催化作用
电解质
纳米颗粒
化学
无机化学
过渡金属
交换电流密度
碳化物
化学工程
碱性燃料电池
氢
阳极
电化学
材料科学
纳米技术
电极
物理化学
有机化学
工程类
塔菲尔方程
作者
Eliran R. Hamo,Ramesh K. Singh,John C. Douglin,Sian Chen,Mohamed Ben Hassine,Enrique Carbó‐Argibay,Shanfu Lu,Haining Wang,Paulo J. Ferreira,Brian A. Rosen,Dario R. Dekel
标识
DOI:10.1021/acscatal.0c03973
摘要
Owing to the sluggish kinetics of the hydrogen oxidation reaction (HOR) in alkaline electrolyte, it is considered a limiting reaction for the development of anion-exchange membrane fuel cell (AEMFC) technology. Studies of alkaline HOR catalysis mainly focus on carbon-supported nanoparticles, which have weak metal–support interactions. In this contribution, we present a unique support based on transition metal carbides (TMCs = Mo2C, Mo2C–TaC, and Mo2C–W2C) for the HOR. PtRu nanoparticles are deposited onto the TMC supports and are characterized by a variety of analytical techniques. The major findings are (i) experimental and theoretical evidence for strong-metal support interaction by both X-ray absorption near-edge structure and density functional theory, (ii) the kinetic current density (jk,s) @25 mV of PtRu/Mo2C–TaC catalyst are 1.65 and 1.50 times higher than that of PtRu/Mo2C and PtRu/Mo2C–W2C, respectively, and (iii) enhanced "tethering" of PtRu nanoparticles on TMC supports. Furthermore, the AEMFC based on the PtRu/Mo2C–TaC anode exhibited a peak power density of 1.2 W cm–2 @70 °C, opening the doors for the development of advanced catalysts based on engineering support materials.
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