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Nanoheterostructured photocatalysts for improving photocatalytic hydrogen production

期刊

CHINESE JOURNAL OF CATALYSIS
卷 38, 期 8, 页码 1295-1306

出版社

SCIENCE PRESS
DOI: 10.1016/S1872-2067(17)62866-3

关键词

Heterojunction; Conduction band; Valence band; Charge transfer; Photocatalytic hydrogen production

资金

  1. National Natural Science Foundation of China [51572253, 21271165]
  2. Scientific Research Grant of Hefei Science Center of CAS [2015SRG-HSC048]
  3. NSFC
  4. Netherlands Organization for Scientific Research [51561135011]

向作者/读者索取更多资源

Rapid industrialization has accordingly increased the demand for energy. This has resulted in the increasingly severe energy and environmental crises. Hydrogen production, based on the photo catalytic water splitting driven by sunlight, is able to directly convert solar energy into a usable or storable energy resource, which is considered to be an ideal alternative energy source to assist in solving the energy crisis and environmental pollution. Unfortunately, the hydrogen production efficiency of single phase photocatalysts is too low to meet the practical requirements. The construction of heterostructured photocatalyst systems, which are comprised of multiple components or multiple phases, is an efficient method to facilitate the separation of electron-hole pairs to minimize the energy-waste, provide more electrons, enhance their redox ability, and hence improve the photo catalytic activity. We summarize the recent progress in the rational design and fabrication of nanoheterostructured photocatalysts. The heterojunction photocatalytic hydrogen generation systems can be divided into type-I, type-II, pn-junction and Z-scheme junction, according to the differences in the transfer of the photogenerated electrons and holes. Finally, a summary and some of the challenges and prospects for the future development of heterojunction photocatalytic systems are discussed. (C) 2017, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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