Coupling of self-healing atomic layer CoAl-LDH onto Mo:BiVO4 photoanode for fast surface charge transfer toward stable and high-performance water splitting

被引:37
|
作者
Zhong, Yi [1 ]
Wu, Chenglin [1 ]
Jia, Xiaofang
Sun, Sijia [1 ]
Chen, Daimei [1 ]
Yao, Wenqing [2 ]
Ding, Hao [1 ]
Zhang, Junying
Ma, Tianyi [3 ,4 ]
机构
[1] China Univ Geosci, Engn Res Ctr, Sch Mat Sci & Technol, Minist Educ Geol Carbon Storage & Low Carbon Util, Beijing 100083, Peoples R China
[2] Beihang Univ, Sch Phys, Beijing 100191, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[4] RMIT Univ, Sch Sci, Melbourne, Vic 3000, Australia
基金
中国国家自然科学基金;
关键词
BiVO4; Ultrathin CoAl-LDH; Charge separation and transfer; OER reaction; OXYGEN EVOLUTION CATALYSTS; BIVO4; PHOTOANODES; DEPOSITION; SEPARATION; OXIDATION; KINETICS;
D O I
10.1016/j.cej.2023.142893
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Herein, Mo doping BiVO4/ultrathin-CoAl-LDH (Mo:BVO/CoAl-LDH-u) photoanode with self-healing property is firstly designed by using the atomic layer CoAl-LDH as cocatalyst to modify Mo:BVO through a simple dipping coating method. The Mo:BVO/CoAl-LDH-u photoanode presents a nearly 100% surface charge separation effi-ciency and extremely outstanding photocurrent density of 5.8 mA/cm2 at 1.23 V vs. reversible hydrogen elec-trode (VRHE) without any scavengers. The CoAl-LDH-u intimately contacted with BiVO4 photoanode significantly improves the surface charge transfer efficiency by passivating the surface state and rapidly extracting holes from Mo:BiVO4, and promotes the oxygen evolution reaction (OER) rate by conversion of Co2+ to Co3+ species. Interestingly, the Mo:BVO/CoAl-LDH-u photoanode has the self-healing peculiarity, due to the easy reparation of oxygen defects in CoAl-LDH-u by the cycle of Co3+/Co2+, and hence the photoelectrochemical (PEC) perfor-mance can be restored naturally in the air. This work presents a facile approach to fabricate high-efficiency BiVO4 photoelectrode for accelerating the PEC water splitting.
引用
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页数:11
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