The effect of oxygen transfer mechanism on the cathode performance based on proton-conducting solid oxide fuel cells
KAUST DepartmentPhysical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/563939
MetadataShow full item record
AbstractTwo types of proton-blocking composites, La2NiO4+δ-LaNi0.6Fe0.4O3-δ (LNO-LNF) and Sm0.2Ce0.8O2-δ-LaNi0.6Fe0.4O3-δ (SDC-LNF), were evaluated as cathode materials for proton-conducting solid oxide fuel cells (H-SOFCs) based on the BaZr0.1Ce0.7Y0.2O3-δ (BZCY) electrolyte, in order to compare and investigate the influence of two different oxygen transfer mechanism on the performance of the cathode for H-SOFCs. The X-ray diffraction (XRD) results showed that the chemical compatibility of the components in both compounds was excellent up to 1000°C. Electrochemical studies revealed that LNO-LNF showed lower area specific polarization resistances in symmetrical cells and better electrochemical performance in single cell tests. The single cell with LNO-LNF cathode generated remarkable higher maximum power densities (MPDs) and lower interfacial polarization resistances (Rp) than that with SDC-LNF cathode. Correspondingly, the MPDs of the single cell with the LNO-LNF cathode were 490, 364, 266, 180 mW cm-2 and the Rp were 0.103, 0.279, 0.587, 1.367 Ω cm2 at 700, 650, 600 and 550°C, respectively. Moreover, after the single cell with LNO-LNF cathode optimized with an anode functional layer (AFL) between the anode and electrolyte, the power outputs reached 708 mW cm-2 at 700°C. These results demonstrate that the LNO-LNF composite cathode with the interstitial oxygen transfer mechanism is a more preferable alternative for H-SOFCs than SDC-LNF composite cathode with the oxygen vacancy transfer mechanism.
CitationHou, J., Qian, J., Bi, L., Gong, Z., Peng, R., & Liu, W. (2015). The effect of oxygen transfer mechanism on the cathode performance based on proton-conducting solid oxide fuel cells. Journal of Materials Chemistry A, 3(5), 2207–2215. doi:10.1039/c4ta04397a
SponsorsThis work was supported by Ministry of Science and Technology of China (Grant no.: 2012CB215403). The project was also supported by the National Science Foundations of China (Grant nos: 51472228 and 21406190).
PublisherRoyal Society of Chemistry (RSC)
JournalJ. Mater. Chem. A