Atomic-Level Reactive Sites for Semiconductor-Based Photocatalytic CO2 Reduction

被引:380
|
作者
Zhang, Yanzhao [1 ]
Xia, Bingquan [1 ]
Ran, Jingrun [1 ]
Davey, Kenneth [1 ]
Qiao, Shi Zhang [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
基金
澳大利亚研究理事会;
关键词
atomic-level reactive sites; carbon dioxide photoreduction; semiconductors; LIGHT-DRIVEN CO2; GRAPHITIC CARBON NITRIDE; FRUSTRATED LEWIS PAIRS; BINUCLEAR RUTHENIUM(II) COMPLEX; VISIBLE-LIGHT; OXYGEN-VACANCY; TIO2; NANOSHEETS; PHOTOCHEMICAL REDUCTION; HIGHLY EFFICIENT; SOLAR FUELS;
D O I
10.1002/aenm.201903879
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic CO2 reduction is an effective means to generate renewable energy. It involves redox reactions, reduction of CO2 and oxidation of water, that leads to the production of solar fuel. Significant research effort has therefore been made to develop inexpensive and practically sustainable semiconductor-based photocatalysts. The exploration of atomic-level active sites on the surface of semiconductors can result in an improved understanding of the mechanism of CO2 photoreduction. This can be applied to the design and synthesis of efficient photocatalysts. In this review, atomic-level reactive sites are classified into four types: vacancies, single atoms, surface functional groups, and frustrated Lewis pairs (FLPs). These different photocatalytic reactive sites are shown to have varied affinity to reactants, intermediates, and products. This changes pathways for CO2 reduction and significantly impacts catalytic activity and selectivity. The design of a photocatalyst from an atomic-level perspective can therefore be used to maximize atomic utilization efficiency and lead to a high selectivity. The prospects for fabrication of effective photocatalysts based on an in-depth understanding are highlighted.
引用
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页数:23
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