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Formation mechanisms of low-dimensional semiconductor nanostructures grown by OMCVD on nonplanar substrates

机译:OMCVD在非平面衬底上生长的低维半导体纳米结构的形成机理

摘要

Semiconductor quantum wires (QWRs) are promising structures for optoelectronics applications, since they can provide quantum confinement for charge carriers in two dimensions. The advantage that they offer over conventional quantum wells (QWs) is due to the sharper density of states characteristic of these structures, yielding narrower spectral lines and higher optical gain. However, to exhibit clear confinement characteristics, QWRs must meet stringent requirements in terms of size, uniformity and interfacial quality. Different methods have been explored for QWR fabrication. Techniques based on etching and regrowth suffer from defect incorporation into the lateral interfaces, since they are not formed in situ, and are limited in size by the lithographic features. On the other hand, growth of fractions of monolayers on vicinal substrates, although overcoming the above limitations, gives rise to size nonuniformities and graded interfaces. In this project, (In)GaAs/AlxGa1-xAs QWRs are obtained by organometallic chemical vapor deposition (OMCVD) growth of quantum wells on patterned, V-grooved substrates. In this way, the lithographically defined pattern serves as a seed for QWR formation. The self-ordering properties of OMCVD on nonplanar surfaces ensure the creation of a self-limiting profile at the bottom of the grooves, on which the wires are grown. This method overcomes the size limitations imposed by lithography, allows the in situ formation of interfaces and, thanks to the self-ordering mechanism, yields structures with high uniformity, whose characteristics are determined solely by the growth conditions. Although nonplanar growth has been employed for more than ten years for QWR fabrication, the understanding of the self-ordering mechanisms originating the profiles at the bottom of the grooves has been until now only phenomenological. The attainment of self-limiting profiles takes place via transients of the growth rates at the bottom of the groove. Current models of nonplanar growth can predict the formation, evolution or disappearance of facets at the 100nm-μm size. However, they cannot describe the transient behaviors at the nm scale that lead to self-limiting growth. This thesis project has been aimed at elucidating the physical mechanisms of this self-organized growth. A fundamental part of the project has been the creation of a wide experimental database to understand the dependence of the self-limiting profiles on the materials and growth conditions. The profiles at the bottom of the groove exhibit a faceted structure, consisting of a central (100) plane, surrounded by two {311}A ones. Cross-sectional transmission electron microscopy (TEM) shows that the bottom facets become wider as the growth temperature increases and as the Al mole fraction x of AlxGa1-xAs layers decreases. It appears therefore that surface diffusion is a key element in determining self-limiting growth. TEM cross sections show also that the establishment of self-limiting profiles takes place via self-adjusting growth rates on these facets. In addition to this geometrical self-ordering, AlxGa1-xAs alloys exhibit also a compositional self-ordering at the bottom of the groove. Due to the higher mobility of Ga species, with respect to the Al ones, the facets at the bottom of the groove are Ga rich, with respect to the sidewall planes, giving rise to so-called vertical quantum wells (VQWs). To determine the composition of the VQWs, we have developed a technique employing cross-sectional atomic force microscopy (AFM) in air. This method is based on the dependence of the AlxGa1-xAs oxidation rates on the Al content x. Through a calibration on a reference sample, we were able to measure compositions with an accuracy of ±0.02. The enhanced Ga content of the VQWs follows classical models of segregation, and reaches a maximum of Δx ≅ 0.15 for x ≅ 0.55 at a growth temperature of 700°C. We also studied the three dimensional structure of the self-limiting surface profiles by top-surface AFM in air of the nonplanar samples after cool-down and removal from the OMCVD reactor. Each of the planes composing the groove presents a monolayer step structure that reflects directly the morphology of surfaces of the same orientation found in planar epitaxy. However, on the facets forming on corrugated substrates the step structure exhibits a higher degree of ordering, with respect to planar epitaxy. This is due to a modification of surface diffusion, when the trench width becomes comparable to or lower than the adatom surface diffusion length. In the last part of the project, we have developed a model ascribing the self-ordering phenomena observed above to local variations of the surface chemical potential μ. Since μ becomes lower as the concavity of the surface increases, it induces a curvature-dependent capillarity flux towards the bottom of the groove. In the absence of capillarity, if the growth rate is higher on the sidewall planes than on the bottom facets, the capillarity-enhanced growth rate at the bottom can balance exactly the sidewall growth rate, thus leading to self-limiting growth. The different behavior of nonplanar OMCVD (where self-ordering is usually observed at the bottom of the grooves) and molecular beam epitaxy (where self-ordering rather takes place at the top of the corrugations) can be explained by the different growth rate anisotropies of the two techniques. In a ternary alloy, the composition is locally different at the bottom of the groove, due to the different diffusion lengths of Ga and Al. The resulting entropy of mixing, which is lower than the one for a uniform composition, tends however to oppose this segregation, thus affecting the alloy self-limiting profiles. The predictions of the model have been successfully verified on our OMCVD-grown profiles. They can be used to design and optimize a variety of nanostructures, including VQWs, QWRs and QWR superlattices in the GaAs/A1GaAs system, and can be further extended to the strained InGaAs/AlGaAs system.
机译:半导体量子线(QWR)是光电子应用的有前途的结构,因为它们可以为二维电荷载流子提供量子限制。它们提供的优于传统量子阱(QW)的优势是由于这些结构的特征态密度更高,产生了更窄的光谱线和更高的光学增益。但是,为了表现出清晰的限制特性,QWR必须满足尺寸,均匀性和界面质量方面的严格要求。已经探索了用于QWR制造的不同方法。基于蚀刻和再生长的技术存在缺陷结合到侧向界面中的问题,因为它们不是原位形成的,并且尺寸受到光刻特征的限制。另一方面,尽管克服了上述限制,但在邻近基底上单层的分数的生长却引起尺寸不均匀和渐变界面。在该项目中,通过在图案化的V形沟槽衬底上量子阱的有机金属化学气相沉积(OMCVD)生长获得(In)GaAs / AlxGa1-xAs QWR。以这种方式,光刻定义的图案用作QWR形成的种子。 OMCVD在非平面表面上的自排序特性可确保在其上生长导线的凹槽底部创建自限制轮廓。该方法克服了光刻技术带来的尺寸限制,允许在界面上原位形成界面,并且由于具有自排序机制,因此可以产生具有高度均匀性的结构,其结构特征仅取决于生长条件。尽管在QWR的制造中采用非平面生长已超过十年,但直到现在,对现象的认识仍是对起源于凹槽底部轮廓的自排序机制的了解。通过在沟槽底部的生长速率的瞬变来实现自限制轮廓。当前的非平面生长模型可以预测100nm-μm尺寸的小面的形成,演化或消失。但是,他们无法描述导致自我限制生长的纳米级瞬态行为。本论文项目旨在阐明这种自组织生长的物理机制。该项目的一个基本部分是创建一个广泛的实验数据库,以了解自我限制型材对材料和生长条件的依赖性。凹槽底部的轮廓显示出多面结构,该结构由中心(100)平面组成,并被两个{311} A平面包围。截面透射电子显微镜(TEM)显示,随着生长温度的升高和AlxGa1-xAs层的Al摩尔分数x降低,底面变宽。因此,表面扩散似乎是决定自限生长的关键因素。 TEM横截面还表明,通过在这些方面进行自我调整的增长率可以建立自我限制的轮廓。除了这种几何自定序之外,AlxGa1-xAs合金还在凹槽底部显示出成分自定序。由于Ga物种相对于Al物种具有更高的迁移率,相对于侧壁平面,凹槽底部的刻面富含Ga,从而产生了所谓的垂直量子阱(VQW)。为了确定VQW的成分,我们开发了一种在空气中采用截面原子力显微镜(AFM)的技术。该方法基于AlxGa1-xAs氧化速率对Al含量x的依赖性。通过对参考样品进行校准,我们能够以±0.02的精度测量成分。 VQW的Ga含量增加,遵循经典的偏析模型,并且在700°C的生长温度下,对于x≤0.55达到最大值Δx0.15 0.15。我们还通过冷却和从OMCVD反应器中移除后,通过非平面样品的空气中的顶表面AFM研究了自限表面轮廓的三维结构。组成凹槽的每个平面都具有单层台阶结构,该结构直接反映了在平面外延中发现的相同方向的表面的形态。然而,相对于平面外延,在波纹状基板上形成的小面上,阶梯结构表现出较高的有序度。当沟槽宽度变得等于或小于吸附原子表面扩散长度时,这是由于表面扩散的改变。在项目的最后一部分,我们开发了一个模型,将上述观察到的自排序现象归因于表面化学势μ的局部变化。由于随着表面凹度的增加,μ变小,因此会引起与曲率有关的毛细管通量流向凹槽底部。没有毛细血管如果侧壁面上的生长速率高于底面上的生长速率,则底部的毛细作用增强的生长速率可以精确地平衡侧壁的生长速率,从而导致自限生长。非平面OMCVD的行为(通常在沟槽的底部通常观察到自序)和分子束外延(在波纹的顶部通常发生在自序而发生)的不同行为可以通过不同的生长速率各向异性来解释。两种技术。在三元合金中,由于Ga和Al的扩散长度不同,其成分在凹槽底部局​​部不同。然而,所产生的混合熵低于均匀组成的混合熵,它趋向于反对这种偏析,从而影响了合金的自限分布。该模型的预测已在我们的OMCVD生长轮廓上得到成功验证。它们可用于设计和优化GaAs / A1GaAs系统中的各种纳米结构,包括VQW,QWR和QWR超晶格,并可进一步扩展到应变InGaAs / AlGaAs系统。

著录项

  • 作者

    Biasiol Giorgio;

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  • 年度 1998
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  • 原文格式 PDF
  • 正文语种 eng
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