分解水
线性扫描伏安法
材料科学
贵金属
电化学
循环伏安法
磷化物
化学工程
纳米结构
制氢
氢
钴
催化作用
纳米技术
金属
无机化学
化学
电极
物理化学
冶金
工程类
光催化
生物化学
有机化学
作者
Jeongwon Kim,Yu Jin Jang,Yoon Hee Jang
出处
期刊:Materials
[MDPI AG]
日期:2023-01-07
卷期号:16 (2): 593-593
被引量:4
摘要
Hydrogen production via water splitting has been extensively explored over the past few decades, and considerable effort has been directed toward finding more reactive and cost-effective electrocatalysts by engineering their compositions, shapes, and crystal structures. In this study, we developed hierarchical cobalt phosphide (Co-P) nanosphere assemblies as non-noble metal electrocatalysts via one-step electrodeposition. The morphologies of the Co-P nanostructures and their electrocatalytic activities towards the hydrogen evolution reactions (HER) were controlled by the applied potentials during electrodeposition. The physicochemical properties of the as-prepared Co-P nanostructures in this study were characterized by field-emission scanning electron microscopy, X-ray photoemission spectroscopy and X-ray diffraction. Linear sweep voltammetry revealed that the Co-P grown at -0.9 V showed the best HER performance exhibiting the highest electrochemical active surface area and lowest interfacial charge transfer resistance. The Co-P electrocatalysts showed superior long-term stability to electrodeposited Pt, indicating their potential benefits.
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