电催化剂
析氧
材料科学
制氢
分解水
催化作用
电解
海水
化学工程
氮化物
电解水
碱性水电解
镍
无机化学
纳米技术
冶金
电极
化学
电化学
光催化
有机化学
物理化学
工程类
地质学
海洋学
电解质
图层(电子)
作者
Huashuai Hu,Xunlu Wang,Zhaorui Zhang,Jiahao Liu,Xiaohui Yan,Xiaoli Wang,Jiacheng Wang,J. Paul Attfield,Minghui Yang
标识
DOI:10.1002/adma.202415421
摘要
Abstract Seawater electrolysis under alkaline conditions is a crucial technology for sustainable hydrogen production. However, achieving the long‐term stability of the electrocatalyst remains a significant challenge. In this study, it is demonstrated that surface reconstruction of a transition metal nitride (TMN) can be used to develop a highly stable oxygen evolution reaction (OER) electrocatalyst. Rapid introduction of phosphate groups (PO 4 3− ) accelerates the in situ surface reconstruction of Ni 3 FeN, generating a catalyst, with a conductive nitride core and Cl − ‐resistant hydroxide shell that demonstrates outstanding performance, maintaining stability for over 2500 h at 1 A cm −2 current density in alkaline seawater. In situ characterization and density functional theory (DFT) calculations reveal the dynamic evolution of active sites, providing insights into the mechanisms driving long‐term stability. This work not only introduces an efficient approach to TMN‐based catalyst design but also advances the development of durable electrocatalysts for industrial‐scale seawater hydrogen production.
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