Understanding the mechanism of synthesis of Pt3Co intermetallic nanoparticles via preferential chemical vapor deposition

被引:22
|
作者
Saedy, S. [1 ,2 ]
Palagin, D. [2 ]
Safonova, O. [3 ]
van Bokhoven, J. A. [2 ,4 ]
Khodadadi, A. A. [1 ,3 ]
Mortazavi, Y. [1 ,5 ]
机构
[1] Univ Tehran, Catalysis & Nanostruct Mat Lab, Sch Chem Engn, POB 11155-4563, Tehran, Iran
[2] Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, Switzerland
[3] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[4] Swiss Fed Inst Technol, Inst Chem & Bioengn, Vladimir Prelog Weg 1, CH-8093 Zurich, Switzerland
[5] Univ Tehran, Oil & Gas Proc Ctr Excellence, Sch Chem Engn, Coll Engn, POB 11155-4563, Tehran, Iran
关键词
OXYGEN REDUCTION REACTION; CARBON-MONOXIDE; PT-CO; FUEL-CELLS; CATALYTIC-PROPERTIES; ENHANCED ACTIVITY; OXIDATION; HYDROGEN; CLUSTERS; COBALT;
D O I
10.1039/c7ta06737b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A detailed study on the synthesis of Pt3Co intermetallic nanoparticles supported on ceria via preferential chemical vapor deposition was conducted, leading to a fundamental understanding of the deposition process and the Co-Pt alloying. This understanding helps us to develop a facile and scalable method for preferential adding of a metal on the surface of another metal already supported on an oxide which facilitates the design of novel structured nanoparticles. The fluidized flow reactor eliminated the deposition profile and resulted in Pt3Co nanoparticles uniformly and homogeneously distributed on ceria. The kinetic study of cobalt deposition on the platinum surface, in accordance with DFT calculations, demonstrates that the platinum surface catalyzes the deposition reaction; while the ceria surface is inert in the preferential deposition temperature window between 150 degrees C and 180 degrees C. The obtained sample was characterized by in situ XRD, HAADF-STEM, FT-IR, and XAS methods. The results indicate the formation of uniform Pt3Co nanoparticles with an average size of 1.1 nm. This sample showed superior catalytic activity in preferential oxidation of CO with an almost twice higher CO conversion rate and CO2 selectivity compared to a classically synthesized sample with successive impregnation.
引用
收藏
页码:24396 / 24406
页数:11
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