过电位
析氧
分解水
催化作用
电催化剂
双功能
无机化学
化学
海水
碱性水电解
氧化物
电解水
电化学
电解
化学工程
光催化
电极
物理化学
电解质
地质学
有机化学
工程类
海洋学
生物化学
作者
Felix Ofori Boakye,Karim Harrath,Mohammad Tabish,Ghulam Yasin,Kwadwo Asare Owusu,Saira Ajmal,Wenbin Zhang,Haining Zhang,Yang‐Gang Wang,Wei Zhao
标识
DOI:10.1016/j.jallcom.2023.172240
摘要
Designing a highly efficient electrocatalyst to realize overall water splitting is vital, yet identifying the active site remains an ongoing challenge. Herein, the electrochemical in situ surface activation of P@Co/Se2-NW/CC was investigated to understand the enhanced OER activity of P@Co/Se2-NW/CC. The incorporation of phosphorus is thought to increase the vacancies surrounding the Co cations in the initial Co/Se2 and speed up the structural change into "active species" like cobalt oxide/oxyhydroxide. The as-synthesized P@Co/Se2-NW/CC required a low overpotential for OER (η100 = 230 and 280 mV) and HER (η100 = 111 and 132 mV), respectively, in alkaline water and alkaline seawater media. In-situ infrared reflection-absorption spectroscopy (IRRAS) and Post characterization unraveled the existence of surface-bounded Co oxide species on P@Co/Se2-NW/CC after OER catalysis, which is responsible for the enhanced electrocatalytic activity. This study offers a valuable strategy for developing noble-metal-free bifunctional catalysts for efficient hydrogen generation from alkaline seawater and alkaline water electrolysis.
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