Rapid charge extraction via hole transfer layer and interfacial coordination bonds on hematite photoanode for efficient photoelectrochemical water oxidation

被引:0
|
作者
Niu H. [1 ]
Gao L. [1 ]
Liu M. [1 ]
Zou Y. [1 ]
Wang J. [1 ]
Hu G. [1 ]
Jin J. [1 ]
机构
[1] State Key Laboratory of Applied Organic Chemistry (SKLAOC), The Key Laboratory of Catalytic Engineering of Gansu Province, Key Laboratory of Advanced Catalysis of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University, Gansu, Lan
基金
中国国家自然科学基金;
关键词
Coordination compound; Hematite photoanode; Hole transfer layer; Interfacial coordination bonds; Photoelectrochemical water oxidation;
D O I
10.1016/j.apcatb.2024.124369
中图分类号
学科分类号
摘要
Enhancing carrier separation and transport efficiency to achieve efficient water oxidation reaction is an important issue in photoelectrochemical (PEC) water splitting field, and introducing hole transfer layer (HTL) is an effective strategy to improve it. However, the difficulty of charge transfer between HTL and oxygen evolution catalyst (OEC) is a problem unresolved. To ameliorate the situation, we choose CoOOH as HTL and the metal–organic coordination compound constructed by 4,5-Imidazoledicarboxylic acid (IA) and Co/Ni ions as OEC. Using the interfacial coordination bonds as carrier transfer channels, the holes were rapidly extracted from HTL to OEC containing abundant active sites and participate in oxidation reaction. In consequence, the unique design results in a photocurrent density of 2.97 times that of α-Fe2O3 at 1.23 VRHE for the IACN/CoOOH/Fe2O3. This study reveals how the advisable design of photoanode promotes interfacial charge transfer and provides a valuable reference for the design of composite photoanode. © 2024 Elsevier B.V.
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