Effect of oleylamine concentration on the structure and oxygen reduction activity of carbon-supported surface-Pt-enriched Pt3Au electrocatalysts

Authors
Lee, Kug-SeungPark, Hee-YoungChung, Young-HoonYoo, Sung JongNam, Suk WooAhn, DocheonSung, Nark-EonJang, Jong Hyun
Issue Date
2015-09-20
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF POWER SOURCES, v.290, pp.130 - 135
Abstract
For carbon-supported Pt-enriched Pt3Au nanoparticles (Pt3Au/C), the effect of oleylamine (OA) concentration during nanoparticle synthesis is investigated. When the OA concentration is increased from 0.12 mM to 1.2 mM, the particle size of Pt3Au gradually decreased from 5.1 nm to 3.3 nm, whereas the crystal structure and surface Pt concentration are not significantly influenced. With higher OA concentration, the oxygen reduction reaction activity of the Pt3Au/C is largely enhanced, which can be explained by the combined effect of increased specific activity and electrochemical surface area of Pt. It is experimentally confirmed using a bulk CO-oxidation technique that smaller particle size (larger OA concentration) leads to decreased OH adsorption strength, which originates from the double layer overlapping effect of closely adjacent nanoparticles. (C) 2015 Elsevier B.V. All rights reserved.
Keywords
ALLOY NANOPARTICLE CATALYSTS; DENSITY-FUNCTIONAL THEORY; FUEL-CELL CATALYSTS; PLATINUM NANOPARTICLES; ELECTRONIC-STRUCTURE; PARTICLE PROXIMITY; METAL-SURFACES; LASER-ABLATION; FORMIC-ACID; SIZE; ALLOY NANOPARTICLE CATALYSTS; DENSITY-FUNCTIONAL THEORY; FUEL-CELL CATALYSTS; PLATINUM NANOPARTICLES; ELECTRONIC-STRUCTURE; PARTICLE PROXIMITY; METAL-SURFACES; LASER-ABLATION; FORMIC-ACID; SIZE; Pt3Au nanoparticle electrocatalyst; Surfactant concentration; Oxygen reduction reaction; Bulk CO oxidation; OH adsorption
ISSN
0378-7753
URI
https://pubs.kist.re.kr/handle/201004/125010
DOI
10.1016/j.jpowsour.2015.04.165
Appears in Collections:
KIST Article > 2015
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

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

BROWSE