阳极
催化作用
材料科学
氧化物
化学工程
兴奋剂
阴极
降级(电信)
氧气
过渡金属
金属
价(化学)
电极
表面改性
无机化学
化学稳定性
质子交换膜燃料电池
膜
氧化还原
析氧
氢
工作(物理)
电化学
反应机理
化学物理
纳米技术
化学反应
交换电流密度
作者
Jiayi Tang,Zijun Fang,Yucheng Huang,Daqin Guan,Bin Chen,Zongping Shao
标识
DOI:10.1002/adma.202521819
摘要
ABSTRACT RuO 2 is a promising alternative to IrO 2 for the oxygen evolution reaction (OER) in proton exchange membrane water electrolyzers (PEMWEs). However, to date, only Ir oxide or IrRu‐oxide based anodes have demonstrated possible stable operation at industrial‐relevant current densities of 2 A cm −2 for practical PEMWE applications. The poor durability of Ir‐free RuO 2 anodes remains a major barrier to its practical use. While metal doping has been extensively explored to stabilize the Ru valence, emerging evidence suggests a multifactorial failure mechanism involving both physical and chemical degradation of RuO 2 anodes. This underscores the need for strategies that stabilize both the catalyst bulk structure and reaction interface in OER. Here, we report a dual‐modification strategy combining bulk Cr substitution with Si surface modification to simultaneously enhance the intrinsic activity and stability of RuO 2 ‐based anode in PEMWE. Cr doping modulates the Ru valence state in the bulk phase, promoting charge transfer while suppressing Ru overoxidation, whereas Si modification stabilizes the reaction interface by inhibiting catalyst reconstruction and protecting the Cr dopant. The resulting catalyst achieves stable operation in PEMWE at 2 A cm −2 and 1.65 V. This work provides new insights into the development of RuO 2 ‐based catalysts and electrodes for PEMWEs.
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