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contributor authorBing Bai
contributor authorNigel M. Sammes
contributor authorAlevtina L. Smirnova
contributor authorGeoff Tompsett
date accessioned2017-05-09T00:38:32Z
date available2017-05-09T00:38:32Z
date copyrightApril, 2010
date issued2010
identifier issn2381-6872
identifier otherJFCSAU-28941#021002_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/143650
description abstractBi2O3 doped scandia stabilized zirconia systems have shown promise for use as electrolytes in intermediate temperature solid oxide fuel cells (IT-SOFC's). Sintering properties, crystal phase transformation, and electrical conductivity of the Bi2O3 doped Sc2O3–ZrO2 systems were investigated. The effect of Bi2O3 doping from 0 mol % to 2.0 mol % and different sintering temperatures on the properties and performance of the electrolyte were examined. The presence of Bi2O3 aided the sintering process and better sintering for the doped system was achieved at lower temperatures. The cubic phase was successfully stabilized at room temperature with concentrations of 1 mol % and 2 mol %Bi2O3 sintered at 1100–1400°C. The achievement of a cubic structure depends on both the Bi2O3 concentration and the sintering temperature. Higher electrical conductivity was achieved with Bi2O3 doped Sc2O3–ZrO2 systems than 10ScSZ below 600°C. A maximum conductivity of 1.68×10−2 S/cm at 700°C was obtained for 2 mol %Bi2O3 doped sample sintered at 1100°C.
publisherThe American Society of Mechanical Engineers (ASME)
titleCharacterization of Scandia Stabilized Zirconia Doped With Various Bi2O3 Additions as an Intermediate Temperature Solid Oxide Fuel Cell Electrolyte
typeJournal Paper
journal volume7
journal issue2
journal titleJournal of Fuel Cell Science and Technology
identifier doi10.1115/1.3117254
journal fristpage21002
identifier eissn2381-6910
keywordsTemperature
keywordsSintering
keywordsSolid oxide fuel cells
keywordsElectrolytes
keywordsConductivity AND Electrical conductivity
treeJournal of Fuel Cell Science and Technology:;2010:;volume( 007 ):;issue: 002
contenttypeFulltext


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