电解
电催化剂
双功能
制氢
奥斯特瓦尔德成熟
分解水
无机化学
化学工程
材料科学
催化作用
电化学
碱性水电解
尿素
化学
电极
纳米技术
电解质
光催化
有机化学
物理化学
工程类
作者
Xiao Xu,Yucheng Dong,Fangfang Liu,Hui Wang,Xuyun Wang,Xiaoyuan Li,Jianwei Ren,Rongfang Wang
标识
DOI:10.1016/j.ijhydene.2023.10.234
摘要
Electrochemical urea electrolysis holds great potential for energy-efficient hydrogen production and wastewater treatment. However, developing cost-effective and highly active catalysts remains a challenge. In this study, a novel bifunctional electrocatalyst of Ni–Zn bimetallic nanosheets (ZnO–Ni2P) was synthesized on Ni foam (NF) for efficient urea decomposition in urea-containing wastewater. The results showed that inactive ZnO phase acted as an "electron pump", which facilitated electron redistribution between Ni and P atoms and created localized vacancies of Ni and P cations. This optimized electronic configuration enhanced the kinetics of both the urea oxidation reaction (UOR) and hydrogen evolution reaction (HER). Additionally, a unique particle-porous structure with abundant grain boundaries was achieved through the utilization of the Kirkendall Effect and Ostwald Ripening. In an alkaline urea electrolysis system, the alkaline urea electrolyzer assembled with ZnO–Ni2P/NF sample as both electrodes exhibited a low driving potential of only 1.424 V to achieve a current density of 10 mA cm−2, which outperformed the commercial noble metal-based electrolyzer (RuO2||Pt/C). The results verify that incorporating an inactive phase to manipulate the electronic structure of the active phase can be an effective strategy in developing catalysts for urea electrolysis.
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