Iacob Ciprian, Matsumoto Atsushi, Brennan Marissa, Liu Hongjun, Paddison Stephen J, Urakawa Osamu, Inoue Tadashi, Sangoro Joshua, Runt James
Department of Materials Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Department of Macromolecular Science, Osaka University, Toyonaka, Osaka 560-0043, Japan.
ACS Macro Lett. 2017 Sep 19;6(9):941-946. doi: 10.1021/acsmacrolett.7b00335. Epub 2017 Aug 16.
The impact of the chemical structure on ion transport, nanoscale morphology, and dynamics in polymerized imidazolium-based ionic liquids is investigated by broadband dielectric spectroscopy and X-ray scattering, complemented with atomistic molecular dynamics simulations. Anion volume is found to correlate strongly with -independent ionic conductivities spanning more than 3 orders of magnitude. In addition, a systematic increase in alkyl side chain length results in about one decade decrease in -independent ionic conductivity correlating with an increase in the characteristic backbone-to-backbone distances found from scattering and simulations. The quantitative comparison between ion sizes, morphology, and ionic conductivity underscores the need for polymerized ionic liquids with small counterions and short alkyl side chain length in order to obtain polymer electrolytes with higher ionic conductivity.
通过宽带介电谱和X射线散射,并辅以原子分子动力学模拟,研究了化学结构对聚合咪唑基离子液体中离子传输、纳米级形态和动力学的影响。发现阴离子体积与跨越三个数量级以上的与频率无关的离子电导率密切相关。此外,烷基侧链长度的系统性增加导致与频率无关的离子电导率下降约一个数量级,这与散射和模拟中发现的特征主链到主链距离的增加相关。离子尺寸、形态和离子电导率之间的定量比较强调了需要具有小抗衡离子和短烷基侧链长度的聚合离子液体,以获得具有更高离子电导率的聚合物电解质。