Rare-earth–platinum alloy nanoparticles in mesoporous zeolite for catalysis
Ryong Ryoo (),
Jaeheon Kim,
Changbum Jo,
Seung Won Han,
Jeong-Chul Kim,
Hongjun Park,
Jongho Han,
Hye Sun Shin and
Jae Won Shin
Additional contact information
Ryong Ryoo: Institute for Basic Science (IBS)
Jaeheon Kim: Institute for Basic Science (IBS)
Changbum Jo: Institute for Basic Science (IBS)
Seung Won Han: Institute for Basic Science (IBS)
Jeong-Chul Kim: Institute for Basic Science (IBS)
Hongjun Park: Institute for Basic Science (IBS)
Jongho Han: Institute for Basic Science (IBS)
Hye Sun Shin: Institute for Basic Science (IBS)
Jae Won Shin: Institute for Basic Science (IBS)
Nature, 2020, vol. 585, issue 7824, 221-224
Abstract:
Abstract Platinum is a much used catalyst that, in petrochemical processes, is often alloyed with other metals to improve catalytic activity, selectivity and longevity1–5. Such catalysts are usually prepared in the form of metallic nanoparticles supported on porous solids, and their production involves reducing metal precursor compounds under a H2 flow at high temperatures6. The method works well when using easily reducible late transition metals, but Pt alloy formation with rare-earth elements through the H2 reduction route is almost impossible owing to the low chemical potential of rare-earth element oxides6. Here we use as support a mesoporous zeolite that has pore walls with surface framework defects (called ‘silanol nests’) and show that the zeolite enables alloy formation between Pt and rare-earth elements. We find that the silanol nests enable the rare-earth elements to exist as single atomic species with a substantially higher chemical potential compared with that of the bulk oxide, making it possible for them to diffuse onto Pt. High-resolution transmission electron microscopy and hydrogen chemisorption measurements indicate that the resultant bimetallic nanoparticles supported on the mesoporous zeolite are intermetallic compounds, which we find to be stable, highly active and selective catalysts for the propane dehydrogenation reaction. When used with late transition metals, the same preparation strategy produces Pt alloy catalysts that incorporate an unusually large amount of the second metal and, in the case of the PtCo alloy, show high catalytic activity and selectivity in the preferential oxidation of carbon monoxide in H2.
Date: 2020
References: Add references at CitEc
Citations: View citations in EconPapers (10)
Downloads: (external link)
https://www.nature.com/articles/s41586-020-2671-4 Abstract (text/html)
Access to the full text of the articles in this series is restricted.
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:585:y:2020:i:7824:d:10.1038_s41586-020-2671-4
Ordering information: This journal article can be ordered from
https://www.nature.com/
DOI: 10.1038/s41586-020-2671-4
Access Statistics for this article
Nature is currently edited by Magdalena Skipper
More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().