Activating photocatalytic hydrogen generation on inorganic lead-free Cs2AgBiBr6 perovskite via reversible Cu2+/Cu+ redox couple

被引:16
作者
Wang, Tian [1 ]
Li, Xin [1 ]
Qin, Zhixiao [1 ]
Wang, Tianfu [1 ]
Zhao, Yixin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
关键词
Perovskite catalysis; H-2; evolution; Cu2+/Cu+ redox couple; Environmental remediation; Carbon neutrality; CU/CU2O NANOPARTICLES; H-2; EVOLUTION; EFFICIENT; PERFORMANCE; NANOSHEETS; ACID;
D O I
10.1016/j.jcat.2022.07.009
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 hydrogen evolution from hydrohalic acid by lead-free metal halide perovskite holds great potential but still faces ineffective charge separation and low solar-to-hydrogen conversion efficiency challenges. In the present study, a reversible Cu2+/Cu+ redox couple is introduced into the inorganic lead-free perovskite Cs2AgBiBr6/(HBr + H3PO2)-based photocatalytic H-2 evolution system to achieve fast hole extraction and effective charge separation. The rapid Cu+ oxidation by photogenerated holes with more favorable thermodynamics and faster kinetics overcomes the intrinsic slow Br oxidation half-reaction, leading to rapid extraction and consumption of holes, which dramatically alleviates the charge recombination and improves the utilization efficiency of electrons for protons reduction. As a result, up to 70 times enhancement of H-2 production is achieved on Cs2AgBiBr6 photocatalyst with the introduction of Cu2+/Cu+ redox couple. (C) 2022 Published by Elsevier Inc.
引用
收藏
页码:509 / 516
页数:8
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