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The significance of in situ conditions in the characterization of GaSb nanopatterned surfaces via ion beam sputtering

机译:原位条件在离子束溅射表征GaSb纳米图案表面中的意义

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摘要

A systematic study is conducted in order to elucidate the underlying mechanism(s) for nanopatterning with low-energy irradiation of GaSb (100) under normal incidence. Ion energies between 50 and 1000 eV of Ar+ and ion fluences of up to 1018 cm"2 were employed. Characterization of the shallow (e.g., 1 to 6 nm) amorphous phase region induced by irradiation and the subsurface crystalline phase region is accomplished with low-energy ion scattering spectroscopy and x-ray photoelectron spectroscopy, respectively. In situ studies are conducted due to the strong chemical affinity for oxygen of GaSb. The studies conclude that at energies below 200 eV, the native oxide layer hampers nanopatterning until it becomes removed at a fluence of approximately 5 x 1016 cm"2. At this energy and threshold fluence, the surface is enriched with Ga atoms during irradiation. At energies above 200 eV, the native oxide layer is efficiently removed in the early irradiation stages, and thus the detrimental effects from the oxide on nanopatterning are negligible. In situ surface concentration quantification indicates that the surface enrichment with Sb atoms in the amorphous phase layer increases with the incident ion energy. Post-air exposure characterization reveals that the measured enrichment of the surface with gallium is due to oxygen reduction by Ga atoms segregated from both the amorphous and the crystalline phase regions as a result of air exposure.
机译:为了阐明在正常入射情况下用GaSb(100)进行低能辐射进行纳米构图的基本机理,进行了系统的研究。使用的Ar +离子能量介于50和1000 eV之间,离子通量高达1018 cm“ 2。通过辐照诱导形成的浅(例如1至6 nm)非晶态相区域和地下结晶相区域的表征可以在较低的条件下完成能量离子散射光谱法和X射线光电子能谱法,由于对GaSb的氧具有很强的化学亲和力,因此进行了原位研究,研究结论是,在能量低于200 eV时,天然氧化物层会阻碍纳米图案的形成,直到被去除为止的能量密度约为5 x 1016 cm“ 2。以这种能量和阈值通量,在辐照期间表面富含Ga原子。在高于200 eV的能量下,天然氧化物层在早期辐照阶段被有效去除,因此,氧化物对纳米图案的有害影响可以忽略不计。原位表面浓度定量分析表明,非晶态相层中Sb原子的表面富集度随入射离子能量的增加而增加。暴露于空气后的特征表明,测得的表面镓的富集归因于由于暴露于空气而导致的Ga原子从非晶相和结晶相区域中析出的氧还原。

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  • 来源
    《Journal of Applied Physics》 |2011年第7期|p.074301.1-074301.6|共6页
  • 作者单位

    School of Materials Engineering, Purdue University, West Lafayette, Indiana 47907, USA,Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana 47907, USA;

    School of Materials Engineering, Purdue University, West Lafayette, Indiana 47907, USA,Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana 47907, USA,School of Nuclear Engineering, Purdue University, West Lafayette, Indiana 47907, USA;

    School of Nuclear Engineering, Purdue University, West Lafayette, Indiana 47907, USA;

    School of Nuclear Engineering, Purdue University, West Lafayette, Indiana 47907, USA;

    School of Electrical Engineering, Purdue University, West Lafayette, Indiana 47907, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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