催化作用
质子交换膜燃料电池
材料科学
钨
化学工程
纳米颗粒
阴极
金属间化合物
烧结
合金
兴奋剂
钯
纳米技术
化学
冶金
物理化学
有机化学
光电子学
工程类
作者
Jiashun Liang,Na Li,Zhonglong Zhao,Liang Ma,Xiaoming Wang,Shenzhou Li,Xuan Liu,Tanyuan Wang,Yaping Du,Gang Lü,Jiantao Han,Yunhui Huang,Dong Su,Qing Li
标识
DOI:10.1002/ange.201908824
摘要
Abstract The commercialization of proton exchange membrane fuel cells (PEMFCs) relies on highly active and stable electrocatalysts for oxygen reduction reaction (ORR) in acid media. The most successful catalysts for this reaction are nanostructured Pt‐alloy with a Pt‐skin. The synthesis of ultrasmall and ordered L1 0 ‐PtCo nanoparticle ORR catalysts further doped with a few percent of metals (W, Ga, Zn) is reported. Compared to commercial Pt/C catalyst, the L1 0 ‐W‐PtCo/C catalyst shows significant improvement in both initial activity and high‐temperature stability. The L1 0 ‐W‐PtCo/C catalyst achieves high activity and stability in the PEMFC after 50 000 voltage cycles at 80 °C, which is superior to the DOE 2020 targets. EXAFS analysis and density functional theory calculations reveal that W doping not only stabilizes the ordered intermetallic structure, but also tunes the Pt‐Pt distances in such a way to optimize the binding energy between Pt and O intermediates on the surface.
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