铱
催化作用
交换电流密度
基质(水族馆)
阳极
碳化物
动力学
氢氧化物
氢
化学计量学
结合能
材料科学
可逆氢电极
化学
化学工程
无机化学
电化学
物理化学
电极
有机化学
塔菲尔方程
冶金
工程类
海洋学
物理
量子力学
参比电极
地质学
核物理学
作者
Jinjie Fang,Haiyong Wang,Qian Dang,Hao Wang,Xingdong Wang,Jiajing Pei,Zhiyuan Xu,Chengjin Chen,Wei Zhu,Hui Li,Yushan Yan,Zhongbin Zhuang
标识
DOI:10.1038/s41467-024-48672-9
摘要
Hydroxide exchange membrane fuel cells (HEMFCs) have the advantages of using cost-effective materials, but hindered by the sluggish anodic hydrogen oxidation reaction (HOR) kinetics. Here, we report an atomically dispersed Ir on Mo2C nanoparticles supported on carbon (IrSA-Mo2C/C) as highly active and stable HOR catalysts. The specific exchange current density of IrSA-Mo2C/C is 4.1 mA cm-2ECSA, which is 10 times that of Ir/C. Negligible decay is observed after 30,000-cycle accelerated stability test. Theoretical calculations suggest the high HOR activity is attributed to the unique Mo2C substrate, which makes the Ir sites with optimized H binding and also provides enhanced OH binding sites. By using a low loading (0.05 mgIr cm-2) of IrSA-Mo2C/C as anode, the fabricated HEMFC can deliver a high peak power density of 1.64 W cm-2. This work illustrates that atomically dispersed precious metal on carbides may be a promising strategy for high performance HEMFCs.
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