过电位
分解水
材料科学
双功能
电极
图层(电子)
催化作用
化学物理
气泡
电极电位
析氧
纳米技术
化学工程
双功能催化剂
电流(流体)
分层(地质)
可逆氢电极
电流密度
分子动力学
电化学
化学
标准电极电位
压力(语言学)
作者
Qian Niu,Fei-Yue Gao,Xiaojie Sun,Hao Liu,Yao Zheng,Shi-Zhang Qiao
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-12-24
卷期号:16 (2): 1303-1311
标识
DOI:10.1021/acscatal.5c07090
摘要
During water electrolysis, overpotential can trigger side reactions that lead to electrode degradation. This issue becomes more pronounced in ampere-level electrolyzers, where intense bubble evolution induces local electrochemical overloading, resulting in elevated local overpotentials. Moreover, stress fluctuations arising from intense bubble evolution impose delamination forces on the overpotential-damaged catalyst layer, thereby further exacerbating electrode degradation. To address these coupled issues, we developed a self-adaptive electrode featuring an engineered catalyst–substrate interface. This self-adaptivity allows the catalyst layer to rapidly modulate its state in response to the elevated overpotential, thereby maintaining a stable performance. Meanwhile, the engineered catalyst–substrate interface suppresses catalyst layer delamination, ensuring structural stability. At the molecular level, such a self-adaptive transformation arises from a locally disordered coordination environment, in which Ni centers are coordinated by different ligands. Beyond self-adaptivity, this locally disordered coordination environment also endows the catalyst layer with superior bifunctional activity toward overall water splitting, surpassing that of conventionally ordered Ni–O–M or Ni–Ni configurations. As a result, the as-prepared electrode demonstrates practical potential under both intermittent and continuous operation, sustaining a stable performance at 0.5 A cm–2 for up to 3000 h. Even under a higher current density of 1.5 A cm–2, considerable stability is retained.
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