Dielectric Barrier Plasma Discharge Exsolution of Nanoparticles at Room Temperature and Atmospheric Pressure

Author:

ul Haq Atta1ORCID,Fanelli Fiorenza23,Bekris Leonidas4,Martin Alex Martinez4,Lee Steve5,Khalid Hessan1,Savaniu Cristian D.6,Kousi Kalliopi7,Metcalfe Ian S.4,Irvine John T. S.6,Maguire Paul1,Papaioannou Evangelos I.4,Mariotti Davide8ORCID

Affiliation:

1. School of Engineering Ulster University Belfast BT37 0QB UK

2. Institute of Nanotechnology (NANOTEC) National Research Council (CNR) via Orabona 4 Bari 70125 Italy

3. Institute of Chemistry of Organometallic Compounds (ICCOM) National Research Council (CNR) via Orabona 4 Bari 70125 Italy

4. School of Engineering Newcastle University Newcastle upon Tyne NE1 7RU UK

5. School of Physics and Astronomy University of St. Andrews Scotland Fife St. Andrews KY16 9SS UK

6. School of Chemistry University of St. Andrews Scotland Fife St. Andrews KY16 9ST UK

7. School of Chemistry & Chemical Engineering University of Surrey Guildford Surrey GU2 7XH UK

8. Department of Design Manufacturing & Engineering Management University of Strathclyde Glasgow G1 1XJ UK

Abstract

AbstractExsolution of metal nanoparticles (NPs) on perovskite oxides has been demonstrated as a reliable strategy for producing catalyst‐support systems. Conventional exsolution requires high temperatures for long periods of time, limiting the selection of support materials. Plasma direct exsolution is reported at room temperature and atmospheric pressure of Ni NPs from a model A‐site deficient perovskite oxide (La0.43Ca0.37Ni0.06Ti0.94O2.955). Plasma exsolution is carried out within minutes (up to 15 min) using a dielectric barrier discharge configuration both with He‐only gas as well as with He/H2 gas mixtures, yielding small NPs (<30 nm diameter). To prove the practical utility of exsolved NPs, various experiments aimed at assessing their catalytic performance for methanation from synthesis gas, CO, and CH4 oxidation are carried out. Low‐temperature and atmospheric pressure plasma exsolution are successfully demonstrated and suggest that this approach could contribute to the practical deployment of exsolution‐based stable catalyst systems.

Funder

UK Catalysis Hub

Royal Academy of Engineering

Henry Royce Institute

Royal Society

Engineering and Physical Sciences Research Council

Publisher

Wiley

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