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000044541 0247_ $$2DOI$$a10.1016/j.ssi.2004.03.045
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000044541 084__ $$2WoS$$aChemistry, Physical
000044541 084__ $$2WoS$$aPhysics, Condensed Matter
000044541 1001_ $$0P:(DE-HGF)0$$aMagrez, A.$$b0
000044541 245__ $$aPreparation, sintering, and water incorporation of proton conducting Ba0.99Zr0.8Y0.2O3-delta: comparison between three different synthesis techniques
000044541 260__ $$aAmsterdam [u.a.]$$bElsevier Science$$c2004
000044541 300__ $$a585 - 588
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000044541 440_0 $$05565$$aSolid State Ionics$$v175$$x0167-2738
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000044541 520__ $$aThree wet chemistry routes were used to synthesize Ba0.99Zr0.8Y0.2O3-delta (BZY20) and to avoid the drawbacks of the conventional mixed oxide route used for its preparation. Pure samples were prepared using the Matrix Trapping and Decomposition (MTD) and Polyacrylamide Gel (PG) processes. The compound as a powder is thermodynamically stable up to 1250 degreesC while the purity of the bulk of a pellet can be maintained up to 1500 degreesC. An expected increase of the lattice parameter (from 0.4193 (BaZrO3) to 0.4228 (1) nm (BZY20)) was observed confirming the dissolution of yttrium in the barium zirconate structure. BZY20 absorbs large amounts of water vapor (H/Ba approximate to 0.19) and pellets can be sintered up to 95% at 1500 degreesC for 10 h. (C) 2004 Elsevier B.V. All rights reserved.
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000044541 65320 $$2Author$$aproton conductor
000044541 65320 $$2Author$$ayttrium-doped barium zirconate
000044541 65320 $$2Author$$awet chemistry route
000044541 65320 $$2Author$$apolyacrylamide gel
000044541 65320 $$2Author$$amatrix trapping and decomposition
000044541 7001_ $$0P:(DE-Juel1)VDB3067$$aSchober, T.$$b1$$uFZJ
000044541 773__ $$0PERI:(DE-600)1500750-9$$a10.1016/j.ssi.2004.03.045$$gVol. 175, p. 585 - 588$$p585 - 588$$q175<585 - 588$$tSolid state ionics$$v175$$x0167-2738$$y2004
000044541 8567_ $$uhttp://dx.doi.org/10.1016/j.ssi.2004.03.045
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