超亲水性
材料科学
电极
化学工程
曲面(拓扑)
氢
纳米技术
润湿
复合材料
化学
有机化学
物理化学
工程类
几何学
数学
作者
Ruihua Ling,Qing Lian,Lianwei Shan,Shengling Xiang,Ouwen Peng,Dongyang Li,Abbas Amini,Ning Wang,Hao Yang,Chun Cheng
出处
期刊:Small
[Wiley]
日期:2024-09-23
标识
DOI:10.1002/smll.202404420
摘要
Wood, as a renewable material, has been regarded as an emerging substrate for self-supporting electrodes in large-scale water electrolysis due to numerous merits such as rich pore structure, abundant hydroxyl groups, etc. However, poor conductivity of wood can greatly suppress the performance of wood-based electrodes. Carbonization process can improve wood's conductivity, but the loss of hydroxyl groups and the required high energy consumption are the drawbacks of such a process. Here, a facile strategy is developed to prepare pristine wood-supported electrode (Ni-NiP/W) for enhanced hydrogen evolution reaction (HER); this improves electrical conductivity of wood while retaining its excellent intrinsic properties. The preparation process involves the deposition of copper on the untreated wood followed with the loading of Ni-NiP catalyst at room temperature. Encouragingly, the Ni-NiP/W exhibits conductive and inherited pristine wood's superhydrophilic and superaerophobic properties, that effectively boost mass and charge transfer. It demonstrates high activity and excellent stability in acidic, alkali, and seawater conditions as well as high current densities of up to 2000 mA cm
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