钴
磷化物
材料科学
多孔性
碳纤维
化学工程
纳米技术
冶金
复合材料
金属
工程类
复合数
作者
Yingjie Jin,Dongli Li,Yanchi Liu,Yabo Fu,Jiazi Shi,Jiaqi Wei
出处
期刊:Journal of physics
[IOP Publishing]
日期:2025-02-01
卷期号:2959 (1): 012005-012005
标识
DOI:10.1088/1742-6596/2959/1/012005
摘要
Abstract In this study, the porous carbon obtained after carbonization of ZIF-67 was employed as the precursor, and three kinds of porous carbon-supported cobalt phosphide materials (CoP@C-600, CoP@C-700, and CoP@C-800) were obtained after phosphidation. The catalysts were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and their electrochemical catalytic performance was tested via an electrochemical workstation. The relationship between the microstructure and the catalytic activity for hydrogen evolution reaction (HER) was investigated. The CoP@C materials prepared under different conditions all retained the dodecahedral structure of ZIF-67. Moreover, compared to Co@C materials, the transition metal phosphides CoP@C exhibited superior electrocatalytic hydrogen evolution performance. Among them, when the current was -10 mA/cm −2 , the overpotential of the CoP@C-600 material was -0.25 V, and its catalytic activity was higher than the other CoP@C materials.
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