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Polarization Anisotropies in Strain-Free Asymmetric and Symmetric Quantum Dots Grown by Droplet Epitaxy

机译:通过液滴外延生长的无应变不对称和对称量子点的极化各向异性

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摘要

We provide an extensive and systematic investigation of exciton dynamics in droplet epitaxial quantum dots comparing the cases of (311)A, (001), and (111)A surfaces. Despite a similar s-shell exciton structure common to the three cases, the absence of a wetting layer for (311)A and (111)A samples leads to a larger carrier confinement compared to (001), where a wetting layer is present. This leads to a more pronounced dependence of the binding energies of s-shell excitons on the quantum dot size and to the strong anti-binding character of the positive-charged exciton for smaller quantum dots. In-plane geometrical anisotropies of (311)A and (001) quantum dots lead to a large electron-hole fine interaction (fine structure splitting (FSS) ∼100 μeV), whereas for the three-fold symmetric (111)A counterpart, this figure of merit is reduced by about one order of magnitude. In all these cases, we do not observe any size dependence of the fine structure splitting. Heavy-hole/light-hole mixing is present in all the studied cases, leading to a broad spread of linear polarization anisotropy (from 0 up to about 50%) irrespective of surface orientation (symmetry of the confinement), fine structure splitting, and nanostructure size. These results are important for the further development of ideal single and entangled photon sources based on semiconductor quantum dots.
机译:我们在液滴外延量子点中提供了广泛而系统地研究了液滴外延量子点的比较(311)A,(001)和(111)的情况。尽管在三种情况下常见的类似S-壳激子结构,但是没有润湿层(311)A和(111)样品,其与(001)相比,较大的载体限制,其中存在润湿层。这导致S-壳激子的结合能量更明显的S-壳激子对量子点尺寸的依赖性以及用于较小量子点的正电激子的强抗结合特征。 (311)A和(001)量子点的面内几何各向异性导致大的电子空穴精细相互作用(细结构分裂(FSS)~100μEV),而对于三倍对称(111)的对应物,这个优点的数字减少了大约一个数量级。在所有这些情况下,我们不观察到细结构分裂的任何尺寸依赖性。所有研究的病例中存在重型孔/光孔混合,导致线性偏振各向异性的广泛扩散(从0到约50%),无论是否表面取向(限制的对称性),细结构分裂和纳米结构尺寸。这些结果对于基于半导体量子点的理想单个和缠结光子源的进一步发展是重要的。

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