催化作用
无定形固体
异质结
尿素
材料科学
化学工程
X射线晶体学
结晶学
无机化学
化学
物理化学
有机化学
衍射
光电子学
物理
光学
工程类
作者
Jiawang Li,Jincheng Liu,Chenmeng Jiang,Jiafeng Tian,Lang Gan,Wei Chen,Jincheng Huang,Jing Zhao,Kang Chen,Yanjie Ren,Qiuping Wei
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-05-16
标识
DOI:10.1021/acs.langmuir.5c00422
摘要
Replacing the kinetically slow oxygen evolution reaction (OER) with urea electro-oxidation significantly reduces the energy requirement for electrolysis of water. However, designing and optimizing efficient electrocatalysts for the industrial application of urea oxidation coupled to hydrogen production remains a challenge. Herein, we construct a C/A-NixP/NiOH heterojunction catalyst with actually abundant amorphous/crystalline interfaces for the urea oxidation reaction (UOR) by an interfacial-sequential treatment method of electrodeposition and low-temperature gas-phase phosphatization on carbon cloth (CC). Remarkably, in UOR, the C/A-NixP/NiOH catalyst required only 1.332 V to reach a current density of 10 mA cm-2 with negligible potential decay over 12 h. The excellent performance is attributed to the synergistic interaction between the inner amorphous NiOH layer and the outer crystalline NixP layer, as well as the abundant amorphous/crystalline interface, an interfacial structure that can expose more active sites as well as enhance the intrinsic activity, thus improving the reaction kinetics and stability of UOR. This work paves the way for the development of low-cost and high-efficiency catalysts for urea oxidation.
科研通智能强力驱动
Strongly Powered by AbleSci AI