Abstract
Developing highly active and stable electrocatalysts for the oxygen evolution reaction (OER) is key to improving the efficiency and practical application of various sustainable energy technologies including water electrolysis, CO2 reduction, and metal air batteries. Here, we use evaporation-induced self-assembly (EISA) to synthesize highly porous fluorite nanocatalysts with a high surface area. In this study, we demonstrate that a 50% rare-earth cation substitution for Ce in the CeO2 fluorite lattice improves the OER activity and stability by introducing oxygen vacancies into the host lattice, which results in a decrease in the adsorption energy of the OH* intermediate in the OER. Among the binary fluorite compositions investigated, Nd2Ce2O7 is shown to display the lowest OER overpotential of 243 mV, achieved at a current density of 10 mA cm-2, and excellent cycling stability in an alkaline medium. Importantly, we demonstrate that rare-earth oxide OER electrocatalysts with high activity and stability can be achieved using the EISA synthesis route without the incorporation of transition and noble metals.
Recommended Citation
S. Paladugu et al., "Mesoporous RE0.5Ce0.5O2-X Fluorite Electrocatalysts For The Oxygen Evolution Reaction," ACS Applied Materials and Interfaces, vol. 16, no. 6, pp. 7014 - 7025, American Chemical Society, Feb 2024.
The definitive version is available at https://doi.org/10.1021/acsami.3c14977
Department(s)
Chemistry
Keywords and Phrases
electrocatalyst; fluorites; mesoporous; OER; oxygen vacancies, high entropy oxides; rare earth cations
International Standard Serial Number (ISSN)
1944-8252; 1944-8244
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2024 American Chemical Society, All rights reserved.
Publication Date
14 Feb 2024
PubMed ID
38308595
Comments
American Chemical Society Petroleum Research Fund, Grant 62728-DNI3