Affiliation:
1. Faculty of Materials Science and Chemistry China University of Geosciences Wuhan 430074 China
2. Shenzhen Research Institute China University of Geosciences Shenzhen 518000 China
3. School of Marine Science and Engineering Hainan University Haikou 570228 China
Abstract
AbstractProtonic ceramic fuel cells (PCFCs) hold potential for sustainable energy conversion, yet their widespread application is hindered by the sluggish kinetics and inferior stability of cathode materials. Here, a facile and efficient reverse atom capture technique is developed to manipulate the surface chemistry of PrBa0.5Sr0.5Co1.5Fe0.5O5+δ (PBSCF) cathode for PCFCs. This method successfully captures segregated Ba and Sr cations on the PBSCF surface using W species, creating a (Ba/Sr)(Co/Fe/W)O3−δ (BSCFW)@PBSCF heterostructure. Benefiting from enhanced kinetics of proton‐involved oxygen reduction reaction and strengthened chemical stability, the single cell using the optimized 2W‐PBSCF cathode demonstrates an exceptional peak power density of 1.32 W cm−2 at 650 °C and maintains durable performance for 240 h. Theoretical calculations unveil that the BSCFW perovskite delivers lower oxygen vacancy formation energy, hydration energy, and proton transfer energy compared to the PBSCF perovskite. This protocol offers new insights into advanced atom capture techniques for sustainable energy infrastructures.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Shenzhen Science and Technology Innovation Program
Cited by
4 articles.
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