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Spectroscopic Understanding of SnO2 and WO3 Metal Oxide Surfaces with Advanced Synchrotron Based; XPS-UPS and Near Ambient Pressure (NAP) XPS Surface Sensitive Techniques for Gas Sensor Applications under Operational Conditions

机译:基于先进的同步加速器的光谱学理解SnO2和WO3金属氧化物表面; XPS-UPS和近环境压力(NAP)XPS在运行条件下用于气体传感器应用的表面敏感技术

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摘要

The most promising and utilized chemical sensing materials, WO and SnO were characterized by means advanced synchrotron based XPS, UPS, NAP-XPS techniques. The complementary electrical resistance and sensor testing experiments were also completed. A comparison and evaluation of some of the prominent and newly employed spectroscopic characterization techniques for chemical sensors were provided. The chemical nature and oxidation state of the WO and SnO thin films were explored at different depths from imminent surface to a maximum of 1.5 nm depth from the surface with non-destructive depth profiling. The adsorption and amount of chemisorbed oxygen species were precisely analyzed and quantified as a function of temperature between 25–400 °C under realistic operating conditions for chemical sensors employing 1–5 mbar pressures of oxygen (O ) and carbon monoxide (CO). The effect of realistic CO and O gas pressures on adsorbed water (H O), OH groups and chemisorbed oxygen species ( ) and chemical stability of metal oxide surfaces were evaluated and quantified.
机译:通过先进的基于同步加速器的XPS,UPS,NAP-XPS技术,对最有前途和最有用的化学传感材料WO和SnO进行了表征。互补电阻和传感器测试实验也已完成。提供了对一些著名的和新近采用的化学传感器光谱表征技术的比较和评估。在无损深度轮廓分析下,从即将到来的表面到距表面最大1.5 nm的深度,研究了WO和SnO薄膜的化学性质和氧化态。在实际工作条件下,对于使用1–5 mbar氧气(O)和一氧化碳(CO)的化学传感器,在实际操作条件下,可以精确地分析和定量化学吸附的氧种类的吸附和数量,作为温度在25-400°C之间的函数。评估并量化了实际CO和O气压对吸附水(H O),OH基团和化学吸附氧种类()以及金属氧化物表面化学稳定性的影响。

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