TY - JOUR
T1 - Attenuating a metal-oxygen bond of a double perovskite oxide
T2 - Via anion doping to enhance its catalytic activity for the oxygen reduction reaction
AU - Zhang, Lihong
AU - Sun, Wang
AU - Xu, Chunming
AU - Ren, Rongzheng
AU - Yang, Xiaoxia
AU - Qiao, Jinshuo
AU - Wang, Zhenhua
AU - Sun, Kening
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2020/7/28
Y1 - 2020/7/28
N2 - Elevating the sluggish oxygen reduction reaction (ORR) activity of the cathode material is crucial to the development and widespread application of intermediate-temperature solid oxide fuel cells (IT-SOFCs). Herein, a novel SOFC cathode, with superior ORR activity, is designed by incorporating F anions at O-sites of a double perovskite oxide (Sr2Fe1.5Mo0.5O6-δ, SFM). The resulting F-doped SFM cathode (Sr2Fe1.5Mo0.5O6-x-δFx, SFMF, x = 0, 0.1, 0.2 and 0.3) exhibits improved crystal structure symmetry and enhanced electrocatalytic activity for the ORR. At 800 °C, the polarization resistance of F-doped SFM is significantly decreased to 0.072 Ω cm2, which can be ascribed to the enhanced oxygen reduction capacity. Moreover, F-doping reduces the metal-oxygen bond energy and accelerates the transportation of O-ions during the electrochemical process, resulting in significantly enhanced ORR activity.
AB - Elevating the sluggish oxygen reduction reaction (ORR) activity of the cathode material is crucial to the development and widespread application of intermediate-temperature solid oxide fuel cells (IT-SOFCs). Herein, a novel SOFC cathode, with superior ORR activity, is designed by incorporating F anions at O-sites of a double perovskite oxide (Sr2Fe1.5Mo0.5O6-δ, SFM). The resulting F-doped SFM cathode (Sr2Fe1.5Mo0.5O6-x-δFx, SFMF, x = 0, 0.1, 0.2 and 0.3) exhibits improved crystal structure symmetry and enhanced electrocatalytic activity for the ORR. At 800 °C, the polarization resistance of F-doped SFM is significantly decreased to 0.072 Ω cm2, which can be ascribed to the enhanced oxygen reduction capacity. Moreover, F-doping reduces the metal-oxygen bond energy and accelerates the transportation of O-ions during the electrochemical process, resulting in significantly enhanced ORR activity.
UR - http://www.scopus.com/inward/record.url?scp=85088703153&partnerID=8YFLogxK
U2 - 10.1039/d0ta04820h
DO - 10.1039/d0ta04820h
M3 - Article
AN - SCOPUS:85088703153
SN - 2050-7488
VL - 8
SP - 14091
EP - 14098
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 28
ER -