Plasma Treatment Induced Oxygen Vacancies and N Doping in the BiVO4 Photoanode toward Improved Charge Transfer and Facilitated Water Oxidation

被引:3
作者
Wang, Anchen [1 ,2 ]
Chen, Yaru [1 ,2 ]
Liu, Xuefeng [1 ,2 ]
Li, Ru [1 ,2 ]
Zhang, Ziyi [1 ,2 ]
Zhang, Fuyang [1 ,2 ]
Cao, Dapeng [1 ,2 ]
Gao, Zhiqiang [1 ,2 ]
Mi, Baoxiu [1 ,2 ]
机构
[1] Nanjing Univ Posts & Telecommun, State Key Lab Organ Elect & Informat Displays, Nanjing 210023, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Inst Adv Mat IAM, Nanjing 210023, Peoples R China
关键词
photoelectrochemical; BiVO4; plasma; N doping; oxygen vacancies; TOTAL-ENERGY CALCULATIONS; PERFORMANCE;
D O I
10.1021/acsami.4c19768
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
BiVO4 is a promising material candidate for photoelectrochemical (PEC) water splitting. However, the BiVO4 photoanode commonly suffers from poor charge carrier transport and sluggish water oxidation kinetics, which limits its PEC performance. Nitrogen (N) doping has been proven as an effective approach to improve electric conductivity and accelerate the water oxidation kinetics of the BiVO4 photoanode. Nevertheless, a simple and mild method for introducing a N dopant into BiVO4 remains lacking. Herein, N-2 plasma treatment is employed as a post-treatment method to achieve effective N doping and induce oxygen vacancies (O-V) in BiVO4 photoanodes. This treatment significantly improves the charge transfer and accelerates the kinetics of water oxidation. The photocurrent density of the N-2-plasma-treated BiVO4 photoanode reaches 1.39 mA cm(-2) at 1.23 V versus the reversible hydrogen electrode (RHE), which surpasses that of pristine BiVO4 (0.30 mA cm(-2)) by a substantial margin. This work provides a facile room-temperature N-2 plasma approach for the simultaneous introduction of N doping and O-V into photoanodes, achieving enhanced charge transport and accelerated water oxidation kinetics.
引用
收藏
页码:12064 / 12073
页数:10
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