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Ju, Young-Wan
GUNS Lab
Research Interests
  • Materials Chemistry
  • Nanotechnology
  • Polymer Chemistry

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Ruddlesden Popper oxides of LnSr(3)Fe(3)O(10-delta) (Ln = La, Pr, Nd, Sm, Eu, and Gd) as active cathodes for low temperature solid oxide fuel cells

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Title
Ruddlesden Popper oxides of LnSr(3)Fe(3)O(10-delta) (Ln = La, Pr, Nd, Sm, Eu, and Gd) as active cathodes for low temperature solid oxide fuel cells
Author
Chaianansutcharit, SoamwadeeHosoi, KoheiHyodo, JunjiJu, Young-WanIshihara, Tatsumi
Issue Date
2015-06
Publisher
ROYAL SOC CHEMISTRYROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.3, no.23, pp.12357 - 12366
Abstract
Ruddlesden Popper type oxides of LnSr(3)Fe(3)O(10-delta) (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-delta), it was found that PrSr3Fe3O10-delta shows the highest activity for the cathode reaction. The prepared LnSr(3)Fe(3)O(10-delta) oxides have a tetragonal crystal structure with the space group I4/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-delta) are reasonably compatible with those of La0.9Sr0.1Ga0.8Mg0.2O3 (LSGM) electrolyte. The catalytic activity as cathodes for H-2-SOFCs depended on Ln ions. A high cathodic activity was achieved on LnSr(3)Fe(3)O(10-delta) (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, PrSr3Fe3O10-delta is highly promising as a cathode for low temperature SOFCs
URI
https://scholarworks.unist.ac.kr/handle/201301/17527
URL
http://pubs.rsc.org/en/Content/ArticleLanding/2015/TA/C5TA01273B#!divAbstract
DOI
10.1039/c5ta01273b
ISSN
2050-7488
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