Hydrogen evolution from water splitting on nanocomposite photocatalysts

The photocatalytic production of H2 in one step is potentially one of the most promising ways for the conversion and storage of solar energy. The paper overviews our recent studies on the photocatalysts splitting water into hydrogen under irradiation. The attention was mainly focused on the promotio...

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Main Author: Wenfeng Shangguan
Format: Article
Language:English
Published: Taylor & Francis Group 2007-01-01
Series:Science and Technology of Advanced Materials
Online Access:http://www.iop.org/EJ/abstract/1468-6996/8/1-2/A14
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spelling doaj-a485162ed9994127a75248a253e05fa72020-11-25T00:34:29ZengTaylor & Francis GroupScience and Technology of Advanced Materials1468-69961878-55142007-01-0181-276Hydrogen evolution from water splitting on nanocomposite photocatalystsWenfeng ShangguanThe photocatalytic production of H2 in one step is potentially one of the most promising ways for the conversion and storage of solar energy. The paper overviews our recent studies on the photocatalysts splitting water into hydrogen under irradiation. The attention was mainly focused on the promotion effects of nanosized modifications in the interlayer and surface of photocatalysts for hydrogen evolution with visible light. The photocatalytic activity depended significantly on modification techniques, such as loading, proton exchange, and intercalation. The formation of a "nest" on the particle surface promoted a uniform distribution and strong combination of the nanosized particles on the surface of catalysts. By the methods of intercalation and pillaring as well as by selecting both host and guest, a large variety of molecular designed host–guest systems were obtained. Cadmium sulfide (CdS)-intercalated composites showed higher activity and stability. This activity of K4Ce2M10O30 (M=Ta, Nb) evolving H2 under visible light irradiation was enhanced by the incorporation of Pt, RuO2 and NiO as co-catalysts. Especially, the nanosized NiOx (Ni–NiO double-layer structure) greatly prompted the photocatalytic H2 evolution significantly.http://www.iop.org/EJ/abstract/1468-6996/8/1-2/A14
collection DOAJ
language English
format Article
sources DOAJ
author Wenfeng Shangguan
spellingShingle Wenfeng Shangguan
Hydrogen evolution from water splitting on nanocomposite photocatalysts
Science and Technology of Advanced Materials
author_facet Wenfeng Shangguan
author_sort Wenfeng Shangguan
title Hydrogen evolution from water splitting on nanocomposite photocatalysts
title_short Hydrogen evolution from water splitting on nanocomposite photocatalysts
title_full Hydrogen evolution from water splitting on nanocomposite photocatalysts
title_fullStr Hydrogen evolution from water splitting on nanocomposite photocatalysts
title_full_unstemmed Hydrogen evolution from water splitting on nanocomposite photocatalysts
title_sort hydrogen evolution from water splitting on nanocomposite photocatalysts
publisher Taylor & Francis Group
series Science and Technology of Advanced Materials
issn 1468-6996
1878-5514
publishDate 2007-01-01
description The photocatalytic production of H2 in one step is potentially one of the most promising ways for the conversion and storage of solar energy. The paper overviews our recent studies on the photocatalysts splitting water into hydrogen under irradiation. The attention was mainly focused on the promotion effects of nanosized modifications in the interlayer and surface of photocatalysts for hydrogen evolution with visible light. The photocatalytic activity depended significantly on modification techniques, such as loading, proton exchange, and intercalation. The formation of a "nest" on the particle surface promoted a uniform distribution and strong combination of the nanosized particles on the surface of catalysts. By the methods of intercalation and pillaring as well as by selecting both host and guest, a large variety of molecular designed host–guest systems were obtained. Cadmium sulfide (CdS)-intercalated composites showed higher activity and stability. This activity of K4Ce2M10O30 (M=Ta, Nb) evolving H2 under visible light irradiation was enhanced by the incorporation of Pt, RuO2 and NiO as co-catalysts. Especially, the nanosized NiOx (Ni–NiO double-layer structure) greatly prompted the photocatalytic H2 evolution significantly.
url http://www.iop.org/EJ/abstract/1468-6996/8/1-2/A14
work_keys_str_mv AT wenfengshangguan hydrogenevolutionfromwatersplittingonnanocompositephotocatalysts
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