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Platinum incorporation into titanate perovskites to deliver emergent active and stable platinum nanoparticles

Authors :
Yukwon Jeon
David Wails
John T. S. Irvine
David Miller
John Kilmartin
Alan V. Chadwick
Maadhav Kothari
Andrea Eva Pascui
Silvia Ramos
EPSRC
University of St Andrews. School of Chemistry
University of St Andrews. Centre for Designer Quantum Materials
University of St Andrews. EaSTCHEM
Publication Year :
2021
Publisher :
Nature Research, 2021.

Abstract

Platinum functions exceptionally well as a nanoparticulate catalyst in many important fields, such as in the removal of atmospheric pollutants, but it is scarce, expensive and not always sufficiently durable. Here, we report a perovskite system in which 0.5 wt% Pt is integrated into the support and its subsequent conversion through exsolution to achieve a resilient catalyst. Owing to the instability of most Pt oxides at high temperatures, a thermally stable platinum oxide precursor, barium platinate, was used to preserve the platinum as an oxide during the solid-state synthesis in an approach akin to the Trojan horse legend. By tailoring the procedure, it is possible to produce a uniform equilibrated structure with active emergent Pt nanoparticles strongly embedded in the perovskite surface that display better CO oxidation activity and stability than those of conventionally prepared Pt catalysts. This catalyst was further evaluated for a variety of reactions under realistic test environments—CO and NO oxidation, diesel oxidation catalysis and ammonia slip reactions were investigated. Nanoparticulate platinum is a highly active catalyst, but it is scarce, expensive and not always sufficiently durable. Now, barium platinate has been used as a vehicle to preserve platinum as an oxide during the solid-state synthesis of a Pt-doped titanate perovskite; this enables the production of a structure with active and stable Pt nanoparticles on the perovskite surface that catalyses CO oxidation.

Details

Language :
English
ISSN :
17554330
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....92af427837d7716b423fb64d7095e233