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Charge-transfer reaction rate at the LiMn2O4 spinel oxide cathode/polymer electrolyte interface

机译:LiMn2O4尖晶石阴极/聚合物电解质界面的电荷转移反应速率

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摘要

Charge-transfer resistance at the LiMn2O4 thin film cathode/polyether based electrolyte interfaces was investigated. The thin film cathodes were prepared by electrostatic spray deposition (ESD) method, and charge-transfer resistances at the cathode/polymer electrolyte interfaces were measured by electrochemical impedance spectroscopy in the poly(ethylene glycol) dimethyl ether (PEGDME) whose average molecular weight is 500 (PEGDME500) dissolving LiCF3SO3 by adding various amounts of polyether having higher average molecular weight of 1000 (PEGDME1000). It was found that the charge-transfer resistance increased with increasing amounts of PEGDME1000. The Gibbs activation energies and the solvation state of lithium ions were almost constant with the amounts of PEGDME1000. On the other hand, the charge-transfer resistance was proportional to the viscosity of the electrolyte. It was suggested that the viscosity of the electrolyte was one of the important factors for the charge-transfer reaction rate at the LiMn2O4 cathode/polyether based electrolytes interfaces. (c) 2005 Published by Elsevier B.V.
机译:研究了LiMn2O4薄膜阴极/聚醚基电解质界面的电荷转移电阻。通过静电喷涂(ESD)方法制备薄膜阴极,并通过电化学阻抗谱法在平均分子量为2的聚乙二醇二甲醚(PEGDME)中测量阴极/聚合物电解质界面处的电荷转移电阻。通过添加各种量的具有更高的平均分子量为1000的聚醚(PEGDME1000)溶解LiCF3SO3的500(PEGDME500)。发现电荷转移电阻随PEGDME1000的量增加而增加。锂离子的吉布斯活化能和溶剂化状态几乎与PEGDME1000的量相同。另一方面,电荷转移电阻与电解质的粘度成比例。提出电解质的粘度是在LiMn2O4阴极/聚醚基电解质界面处电荷转移反应速率的重要因素之一。 (c)2005年由Elsevier B.V.

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