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Nanocrystalline BaSnO3 as an Alternative Gas Sensor Material: Surface Reactivity and High Sensitivity to SO2

机译:纳米晶BaSnO3作为替代气体传感器材料:表面反应性和对SO2的高敏感性

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摘要

Nanocrystalline perovskite-type BaSnO3 was obtained via microwave-assisted hydrothermal route followed by annealing at variable temperature. The samples composition and microstructure were characterized. Particle size of 18–23 nm was unaffected by heat treatment at 275–700 °C. Materials DC-conduction was measured at variable temperature and oxygen concentration. Barium stannate exhibited n-type semiconductor behavior at 150–450 °C with activation energy being dependent on the materials annealing temperature. Predominant ionosorbed oxygen species types were estimated. They were shown to change from molecular to atomic species on increasing temperature. Comparative test of sensor response to various inorganic target gases was performed using nanocrystalline SnO2-based sensors as reference ones. Despite one order of magnitude smaller surface area, BaSnO3 displayed higher sensitivity to SO2 in comparison with SnO2. DRIFT spectroscopy revealed distinct interaction routes of the oxides surfaces with SO2. Barium-promoted sulfate formation favoring target molecules oxidation was found responsible for the increased BaSnO3 sensitivity to ppm-range concentrations of SO2 in air.
机译:纳米晶钙钛矿型BaSnO3是通过微波辅助水热途径,然后在可变温度下退火而获得的。表征了样品的组成和微观结构。在275-700°C下进行热处理不会影响18-23 nm的粒径。在可变的温度和氧气浓度下测量材料的直流传导。锡酸钡在150–450°C时表现出n型半导体行为,其活化能取决于材料的退火温度。估计了主要的离子吸附氧种类类型。结果表明,随着温度的升高,它们从分子种类转变为原子种类。使用基于纳米晶SnO2的传感器作为参考传感器,对传感器对各种无机目标气体的响应进行了对比测试。尽管表面积减小了一个数量级,但与SnO2相比,BaSnO3对SO2的敏感性更高。 DRIFT光谱显示了氧化物表面与SO2的独特相互作用路径。发现钡促进的硫酸盐形成有利于目标分子的氧化,这导致BaSnO3对空气中ppm浓度的SO2的敏感性增加。

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