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作为低成本析氢电催化剂的FeC纳米颗粒:Co替代的重要性

FeC nanoparticles as low-cost HER electrocatalyst: the importance of Co substitution.

作者信息

Li Siwei, Ren Pengju, Yang Ce, Liu Xi, Yin Zhen, Li Weizhen, Yang Hanjun, Li Jian, Wang Xiaoping, Wang Yi, Cao Ruochen, Lin Lili, Yao Siyu, Wen Xiaodong, Ma Ding

机构信息

College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China; Syncat@Beijing, Synfuels China Technology Co., Ltd, Beijing 101407, China.

出版信息

Sci Bull (Beijing). 2018 Oct 30;63(20):1358-1363. doi: 10.1016/j.scib.2018.09.016. Epub 2018 Sep 22.

Abstract

Constructing and understanding the doping effect of secondary metal in transition metal carbide (TMC) catalysts is pivotal for the design of low-cost hydrogen evolution reaction (HER) electrocatalysts. In this work, we developed a wet-chemistry strategy for synthesizing Co-modified FeC nanoparticles ((FeCo)C NPs) as highly active HER electrocatalysts in basic solution. The structure of (FeCo)C NPs was characterized by X-ray diffraction (XRD), extended X-ray absorption fine structure spectra (EXAFS) and scanning/transmission electron microscopy (S/TEM), indicating that the isomorphous substitution of cobalt in the lattice of FeC. (FeCo)C exhibited the best HER activity (174 mV for j = -10 mA/cm). Computational calculation results indicate that Co provides the most active site for HER. X-ray adsorption spectra (XAS) studies further suggested that the electron transfer in Fe-C bonds are enhanced by the substitution of Co, which modulates the hydrogen adsorption on the adjacent electronic-enriched carbon, and therefore promotes HER activity. Our results affirm the design of low-cost bimetallic TMCs based HER catalysts.

摘要

构建并理解过渡金属碳化物(TMC)催化剂中第二金属的掺杂效应对于设计低成本析氢反应(HER)电催化剂至关重要。在这项工作中,我们开发了一种湿化学策略来合成Co修饰的FeC纳米颗粒((FeCo)C NPs),作为碱性溶液中高活性的HER电催化剂。通过X射线衍射(XRD)、扩展X射线吸收精细结构光谱(EXAFS)和扫描/透射电子显微镜(S/TEM)对(FeCo)C NPs的结构进行了表征,表明钴在FeC晶格中发生了同晶取代。(FeCo)C表现出最佳的HER活性(j = -10 mA/cm²时为174 mV)。计算结果表明,Co为HER提供了最活跃的位点。X射线吸收光谱(XAS)研究进一步表明,Co的取代增强了Fe-C键中的电子转移,这调节了氢在相邻富电子碳上的吸附,从而促进了HER活性。我们的结果证实了基于低成本双金属TMCs的HER催化剂的设计。

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