电流(流体)
氢
制氢
化学
比例(比率)
生产(经济)
材料科学
无机化学
化学工程
热力学
物理
有机化学
工程类
宏观经济学
量子力学
经济
作者
Qiansen Wang,Wenhui Ling,Yang Lu,Hao Zhao,Qingqing Cheng,Yifan Huang,Lianhai Zu,Bo Yang,Hui Yang
标识
DOI:10.1002/ange.202506619
摘要
Pt single‐atom (SA) catalysts are considered ideal cathodic materials for PEM water electrolysis (PEMWE) due to their excellent atom utilization and tunable local coordination environment, yet their durability for practical applications remains unresolved challenge. Herein we report the Pt SAs, synergistically stabilized by Cl‐ligand and Ru nanoparticles, exhibit both high activity and durability for hydrogen evolution reaction. A key finding is that dynamically evolved Pt‐Cl‐Pt coordination structure protects Pt SAs against aggregation. Theoretical analysis reveals the unique electronic structure of Pt SAs is finely tuned through the synergistic role of Ru and Cl, resulting in a notable stabilization of Pt SAs. PEMWE with such a catalyst at an ultra‐low Pt loading delivers a cell voltage of only 1.66 V at a current density of 1.0 A cm‐2, while maintaining the outstanding electrocatalytic and structural stability of the Pt‐Cl‐Pt coordination over 1000 h, thus providing an application potential of SA catalysts.
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