质子交换膜燃料电池
催化作用
溶解
铂金
金属
阴极
化学
材料科学
化学工程
分析化学(期刊)
无机化学
冶金
色谱法
物理化学
有机化学
工程类
作者
Hsiwen Wu,Fei Xiao,Jing Wang,Meng Gu,Minhua Shao
出处
期刊:Nano Research
[Springer Nature]
日期:2023-12-06
卷期号:17 (10): 8772-8784
被引量:10
标识
DOI:10.1007/s12274-023-6297-3
摘要
This work presents simple post-treatment methods to selectively and partially remove the Pd core of Pd-Pt core-shell (Pt@Pd/C) catalysts. The proton exchange membrane fuel cell with the post-treated Pt@Pd/C cathode (Pt loading: 0.10 mg center dot cm-2) delivers an impressive peak power density of 1.2 W center dot cm-2. The partial removal of Pd core endows an ultrahigh oxygen reduction reaction (ORR) mass activity of 0.32 A center dot mgPGM-1 when normalized to the platinum group metal (PGM) mass, or equivalently 0.55 A center dot mgPt-1 at 0.9 V measured in a fuel cell. The post-treatment thickens the Pt shells and mitigates the Pd dissolution during potential cycling. As a result, the post-treated core-shell catalyst demonstrates superior durability in ORR mass activity and polarization power density retention than untreated core-shell catalyst and benchmark Pt/C. In-situ inductively coupled plasma-mass spectrometry (ICP-MS) results highlight that the amount of dissolved Pd in post-treated core-shell catalyst is 17-times lower than that of the untreated one. Our findings highlight the importance of structural tuning of catalysts in enhancing their mass activity and durability.
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