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High performance of Mo-doped La0.6Sr0.4Fe0.9Ni0.1O3-δ perovskites as anode for solid oxide fuel cells.

Authors :
Hou, Yunting
Wang, Lijun
Bian, Liuzhen
Chen, Ning
Chou, Kuochih
Source :
Electrochimica Acta. Dec2018, Vol. 292, p540-545. 6p.
Publication Year :
2018

Abstract

Abstract The Mo-doped La 0.6 Sr 0.4 Fe 0.9 Ni 0.1 O 3-δ (LSFNM) material is synthesized by a sol-gel method as a SOFC anode. XRD results explain that La 0.6 Sr 0.4 Fe 0.9 Ni 0.1 O 3-δ (LSFN) is decomposed severely above 800 °C in reducing atmosphere, while LSFNM basically maintains the cubic perovskite main phase, and only a small quantity of heterophase appears. Apparently, Mo doping can improve the reduction stability of material. Meanwhile, Mo6+ effectively suppresses the reduction of the Fe4+/Fe3+ electron pair in reducing atmosphere, which enhances the electrical conductivity. In 5% H 2 -Ar, the conductivity of Mo-doped sample is increased from 0.75 to 2.8 S cm−1 at 800 °C, which is more in line with the requirement of the anode. LSFNM exhibits lower polarization resistance (R p) than LSFN in wet H 2 ; for example, the R p values of LSFN and LSFNM at 850 °C are 0.25 and 0.18 Ω cm2. The maximum power density (P max) of the LSGM-supported single cell is increased from 740 to 975 mW cm−2 in H 2 at 850 °C, and the cell exhibits reasonable stability at 700 °C for 100 h. Thus, it is rational to consider that the LSFNM is a potential material for IT–SOFC anode. Graphical abstract Image Highlights • La 0.6 Sr 0.4 Fe 0.8 Ni 0.1 Mo 0.1 O 3-δ (LSFNM) is used as anode electrode for SOFC. • Mo doping significantly improves stability in reducing atmosphere. • The conductivity of LSFNM reaches 2.8 S cm−2 at 800 °C in 5% H 2 -Ar. • LSFNM exhibits higher hydrogen oxidation reaction (HOR) activity than LSFN. • Maximum power density of 975 mW cm−2 in H 2 is obtained at 850 °C for LSFNM. [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
*SOLID oxide fuel cells
*ANODES

Details

Language :
English
ISSN :
00134686
Volume :
292
Database :
Academic Search Index
Journal :
Electrochimica Acta
Publication Type :
Academic Journal
Accession number :
132919667
Full Text :
https://doi.org/10.1016/j.electacta.2018.09.190