Published April 15, 2016 | Version v1
Journal article

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

  • 1. División de Materiales Avanzados, IPICYT, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa San José 2055 Col. Lomas 4a. sección C.P. 78216, San Luis Potosí, S.L.P., México (Mexico)
  • 2. Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México, Circuito Exterior S/N, Ciudad Universitaria, A. P. 70-186, Delegación Coyoacán, C.P. 04510, México D. F., México (Mexico)

Description

Graphical abstract: - Highlights: • Nickel-doped TiO2 catalysts (1 wt. %) drive the CO oxidation at low temperature. • DRIFTS reveals the participation of nickel during the CO oxidation. • Ni(CO)2 bridged species are detected by DRIFTS. • Au/TiO2-Ni 1 is the most active and stable catalyst with respect to undoped TiO2. • Ti3+ species corroborate Ni doped TiO2 and surface oxygen vacancies. - Abstract: Nickel-doped-TiO2 catalysts were prepared by the sol–gel 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, N2 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 °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 °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 sol–gel-doped TiO2 improved the catalytic behavior during the performance of CO oxidation reactions, and inhibited the AuNP sintering.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2016.01.285

Additional details

Identifiers

DOI
10.1016/j.apsusc.2016.01.285;
PII
S0169-4332(16)30146-5;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
368
Journal Page Range
p. 224-232
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.