Electron transfer dynamics and enhanced H2 production activity of hydrangea-like BiOBr/Bi2S3-based photocatalysts with Cu-complex as a redox mediator

被引:21
作者
Chang, Chi-Jung [1 ]
Huang, Chieh-Lin [1 ]
Yu, Yuan-Hsiang [2 ]
Teng, Ming-Chun [1 ]
Chiang, Chao-Lung [3 ]
Lin, Yan-Gu [1 ]
机构
[1] Feng Chia Univ, Dept Chem Engn, 100 Wenhwa Rd, Taichung 40724, Taiwan
[2] Fu Jen Catholic Univ, Dept Chem, New Taipei 24205, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
关键词
Photocatalyst; Hydrogen production; BiOBr/Bi2S3; X-ray absorption-spectra; Complex; HYDROGEN-PRODUCTION; COMPOSITE; BIOBR; HETEROJUNCTION; CONSTRUCTION; DEGRADATION; ULTRATHIN; CATALYST; SPHERES; MIMICS;
D O I
10.1016/j.apsusc.2021.151870
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
A composite photocatalyst consisting of the BiOBr/Bi2S3 heterojunction and a Cu complex exhibited high H-2 production activity through an efficient transport of charge by redox couple Cu(II)/Cu(I) of the complex. BiOBr was prepared by a microwave solvothermal method. Then, the BiOBr/Bi2S3 composite was prepared as a heterojunction photocatalyst by an ion-exchange process. The copper complex was then introduced as a co-catalyst or a redox mediator. The morphology, crystal properties, optical properties, surface chemistry, photocurrent response, and photocatalytic activity of these BiOBr/Bi2S3/copper complex composites were investigated. The formation of a BiOBr/Bi2S3 heterojunction and the introduction of Cu complex improved the performance of the photocatalysts. For the first time, operando X-ray absorption spectra were recorded in situ to unveil the local interaction at the reactant-photocatalyst interface toward the photocatalysis reaction of BiOBr/Bi2S3-Cu complex photocatalyst in the sacrificial agent solution (Na2S, Na2SO3).
引用
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页数:12
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