Z-scheme transition metal bridge of Co9S8/Cd/CdS tubular heterostructure for enhanced photocatalytic hydrogen evolution

被引:151
作者
Zhang, Tianxi [1 ]
Meng, Fanlu [2 ]
Cheng, Yin [2 ]
Dewangan, Nikita [1 ]
Ho, Ghim Wei [2 ,3 ]
Kawi, Sibudjing [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117585, Singapore
[2] Natl Univ Singapore, Dept Elect & Comp Engn, 4 Engn Dr 3, Singapore 117583, Singapore
[3] ASTAR, Inst Mat Res & Engn, 3 Res Link, Singapore 117602, Singapore
基金
新加坡国家研究基金会;
关键词
Cadmium sulfide; Cobalt sulfide; Photocatalytic H(2)evolution; Light absorption; Charge transfer;
D O I
10.1016/j.apcatb.2020.119853
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
Narrow band gap semiconductors heterojunction with superior coupling and composition matching can enhance light absorption, reduce carrier recombination and increase redox activity. Here, we report Co9S8/Cd/CdS Z-scheme type heterojunctions with hierarchical tubular heterostructure and inexpensive transition metallic electronic bridge between two distinct semiconductors by a simultaneous immobilization and in-situ reduction strategy. The designed heterostructure greatly promotes the redox activity owing to high-density catalytic sites, excellent visible light capture by small band gap Co9S8/CdS and hollow framework in conjunction with fast charge separation and smooth transfer through intermediary conductive Cd. The optimized photocatalyst exhibits a hydrogen generation rate up to 10.42 mu mol h(-1) without obvious drop in performance over multiple cycles. The structural design, matching tandem constituent and continuous phase mediator are the pivotal factors to engender an efficient solid-state Z-scheme photocatalysis. The facile synthetic approach and noble metal free tandem structure of this work provide alternative avenues for the development of heterojunction photocatalysts for efficient solar-to-chemical conversion.
引用
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页数:8
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