催化作用
贵金属
电解质
化学
制氢
基质(水族馆)
吸附
电催化剂
氢
无机化学
化学工程
X射线光电子能谱
密度泛函理论
电子转移
材料科学
物理化学
有机化学
计算化学
电化学
地质学
工程类
电极
海洋学
作者
Peitao Zhao,Yanling Zhao,Huagen Liang,Xueping Song,Bo Yu,Fang Liu,Arthur J. Ragauskas,Cuiping Wang
标识
DOI:10.1016/j.cej.2023.143140
摘要
Carbon substrate support is a promising approach to facilitate catalytic activity of non-noble metal catalysts in hydrogen evolution reactions (HER). Here, we report a waste-derived electrocatalyst P-CoNiO2@NC synthesized under mild condition. It exhibits outstanding HER performance in both acid (η10 = 64.6 mV) and alkaline (η10 = 96.4 mV) condition with good stability. Especially, it begins to outperform commercial Pt/C when the current density is over 74 mA/cm2 in acid electrolyte and 29 mA/cm2 in alkaline electrolyte. Moreover, the waste-derived carbon substrate could effectively promote HER activity of other dual 3d TMOs such as Fe and Co, Fe and Ni. The improved HER activity originates from electron transfer, electronic structure adjustment and optimization of intermediates adsorption according to X -ray photoelectron spectroscopy and density functional theory calculations. This work provides a new insight for converting wastes into value-added products and a sustainable and friendly strategy to facilitate hydrogen energy production.
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