Atomic Scale Responses of High Entropy Oxides to Redox Environments

• Published in: Nano letters 2024-09, Vol.24 (37), p.11537-11543
• Main Authors: Huang, Zhennan, Wang, Lu, Li, Tangyuan, Venkatraman, Kartik, He, Yang, Polo-Garzon, Felipe, Smith, Jacob, Du, Yiheng, Hu, Liangbing, Wu, Zili, Jiang, De-en, Chi, Miaofang
• Format: Article
• Language: English
• ISSN: 1530-6984; 1530-6992; 1530-6992
• DOI: 10.1021/acs.nanolett.4c02985

The potential of high entropy oxides (HEOs) as high-performance energy storage materials and catalysts has been mainly understood through their bulk structures. However, the importance of their surfaces, which may play an even more critical role, remains largely unknown. In this study, we employed advanced scanning transmission electron microscopy to investigate the atomic-scale structural and chemical responses of CeYLaHfTiZrO x HEOs to high-temperature redox environments. Our observations reveal dynamic elemental and structural reconstructions in the surface of HEOs under different gas environments, contrasting with the high stability of the bulk structure. Notably, the surfaces of HEO particles consistently exhibit abundant oxygen vacancies, regardless of the redox environment. These findings indicate that HEOs offer distinct advantages in facilitating chemical and electrochemical reactions, relying on oxygen vacancies. Our results also suggest that the exceptional performance of HEOs in energy storage applications arises from surface structural and chemical adaptability.