Back to Search Start Over

Preparation of LaNiO powders as a cathode material for SOFC via a PVP-assisted hydrothermal route.

Authors :
Lou, Zhongliang
Hao, Xiaoming
Peng, Jun
Wang, Zhenhua
Rooney, David
Sun, Kening
Source :
Journal of Solid State Electrochemistry; Apr2015, Vol. 19 Issue 4, p957-965, 9p
Publication Year :
2015

Abstract

Uniform submicron LaNiO (sm-LNO) powders have been synthesized by a facile polyvinylpyrrolidone (PVP)-assisted hydrothermal route. In the presence of PVP, sm-LNO of pure phase has been obtained by calcination at the relatively low temperature of 900 °C for 8 h. Compared micron-sized LNO (m-LNO) particles obtained at 1,000 °C by hydrothermal synthesis route without PVP assisted, the sm-LNO-PVP displays regularly shaped and well-distributed particles in the range of 0.3-0.5 μm. The scanning electron microscopy (SEM) results showed that the sm-LNO sample is submicronic and that the m-LNO sample shows agglomerates with a broad size distribution. The electrochemical performance of m-LNO and sm-LNO-PVP has been investigated by electrochemical impedance spectroscopy. The polarization resistance of the sm-LNO-PVP cathode reaches a value of 0.40 Ω cm at 750 °C, which is lower than that of m-LNO (0.62 Ω cm). This result indicates that a fine electrode microstructure with submicron particles can help to increase the active sites, accelerate oxygen diffusion, and reduce polarization resistance. An anode-supported single cell with sm-LNO cathode has been fabricated and tested over a temperature range from 650 to 800 °C. The maximum power density of the cell has achieved 834 mW cm at 750 °C. These results therefore show that this PVP-assisted hydrothermal method is an effective approach to construct submicron-structured cathode and enhance the performance of intermediate temperature solid oxide fuel cell. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14328488
Volume :
19
Issue :
4
Database :
Complementary Index
Journal :
Journal of Solid State Electrochemistry
Publication Type :
Academic Journal
Accession number :
101714687
Full Text :
https://doi.org/10.1007/s10008-014-2667-9