Author
Listed:
- Wei-Zhen Li
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory)
- Libor Kovarik
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory)
- Donghai Mei
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory)
- Jun Liu
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory)
- Yong Wang
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory
The Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University)
- Charles H. F. Peden
(Institute for Integrated Catalysis, Pacific Northwest National Laboratory)
Abstract
The development of thermally stable, nanometer-sized precious metal-based catalysts remains a daunting challenge. Such materials, especially those based on the use of costly platinum metal, are essential and, to date, non-replaceable for a large number of industrially important catalytic processes. Here we report a well-defined cuboctahedral MgAl2O4 spinel support material that is capable of stabilizing platinum particles in the range of 1–3 nm on its relatively abundant {111} facets during extremely severe aging at 800 °C in air for 1 week. The aged catalysts retain platinum dispersions of 15.9% with catalytic activities for methanol oxidation being ~80% of that of fresh ones, whereas a conventional Pt/γ-Al2O3 catalyst is severely sintered and nearly inactive. We reveal the origin of the markedly superior ability of spinel {111} facets, resulting from strong interactions between spinel surface oxygens and epitaxial platinum {111} facets, inspiring the rational design of anti-sintering supported platinum group catalysts.
Suggested Citation
Wei-Zhen Li & Libor Kovarik & Donghai Mei & Jun Liu & Yong Wang & Charles H. F. Peden, 2013.
"Stable platinum nanoparticles on specific MgAl2O4 spinel facets at high temperatures in oxidizing atmospheres,"
Nature Communications, Nature, vol. 4(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3481
DOI: 10.1038/ncomms3481
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