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Impact of air exposure and annealing on the chemical and electronic properties of the surface of SnO2 nanolayers deposited by rheotaxial growth and vacuum oxidation

机译:暴露于空气中和退火对通过流变生长和真空氧化沉积的SnO2纳米层表面化学和电子性能的影响

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摘要

In this paper the SnO2 nanolayers were deposited by rheotaxial growth and vacuum oxidation (RGVO) and analyzed for the susceptibility to ambient-air exposure and the subsequent recovery under vacuum conditions. Particularly the surface chemistry of the layers, stoichiometry and level of carbon contamination, was scrutinized by X-ray photoelectron spectroscopy (XPS). The layers were tested i) pristine, ii) after air exposure and iii) after UHV annealing to validate perspective recovery procedures of the sensing layers. XPS results showed that the pristine RGVO SnO2 nanolayers are of high purity with a ratio [O]/[Sn] = 1.62 and almost no carbon contamination. After air exposure the relative [O]/[Sn] concentration increased to 1.80 while maintaining a relatively low level of carbon contaminants. Subsequent UHV annealing led to a relative [O]/[Sn] concentration comparable to the pristine samples. The oxidation resulted in a variation of the distance between the valence band edge and the Fermi level energy. This was attributed to oxygen diffusion through the porous SnO2 surface as measured by atomic force microscopy.
机译:在本文中,通过流变生长和真空氧化(RGVO)沉积了SnO2纳米层,并分析了其对环境空气暴露的敏感性以及随后在真空条件下的回收率。特别地,通过X射线光电子能谱法(XPS)仔细检查层的表面化学,化学计量和碳污染水平。在i)原始,ii)空气暴露后和iii)UHV退火后测试层,以验证传感层的透视恢复程序。 XPS结果表明,原始的RGVO SnO2纳米层具有高纯度,比率[O] / [Sn] = 1.62,几乎没有碳污染。暴露于空气后,相对[O] / [Sn]浓度增加到1.80,同时保持相对较低的碳污染物含量。随后的UHV退火导致相对[O] / [Sn]浓度与原始样品相当。氧化导致价带边缘和费米能级之间的距离发生变化。这归因于通过原子力显微镜测得的氧通过多孔SnO2表面的扩散。

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