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Conductivity Induced Polarization in a Semicrystalline Ferroelectric Polymer

机译:半结晶铁电聚合物中的电导诱导极化

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It is commonly believed that formation of polarization and its switching in ferroelectrics under high electric field strength is a fast process in the microsecond range governed by a well known activation field. We have found, however, that in semicrystalline ferroelectric polymers, containing both crystalline and amorphous phases, polarization continues to grow during times 5 to 6 orders of magnitude longer than the estimated switching times. The controversy has been resolved by taking into account the effect of conductivity in such materials. It has been shown that there are two components of the ferroelectric polarization, of which the first one is essentially field dependent and originates from a fast alignment of dipoles in crystalline regimes, while the second slow component is controlled by the conductivity of the material. Appropriate modeling showed that charge accumulation at the interfacial boundaries is an important component of the slow polarization. Good agreement between calculated and measured polarization has been observed for poly(vinylidene fluoride) (PVDF). However, it is believed that the phenomenon is probably common for all two-phase ferroelectrics such as ceramics and ceramics-polymer composites.
机译:通常认为,在高电场强度下铁电体中极化的形成及其转换是在微秒范围内由众所周知的激活场控制的快速过程。但是,我们发现,在同时含有结晶相和非晶相的半结晶铁电聚合物中,极化比预计的转换时间长5至6个数量级,并且持续增长。通过考虑此类材料中电导率的影响,解决了这一争议。已经表明,铁电极化有两个分量,第一个分量基本上是场相关的,并且源于晶格中偶极子的快速排列,而第二个慢分量由材料的电导率控制。适当的建模表明,界面边界处的电荷积累是慢极化的重要组成部分。对于聚偏二氟乙烯(PVDF),已观察到极化与计算极化之间的良好一致性。然而,据信该现象可能对于所有两相铁电体都是常见的,例如陶瓷和陶瓷-聚合物复合材料。

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