聚苯胺
聚合
结晶度
质子化
极化子
材料科学
分散性
高分子化学
活化能
化学工程
物理化学
聚合物
化学
离子
有机化学
复合材料
工程类
物理
量子力学
电子
作者
Ku-Yen Lin,Lun-Wei Hu,Ko-Lun Chen,Ming‐Deng Siao,Wei-Fu Ji,Chun‐Chuen Yang,Jui‐Ming Yeh,Kuan‐Cheng Chiu
标识
DOI:10.1016/j.eurpolymj.2017.01.035
摘要
We report on the effects from polymerization temperature (TP) on the thermal de-protonation of anilinium cations into neutral anilines and on the structural and electrical properties of polyaniline emeraldine salt (PANI ES) samples synthesized from chemical oxidative polymerization with ammonium peroxydisulfate as oxidant and with [HCl] varied from 0.7, 1.0, and 2.0 M. From the TP–dependence of induction period the activation energy associated with this thermal de-protonation is evaluated. With increasing TP to increase the de-protonation rate, the as-synthesized PANI ES samples possess a weaker hardness, a less crystallinity, a lower molecular weight and a smaller dispersity. From the temperature-dependence of electrical conductivity measured on these doped PANI ES samples and with application of the nearest-neighbor hopping model, the corresponding activation energy for charge transport increases with increasing TP. Above results reveal that the distribution of polaron states induced by counter-ions in the PANI ES sample synthesized at higher TP becomes more disorder and hence results in a broader polaron bandwidth.
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