催化作用
吸附
基质(水族馆)
材料科学
氢
化学工程
化学
物理化学
生物化学
海洋学
地质学
工程类
有机化学
作者
Zihao Dong,Nan Yang,Tang Tang,Xiaozhi Liu,Jiaju Fu,Hai‐Rui Pan,Zhe Jiang,Liang Ding,Xing Cheng,Lirong Zheng,Jianan Zhang,Xiaoxia Chang,Bingjun Xu,Jin‐Song Hu
标识
DOI:10.1021/acscatal.3c01466
摘要
Developing CO-tolerant Pt-based catalysts for the hydrogen oxidation reaction (HOR) is critical for the commercialization of fuel cells and thus receiving increasing interest. Although it is known that weakening the CO adsorption on Pt can improve CO tolerance, efficient strategies are still needed. Inspired by theoretical simulations, we propose here a cascade strategy to synergistically mitigate electron back-donation of Pt 5d → CO 2π* by introducing single-atomic Fe–N–C substrate and alloying, which significantly boosts the CO-tolerance of Pt-based HOR catalysts. The obtained PtNiMo/Fe–N–C can maintain above 80% HOR current density after 2000 s in 1000 ppm CO/H2, substantially outperforming control catalysts and ranking among the state-of-the-art catalysts. The in situ surface-enhanced infrared adsorption spectroscopy validates that the effectively weakened CO adsorption contributes to improved CO tolerance. This strategy opens up opportunities for designing advanced HOR catalysts with desired CO tolerance.
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