Please use this identifier to cite or link to this item:
https://idr.l1.nitk.ac.in/jspui/handle/123456789/12595
Title: | Praseodymium doped ceria as electrolyte material for IT-SOFC applications |
Authors: | Shajahan, I. Ahn, J. Nair, P. Medisetti, S. Patil, S. Niveditha, V. Uday, Bhaskar, Babu, G. Dasari, Hari Prasad Lee, J.-H. |
Issue Date: | 2018 |
Citation: | Materials Chemistry and Physics, 2018, Vol.216, , pp.136-142 |
Abstract: | Praseodymium-doped ceria (PDC, Ce0.9Pr0.1O2) electrolyte material for intermediate temperature solid oxide fuel cells (IT-SOFCs) has been successfully synthesised by EDTA-citrate method. From X-Ray diffraction (XRD), fluorite structure along with a crystallite size of 5.4 nm is obtained for PDC nanopowder calcined at 350 C/24 h. Raman spectroscopy confirmed the structure, presence of oxygen vacancies with the manifestation of the main peak at 457 cm?1 and with a secondary peak at 550 cm?1. From Transmission Electron Microscopy (TEM) analysis, the average particle size is around 7 10 nm and selected area electron diffraction (SAED) patterns further confirmed the fluorite structure of PDC nanopowder. The PDC nanopowder displayed a BET surface area of 65 m2/g with a primary particle size of ?13 nm (calculated from BET surface area). Dilatometer studies revealed a multi-step shrinkage behaviour with the multiple peaks at 522, 1171 and 1461 C which may be originated due to the presence of multiple size hard agglomerates. The PDC electrolyte pellet sintered at 1500 C displayed an ionic conductivity of 1.213E-03 S cm?1 along with an activation energy of 1.28eV. Instead of a single fluorite structure, XRD of sintered PDC pellet showed multiple structures (Fluorite structure (CeO2) and cubic structure (PrO2). 2018 Elsevier B.V. |
URI: | https://idr.nitk.ac.in/jspui/handle/123456789/12595 |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
7 Praseodymium doped ceria.pdf | 1.79 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.