首页> 外文期刊>Electrochimica Acta >Polymer dynamics in thin p-type conducting films investigated by ac-electrogravimetry. Kinetics aspects on anion exclusion, free solvent transfer, and conformational changes in poly(o-toluidine)
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Polymer dynamics in thin p-type conducting films investigated by ac-electrogravimetry. Kinetics aspects on anion exclusion, free solvent transfer, and conformational changes in poly(o-toluidine)

机译:通过交流电重力法研究了薄p型导电膜中的聚合物动力学。阴离子(排除),自由溶剂转移和聚(邻甲苯胺)构象变化的动力学方面

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摘要

A new transfer model is proposed to explain ac-electrogravimetry response of p-doped films. This model takes into account the exclusion effect occurring as a result of the anion transfer. The insertion/expulsion of anions inside a film involves simultaneously the expulsion/insertion of free solvent molecules. The number of solvent molecules excluded depends on the volume of anion transferred. Solvent transfer stimulated by the conformational changes of films constitutes the remaining electrogravimetric response when the exclusion process cannot explain by itself this response. Consequently, the kinetics of this free solvent transfer can be directly related to the kinetics of conformational changes. This model was validated in poly(o-toluidine) thin films where electrochemical kinetics were quantitatively investigated as a function of the applied potential. As far as we know, for the first time, charge transfer and conformational changes could be kinetically separated. This new transfer model may respond to fundamental questions on the electrochemistry of conducting polymers, which may have a significant impact on a large number of applications. (C) 2014 Elsevier Ltd. All rights reserved.
机译:提出了一种新的传递模型来解释p掺杂薄膜的交流电重分析。该模型考虑了由于阴离子转移而产生的排斥效应。阴离子在膜内的插入/排出同时涉及游离溶剂分子的排出/插入。排除的溶剂分子数量取决于转移的阴离子量。当排除过程不能自己解释这种反应时,由膜的构象变化所激发的溶剂转移构成了剩余的电重量反应。因此,这种自由溶剂转移的动力学可以与构象变化的动力学直接相关。该模型在聚(邻甲苯胺)薄膜中得到验证,在该薄膜中,电化学动力学作为施加电势的函数进行了定量研究。据我们所知,电荷转移和构象变化首次可以动力学分离。这种新的转移模型可能会回答有关导电聚合物电化学的基本问题,这可能会对大量应用产生重大影响。 (C)2014 Elsevier Ltd.保留所有权利。

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