催化作用
耐久性
纳米颗粒
质子交换膜燃料电池
碳纤维
材料科学
化学工程
铂金
无定形碳
烧结
氧还原反应
原电池
无定形固体
化学
纳米技术
电化学
冶金
复合材料
有机化学
物理化学
工程类
复合数
电极
作者
Haoyan Cheng,Zhenming Cao,Zitao Chen,Ming Zhao,Minghao Xie,Zhiheng Lyu,Zhihong Zhu,Miaofang Chi,Younan Xia
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-07-15
卷期号:19 (8): 4997-5002
被引量:75
标识
DOI:10.1021/acs.nanolett.9b01221
摘要
Carbon-supported Pt nanoparticles are used as catalysts for a variety of reactions including the oxygen reduction reaction (ORR) key to proton-exchange membrane fuel cells, but their catalytic performance has long been plagued by detachment and sintering. Here we report the in situ growth of sub-2 nm Pt particles on a commercial carbon support via the galvanic reaction between a Pt(II) precursor and a uniform film of amorphous Se predeposited on the support. The residual Se could serve as a linker to strongly anchor the Pt nanoparticles to the carbon surface, leading to a catalytic system with extraordinary activity and durability toward ORR. Even after 20 000 cycles of accelerated durability test, the sub-2 nm Pt particles were still dispersed well on the carbon support and maintained a mass activity more than three-times as high as the pristine value of a commercial Pt/C catalyst.
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