Electric and magnetic properties of polymer electrolyte/carbon black composites

被引:11
作者
Franco, RWA
Donoso, JP
Magon, CJ
Rodella, CB
Florentino, AO
Saeki, MJ
Pernaut, JM
de Oliveira, AL
机构
[1] Univ Sao Paulo, IFSC, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Estadual Paulista, UNESP, BR-17013410 Bauru, SP, Brazil
[3] Univ Fed Minas Gerais, ICEx, BR-31270901 Belo Horizonte, MG, Brazil
关键词
composite; polymer electrolyte; carbon black; nuclear magnetic resonance; electron paramagnetic resonance; impedance spectroscopy; conductivity;
D O I
10.1016/S0167-2738(98)00284-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Measurements of H-1 Nuclear Magnetic Resonance (NMR) relaxation times, Electron Paramagnetic Resonance (EPR) and AC Impedance Spectroscopy (IS) are reported for composites based on PEO8:LiClO4 and carbon black (CB), prepared by two methods: solvent and fusion processing. Three nuclear relaxation processes were identified for H-1 nuclei: (i) belonging to the polymer chains in the amorphous phase, loosely bound to the CB particles, whose dynamics is almost the same as fbr unfilled polymer, (ii) belonging to the polymer chains which are tightly attached to the CB particles, and (iii) belonging to the crystalline phase in the loose polymer chain. The paramagnetic electronic susceptibility of the composite samples, measured by EPR, was interpreted by assuming a contribution of localized spin states that follow a Curie law, and a Pauli-like contribution of delocalized spins. A significant change of the EPR linewidth was observed at 40 K, which is the temperature where the Curie and Pauli susceptibilities equally contribute to the paramagnetic electronic susceptibility. The electrical properties are very sensitive to the preparation methods of the composites, which conditions the interaction between carbon particle-carbon particle and carbon particle-polymer chain. Classical statistic models to describe the conductivity in these media were not satisfactory. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 160
页数:12
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