Gold-TiO2-Nickel catalysts for low temperature-driven CO oxidation reaction

被引:13
作者
Hinojosa-Reyes, Mariana [1 ]
Zanella, Rodolfo [2 ]
Maturano-Rojas, Viridiana [2 ]
Rodriguez-Gonzalez, Vicente [1 ]
机构
[1] IPICYT, Div Mat Avanzados, Camino Presa San Jose 2055 Col Lomas 4a Secc, San Luis Potosi 78216, Slp, Mexico
[2] Univ Nacl Autonoma Mexico, Ctr Ciencias Aplicadas & Desarrollo Tecnol, Circuito Exterior S-N,Ciudad Univ,AP 70-186, Mexico City 04510, DF, Mexico
关键词
CO oxidation; Gold nanoparticles; Nickel-doped TiO2; DRIFTS; Low temperature oxidation; DEPOSITION-PRECIPITATION; CARBON-MONOXIDE; GOLD CATALYSTS; NICKEL; HYDROGEN; ADSORPTION; PARTICLES; STABILITY; WATER; RAMAN;
D O I
10.1016/j.apsusc.2016.01.285
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
Nickel-doped-TiO2 catalysts were prepared by the solgel method and surface modified with gold nanoparticles (AuNPs) by the urea-deposition-precipitation technique. The as-synthesized catalysts were characterized by X-ray diffraction, Raman and XPS spectroscopies, N-2 physisorption, STEM-HAADF microscopy and TPR hydrogen consumption. The Au/TiO2-Ni catalysts were evaluated catalytically performing CO oxidation reactions. The catalyst with nickel content of 1 wt. % (Au/TiO2-Ni 1) showed the highest CO conversion with respect to the high-nickel-content or bare/commercial TiO2 at 0 degrees C. In situ DRIFTS showed a strong participation of both nickel due to the presence of surface-nickel-metallic nanoparticles formed during the CO adsorption process at reaction temperatures above 200 degrees C, and surface-bridged-nickel-CO species. A minor deactivation rate was observed for the Au/TiO2-Ni 1 catalyst in comparison with the Au/TiO2 one. The oxygen vacancies that were created on the solgel-doped TiO2 improved the catalytic behavior during the performance of CO oxidation reactions, and inhibited the AuNP sintering. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:224 / 232
页数:9
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