多面体
催化作用
氮气
氢
碳纤维
材料科学
制氢
化学
兴奋剂
化学工程
数学
有机化学
组合数学
复合材料
光电子学
复合数
工程类
作者
Ramakrishna Reddy Ayyaluri,B.N. Vamsi Krishna,Mohit Kumar,Obula Reddy Ankinapalli,Jae Su Yu
标识
DOI:10.1016/j.ijhydene.2024.05.204
摘要
The development of stable non-noble and cost-effective metal sulfide-based electrocatalyst materials for hydrogen evolution reaction (HER) is still a great challenge. Herein, we report the rationally designed electrocatalysts containing Co3S4/Co9S8 co-doped nitrogen-enriched porous carbon polyhedrons (Co3S4/Co9S8/NC PHs). The Co3S4/Co9S8/NC PHs were achieved from Zeolitic imidazolate framework-67 PHs by adding sulfur powder and then placing them in an inert atmosphere at 375 °C for 2 h. The prepared electrocatalyst materials were analyzed using X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy techniques. The HER catalytic activity of the Co3S4/Co9S8/NC PHs exhibited the superior overpotential performance of 134 mV at a current density of 10 mA cm−2 with the Tafel slope of −119 mV dec−1. Additionally, the results from chronopotentiometry maintained a strong kinetic response as well as the long cycling stability of 100 h for the Co3S4/Co9S8/NC PHs electrocatalyst at a constant current density of −10 mA cm−2 with 8.4% decay rate. This study demonstrates a new strategy for hydrogen generation synthesizing non-noble catalyst materials with excellent HER activities.
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