材料科学
阳极
氧化还原
氨
电化学
化学工程
纳米颗粒
氢
陶瓷
无机化学
纳米技术
电极
冶金
化学
物理化学
有机化学
工程类
作者
Zuoqing Liu,Haosong Di,Dongliang Liu,Guangming Yang,Yinlong Zhu,Zhixin Luo,Ran Ran,Yan Wang,Wei Zhou,Zongping Shao
标识
DOI:10.1002/adfm.202420214
摘要
Abstract Ammonia, with high hydrogen content and carbon neutrality, is an ideal fuel for protonic ceramic fuel cells (PCFCs). However, the limited electrochemical efficiency and durability of ammonia‐based PCFCs have posed challenges for broader implementation. Herein, a novel anode material, Ni‐Ba(Zr 0.1 Ce 0.7 Y 0.1 Yb 0.1 ) 0.94 Ru 0.03 Fe 0.03 O 3‐δ (BZCYYbRF), developed by co‐doping with Ru and Fe is introduced, which promotes the exsolution of RuFe nanoparticles under reducing conditions. A secondary redox process further enhances nanoparticle redistribution, increasing catalytic activity and improving ammonia decomposition and hydrogen oxidation, as well as the charge transfer at the heterointerface, leading to a marked improvement in the electrochemical performance of the PCFC under both hydrogen and ammonia fuel conditions. A single cell utilizing BZCYYbRF as the anode achieves a peak power density of 700 mW cm⁻ 2 at 650 °C under NH 3 fuel, with stable operation for up to 150 h. Additionally, secondary redox treatment improved performance to 807 mW cm⁻ 2 at 650 °C. The innovation lies in the co‐doping and redox‐driven nanoparticle exsolution strategy, significantly boosting PCFC performance and stability, positioning this anode as a breakthrough for direct ammonia fuel cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI