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Ionic Space Charge Relaxation and High Dielectric Permittivity in Polyethylene Oxide

机译:聚环氧乙烷中离子空间电荷弛豫和高介电常数

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Thin films of polyethylene Oxide with molecular weights from 6*10~3 to 4*10~5 were prepared from aqueous solutions y a spin technique as AL-PEO-Al structures, or as AL-PEO-Si structures. Dielectric measurements were carried out in a frequency range 3 mHz<=f<=1 MHz in atmoshperes of different relative humidity and at different temepratures. The nominal dielectric permittivity exhibits a remarkable dependence on the sample thickness and the relative humidity. We find a ture volume polarization in the high frequency range and a thermally activated relaxation process in the low frequeny rnage, whose time constant is shifted towards high frequencies with increasing r.h.. It is ocnsidered that due to the absorbed dipolar water molecules chemical bonds within the sample are broken and quasi-free ions are generated. These ions move through the sample to the electrode interfaces and form an ionic space charge. We assume that at the PEO-Al interface an oxide layer is formed, which is impermeable for these ions. The transit times and the drift velovities of the ions are almost independent of the electric field strength in the low-field limit. Therefore we conclude that the movement of the ions can be described by a multiwell potential model, where the transition probability between neighbored wells is thermally activated.
机译:采用自旋技术制备水溶液,以AL-PEO-Al结构或AL-PEO-Si结构制备了分子量为6 * 10〜3至4 * 10〜5的聚环氧乙烷薄膜。在不同的相对湿度和不同的温度下,在3 mHz <= f <= 1 MHz的频率范围内进行介电测量。标称介电常数对样品厚度和相对湿度表现出显着的依赖性。我们发现在高频范围内存在体积极化,而在低频范围内存在热活化弛豫过程,其时间常数随着rh的增加而向高频移动,这可能是由于吸收了偶极水分子内部的化学键所致。样品破裂并生成准无离子。这些离子穿过样品移动到电极界面并形成离子空间电荷。我们假设在PEO-Al界面处形成了一层氧化层,这些离子不可渗透。离子的迁移时间和漂移速度几乎与低电场极限中的电场强度无关。因此,我们得出结论,离子的运动可以通过多孔势模型来描述,其中相邻阱之间的跃迁概率被热激活。

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