外延ZnO热电子输运研究中带电缺陷密度的估计

IF 0.3 4区 物理与天体物理 Q4 PHYSICS, MULTIDISCIPLINARY Lithuanian Journal of Physics Pub Date : 2020-02-05 DOI:10.3952/physics.v60i1.4163
L. Ardaravičius, O. Kiprijanovič, M. Ramonas, E. Šermukšnis, A. Simukovic, A. Matulionis
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引用次数: 1

摘要

报道了通过在名义上未掺杂的n型Zn极性ZnO外延层上施加短(几个ns)电压脉冲进行的高场电子输运测量,并根据玻尔兹曼动力学方程进行了解释。瞬态测量没有显示高达320kV/cm电场的电子密度的显著变化。这一结果与电流的实验数据一起使我们能够从测量的电流中估计电子漂移速度:对于电子密度为1.5×1017 cm–3的ZnO层,在320 kV/cm的预击穿场下获得了最高值~2.9×107 cm/s。假设双电荷氧空位(~1.6×1017 cm–3)和其他带电中心(~1.7×1017厘米–3)的密度最适合模拟和测量的热电子效应。证明了与外延层生长条件的相关性:较高的锌电池温度有利于形成更高密度的氧空位(347°C时为1.9×1017 cm–3)。
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Estimation of the charged defect density from hot-electron transport studies in epitaxial ZnO
High-field electron transport measurements by applying short (few ns) voltage pulses on nominally undoped n-type Zn-polar ZnO epilayers are reported and interpreted in terms of the Boltzmann kinetic equation. The transient measurements do not demonstrate a significant change in the electron density up to 320 kV/cm electric field. This result together with the experimental data on the current allows one to estimate the electron drift velocity from the measured current: the highest value of ~2.9 × 107 cm/s is obtained at the pre-breakdown field of 320 kV/cm for the ZnO layer with the electron density of 1.5 × 1017 cm–3. The densities of double-charged oxygen vacancies (~1.6 × 1017 cm–3) and other charged centres (~1.7 × 1017 cm–3) are assumed for the best fit of the simulated and measured hot-electron effect. A correlation with the epilayer growth conditions is demonstrated: the higher Zn cell temperature favours the formation of a higher density of the oxygen vacancies (1.9 × 1017 cm–3 at 347°C).
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来源期刊
Lithuanian Journal of Physics
Lithuanian Journal of Physics 物理-物理:综合
CiteScore
0.90
自引率
16.70%
发文量
21
审稿时长
>12 weeks
期刊介绍: The main aim of the Lithuanian Journal of Physics is to reflect the most recent advances in various fields of theoretical, experimental, and applied physics, including: mathematical and computational physics; subatomic physics; atoms and molecules; chemical physics; electrodynamics and wave processes; nonlinear and coherent optics; spectroscopy.
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