species accompanied by the formation of surface oxygen vacancies (Vo). The residual carbon-related species on the surface of CV-TiO(2) favored its adsorption of organic dyes. Compared with TiO(2) and CA-TiO(2), CV-TiO(2) exhibited an improved charge carrier separation with surface Vo as trapping sites for electrons. Vacuum annealing-induced improvement of crystallinity, enhancement of adsorption capacity, and formation of surface Vo contributed to the excellent photocatalytic activity of CV-TiO(2), which was superior to that of commercial TiO(2) (P25, Degussa). Obviously, vacuum annealing-triggered decomposition of ethanol played an important role in the modification of TiO(2). In the presence of ethanol, vacuum annealing was also suitable for the introduction of Vo into P25. Therefore, the current work offers an easy approach for the modification of TiO(2) to enhance its photocatalytic performance by facile vacuum annealing in the presence of ethanol. |
format | Online Article Text |
id | pubmed-8529652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85296522021-10-22 Facile Vacuum Annealing-Induced Modification of TiO(2) with an Enhanced Photocatalytic Performance Cui, Zhenpeng Zhao, Min Que, Xueyan Wang, Jingjing Xu, Yang Ghazzal, Mohamed Nawfal Colbeau-Justin, Christophe Pan, Duoqiang Wu, Wangsuo ACS Omega [Image: see text] In this work, the photocatalytic performance enhancement of hydrothermally prepared TiO(2) was achieved by facile vacuum annealing treatment. Calcination of TiO(2) powder in air (CA-TiO(2)) maintained its white color, while gray powder was obtained when the annealing was performed under vacuum (CV-TiO(2)). Fourier transform infrared, total organic carbon, X-ray photoelectron spectroscopy, and electron paramagnetic resonance analyses proved that vacuum annealing transformed ethanol adsorbed on the surface of TiO(2) into carbon-related species accompanied by the formation of surface oxygen vacancies (Vo). The residual carbon-related species on the surface of CV-TiO(2) favored its adsorption of organic dyes. Compared with TiO(2) and CA-TiO(2), CV-TiO(2) exhibited an improved charge carrier separation with surface Vo as trapping sites for electrons. Vacuum annealing-induced improvement of crystallinity, enhancement of adsorption capacity, and formation of surface Vo contributed to the excellent photocatalytic activity of CV-TiO(2), which was superior to that of commercial TiO(2) (P25, Degussa). Obviously, vacuum annealing-triggered decomposition of ethanol played an important role in the modification of TiO(2). In the presence of ethanol, vacuum annealing was also suitable for the introduction of Vo into P25. Therefore, the current work offers an easy approach for the modification of TiO(2) to enhance its photocatalytic performance by facile vacuum annealing in the presence of ethanol. American Chemical Society 2021-09-28 /pmc/articles/PMC8529652/ /pubmed/34693132 http://dx.doi.org/10.1021/acsomega.1c03762 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Cui, Zhenpeng Zhao, Min Que, Xueyan Wang, Jingjing Xu, Yang Ghazzal, Mohamed Nawfal Colbeau-Justin, Christophe Pan, Duoqiang Wu, Wangsuo Facile Vacuum Annealing-Induced Modification of TiO(2) with an Enhanced Photocatalytic Performance |
title | Facile Vacuum Annealing-Induced Modification of TiO(2) with
an Enhanced Photocatalytic Performance |
title_full | Facile Vacuum Annealing-Induced Modification of TiO(2) with
an Enhanced Photocatalytic Performance |
title_fullStr | Facile Vacuum Annealing-Induced Modification of TiO(2) with
an Enhanced Photocatalytic Performance |
title_full_unstemmed | Facile Vacuum Annealing-Induced Modification of TiO(2) with
an Enhanced Photocatalytic Performance |
title_short | Facile Vacuum Annealing-Induced Modification of TiO(2) with
an Enhanced Photocatalytic Performance |
title_sort | facile vacuum annealing-induced modification of tio(2) with
an enhanced photocatalytic performance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529652/ https://www.ncbi.nlm.nih.gov/pubmed/34693132 http://dx.doi.org/10.1021/acsomega.1c03762 |
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