Ruddlesden Popper oxides of LnSr 3 Fe 3 O 10−δ (Ln = La, Pr, Nd, Sm, Eu, and Gd) as active cathodes for low temperature solid oxide fuel cells
Ruddlesden Popper type oxides of LnSr 3 Fe 3 O 10−δ (Ln = La, Pr, Nd, Sm, Eu, and Gd) have been investigated as active cathodes for solid oxide fuel cells (SOFCs). Among the examined LnSr 3 Fe 3 O 10−δ , it was found that PrSr 3 Fe 3 O 10−δ shows the highest activity for the cathode reaction. The pr...
Saved in:
Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 3; no. 23; pp. 12357 - 12366 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
2015
|
Online Access | Get full text |
Cover
Loading…
Summary: | Ruddlesden Popper type oxides of LnSr
3
Fe
3
O
10−δ
(Ln = La, Pr, Nd, Sm, Eu, and Gd) have been investigated as active cathodes for solid oxide fuel cells (SOFCs). Among the examined LnSr
3
Fe
3
O
10−δ
, it was found that PrSr
3
Fe
3
O
10−δ
shows the highest activity for the cathode reaction. The prepared LnSr
3
Fe
3
O
10−δ
oxides have a tetragonal crystal structure with the space group
I
4/
mmm
. With decreasing the ionic size of Ln
3+
, the unit cell volume and crystallite size decrease. The temperature and
P
O2
dependences of electrical conductivities indicate the metal-like behaviour and the predominant hole conduction. The thermal expansion coefficient (TEC) values derived from the non-linear expansion curves of LnSr
3
Fe
3
O
10−δ
are reasonably compatible with those of La
0.9
Sr
0.1
Ga
0.8
Mg
0.2
O
3
(LSGM) electrolyte. The catalytic activity as cathodes for H
2
-SOFCs depended on Ln ions. A high cathodic activity was achieved on PrSr
3
Fe
3
O
10−δ
(PSFO10) and a maximum power density of 0.51 W cm
−2
was achieved at 1073 K when 0.3 mm thick LSGM electrolyte was used. The surface exchange coefficient,
k
, also confirms the high activity for the dissociation of oxygen on PSFO10. Therefore, PrSr
3
Fe
3
O
10−δ
is highly promising as a cathode for low temperature SOFCs. |
---|---|
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C5TA01273B |