Ni-SDC cermet anode for medium-temperature solid oxide fuel cell with lanthanum gallate electrolyte

Citation
Xg. Zhang et al., Ni-SDC cermet anode for medium-temperature solid oxide fuel cell with lanthanum gallate electrolyte, J POWER SOU, 83(1-2), 1999, pp. 170-177
Citations number
31
Categorie Soggetti
Physical Chemistry/Chemical Physics","Environmental Engineering & Energy
Journal title
JOURNAL OF POWER SOURCES
ISSN journal
03787753 → ACNP
Volume
83
Issue
1-2
Year of publication
1999
Pages
170 - 177
Database
ISI
SICI code
0378-7753(199910)83:1-2<170:NCAFMS>2.0.ZU;2-F
Abstract
The polarization properties and microstructure of Ni-SDC (samaria-doped cer ia) cermet anodes prepared from spray pyrolysis (SP) composite powder, and element interface diffusion between the anode and a La0.9Sr0.1Ga0.8Mg0.2O2- delta (LSGM) electrolyte are investigated as a function of anode sintering temperature. The anode sintered at 1250 degrees C displays minimum anode po larization (with anode ohmic loss), while the anode prepared at 1300 degree s C has the best electrochemical overpotential, viz., 27 mV at 300 mA cm(-2 ) operating at 800 degrees C. The anode ohmic loss gradually increases with increase in the sintering temperature at levels below 1300 degrees C, and sharply increases at 1350 degrees C. Electron micrographs show a clear grai n growth at sintering temperatures higher than 1300 degrees C. The anode mi crostructure appears to be optimized at 1300 degrees C, in which nickel par ticles form a network with well-connected SDC particles finely distributed over the surfaces of the nickel particles. The anode sintered at 1350 degre es C has severe grain growth and an apparent interface diffusion of nickel from the anode to the electrolyte. The nickel interface diffusion is assume d to be the main reason for the increment in ohmic loss, and the resulting loss in anode performance. The findings suggest that sintering Ni-SDC compo site powder near 1250 degrees C is the best method to prepare the anode on a LSGM electrolyte, (C) 1999 Elsevier Science S.A. All rights reserved.