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Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites
Metal-halide perovskite nanocrystals have emerged as one of the promising photocatalysts in the photocatalysis field owing to their low-cost and excellent optoelectronic properties. However, this type of nanocrystals generally displays low activity in photocatalytic CO(2) reduction owing to the lack...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074081/ https://www.ncbi.nlm.nih.gov/pubmed/35529999 http://dx.doi.org/10.1039/c9ra07236e |
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author | Guo, Xiao-Xuan Tang, Shang-Feng Mu, Yan-Fei Wu, Li-Yuan Dong, Guang-Xing Zhang, Min |
author_facet | Guo, Xiao-Xuan Tang, Shang-Feng Mu, Yan-Fei Wu, Li-Yuan Dong, Guang-Xing Zhang, Min |
author_sort | Guo, Xiao-Xuan |
collection | PubMed |
description | Metal-halide perovskite nanocrystals have emerged as one of the promising photocatalysts in the photocatalysis field owing to their low-cost and excellent optoelectronic properties. However, this type of nanocrystals generally displays low activity in photocatalytic CO(2) reduction owing to the lack of intrinsic catalytic sites and insufficient charge separation. Herein, we functionalized CsPbBr(3) nanocrystals with graphitic carbon nitride, containing titanium-oxide species (TiO-CN) to develop an efficient composite catalyst system for photocatalytic CO(2) reduction using water as the electron source. Compared to its congener with pristine CsPbBr(3), the introduction of TiO-CN could not only increase the number of active sites, but also led to a swift interfacial charge separation between CsPbBr(3) and TiO-CN due to their favorable energy-offsets and strong chemical bonding behaviors, which endowed this composite system with an obviously enhanced photocatalytic activity in the reduction of CO(2) to CO with water as the sacrificial reductant. Over 3-fold and 6-fold higher activities than those of pristine CsPbBr(3) nanocrystals and TiO-CN nanosheets, respectively, were observed under visible light irradiation. Our study provides an effective strategy for improving the photocatalytic activity of metal-halide perovskite nanocrystals, thus promoting their photocatalytic application in the field of artificial photosynthesis. |
format | Online Article Text |
id | pubmed-9074081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90740812022-05-06 Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites Guo, Xiao-Xuan Tang, Shang-Feng Mu, Yan-Fei Wu, Li-Yuan Dong, Guang-Xing Zhang, Min RSC Adv Chemistry Metal-halide perovskite nanocrystals have emerged as one of the promising photocatalysts in the photocatalysis field owing to their low-cost and excellent optoelectronic properties. However, this type of nanocrystals generally displays low activity in photocatalytic CO(2) reduction owing to the lack of intrinsic catalytic sites and insufficient charge separation. Herein, we functionalized CsPbBr(3) nanocrystals with graphitic carbon nitride, containing titanium-oxide species (TiO-CN) to develop an efficient composite catalyst system for photocatalytic CO(2) reduction using water as the electron source. Compared to its congener with pristine CsPbBr(3), the introduction of TiO-CN could not only increase the number of active sites, but also led to a swift interfacial charge separation between CsPbBr(3) and TiO-CN due to their favorable energy-offsets and strong chemical bonding behaviors, which endowed this composite system with an obviously enhanced photocatalytic activity in the reduction of CO(2) to CO with water as the sacrificial reductant. Over 3-fold and 6-fold higher activities than those of pristine CsPbBr(3) nanocrystals and TiO-CN nanosheets, respectively, were observed under visible light irradiation. Our study provides an effective strategy for improving the photocatalytic activity of metal-halide perovskite nanocrystals, thus promoting their photocatalytic application in the field of artificial photosynthesis. The Royal Society of Chemistry 2019-10-25 /pmc/articles/PMC9074081/ /pubmed/35529999 http://dx.doi.org/10.1039/c9ra07236e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Guo, Xiao-Xuan Tang, Shang-Feng Mu, Yan-Fei Wu, Li-Yuan Dong, Guang-Xing Zhang, Min Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title | Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title_full | Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title_fullStr | Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title_full_unstemmed | Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title_short | Engineering a CsPbBr(3)-based nanocomposite for efficient photocatalytic CO(2) reduction: improved charge separation concomitant with increased activity sites |
title_sort | engineering a cspbbr(3)-based nanocomposite for efficient photocatalytic co(2) reduction: improved charge separation concomitant with increased activity sites |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074081/ https://www.ncbi.nlm.nih.gov/pubmed/35529999 http://dx.doi.org/10.1039/c9ra07236e |
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