过电位
析氧
碲化物
阴极保护
电化学
分解水
催化作用
吸附
化学
材料科学
图层(电子)
化学工程
无机化学
纳米技术
冶金
电极
光催化
工程类
物理化学
有机化学
作者
Peng Guo,Shoufu Cao,Yijin Wang,Xiaoqing Lü,Youzi Zhang,Xu Xin,Xiao Chi,Xiaojiang Yu,Ilhom Tojiboyev,Hadi Salari,Ana Jorge Sobrido,Maria‐Magdalena Titirici,Xuanhua Li
标识
DOI:10.1016/j.apcatb.2022.121355
摘要
Metal tellurides attract recent attention because of their promising applications as effective catalysts for the oxygen evolution reaction (OER). However, inappropriate adsorption energy between OER intermediates and telluride leads to an unsatisfactory electrocatalytic intrinsic activity. Herein, we adopt a unique in-situ cathodic electrochemical activation process to facilitate the surface self-reconstruction to form oxygen vacancy (OV)-rich TeO2 layer onto Fe-doped NiTe (OV@Fe-NiTe). Characterizations and theoretical calculation demonstrate that the presence of the OV-rich TeO2 layer realizes the adjustment of d-band center of the active site that translates into an enhancement of the adsorption of *OOH intermediate and thus the optimization of the OER pathway. Consequently, the OV@Fe-NiTe only requires an ultralow overpotential of 245 mV to drive 100 mA cm-2 in 1 M KOH, 95 mV lower than that of Fe-NiTe, and hence becoming the best water oxidation electrocatalysts amongst recently reported telluride electrocatalysts. This study presents a unique strategy to exploit telluride-based catalysts through electrochemical surface engineering.
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