光电流
双金属片
析氧
磷化物
催化作用
材料科学
钴
电解质
分解水
化学工程
镍
纳米技术
金属
化学
电极
电化学
光电子学
物理化学
工程类
冶金
生物化学
光催化
作者
Junyi Cui,Mátyás Dabóczi,Zhenyu Cui,Mengjun Gong,Joseph M. Flitcroft,Jonathan M. Skelton,Stephen C. Parker,Salvador Eslava
出处
期刊:Small
[Wiley]
日期:2023-10-06
卷期号:20 (7): e2306757-e2306757
被引量:21
标识
DOI:10.1002/smll.202306757
摘要
Abstract Achieving highly performant photoanodes for oxygen evolution is key to developing photoelectrochemical devices for solar water splitting. In this work, BiVO 4 photoanodes are enhanced with a series of core–shell structured bimetallic nickel‐cobalt phosphides (MPs), and key insights into the role of co‐catalysts are provided. The best BiVO 4 /Ni 1.5 Co 0.5 P and BiVO 4 /Ni 0.5 Co 1.5 P photoanodes achieve a 3.5‐fold increase in photocurrent compared with bare BiVO 4 . It is discovered that this enhanced performance arises from a synergy between work function, catalytic activity, and capacitive ability of the MPs. Distribution of relaxation times analysis reveals that the contact between the MPs, BiVO 4 , and the electrolyte gives rise to three routes for hole injection into the electrolyte, all of which are significantly improved by the presence of a second metal cation in the co‐catalyst. Kinetic studies demonstrate that the significantly improved interfacial charge injection is due to a lower charge‐transfer resistance, enhanced oxygen‐evolution reaction kinetics, and larger surface hole concentrations, providing deeper insights into the carrier dynamics in these photoanode/co‐catalyst systems for their rational design.
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