Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation

We report a new type of Au@TiO2-CdS ternary nanostructures by decorating CdS nanoparticles onto Au@TiO2 core-shell structures. Comparing to the binary structures, such as CdS-TiO2 and Au@TiO2, these ternary nanostructures exhibit remarkably high photocatalytic H2 generation rate under visible-light...

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Main Authors: Yin, Li-Sha, Fang, Jun, Xu, Lin, Zhang, Zhenyi, Yuan, Yu-Peng, Cao, Shao-Wen, Wang, Zheng, Liao, Yusen, Xue, Can
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2013
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Online Access:https://hdl.handle.net/10356/99458
http://hdl.handle.net/10220/17593
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-994582023-07-14T15:54:35Z Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation Yin, Li-Sha Fang, Jun Xu, Lin Zhang, Zhenyi Yuan, Yu-Peng Cao, Shao-Wen Wang, Zheng Liao, Yusen Xue, Can School of Materials Science & Engineering DRNTU::Engineering::Materials::Nanostructured materials We report a new type of Au@TiO2-CdS ternary nanostructures by decorating CdS nanoparticles onto Au@TiO2 core-shell structures. Comparing to the binary structures, such as CdS-TiO2 and Au@TiO2, these ternary nanostructures exhibit remarkably high photocatalytic H2 generation rate under visible-light irradiation. The enhanced photocatalytic activity is attributed to the unique ternary design, which builds up a transfer path for the photoexcited electrons of CdS to the core Au particles via the TiO2 nanocrystal bridge, and thus effectively suppressed the electron-hole recombination on the CdS photocatalyst. This internal electron transfer pathway (CdS→TiO2→Au) eliminates the needs of post-deposition of metal co-catalyst since the core Au nanoparticle can act as the interior active catalyst for proton reduction towards hydrogen evolution. We believe that our work demonstrates a promising way for rational design of metal-semiconductor hybrid photocatalysts to achieve high photocatalytic efficiency for solar fuels production. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Accepted version 2013-11-12T04:13:07Z 2019-12-06T20:07:43Z 2013-11-12T04:13:07Z 2019-12-06T20:07:43Z 2013 2013 Journal Article Fang, J., Xu, L., Zhang, Z., Yuan, Y.-P., Cao, S.-W., Wang, Z., et al. (2013). Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation. ACS applied materials & interfaces, 5(16), 8088-8092. https://hdl.handle.net/10356/99458 http://hdl.handle.net/10220/17593 10.1021/am4021654 en ACS applied materials & interfaces © 2013 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by ACS Applied Materials & Interfaces, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/am4021654]. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Materials::Nanostructured materials
spellingShingle DRNTU::Engineering::Materials::Nanostructured materials
Yin, Li-Sha
Fang, Jun
Xu, Lin
Zhang, Zhenyi
Yuan, Yu-Peng
Cao, Shao-Wen
Wang, Zheng
Liao, Yusen
Xue, Can
Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
description We report a new type of Au@TiO2-CdS ternary nanostructures by decorating CdS nanoparticles onto Au@TiO2 core-shell structures. Comparing to the binary structures, such as CdS-TiO2 and Au@TiO2, these ternary nanostructures exhibit remarkably high photocatalytic H2 generation rate under visible-light irradiation. The enhanced photocatalytic activity is attributed to the unique ternary design, which builds up a transfer path for the photoexcited electrons of CdS to the core Au particles via the TiO2 nanocrystal bridge, and thus effectively suppressed the electron-hole recombination on the CdS photocatalyst. This internal electron transfer pathway (CdS→TiO2→Au) eliminates the needs of post-deposition of metal co-catalyst since the core Au nanoparticle can act as the interior active catalyst for proton reduction towards hydrogen evolution. We believe that our work demonstrates a promising way for rational design of metal-semiconductor hybrid photocatalysts to achieve high photocatalytic efficiency for solar fuels production.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Yin, Li-Sha
Fang, Jun
Xu, Lin
Zhang, Zhenyi
Yuan, Yu-Peng
Cao, Shao-Wen
Wang, Zheng
Liao, Yusen
Xue, Can
format Article
author Yin, Li-Sha
Fang, Jun
Xu, Lin
Zhang, Zhenyi
Yuan, Yu-Peng
Cao, Shao-Wen
Wang, Zheng
Liao, Yusen
Xue, Can
author_sort Yin, Li-Sha
title Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
title_short Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
title_full Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
title_fullStr Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
title_full_unstemmed Au@TiO2–CdS ternary nanostructures for efficient visible-light-driven hydrogen generation
title_sort au@tio2–cds ternary nanostructures for efficient visible-light-driven hydrogen generation
publishDate 2013
url https://hdl.handle.net/10356/99458
http://hdl.handle.net/10220/17593
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