光电流
材料科学
酞菁
吸收(声学)
光化学
电子转移
半导体
电解质
析氧
分解水
载流子
铜
化学工程
纳米技术
电化学
光电子学
催化作用
光催化
电极
化学
物理化学
有机化学
工程类
复合材料
冶金
作者
Mengmeng Fan,Ziyang Tao,Qiang Zhao,Jinping Li,Guang Liu,Chuan Zhao
标识
DOI:10.1002/admt.202201835
摘要
Abstract The limited performance of BiVO 4 for photoelectrochemical (PEC) water splitting is currently restricted to limited light absorption and rapid carrier recombination. Herein, molecular copper phthalocyanine (CuPc) and FeOOH co‐integrated BiVO 4 photoanode are prepared by a simple dipping method and demonstrate significantly improved PEC water oxidation activities. The optimized BiVO 4 /CuPc/FeOOH photoanode attains a photocurrent density of 3.67 mA cm −2 at 1.23 V RHE and maintains the PEC performance without significant decay over a long period of time. In addition, significant increase of charge separation efficiency and decrease of charge transfer resistance of the BiVO 4 /CuPc/FeOOH photoanode also demonstrate that the hole–electron transfer and water oxidation reaction are promoted. It is found that CuPc has a similar structure to photosensitized chlorophyll, which can broaden the absorption range of BiVO 4 in the visible region and improve the photo‐generated carriers transfer in the semiconductor. Whereas the FeOOH layer can rapidly transfer the photo‐generated holes into the electrolyte to participate in the water oxidation reaction as oxygen evolution cocatalyst. This work provides a feasible pathway to improve the PEC water splitting performance of BiVO 4 by increasing light absorption and accelerating carrier transfer.
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