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Synthesis of bimetallic AuPt/CeO2 catalysts and their comparative study in CO oxidation under different reaction conditions.

Authors :
Plyusnin, Pavel E.
Slavinskaya, Elena M.
Kenzhin, Roman M.
Kirilovich, Anastasiya K.
Makotchenko, Evgeniya V.
Stonkus, Olga A.
Shubin, Yury V.
Vedyagin, Aleksey A.
Source :
Reaction Kinetics, Mechanisms & Catalysis; Jun2019, Vol. 127 Issue 1, p69-83, 15p
Publication Year :
2019

Abstract

In the present work, ceria-supported Au–Pt catalyst with metal ratio 3:2 was prepared using a "single-source precursor" concept. The double complex salt [AuEn<subscript>2</subscript>]<subscript>2</subscript>[Pt(NO<subscript>2</subscript>)<subscript>4</subscript>]<subscript>3</subscript>·6H<subscript>2</subscript>O was used as such precursor. CeO<subscript>2</subscript> of unique morphology with developed surface area (120 m<superscript>2</superscript>/g) obtained by urea precipitation technique was used as a support. According to XRD data, size of the alloyed Au–Pt particles was estimated to be less than 3 nm. It was shown that bimetallic Au–Pt system intensifies release of oxygen from the CeO<subscript>2</subscript> lattice. The 0.5%Au2Pt3/CeO<subscript>2</subscript> catalyst was comparatively studied in low temperature CO oxidation (simplified model reaction mixture) and under prompt thermal aging conditions (complex reaction mixture) with regard to monometallic reference samples 0.2%Au/CeO<subscript>2</subscript> and 0.3%Pt/CeO<subscript>2</subscript>. The catalytic performance of the samples was found to be significantly dependent on the reaction and pre-treatment conditions. In the case of the bimetallic catalyst, reversible redistribution and enrichment of the nanoparticle surface with Pt or Au were shown to be the key factor defining the activity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18785190
Volume :
127
Issue :
1
Database :
Complementary Index
Journal :
Reaction Kinetics, Mechanisms & Catalysis
Publication Type :
Academic Journal
Accession number :
136503865
Full Text :
https://doi.org/10.1007/s11144-019-01545-5