TY - JOUR
T1 - Co-free and Sr-free double-perovskite oxide PrBaFe1.9Nb0.1O5+δ as a potential electrode material for symmetrical solid oxide fuel cells
AU - Wang, Feng
AU - Qi, Jinyan
AU - Shan, Pengkai
AU - Qian, Bin
AU - Xie, Lishuai
AU - Zheng, Yifeng
AU - Chen, Han
AU - Ge, Lin
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
PY - 2024/10
Y1 - 2024/10
N2 - Double-perovskite oxide PrBaFe2O5+δ (PBF) is considered as a potential electrode material because of its superior oxygen reduction reaction (ORR) activity in air and excellent stability in wet hydrogen atmospheres. However, the electrochemical activities of Fe-based electrode materials are constrained by the oxygen vacancy concentration and oxy-ion transport properties. Herein, PrBaFe2-xNbxO5+δ (PBFNx, x = 0, 0.05, 0.1, 0.15) oxides are synthesized and evaluated as electrodes for symmetrical solid oxide fuel cell (SSOFC). X-ray diffraction (XRD) indicates that PBFNx samples have an orthorhombic structure and good chemical compatibility with electrolyte. Among all the samples, the PBFN0.1 symmetrical half-cell shows the lowest polarization resistance at 800 °C, which decreases by 29.2% compared with that of PBF in air and decreases by 59.9% compared with that of PBF in wet hydrogen atmospheres. The output performance of the single cell with PBFN0.1 as symmetrical electrodes achieves 197.10 mW cm−2 in wet hydrogen atmospheres at 800 °C, which is an improvement of 31.97% compared with that of PBF. The enhanced electrochemical performance can be attributed to an increase in oxygen vacancy concentrations. The results suggest that the PBFN0.1 material is a potential candidate for SSOFC.
AB - Double-perovskite oxide PrBaFe2O5+δ (PBF) is considered as a potential electrode material because of its superior oxygen reduction reaction (ORR) activity in air and excellent stability in wet hydrogen atmospheres. However, the electrochemical activities of Fe-based electrode materials are constrained by the oxygen vacancy concentration and oxy-ion transport properties. Herein, PrBaFe2-xNbxO5+δ (PBFNx, x = 0, 0.05, 0.1, 0.15) oxides are synthesized and evaluated as electrodes for symmetrical solid oxide fuel cell (SSOFC). X-ray diffraction (XRD) indicates that PBFNx samples have an orthorhombic structure and good chemical compatibility with electrolyte. Among all the samples, the PBFN0.1 symmetrical half-cell shows the lowest polarization resistance at 800 °C, which decreases by 29.2% compared with that of PBF in air and decreases by 59.9% compared with that of PBF in wet hydrogen atmospheres. The output performance of the single cell with PBFN0.1 as symmetrical electrodes achieves 197.10 mW cm−2 in wet hydrogen atmospheres at 800 °C, which is an improvement of 31.97% compared with that of PBF. The enhanced electrochemical performance can be attributed to an increase in oxygen vacancy concentrations. The results suggest that the PBFN0.1 material is a potential candidate for SSOFC.
KW - Double perovskite
KW - Electrochemical performance
KW - Nb doping
KW - Symmetrical solid oxide fuel cells
UR - http://www.scopus.com/inward/record.url?scp=85199903420&partnerID=8YFLogxK
U2 - 10.1007/s11581-024-05724-w
DO - 10.1007/s11581-024-05724-w
M3 - 文章
AN - SCOPUS:85199903420
SN - 0947-7047
VL - 30
SP - 6305
EP - 6319
JO - Ionics
JF - Ionics
IS - 10
ER -