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Universal Behavior of Dielectric Responses of Glass Formers: Role of Dipole-Dipole Interactions

机译:玻璃形成者的介电响应的普遍行为:偶极-偶极相互作用的作用

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摘要

From an exhaustive examination of the molecular dynamics in practically all van der Waals molecular glass formers ever probed by dielectric spectroscopy, we found that the width of the a-loss peak at or near the glass transition temperature T-g is strongly anticorrelated with the polarity of the molecule. The larger the dielectric relaxation strength Delta epsilon(T-g) of the system, the narrower is the a-loss peak. This remarkable property is explained by the contribution from the dipole-dipole interaction potential V-dd(r) = -Dr(-6) to the attractive part of the intermolecular potential, making the resultant potential more harmonic, and the effect increases rapidly with the dipole moment mu and Delta epsilon(T-g) in view of the relation, D proportional to (mu(4)/kT(g)) proportional to kT(g)[Delta epsilon(T-g)](2). Since the novel correlation discovered encompasses practically all van der Waals molecular glass formers studied by dielectric spectroscopy, it impacts the large dielectric research community as well as those engaged in solving the glass transition problem.
机译:通过对介电谱法研究的几乎所有范德华分子玻璃形成剂中的分子动力学进行详尽的检查,我们发现在玻璃化转变温度Tg或附近的a-损失峰的宽度与玻璃的极性密切相关。分子。系统的介电弛豫强度Δε(T-g)越大,a损耗峰越窄。偶极子-偶极子相互作用势V-dd(r)= -Dr(-6)对分子间电势的吸引部分的贡献,使得所得电势更加谐波,并且随着偶极矩mu和Delta epsilon(Tg)鉴于关系D与kT(g)[Delta epsilon(Tg)](2)成比例的(mu(4)/ kT(g))成正比。由于发现的新型相关性实际上涵盖了所有通过介电谱研究的范德华分子玻璃形成剂,因此它影响了大型介电研究界以及从事解决玻璃化转变问题的人们。

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  • 来源
    《Physical review letters》 |2016年第2期|025702.1-025702.6|共6页
  • 作者单位

    Univ Silesia, Inst Phys, PL-40007 Katowice, Poland|Silesian Ctr Educ & Interdisciplinary Res, PL-41500 Chorzow, Poland;

    Univ Silesia, Inst Phys, PL-40007 Katowice, Poland|Silesian Ctr Educ & Interdisciplinary Res, PL-41500 Chorzow, Poland;

    Univ Silesia, Inst Phys, PL-40007 Katowice, Poland|Silesian Ctr Educ & Interdisciplinary Res, PL-41500 Chorzow, Poland;

    Univ Silesia, Inst Phys, PL-40007 Katowice, Poland|Silesian Ctr Educ & Interdisciplinary Res, PL-41500 Chorzow, Poland;

    Univ Pisa, Dipartimento Fis, CNR IPCF, I-56127 Pisa, Italy;

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