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Activity and Stability Boosting of an Oxygen‐Vacancy‐Rich BiVO 4 Photoanode by NiFe‐MOFs Thin Layer for Water Oxidation
Author(s) -
Pan JinBo,
Wang BingHao,
Wang JinBo,
Ding HongZhi,
Zhou Wei,
Liu Xuan,
Zhang JinRong,
Shen Sheng,
Guo JunKang,
Chen Lang,
Au ChakTong,
Jiang LiLong,
Yin ShuangFeng
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202012550
Subject(s) - photocurrent , oxygen evolution , materials science , chemical engineering , oxidizing agent , oxygen , catalysis , water splitting , thin film , layer (electronics) , metal , nanotechnology , chemistry , photocatalysis , optoelectronics , metallurgy , electrochemistry , electrode , biochemistry , engineering , organic chemistry
The introduction of oxygen vacancies (Ov) has been regarded as an effective method to enhance the catalytic performance of photoanodes in oxygen evolution reaction (OER). However, their stability under highly oxidizing environment is questionable but was rarely studied. Herein, NiFe‐metal–organic framework (NiFe‐MOFs) was conformally coated on oxygen‐vacancy‐rich BiVO 4 (Ov‐BiVO 4 ) as the protective layer and cocatalyst, forming a core–shell structure with caffeic acid as bridging agent. The as‐synthesized Ov‐BiVO 4 @NiFe‐MOFs exhibits enhanced stability and a remarkable photocurrent density of 5.3±0.15 mA cm −2 at 1.23 V (vs. RHE). The reduced coordination number of Ni(Fe)‐O and elevated valence state of Ni(Fe) in NiFe‐MOFs layer greatly bolster OER, and the shifting of oxygen evolution sites from Ov‐BiVO 4 to NiFe‐MOFs promotes Ov stabilization. Ovs can be effectively preserved by the coating of a thin NiFe‐MOFs layer, leading to a photoanode of enhanced photocurrent and stability.