化学
电解质
钴
析氧
碲化物
金属
无机化学
氧气
对偶(语法数字)
兴奋剂
电化学
物理化学
电极
有机化学
光电子学
艺术
文学类
物理
作者
Xiaoxiao Jing,Jinyuan Dong,Yuguang Mao,Lingyan Zhou,Jiabao Ding,Huilong Dong,Linjuan Zhang,Yuxuan Zhang,Weifeng Zhang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-07-01
卷期号:63 (28): 12764-12773
被引量:9
标识
DOI:10.1021/acs.inorgchem.4c00921
摘要
Cobalt (Co)-based materials have been widely investigated as hopeful noble-metal-free alternatives for the oxygen evolution reaction (OER) in alkaline electrolytes, which is crucial for generating hydrogen by water electrolysis. Herein, cobalt-based telluride particles with good electronic conductivity as anodic electrocatalysts were prepared under vacuum by the solid-state strategy, which display remarkable activities toward the OER. Nickel (Ni) and iron (Fe) codoped cobalt telluride (NiFe-CoTe) exhibits an overpotential of 321 mV to achieve a current density of 10 mA cm-2 and a Tafel slope of 51.8 mV dec-1, outperforming the performances of CoTe, CoTe2, and IrO2. According to the DFT calculation, the adsorbed hydroxyl-assisted adsorbate evolution mechanism was proposed for the OER process of NiFe-CoTe, which reveals the synergetic effect toward OER induced by codoping of the Ni and Fe atoms. This work proposes a rational strategy to prepare cobalt-based tellurides as efficient OER catalysts in alkaline electrolytes, providing a new strategy to prepare and regulate metal-based tellurides for catalysis and beyond.
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