过电位
催化作用
碳化
沸石咪唑盐骨架
过渡金属
钴
材料科学
化学工程
电化学
电催化剂
电解
碳纤维
制氢
咪唑酯
无机化学
金属有机骨架
化学
物理化学
电极
有机化学
吸附
冶金
复合材料
电解质
工程类
复合数
扫描电子显微镜
作者
Robin N. Dürr,E.F. Stephan,Jocelyne Leroy,Frédéric Oswald,B. Verhaeghe,Bruno Jousselme
标识
DOI:10.1002/celc.202300205
摘要
Abstract Herein we present non‐noble metal single‐atom catalysts (SACs) based on carbonized transition metal‐doped zeolitic imidazolate frameworks (ZIFs) as stable and efficient electrocatalysts for the hydrogen evolution reaction in acidic media. In this work, earth‐abundant metals are embedded in a porous N‐rich carbon matrix by pyrolyzing metal‐doped ZIF structures and characterized by spectroscopic, microscopic, and electrochemical methods. The complete synthesis of these high surface area SACs was carried out without any solvents and hence offers a promising route for a more sustainable catalyst production and industrial upscaling. As the best‐performing catalyst, cobalt SAC illustrated already with a low cobalt loading of <0.3 at.% a substantial increase in activity with an overpotential of −322 mV for −10 mA cm −2 , and high stability during electrolysis at −10 mA cm −2 for 12 h in acidic media, with only a small decrease of 33 mV to more negative potentials after the initiation period.
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