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Ex-solution of Ni nanoparticles in a La0.2Sr0.8Ti1-xNixO3-delta alternative anode for solid oxide fuel cell SCIE SCOPUS

Title
Ex-solution of Ni nanoparticles in a La0.2Sr0.8Ti1-xNixO3-delta alternative anode for solid oxide fuel cell
Authors
Byung Hyun ParkChoi, GM
Date Issued
2014-09-01
Publisher
Elsevier
Abstract
Electro-catalytic nanoparticles can be produced in oxide anodes for solid oxide fuel cell (SOFC) by an-ex-solution method, i.e., by incorporating metals into a perovskite oxide phase in air followed by the reduction of the perovskite oxide. In this study, we used a Ni ex-solution method with a La and Ni co-doped SrTiO3 (La0.2Sr0.8Ti1 - xNixO3 - delta, x = 0-02) anode for SOFC The parameters and mechanisms of the Ni ex-solution were investigated by varying the ex-solution temperature (800-1300 degrees C) and time (3-24 h). The degrees of Ni ex-solution and Ti reduction were dependent on time and temperature. Ni ex-solution reaction was relatively faster than Ti reduction which required a higher temperature or a longer time. XRD analysis was used to observe the changes in the lattice parameter of La0.2Sr0.8Ti1 - xNixO3 - delta after the ex-solution process. The electrochemical performance of an electrolyte (Sc-stabilized zirconia)-supported cell with the La0.2Sr0.8Ti1 - xNixO3 - delta anode with x = 0.1 showed that the total cell resistance is high, due mostly to the anode resistance. The maximum power density at 800 degrees C is also relatively low, similar to 150 mW/cm(2), due to the thick (similar to 300 mu m) electrolyte and the low level of anodic performance. (C) 2013 Elsevier B.V. All rights reserved.
Keywords
SOFC; Stability; Anode; Ex-solution; AUTOMOTIVE EMISSIONS CONTROL; RARE-EARTH VANADATES; SOFC ANODE; PERFORMANCE; TEMPERATURE; PRECIPITATION; ENHANCEMENT; EXSOLUTION; CATALYST; TITANATE
URI
https://oasis.postech.ac.kr/handle/2014.oak/13664
DOI
10.1016/J.SSI.2013.10.016
ISSN
0617-2738
Article Type
Article
Citation
SOLID STATE IONICS, vol. 262, page. 345 - 348, 2014-09-01
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최경만CHOI, GYEONG MAN
Dept of Materials Science & Enginrg
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