Published January 2019 | Version v1
Journal article

Facile construction of Mn2O3@CeO2 core@shell cubes with enhanced catalytic activity toward CO oxidation

  • 1. Jiangsu Province Engineering Laboratory of High Efficient Energy Storage Technology and Equipments, Xuzhou City Key Laboratory of High Efficient Energy Storage Technology and Equipments, China University of Mining and Technology, Xuzhou 221008 (China)
  • 2. Low Carbon Energy Institute, China University of Mining and Technology, Xuzhou 221008 (China)
  • 3. School of Chemical Engineering and Technology, China University of Mining and Technology, Xuzhou 221116 (China)

Description

Highlights: • Mn2O3@CeO2 core@shell cubes were fabricated by a facile three-step process. • CeO2 shell thickness could be tuned by variying the feeding amount of Ce(NO3)3. • Mn2O3@CeO2 core@shell cubes exhibted enhanced CO catalytic oxidation activity. • High activity can be attibuted to the synergistic action between Mn2O3 and CeO2. -- Abstract: Heterogeneous core@shell nanostructures bring unique synergetic catalytic properties in comparison with their single-component materials, because the two-phase interface could render hybrid junctions with rich redox reactions. Herein, a series of Mn2O3@CeO2 core@shell cubes with tunable CeO2 shell thickness have been controllably synthesized by a facile multi-step process, which involved the annealing treatment of MnCO3 precursor to produce Mn2O3 microcubes, followed by a refuxing process to deposit a uniform CeO2 layer on the Mn2O3 surface. The CeO2 shell was assembled by nanoparticles with sizes in the range of 2–10 nm, and the thickness could be facilely manipulated by changing the Mn/Ce molar ratios of reactants used in the synthetic process. The Mn2O3@CeO2 core@shell cubes exhibited enhanced catalytic activity toward CO oxidation compared with both pure CeO2 and Mn2O3, which was attributed to the synergistic interaction between CeO2 and Mn2O3. Impressively, Mn2O3@CeO2-0.1 sample with a proper CeO2 thickness exhibited the highest catalytic performance, attaining 100% CO conversion at 220 °C.

Additional details

Identifiers

DOI
10.1016/j.jssc.2018.10.024;
PII
S0022459618304572;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
269
Journal Page Range
p. 419-427
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.