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摘要
通过在电镀过程实现P体相掺杂制备P-BiVO4光阳极,P-BiVO4光阳极的起始电位相比于BiVO4光阳极发生明显的阴极位移。在光电化学分解水反应中,P-BiVO4表现出高效的选择性和活性。EIS和UPS测试结果表明,P掺杂能够显著加快光阳极的电荷转移,加速BiVO4光阳极载流子的分离,从而延长了空穴寿命和促使空穴向表面转移,能够有效地提升光电化学分解水的OER动力学。
Abstract
P-BiVO4 photoanode is prepared through P-phase doping during electroplating.The initial potential of P-BiVO4 photoanode shifts significantly compared with that of BiVO4 photoanode.P-BiVO4 exhibits high selectivity and activity in the photoelectrochemical water-splitting reaction.EIS and UPS tests indicate that P doping can significantly accelerate the charge transfer and carrier separation of BiVO4 photoanode,thus extending the hole life and promoting the hole transfer to the surface,and effectively improving the OER kinetics of photoelectrochemical water-splitting.
关键词
钒酸铋
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电催化
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光催化
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分解水
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光电化学
Key words
BiVO4
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electrocatalysis
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photocatalysis
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water splitting
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photoelectrochemical
Author summay
王宇宏(1993-),男,博士,讲师,研究方向为光电化学分解水,wangyuhong@tyust.edu.cn;郭少青(1972-),女,博士,教授,博士生导师,研究方向为能源清洁利用,通讯联系人,guosq@tyust.edu.cn。
磷原子诱导钒酸铋光阳极高效光电化学分解水的研究[J].
现代化工, 2024, 44(11): 165-169 DOI:10.16606/j.cnki.issn0253-4320.2024.11.030