| Literature DB >> 31305086 |
Haoyan Cheng1,2, Zhenming Cao1, Zitao Chen1, Ming Zhao3, Minghao Xie3, Zhiheng Lyu3, Zhihong Zhu2, Miaofang Chi4, Younan Xia1,3.
Abstract
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.Entities:
Keywords: Oxygen reduction reaction; Pt nanoparticles; catalytic durability; galvanic reaction; selenium
Year: 2019 PMID: 31305086 DOI: 10.1021/acs.nanolett.9b01221
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189