电解
尿素
催化作用
无机化学
材料科学
碳纤维
煅烧
离解(化学)
制氢
解吸
电流密度
化学工程
吸附
化学
电解质
物理化学
有机化学
复合材料
电极
工程类
物理
复合数
量子力学
作者
Guangfu Qian,Jinli Chen,Wenjie Jiang,Tianqi Yu,Kexin Tan,Shibin Yin
摘要
Abstract Exploiting efficient urea oxidation reaction (UOR) and hydrogen evolution reaction (HER) catalysts are significant for energy‐saving H 2 production through urea‐assisted water electrolysis, but it is still challenging. Herein, carbon‐encapsulated CoNi coupled with CoNiMoO (CoNi@CN‐CoNiMoO) is prepared by solvothermal method and calcination to enhance the activity/stability of urea‐assisted water electrolysis at large current density. It exhibits good activity for UOR ( E 10/1,000 = 1.29/1.40 V) and HER ( E −10/−1000 = −45/−245 mV) in 1.0 M KOH + 0.5 M urea solution. For the UOR||HER system, CoNi@CN‐CoNiMoO only needs 1.58 V at 500 mA cm −2 and shows good stability. Density functional theory calculation suggests that the strong electronic interaction at the interface between NiCo alloy and N‐doping‐carbon layers can optimize the adsorption/desorption energy of UOR/HER intermediates and accelerate the water dissociation, which can expedite urea decomposition and Volmer step, thus increasing the UOR and HER activity, respectively. This work provides a new solution to design UOR/HER catalysts for H 2 production through urea‐assisted water electrolysis.
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