钴
塔菲尔方程
催化作用
掺杂剂
异质结
碳纤维
材料科学
化学工程
化学
无机化学
兴奋剂
有机化学
复合数
物理化学
电化学
电极
光电子学
工程类
复合材料
作者
J. C. Li,Qichang Wang,Wenjie Zhang,Kai Zhang,Dekui Shen
标识
DOI:10.1016/j.ijhydene.2024.02.171
摘要
The coupling of cobalt and cobalt phosphides has been demonstrated to be an efficient strategy to enhance the catalytic activity for hydrogen evolution reaction (HER). Herein, the lignin-based carbon encapsulated cobalt/cobalt phosphides heterojunctions (Co/Co2P@LGC) was synthesized successfully on the lignin-based carbon by carbothermal reduction integrated with post-phosphidation. The strong coupling interaction in the heterostructure promoted the establishment of a distinct synergy effect between Co and P atoms, resulting in the redistribution of electronic structure. The outstanding porous sheet structure of lignin-derived carbon facilitated the exposure of more accessible active sites and self-dopants were conducive to the formation of more carbon defects. As expected, the best catalysts, Co/Co2P@LGC-450 exhibited excellent HER performance in 0.5 M H2SO4, which afford a current density of 10 mA/cm2 with only 150 mV and a Tafel slope of 86 mV dec−1, as well as a robust stability for 120 h at 10 mA cm−2. This research not only presented a facile method for heterostructure electrocatalysts preparation, but also offered crucial insights into the lignin valorisation.
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