材料科学
金属
氢
电流(流体)
安培
电流密度
电催化剂
化学工程
纳米技术
无机化学
化学物理
冶金
电化学
电极
热力学
物理化学
化学
有机化学
工程类
物理
量子力学
作者
Hao Xiong,Rong Zhuang,Bowen Cheng,Dengke Liu,Yuxuan Du,Hongyue Wang,Ye Liu,Fei Xu,Hongqiang Wang
标识
DOI:10.1002/aenm.202404077
摘要
Abstract Electrocatalytic water splitting is an attractive approach for large‐scale hydrogen generation, critical for global carbon neutrality. However, the prevalent commercialized alkaline water electrolysis is generally conducted at low current densities due to sluggish kinetics and high overpotential, severely hampering high‐efficiency hydrogen production. Exploration of hydrogen evolution reaction (HER) electrocatalysts that can reliably operate at ampere‐level current densities under low overpotentials is thus a primary challenge. In contrast to extensive studies using powdery electrocatalysts, the self‐supported metallic catalytic cathode has become a burgeoning direction toward ampere‐level current densities, owing to their integrated design with intensive interfacial binding, high conductivity and mechanical stability with industrial tolerance/adaption. Recent years have witnessed tremendous research advances in designing self‐supported metallic electrocatalysts. Therefore, this flourishing area is specially summarized. Beginning with the introduction to the theory and mechanism of alkaline HER, the engineering strategies on self‐supported metallic electrodes are systematically summarized, including metal and alloy construction, heterostructure engineering, doping manipulation, and surface design. Meanwhile, particular emphasis is focused on the relationship between structure, activity, and stability under ampere‐level HER. Finally, the existing challenges, requirements of industrial‐scale application, and future direction for designing electrocatalysts are summarized, aiming to provide a better solution for industrial alkaline water electrolysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI