Au-Ru/TiO2 prepared by deposition-precipitation with urea: Relevant synthesis parameters to obtain bimetallic particles

被引:20
|
作者
Calzada, Lina A. [1 ]
Louis, Catherine [2 ]
Han, Chang Wan [3 ]
Ortalan, Volkan [4 ,5 ]
Zanella, Rodolfo [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Ciencias Aplicadas & Tecnol, Circuito Exterior S-N, Mexico City 04510, DF, Mexico
[2] Sorbonne Univ, CNRS, LRS, F-75005 Paris, France
[3] Purdue Univ, Sch Mat Engn, W Lafayette, IN 47907 USA
[4] Univ Connecticut, Mat Sci & Engn, Storrs, CT 06269 USA
[5] Univ Connecticut, Inst Mat Sci, Storrs, CT 06269 USA
关键词
Gold; Ruthenium; Bimetallic catalysts; Au-Ru; Deposition-Precipitation with urea; CO oxidation; SUPPORTED RUTHENIUM CATALYSTS; CO OXIDATION; GOLD NANOPARTICLES; SELECTIVE HYDROGENATION; CARBON-MONOXIDE; RU NANOPARTICLES; AU CATALYSTS; ADSORPTION; TIO2; SIZE;
D O I
10.1016/j.apcatb.2019.118503
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
Although Au and Ru are not miscible in the bulk, the paper focusses on the attempts to prepare bimetallic Au-Ru/TiO2 catalysts by deposition-precipitation with urea (co-DPU and sequential DPU, Au then Ru and vice versa). Gold was found already reduced after the preparations of co-DPU and Ru then Au DPU, leading to large gold particles and to catalysts as poorly active as Ru/TiO2 in CO oxidation. The Au-Ru/TiO2 catalysts prepared by Au then Ru DPU provided the most interesting results: small bimetallic particles were formed; after reduction in H-2 at 300 degrees C, their structure was Janus-type and Au core - Ru shell, and the catalyst was poorly active, whereas after reduction at 500 degrees C, the particles became mainly Ru core - Au shell, and the catalyst showed higher activity than Au/TiO2 and a synergetic effect in CO oxidation compared to the monometallic counterparts.
引用
收藏
页数:14
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