材料科学
异质结
氢
无机化学
光电子学
化学
有机化学
作者
S. Q. Zhang,Renjie Ren,Jing Cao,Dezheng Zhang,Jingsen Bai,Ce Han,Li Xiao,Lin Zhuang,Ping Song,Weilin Xu
标识
DOI:10.1002/aenm.202404266
摘要
Abstract Designing efficient and CO‐tolerant catalysts for hydrogen oxidation reaction (HOR) in anode is one of the challenges for alkaline exchange membrane fuel cells in practical application. Herein, Ru‐MnO heterostructure with two adjacent clusters supported on commercial carbon (BP 2000) (denoted as Ru‐MnO/C) is designed to accelerate the sluggish kinetics of alkaline HOR. The cluster–cluster heterostructure interface modifies the electronic structure of Ru sites with electron transfer from Ru to MnO, then optimizes the adsorption of intermediates on Ru sites. Consequently, this catalyst exhibits high catalytic HOR activities in alkaline media with high exchange current density (3.71 mA cm −2 ) and mass activity (0.78 A mg Ru −1 ). Meanwhile, the alkaline exchange membrane fuel cell delivers a specific peak power density (PPD) of 7.0 W mg −1 Ru under H 2 /O 2 condition, which is higher than that of most reported catalysts. More importantly, the catalyst also demonstrates the remarkable stability and CO‐tolerance. This work presents the superiority of cluster–cluster heterostructure interface toward efficient HOR, which is expected to further enlighten the design of advanced catalysts for electrocatalysis.
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