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SiO2 supported highly dispersed Pt atoms on LaNiO3 by reducing a perovskite-type oxide as the precursor and used for CO oxidation.

Authors :
Zhang, Siran
An, Kang
Fang, Chunyu
Zhang, Ziyang
Liu, Qiang
Lu, Suhong
Liu, Yuan
Source :
Catalysis Today. Sep2020, Vol. 355, p222-230. 9p.
Publication Year :
2020

Abstract

• LaNi 1- x Pt x O 3 /SiO 2 were prepared by a facile method of citrate acid complexation combined with impregnation. • Pt/LaNiO 3 loaded on SiO 2 was obtained by reducing LaNi 1- x Pt x O 3 /SiO 2. • Pt atoms were highly dispersed on a support by using a perovskite-type oxide as the precursor. • Pt/LaNiO 3 /SiO 2 showed excellent activity and stability for CO oxidation. A new facile method for preparing highly dispersed precious metal catalysts was proposed in this work. Highly dispersed Pt supported on LaNiO 3 /SiO 2 were prepared by using LaNi 1- x Pt x O 3 perovskite as precursors. The catalytic performances of CO oxidation over the prepared catalytsts were investigated. The structural features of the catalysts were characterized by N 2 adsorption-desorption, XRD, H 2 -TPR, TEM, EXAFS, CO-TPD and O 2 -TPD techniques. The result indicated that nanocrystalline of LaNi 1- x Pt x O 3 was supported on SiO 2. Reducing LaNi 1- x Pt x O 3 /SiO 2 could make Pt from the interior of the perovskite crystal lattice onto the surface and then form highly dispersed Pt on the support of LaNiO 3 /SiO 2. As the platinum content was 0.5% or less, platinum atoms could distribute highly even maybe in single atoms. The catalytic test revealed that LaNi 0.95 Pt 0.05 O 3 /SiO 2 exhibited a significant activity and stability for CO oxidation, as well as excellent performance in the presence of both 15 vol.% H 2 O and 12.5 vol.% CO 2. It has been demonstrated that the highly dispersed Pt, the easy reducibility, and sufficient surface oxygen species were responsible for the high catalytic activity of LaNi 0.95 Pt 0.05 O 3 /SiO 2 catalyst. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09205861
Volume :
355
Database :
Academic Search Index
Journal :
Catalysis Today
Publication Type :
Academic Journal
Accession number :
146558833
Full Text :
https://doi.org/10.1016/j.cattod.2019.04.041