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首页> 外文期刊>IEEE Transactions on Dielectrics and Electrical Insulation >Extending an Asymmetric Double Well Potential Model to Hfo2
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Extending an Asymmetric Double Well Potential Model to Hfo2

机译:将非对称双阱势能模型扩展到Hfo2

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摘要

Previously an asymmetric double well potential model was successfully applied to interpret the nonlinear relaxational polarization of Al2O3. Here we extend this model to HfO2. The capacitance measurements on HfO2 based metal-insulator-metal MIM capacitors were performed. To study this relaxational polarization the thickness of the dielectric, device temperature, frequency and electric field were varied systematically. It was revealed that at lower temperatures T ≤ 180 K the relaxation happens via proton tunneling transition in asymmetric double wells. Incorporation of protons in HfO2 is illustrated by monitoring the mass spectra during oxide evaporation. Above 180 K the thermal activation transition comes in a play but the relaxation process is also found to be influenced by electrode space charges. One of our goals here was to show that our model is not specific to Al2O3 and it has the ability to explain the nonlinearity of other metal oxides.
机译:以前,成功地将非对称双阱势模型用于解释Al2O3的非线性弛豫极化。在这里,我们将此模型扩展到HfO2。在基于HfO2的金属绝缘体金属MIM电容器上进行了电容测量。为了研究这种松弛极化,系统地改变了电介质的厚度,器件温度,频率和电场。结果表明,在较低的温度T≤180 K时,通过非对称双阱中的质子隧穿跃迁发生了弛豫。通过监测氧化物蒸发过程中的质谱图说明了质子在HfO2中的结合。高于180 K时,会发生热活化转变,但还发现弛豫过程受电极空间电荷的影响。我们的目标之一是证明我们的模型并非特定于Al2O3,并且能够解释其他金属氧化物的非线性。

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