Exploring Topochemical Oxidation Reactions for Reversible Tuning of Thermal Conductivity in Perovskite Fe Oxides
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American Chemical Society
Abstract
We present a study on the reversibility of thermal conductivity in iron oxides through topochemical oxygen exchange between brownmillerite (BM) (Ca,Sr)FeO2.5 and perovskite (PV) (Ca,Sr)FeO3.0. By using different oxidation methods, including gas phase (O2/O3), liquid phase (NaOCl in H2O), and solid electrolyte (Y2O3:ZrO2), we demonstrate that the oxidation pathway has a critical influence on the reversibility of the ionic-exchange process. Cyclic oxidation and reduction using O2/O3 or NaOCl lead to an important accumulation of structural defects, undermining the reversibility of thermal conductivity. In the case of wet oxidation, we demonstrate an inherent tendency of negative charge-transfer oxides toward amorphization and elucidate the origin of this effect. Conversely, the electrochemical injection of the O2– ions via a Y2O3:ZrO2 solid electrolyte reduces structural damage significantly, enhancing both reversibility and durability. This study underscores the importance of selecting appropriate topochemical oxygen exchange methods to maintain structural integrity and optimize functional performance in oxide-based tunable devices.
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The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.chemmater.4c02023.
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Varela-Domínguez, N., S. Claro, M., Carbó-Argibay, E., Magén, C. & Rivadulla, F. (2024). Exploring Topochemical Oxidation Reactions for Reversible Tuning of Thermal Conductivity in Perovskite Fe Oxides. "Chemistry of Materials", 36(20), 10249-10258. DOI: 10.1021/acs.chemmater.4c02023
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https://doi.org/10.1021/acs.chemmater.4c02023Sponsors
This work has received financial support from Agencia Estatal de Investigación (Spain), project PID2019-104150RB-I00, PID2022-138883NB-I00, TED2021-130930B-I00, Xunta de Galicia (Centro de investigación do Sistema universitario de Galicia accreditation 2023-2027, ED431G 2023/03), Gobierno de Aragón through grant E13_20R and the European Union (European Regional Development Fund – ERDF). The research of F.R. receives financial support from the Oportunius Program, Xunta de Galicia. N.V.-D. acknowledges financial support from Agencia Estatal de Investigación (Spain) through an FPI fellowship (PRE2020-096467). This work was carried out in part through the use of the INL User Facilities. The authors would like to thank the use of the USC Research Infrastructures (RIAIDT) analytical facilities. The authors acknowledge the use of instrumentation as well as the technical advice provided by the National Facility ELECMI ICTS, node Laboratorio de Microscopias Avanzadas (LMA) at Universidad de Zaragoza.
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© 2024 The Authors. Published by American Chemical Society. Attribution 4.0 International








