Mitigating A-Site Segregation in Pyrochlore Oxides : Enhancing Oxygen Evolution Reaction Performance through Surface Engineering
Significant progress has been achieved in enhancing the oxygen evolution reaction (OER) performance of pyrochloric oxides through geometric and electronic structure regulation. However, the issue of A-site cation segregation in these materials remains underexplored. In this study, Bi2Ru2O7, a promis...
| Publié dans: | Langmuir : the ACS journal of surfaces and colloids. - 1985. - 41(2025), 6 vom: 18. Feb., Seite 4249-4258 |
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| Auteur principal: | |
| Autres auteurs: | , , , , , , |
| Format: | Article en ligne |
| Langue: | English |
| Publié: |
2025
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| Accès à la collection: | Langmuir : the ACS journal of surfaces and colloids |
| Sujets: | Journal Article |
| Résumé: | Significant progress has been achieved in enhancing the oxygen evolution reaction (OER) performance of pyrochloric oxides through geometric and electronic structure regulation. However, the issue of A-site cation segregation in these materials remains underexplored. In this study, Bi2Ru2O7, a promising OER electrocatalyst, is synthesized via a sol-gel method, and its surface is modified using l-ascorbic acid to address Bi3+ segregation. This treatment selectively removes the Bi2O3 passivation layer, inducing an amorphous RuOx layer that forms a heterostructure with crystalline Bi2Ru2O7. This engineered structure significantly enhances catalytic performance, reducing the overpotential to 259 mV at 10 mA cm-2 and maintaining stability after continuous operation for >30 h. Comprehensive characterization, electrochemical testing, and density functional theory calculations reveal that the improvements stem from an increased number of oxygen vacancies and enhanced electron transfer. This work underscores the importance of surface engineering to mitigate A-site segregation, providing a new strategy for optimizing Ru-based pyrochlores in energy conversion technologies |
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| Description: | Date Revised 18.02.2025 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
| ISSN: | 1520-5827 |
| DOI: | 10.1021/acs.langmuir.4c04886 |