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通过原位催化剂调谐实现用于析氧催化剂的氢氧化镍/钒酸铋光阳极的长期光稳定性

Towards Long-Term Photostability of Nickel Hydroxide/BiVO Photoanodes for Oxygen Evolution Catalysts via In Situ Catalyst Tuning.

作者信息

Gao Rui-Ting, He Dan, Wu Lijun, Hu Kan, Liu Xianhu, Su Yiguo, Wang Lei

机构信息

School of Chemistry and Chemical Engineering & Inner Mongolia Engineering and Technology Research Center for Catalytic Conversion and Utilization of Carbon Resource Molecules, Inner Mongolia University, 235 West University Street, Hohhot, 010021, China.

Key Laboratory of Materials Processing and Mold, Ministry of Education, Zhengzhou University, Zhengzhou, 450002, China.

出版信息

Angew Chem Int Ed Engl. 2020 Apr 6;59(15):6213-6218. doi: 10.1002/anie.201915671. Epub 2020 Feb 12.

Abstract

Increasing long-term photostability of BiVO photoelectrode is an important issue for solar water splitting. The NiOOH oxygen evolution catalyst (OEC) has fast water oxidation kinetics compared to the FeOOH OEC. However, it generally shows a lower photoresponse and poor stability because of the more substantial interface recombination at the NiOOH/BiVO junction. Herein, we utilize a plasma etching approach to reduce both interface/surface recombination at NiOOH/BiVO and NiOOH/electrolyte junctions. Further, adding Fe into the borate buffer electrolyte alleviates the active but unstable character of etched-NiOOH/BiVO , leading to an outstanding oxygen evolution over 200 h. The improved charge transfer and photostability can be attributed to the active defects and a mixture of NiOOH/NiO/Ni in OEC induced by plasma etching. Metallic Ni acts as the ion source for the in situ generation of the NiFe OEC over long-term durability.

摘要

提高BiVO光电极的长期光稳定性是太阳能水分解的一个重要问题。与FeOOH析氧催化剂(OEC)相比,NiOOH析氧催化剂具有更快的水氧化动力学。然而,由于NiOOH/BiVO结处更严重的界面复合,它通常表现出较低的光响应和较差的稳定性。在此,我们采用等离子体蚀刻方法来减少NiOOH/BiVO和NiOOH/电解质结处的界面/表面复合。此外,在硼酸盐缓冲电解质中添加铁可减轻蚀刻后的NiOOH/BiVO的活性但不稳定的特性,从而实现超过200小时的出色析氧性能。电荷转移和光稳定性的提高可归因于等离子体蚀刻在OEC中诱导产生的活性缺陷以及NiOOH/NiO/Ni的混合物。金属Ni作为原位生成具有长期耐久性的NiFe OEC的离子源。

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