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通过夹入氧空位层抑制BiVO||NiOOH结处的光生电荷复合以实现高效光电化学水氧化。

Suppressing photoinduced charge recombination at the BiVO||NiOOH junction by sandwiching an oxygen vacancy layer for efficient photoelectrochemical water oxidation.

作者信息

Peng Yong, Du Minshu, Zou Xingli, Jia Guohua, Permatasari Santoso Shella, Peng Xiang, Niu Wenxin, Yuan Mingjian, Hsu Hsien-Yi

机构信息

School of Energy and Environment, Department of Materials Science and Engineering, City University of Hong Kong, Kowloon Tong, Hong Kong, China; Shenzhen Research Institute of City University of Hong Kong, Shenzhen 518057, China.

School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, Shaanxi 710072, China.

出版信息

J Colloid Interface Sci. 2022 Feb 15;608(Pt 2):1116-1125. doi: 10.1016/j.jcis.2021.10.063. Epub 2021 Oct 23.

Abstract

Nickel oxyhydroxide (NiOOH) is regarded as one of the promising cocatalysts to enhance the catalytic performance of photoanodes but suffers from serious interfacial charge-carrier recombination at the photoanode||NiOOH interface. In this work, surface-engineered BiVO photoanodes are fabricated by sandwiching an oxygen vacancy (O) interlayer between BiVO and NiOOH. The surface O interlayer is introduced on BiVO by a chemical reduction treatment using a mild reducing agent, sodium hypophosphite. The induced O can alleviate the interfacial charge-carrier recombination at the BiVO4||NiOOH junction, resulting in efficient charge separation and transfer efficiencies, while an outer NiOOH layer is coated to prevent the O layer from degradation. As a result, the as-prepared NiOOH-P-BiVO photoanode exhibits a high photocurrent density of 3.2 mA cm at 1.23 V vs. RHE under the irradiation of 100 mW/cm AM 1.5G simulated sunlight, in comparison to those of bare BiVO, P-BiVO and NiOOH-BiVO photoanodes (1.1, 2.1 and 2.3 mA cm, respectively). In addition to the superior photoactivity, the 5-h amperometric measurements illustrate improved stability of the surface-engineered NiOOH-P-BiVO photoanode. Our work showcases the feasibility of combining cocatalysts with O, for improved photoactivity and stability of photoelectrodes.

摘要

羟基氧化镍(NiOOH)被认为是增强光阳极催化性能的有前景的助催化剂之一,但在光阳极||NiOOH界面处存在严重的界面电荷载流子复合问题。在这项工作中,通过在BiVO和NiOOH之间夹入一个氧空位(O)中间层来制备表面工程化的BiVO光阳极。使用温和的还原剂次磷酸钠通过化学还原处理在BiVO上引入表面O中间层。诱导产生的O可以减轻BiVO4||NiOOH结处的界面电荷载流子复合,从而实现高效的电荷分离和转移效率,同时涂覆一层外部NiOOH层以防止O层降解。结果,所制备的NiOOH-P-BiVO光阳极在100 mW/cm² AM 1.5G模拟太阳光照射下,相对于可逆氢电极(RHE)在1.23 V时表现出3.2 mA/cm²的高光电流密度,相比之下,裸BiVO、P-BiVO和NiOOH-BiVO光阳极的光电流密度分别为1.1、2.1和2.3 mA/cm²。除了优异的光活性外,5小时的安培测量表明表面工程化的NiOOH-P-BiVO光阳极的稳定性得到了提高。我们的工作展示了将助催化剂与O相结合以提高光电极的光活性和稳定性的可行性。

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