File Download

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

안광진

An, Kwangjin
Advanced Nanocatalysis Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Boosting hot electron flux and catalytic activity at metal-oxide interfaces of PtCo bimetallic nanoparticles

Author(s)
Lee, HyosunLim, JuhyungLee, ChanghwanBack, SeoinAn, KwangjinShin, Jae WonRyoo, RyongJung, YousungPark, Jeong Young
Issued Date
2018-06
DOI
10.1038/s41467-018-04713-8
URI
https://scholarworks.unist.ac.kr/handle/201301/24339
Fulltext
https://www.nature.com/articles/s41467-018-04713-8
Citation
NATURE COMMUNICATIONS, v.9, pp.2235
Abstract
Despite numerous studies, the origin of the enhanced catalytic performance of bimetallic nanoparticles (NPs) remains elusive because of the ever-changing surface structures, compositions, and oxidation states of NPs under reaction conditions. An effective strategy for obtaining critical clues for the phenomenon is real-time quantitative detection of hot electrons induced by a chemical reaction on the catalysts. Here, we investigate hot electrons excited on PtCo bimetallic NPs during H-2 oxidation by measuring the chemicurrent on a catalytic nanodiode while changing the Pt composition of the NPs. We reveal that the presence of a CoO/Pt interface enables efficient transport of electrons and higher catalytic activity for PtCo NPs. These results are consistent with theoretical calculations suggesting that lower activation energy and higher exothermicity are required for the reaction at the CoO/Pt interface.
Publisher
NATURE PUBLISHING GROUP
ISSN
2041-1723
Keyword
INITIO MOLECULAR-DYNAMICSCORE-SHELL NANOPARTICLESAUGMENTED-WAVE METHODHYDROGEN OXIDATIONSURFACE-CHEMISTRYCHEMICAL-REACTIONNANOCRYSTALSNANOSTRUCTURESEXCITATIONSADSORPTION

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.