Photocatalytic Reduction on Bismuth-Based p-Block Semiconductors

被引:76
作者
Cui, Dandan [1 ,2 ]
Wang, Liang [3 ]
Du, Yi [1 ,3 ]
Hao, Weichang [1 ]
Chen, Jun [2 ]
机构
[1] Beihang Univ, BUAA UOW Joint Res Ctr, Sch Phys, Xueyuan Rd 37, Beijing 100191, Peoples R China
[2] Univ Wollongong, Australian Inst Innovat Mat, Intelligent Polymer Res Inst, ARC Ctr Excellence Electromat Sci, Innovat Campus, Wollongong, NSW 2500, Australia
[3] Univ Wollongong, AIIM, ISEM, Wollongong, NSW 2500, Australia
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
Photocatalysis; p-Block semiconductor; Bismuth-based photocatalysts; Photoreduction; VISIBLE-LIGHT PHOTOCATALYSIS; MOLECULAR-OXYGEN ACTIVATION; PURE WATER; BIOX X; EXCITON DISSOCIATION; ABSORPTION-SPECTRA; OPTICAL-PROPERTIES; NITROGEN-FIXATION; VACANCY FORMATION; CO2;
D O I
10.1021/acssuschemeng.8b04977
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
With the constant increase in demand for fuel energy, research on the exploration of renewable energy sources is becoming significantly critical. Herein, photocatalysis for the direct conversion of solar to chemical energy has attracted tremendous attention. In particular, because of the energy band edges mainly formed by p orbitals or s-p hybridized states, resulting in narrow band gaps and highly dispersive band structures, photocatalysts constructed from p-block elements exhibit remarkable visible-light photocatalytic activity. Taking bismuth oxyhalide-based photo catalysts, a typical family of p-block semiconductors, as an example, the following perspective mainly focuses on three significant strategies, including constituent adjustment, vacancy engineering, and the construction of heterostructures, on the design and construction of bismuth-based solar-conversion systems with high efficiencies in terms of H-2 evolution, CO2 reduction, and N-2 fixation. Finally, our thoughts on future challenges to be overcome for the development of advanced photoreduction systems are presented.
引用
收藏
页码:15936 / 15953
页数:35
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