偏钒酸铵
化学计量学
材料科学
钒
析氧
表面光电压
表面改性
氧气
半导体
化学物理
涂层
化学工程
纳米技术
光电子学
电极
化学
冶金
电化学
物理化学
物理
工程类
量子力学
有机化学
光谱学
作者
Qingjie Wang,Zeyuan Wang,Nan Liao,Salvador Montilla-Verdú,Maxime Contreras,Néstor Guijarro,Jingshan Luo
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-06-11
卷期号:9 (7): 3308-3315
被引量:12
标识
DOI:10.1021/acsenergylett.4c01240
摘要
Altering the surface stoichiometry of semiconductor electrodes is known to affect the photoelectrochemical (PEC) response. To date, several reports have hinted at the influence of the surface Bi:V ratio on the solar water oxidation performance of BiVO4 photoanodes, but only a handful of strategies have been reported to afford tuning of such surface stoichiometry, while a comprehensive understanding at an atomic level of the role of the surface termination remains elusive. Herein, we report a new methodology that modulates the surface Bi:V ratio and maximizes the PEC performance toward the oxygen evolution reaction (OER). The presence of ammonium metavanadate drastically reduces the surface recombination while improving the charge separation. Detailed characterization revealed that this treatment filled the native surface vanadium vacancies, which usually act as recombination centers, while inducing a significant increase in the density of oxygen vacancies, which reinforced the built-in electric field that drives the charge separation. Interestingly, coating with NiFeOx improves, especially, the charge separation in surface V-modified BiVO4. Results suggest that the V-modified surface termination altered the surface energetics of BiVO4, leading to an improved band alignment across the interface. Overall, these results provide a new platform to modulate the surface stoichiometry of BiVO4 thin films while shedding new light on the mechanisms by which the surface termination governs the PEC response.
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