Concurrent Amorphization and Nanocatalyst Formation in Cu-Substituted Perovskite Oxide Surface : Effects on Oxygen Reduction Reaction at Elevated Temperatures

© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2024) vom: 09. Aug., Seite e2404103
1. Verfasser: Jeon, SungHyun (VerfasserIn)
Weitere Verfasser: Jung, Wan-Gil, Bae, Hohan, Ahn, Sejong, Koo, Bonjae, Yu, WonJeong, Kim, Seunghyun, Oh, DongHwan, Kim, Uisik, Barnett, Scott A, Seo, Jongsu, Kim, Bong-Joong, Jung, WooChul
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article ex‐solution in situ observation oxygen reduction reaction solid oxide fuel cell surface amorphization
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520 |a The activity and durability of chemical/electrochemical catalysts are significantly influenced by their surface environments, highlighting the importance of thoroughly examining the catalyst surface. Here, Cu-substituted La0.6Sr0.4Co0.2Fe0.8O3-δ is selected, a state-of-the-art material for oxygen reduction reaction (ORR), to explore the real-time evolution of surface morphology and chemistry under a reducing atmosphere at elevated temperatures. Remarkably, in a pioneering observation, it is discovered that the perovskite surface starts to amorphize at an unusually low temperature of approximately 100 °C and multicomponent metal nanocatalysts additionally form on the amorphous surface as the temperature raises to 400 °C. Moreover, this investigation into the stability of the resulting amorphous layer under oxidizing conditions reveals that the amorphous structure can withstand a high-temperature oxidizing atmosphere (≥650 °C) only when it has undergone sufficient reduction for an extended period. Therefore, the coexistence of the active nanocatalysts and defective amorphous surface leads to a nearly 100% enhancement in the electrode resistance for the ORR over 200 h without significant degradation. These observations provide a new catalytic design strategy for using redox-dynamic perovskite oxide host materials 
650 4 |a Journal Article 
650 4 |a ex‐solution 
650 4 |a in situ observation 
650 4 |a oxygen reduction reaction 
650 4 |a solid oxide fuel cell 
650 4 |a surface amorphization 
700 1 |a Jung, Wan-Gil  |e verfasserin  |4 aut 
700 1 |a Bae, Hohan  |e verfasserin  |4 aut 
700 1 |a Ahn, Sejong  |e verfasserin  |4 aut 
700 1 |a Koo, Bonjae  |e verfasserin  |4 aut 
700 1 |a Yu, WonJeong  |e verfasserin  |4 aut 
700 1 |a Kim, Seunghyun  |e verfasserin  |4 aut 
700 1 |a Oh, DongHwan  |e verfasserin  |4 aut 
700 1 |a Kim, Uisik  |e verfasserin  |4 aut 
700 1 |a Barnett, Scott A  |e verfasserin  |4 aut 
700 1 |a Seo, Jongsu  |e verfasserin  |4 aut 
700 1 |a Kim, Bong-Joong  |e verfasserin  |4 aut 
700 1 |a Jung, WooChul  |e verfasserin  |4 aut 
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