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Preparation and conductive properties of double perovskite Ba3Sr1+xTa2-xO9-delta and application for hydrogen sensor

作   者:
Huang, WenlongLi, YingDing, YushiLi, Hongzheng
作者机构:
Peoples R China Liaoning Key Lab Met Sensor & Technol Shenyang 110819Northeastern Univ Liaoning Sch Met
关键词:
Ionic conductionConductivityHydrogen sensorPerovskitesTransport number
期刊名称:
Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics
i s s n:
0925-8388
年卷期:
2019 年 792 卷
页   码:
759-769
页   码:
摘   要:
A series of Ba3Sr1+xTa2-xO9-delta (x = 0,0.1,0.2,0.3,0.4) double perovskite proton conductors were fabricated at 1400 degrees C for 10 h and further sintered at 1650 degrees C for 10 h via a solid-state reaction process. Their phase composition, microstructure characterization and valence were investigated by XRD, FESEM and XPS techniques. Conductivities of these proton conductors were measured under the atmosphere of various water vapor and oxygen pressures by the electrochemical impedance spectra technique. It was found that the grain boundary thicknesses of Ba3Sr1+xTa2-xO9-delta were significantly higher than other perovskite proton conductors. The total conductivities of Ba3Sr1+xTa2-xO9-delta increased with the increase of both temperature and stoichiometric proportion of Sr, and Ba3Sr1.4Ta1.6O8.4 exhibited the highest conductivity of about 4.4 x 10(-3) S cm(-1) at 750 degrees C. Additionally, the transport numbers of proton, oxide ion and hole were measured using defect equilibria model. The results indicated that Ba3Sr1+xTa2-xO9-delta oxides were almost pure proton conductors at 400-550 degrees C and mixed proton-oxide ion-hole conductors at 550-850 degrees C, and Ba3Sr1.3Ta1.7O8.55 exhibited the highest protonic transport number. The performance of the hydrogen sensor using Ba3Sr1.3Ta1.7O8.55 was also measured in various hydrogen partial pressure, a good linear relationship between EMF and P-H2 was observed at 400-800 degrees C, and the response time was around 10s. (C) 2019 Elsevier B.V. All rights reserved.
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