Noble metal alloy-Zr(Sc)O-2 cermet cathode for reduced-temperature SOFCs

Citation
K. Sasaki et al., Noble metal alloy-Zr(Sc)O-2 cermet cathode for reduced-temperature SOFCs, SOL ST ION, 144(3-4), 2001, pp. 233-240
Citations number
23
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
SOLID STATE IONICS
ISSN journal
01672738 → ACNP
Volume
144
Issue
3-4
Year of publication
2001
Pages
233 - 240
Database
ISI
SICI code
0167-2738(200112)144:3-4<233:NMACCF>2.0.ZU;2-B
Abstract
Polarization characteristics of noble metal alloy-(Sc0.10Ce0.01)Zr0.89O2 (S SZ) cermet cathodes were studied in order to develop a new cathode for redu ced-temperature solid oxide fuel cells (SOFCs). Several noble metal alloy-S SZ cermet cathodes were prepared by mixing Pt, Pd, Rh and/or Ag and their a lloy powders with SSZ powder using a high-energy ball mill in vacuum and pa sting the cermet onto yttria stabilized zirconia (YSZ) electrolyte. A Pt-Ag /SSZ cermet cathode achieved as high as 12 S/cm(2) of interfacial conductiv ity, sigma (E), at 973 K and 1.5 S/cm(2) at 873 K in air. The results sugge st that this Pt-Ag/SSZ cermet cathode has enough activity not only at 973 K but also at 873 K. This high activity can be obtained by selecting a suita ble alloy composition, ball milling a proper ratio of SSZ/noble metal mixtu re in vacuum and controlling the cathode thickness and the sintering temper ature. By replacing the metallic component of cermet from Pt to Pt-Ag alloy (50 wt.% Pt), the quantity of Pt in cermet can be reduced to 19 from 40 Mg /cm(2) in addition to the improvement of activity from 6.7 S/cm(2) at 973 K to 12 S/cm(2) of sigma (E) at 973 K. The activation energies, E-a, of Pt-A g and Pd-Ag/SSZ cermet were smaller than that of Pt/SSZ cermet. In the case of Pt-Ag/SSZ cermet, the E-a decreased with increasing Ag ratio in the Pt- Ag alloy. The E-a also depends on the SSZ/Pt-Ag ratio. This cathode showed two optima of sigma (E) versus the SSZ/Pt-Ag ratio and a remarkable depende nce on cathode thickness. It was considered that the first optimum is based on two-dimensional reaction sites on YSZ electrolyte and the second optimu m originates from three-dimensional expansion of reaction sites into the ce rmet cathode layer. (C) 2001 Elsevier Science B.V. All rights reserved.