Phase-dependent dielectric properties and proton conduction of neopentyl glycol

新戊二醇的相依赖介电特性和质子传导

阅读:1

Abstract

Phase-dependent dielectric properties and proton conduction of neopentyl glycol (NPG), which is an organic molecular plastic crystal, were studied via variable-temperature broadband dielectric spectroscopy (BDS). Permittivity and conductivity data show the phase transformations of NPG from the crystalline state to the plastic crystalline state at 315 K and then to the molten state at 402 K across the temperature range of 293-413 K. The Vogel temperatures (T (v)) fitted from the Vogel-Fulcher-Tammann (VFT) equation agree well with the values extrapolated by the Stickel plot (linearized Vogel plot). Impedance and modulus data display a separation of the -Z'' (the imaginary part of the complex impedance) and M'' (the imaginary part of the complex electric modulus) peaks in the crystalline phase. However, they overlap in both the plastic crystalline phase and the molten phase, indicating long-range proton conduction. In both the molten phase and the plastic crystalline phase, the temperature dependence of direct current conductivity (σ (dc)) obeys the VFT equation very well. While the vehicle mechanism (translational diffusion) is an intrinsic mechanism for ionic or protonic conduction in the molten phase, it is speculated that the Grotthuss mechanism also works due to the self-dissociation of NPG molecules, which are similar to water molecules. In the plastic crystalline phase, the proton hopping mechanism is most likely the underlying ion-conducting mechanism because of the rotational disorder and intrinsic defects (vacancies) of the NPG molecules. In the ordered crystalline phase, the proton conduction is presumed to follow the proton hopping mechanism as determined from the localized relaxation and the temperature dependence of σ (dc) (Arrhenius behavior).

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。