Highly active FexCo1-xP cocatalysts modified CdS for photocatalytic hydrogen production

被引:21
作者
Zhang, Jun [1 ]
Zhao, Qi [2 ,3 ]
Zhang, Jinxing [1 ]
Shi, Ying [1 ]
Huang, Cunping [4 ]
Xia, Ligang [1 ]
Wu, Qiang [1 ]
Yao, Weifeng [1 ,5 ]
机构
[1] Shanghai Univ Elect Power, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, Shanghai, Peoples R China
[2] City Univ Hong Kong, Ctr Super Diamond & Adv Films COSDAF, Kowloon, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[3] City Univ Hong Kong, Dept Chem, Kowloon, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[4] Fed Aviat Adm William J Hughes Tech Ctr, Aviat Fuels Res Lab, Atlantic City, NJ USA
[5] Shanghai Inst Pollut Control & Ecol Secur, Shanghai, Peoples R China
基金
上海市自然科学基金;
关键词
Photocatalytic hydrogen production; Non-noble-metal photocatalysts; Ternary FexCo1-xP nanoparticles; Phosphide cocatalysts; EVOLUTION REACTION; NANOWIRES; CATALYST; COMPLEX; ARRAY;
D O I
10.1016/j.ijhydene.2020.06.090
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
In this paper, we report a ternary FexCo1-xP co-catalyst, which can greatly improve the photocatalytic performance of CdS photocatalyst for hydrogen production under visible light irradiation. The high efficiency of ternary FexCo1-xP loaded CdS is mainly due to the high electrochemical activity and efficient charge transfer between FexCo1-xP cocatalyst and CdS. Experimental results have shown that the substitution of Fe ions for some Co ions in CoP can change the electrochemical properties of FexCo1-xP. The electrocatalytic performance of FexCo1-xP and the photocatalytic activity of FexCo1- P-x/CdS are both dependent on the molar concentration x of Fe. When x = 0.4 the hydrogen generation rate (18.27 mmol h(-1) g(-1)) and the quantum efficiency (50.6% at 420 nm) for 0.5 wt% Fe0.4Co0.6P/CdS photocatalyst is 5.85 times higher than that of pure CdS and 1.35 times higher than that of 0.5 wt% CoP/CdS. This new noble-metal-free FexCo1-xP cocatalyst is beneficial for the solar hydrogen economy. (c) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:22722 / 22731
页数:10
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