Abstract
The search for new functional materials that combine high stability and efficiency with reasonable cost and ease of synthesis is critical for their use in renewable energy applications. Specifically in catalysis, nanoparticles, with their high surface-To-volume ratio, can overcome the cost implications associated with otherwise having to use large amounts of noble metals. However, commercialized materials, that is, catalytic nanoparticles deposited on oxide supports, often suffer from loss of activity because of coarsening and carbon deposition during operation. Exsolution has proven to be an interesting strategy to overcome such issues. Here, the controlled emergence, or exsolution, of faceted iridium nanoparticles from a doped SrTiO3 perovskite is reported and their growth preliminary probed by in situ electron microscopy. Upon reduction of SrIr0.005Ti0.995O3, the generated nanoparticles show embedding into the oxide support, therefore preventing agglomeration and subsequent catalyst degradation. The advantages of this approach are the extremely low noble metal amount employed (0.5% weight) and the catalytic activity reported during CO oxidation tests, where the performance of the exsolved SrIr0.005Ti0.995O3 is compared to the activity of a commercial catalyst with 1% loading (1% Ir/Al2O3). The high activity obtained with such low doping shows the possibility of scaling up this new catalyst, reducing the high cost associated with iridium-based materials.
Original language | English |
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Pages (from-to) | 37444-37453 |
Number of pages | 10 |
Journal | ACS Applied Materials and Interfaces |
Volume | 12 |
Issue number | 33 |
DOIs | |
State | Published - Aug 19 2020 |
Bibliographical note
Funding Information:This work was performed as part of the Engineering and Physical Science Research Council grant numbers EP/R023522/1, EP/R023646/1 and EP/R023921/1. D.J.P. was supported by The Royal Society grant numbers UF100105 and UF150693 during this work. Nion UltraSTEM 100 characterization was conducted at the Centre for Nanophase Materials Sciences at Oak Ridge National Laboratory (US), which is a DOE Office of Science User Facility and this work was supported in part by the National Science Foundation under DMR 1455154 (M.P.T., B.S.G.). The authors are grateful to all the members of the Emergent Nanomaterials (EPSRC Critical Mass Proposal) project for useful discussion.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
Keywords
- catalysis
- exsolution
- in situ TEM
- iridium
- nanoparticles
ASJC Scopus subject areas
- Materials Science (all)