TY - JOUR
T1 - Boosting Ammonia-Fueled Protonic Ceramic Fuel Cells with RuFe Nanoparticle Exsolution
T2 - Enhanced Performance via Secondary Redox Treatment
AU - Liu, Zuoqing
AU - Di, Haosong
AU - Liu, Dongliang
AU - Yang, Guangming
AU - Zhu, Yinlong
AU - Luo, Zhixin
AU - Ran, Ran
AU - Wang, Wei
AU - Zhou, Wei
AU - Shao, Zongping
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/4/10
Y1 - 2025/4/10
N2 - 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(Zr0.1Ce0.7Y0.1Yb0.1)0.94Ru0.03Fe0.03O3-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 NH3 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.
AB - 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(Zr0.1Ce0.7Y0.1Yb0.1)0.94Ru0.03Fe0.03O3-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 NH3 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.
KW - RuFe nanoparticle
KW - ammonia decomposition catalyst
KW - ammonia fuel
KW - anode
KW - direct ammonia protonic ceramic fuel cells
UR - http://www.scopus.com/inward/record.url?scp=105002488659&partnerID=8YFLogxK
U2 - 10.1002/adfm.202420214
DO - 10.1002/adfm.202420214
M3 - 文章
AN - SCOPUS:105002488659
SN - 1616-301X
VL - 35
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 15
M1 - 2420214
ER -