材料科学
阳极
催化作用
燃料电池
质子交换膜燃料电池
氢
化学工程
氢燃料
功率密度
直接乙醇燃料电池
动力学
离子交换
氧化还原
碱性燃料电池
离子
纳米技术
膜
无机化学
电池电压
交换电流密度
钌
开路电压
再生燃料电池
氢气储存
化学动力学
纳米颗粒
壳体(结构)
作者
Liangbin Liu,Renjie Ren,Y. Cheng,Zhongliang Huang,Lin Zhuang,Jing Xia,Xiaoqing Huang,Nanjun Chen
标识
DOI:10.1002/aenm.202506035
摘要
ABSTRACT Developing highly efficient and durable Ru‐based hydrogen oxidation reaction (HOR) catalysts is essential for advancing anion exchange membrane fuel cell (AEMFC) technology. However, Ru‐type catalysts have suffered from unbalanced intermediate adsorption/desorption, resulting in suboptimal HOR activity and limited long‐term stability, particularly under practical AEMFC operating conditions. Here, we present a RuCo core–shell nanoplate featuring a Co core and an atomically scaled Ru skin shell (Co@Ru NPs), in which the unique core–shell structure and atomic Ru skin effectively optimize the adsorption/desorption balance of H * and OH * species while enhancing reaction kinetics in AEMFCs. Consequently, the Co@Ru NPs‐based fuel cell delivers an excellent peak power density (PPD) of 1.57 W cm −2 in H 2 ‐O 2 with an ultralow Ru loading of 0.05 mg cm −2 , which enables an exceptional anode specific power of 31.4 W mg Ru −1 , outperforming those of state‐of‐the‐art Ru‐type AEMFCs. Moreover, the Co@Ru NPs‐based fuel cell can be run stably at 0.5 A cm −2 for over 300 h, demonstrating the excellent stability of Co@Ru NPs for practical fuel cell applications.
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