Simultaneously Tuning Charge Separation and Surface Reaction Kinetics on ZnIn2S4 Photoanode by P-Doping for Highly Efficient Photoelectrochemical Water Splitting and Urea Oxidation

被引:1
|
作者
Sun, Jiamin [1 ]
Tang, Ling [1 ]
Li, Chenglong [1 ]
Quan, Jingjing [1 ]
Xu, Li [1 ]
Ning, Xingming [1 ]
Chen, Pei [1 ]
Weng, Qiang [1 ]
An, Zhongwei [1 ]
Chen, Xinbing [1 ]
机构
[1] Shaanxi Normal Univ, Sch Mat Sci & Engn, Key Lab Appl Surface & Colloid Chem MOE, Shaanxi Key Lab Adv Energy Devices,Shaanxi Engn La, Xian 710119, Peoples R China
基金
中国国家自然科学基金;
关键词
charge recombination; sulfur vacancies; element doping; charge transfer; photoelectrochemical;
D O I
10.3390/separations11090268
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
ZnIn2S4 nanosheets are a promising photoanode for driving photoelectrochemical (PEC) hydrogen fuel production; nevertheless, poor charge separation and sluggish surface reaction kinetics hinder its PEC performance to an extreme degree. Herein, a facile element doping strategy (i.e., P element) was developed to obtain the desired photoanode. As a result, the ZnIn2S4-P (ZIS-P-5) photoanode exhibits a remarkable photocurrent density of 1.66 mA cm(-2) at 1.23 V versus a reversible hydrogen electrode (V-RHE) and a much lower onset potential of 0.12 V vs. RHE for water oxidation. Careful electrochemical analysis confirms that the P doping and sulfur vacancies (Sv) not only facilitate the hole transfer, but also boost surface reaction kinetics. Finally, the "killing two birds with one stone" goal can be achieved. Moreover, the optimized photoanode also presents high PEC performance for urea oxidation, obtaining a photocurrent density of 4.13 mA cm(-2) at 1.23 V vs. RHE. This work provides an eco-friendly, simple and effective method to realize highly efficient solar-to-hydrogen conversion.
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页数:12
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