Interfacial and Vacancy Engineering on 3D-Interlocked Anode Catalyst Layer for Achieving Ultralow Voltage in Anion Exchange Membrane Water Electrolyzer

被引:1
作者
Wan, Lei [1 ]
Lin, Dongcheng [1 ]
Liu, Jing [1 ]
Xu, Ziang [1 ]
Xu, Qin [1 ]
Zhen, Yihan [1 ]
Pang, Maobin [1 ]
Wang, Baoguo [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
oxygen evolution reaction; interfacial engineering; vacancy engineering; membrane electrode assembly; anion exchange membrane waterelectrolysis; OXYGEN EVOLUTION; HIGH-PERFORMANCE; HYDROGEN-PRODUCTION; ACTIVE-SITE; NANOPARTICLES;
D O I
10.1021/acsnano.4c03668
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing a high-efficiency and stable anode catalyst layer (CL) is crucial for promoting the practical applications of anion exchange membrane (AEM) water electrolyzers. Herein, a hierarchical nanosheet array composed of oxygen vacancy-enriched CoCrOx nanosheets and dispersed FeNi layered double hydroxide (LDH) is proposed to regulate the electronic structure and increase the electrical conductivity for improving the intrinsic activity of the oxygen evolution reaction (OER). The CoCrOx/NiFe LDH electrodes require an overpotential of 205 mV to achieve a current density of 100 mA cm(-2), and they exhibit long-term stability at 1000 mA cm(-2) over 7000 h. Notably, a breakthrough strategy is introduced in membrane electrode assembly (MEA) fabrication by transferring CoCrOx/NiFe LDH to the surface of an AEM, forming a 3D-interlocked anode CL, significantly reducing the overall cell resistance and enhancing the liquid/gas mass transfer. In AEM water electrolysis, it exhibits an ultralow cell voltage of 1.55 V-cell to achieve a current density of 1.0 A cm(-2) in 1 M KOH, outperforming the state-of-the-art Pt/C//IrO2. This work provides a valuable approach to designing high-efficiency electrocatalysts at the single-cell level for advanced alkaline water electrolysis technologies.
引用
收藏
页码:22901 / 22916
页数:16
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