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Defect characterization in cadmium telluride and cadmium-zinc-tellurium crystals.

机译:碲化镉和镉锌碲晶体的缺陷表征。

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摘要

Intrinsic defects and impurities in undoped CdTe and Cd1−x ZnxTe semiconductor compounds have been investigated using thermally stimulated spectroscopy with the general aim of identifying and then understanding the effects of the defects on the electrical and optical properties of these compounds. In order to identify and understand the effects of these defects (trapping levels), the samples were subjected to room temperature deformation, high temperature annealing, and dopants diffusion. The samples were always analyzed before and after any process. It is found that the trapping levels observed at ∼61 K and ∼114 K with thermal ionization energies of 0.12 ± 0.01 eV and 0.23 ± 0.01 eV and trapping cross-sections of 4.7 × 10−16 and 7.8 × 10−17 cm2 are associated with the isolated first and second ionized state of the cadmium vacancy, while trapping levels observed at ∼51 K and ∼94 K with thermal ionization energies of 0.09 ± 0.01 eV and 0.18 ± 0.01 eV and trapping cross-sections of 9.3 × 10 −17 and 6.8 × 10−17 cm2 are associated with first and second states of the isoelectronic oxygen-cadmium vacancy complex (VCd-OTe) respectively. In addition, we found that deep level trapping states located near the middle of the band gap (in the region between 230 K and 267 K) in undoped as grown CdTe are related to the tellurium antisite-cadmium vacancy complex (TeCd-V Cd) where the lowest thermal ionization state is 0.78 ± 0.01 eV. The thermal ionization energies (transition energies) were extracted using variable heating rate and/or initial rise methods. Our results have been reinforced with theoretical calculations using linearized augmented plane wave (LAPW) within the local density approximation (LDA). Also, from our room temperature deformation, we have found evidence of three levels of dislocation defects in CdTe crystals. The first two energy levels, with ionization energies of E1 = 0.06 ± 0.01 eV and E2 = 0.38 ± 0.01 eV are due to Cd dislocations. The third deeper level, with ionization energy of E3 = 0.49 ± 0.01 eV, is related to Te dislocations. In addition, we have found that the intensity of the induced dislocations, photoconductivity, and resistivity of the crystals are proportional to the deformation rate and the direction of the applied compression load. The annealing result showed that the applied load did not reach the yield point of the crystals; therefore, the induced deformation is elastic.
机译:使用热激发光谱法研究了未掺杂的CdTe和Cd 1-x Zn x Te半导体化合物的本征缺陷和杂质,其主要目的是识别并理解这些化合物的电学和光学性能上的缺陷。为了识别和理解这些缺陷(陷阱能级)的影响,对样品进行了室温变形,高温退火和掺杂剂扩散。始终在任何过程之前和之后对样品进行分析。发现在电离能为0.12±0.01 eV和0.23±0.01 eV且截面积为4.7×10 −16 和7.8的热电离能下,在〜61 K和〜114 K处观察到的俘获能级×10 −17 cm 2 与分离的镉空位的第一和第二电离态有关,而在热电离下,在〜51 K和〜94 K处能捕获能级能量为0.09±0.01 eV和0.18±0.01 eV,俘获截面为9.3×10 -17 和6.8×10 −17 cm 2 分别与等电子氧-镉空位络合物(V Cd -O Te )的第一和第二状态相关。此外,我们发现未掺杂的CdTe生长在带隙中间(在230 K和267 K之间的区域)附近的深能级俘获状态与碲抗位-镉空位复合物(Te -V Cd ),其中最低的热电离状态为0.78±0.01 eV。使用可变的加热速率和/或初始上升方法提取热电离能(跃迁能)。我们的结果在局部密度近似(LDA)范围内使用线性化的增强平面波(LAPW)进行理论计算得到了加强。同样,从我们的室温变形中,我们发现了CdTe晶体中位错缺陷的三个水平的证据。前两个能级的电离能分别为E1 = 0.06±0.01 eV和E2 = 0.38±0.01 eV,这归因于Cd的位错。第三个更深的水平,其电离能为E3 = 0.49±0.01 eV,与Te位错有关。此外,我们发现晶体的位错强度,光电导率和电阻率与变形率和施加压缩载荷的方向成正比。退火结果表明,所施加的载荷没有达到晶体的屈服点。因此,引起的变形是弹性的。

著录项

  • 作者

    Awadalla, Salah Abdo.;

  • 作者单位

    Washington State University.;

  • 授予单位 Washington State University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 113 p.
  • 总页数 113
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学 ;
  • 关键词

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