Peng Yong, Du Minshu, Zou Xingli, Jia Guohua, Permatasari Santoso Shella, Peng Xiang, Niu Wenxin, Yuan Mingjian, Hsu Hsien-Yi
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.
J Colloid Interface Sci. 2022 Feb 15;608(Pt 2):1116-1125. doi: 10.1016/j.jcis.2021.10.063. Epub 2021 Oct 23.
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.
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。