Ion Solvation in Polymer Blends and Block Copolymer Melts: Effects of Chain Length and Connectivity on the Reorganization of Dipoles

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• 作者：Issei Nakamura
• 刊名：Journal of Physical Chemistry B
• 出版年：2014
• 出版时间：May 29, 2014
• 年：2014
• 卷：118
• 期：21
• 页码：5787-5796
• 全文大小：416K
• 年卷期：v.118,no.21(May 29, 2014)
• ISSN：1520-5207

文摘

We studied the thermodynamic properties of ion solvation in polymer blends and block copolymer melts and developed a dipolar self-consistent field theory for polymer mixtures. Our theory accounts for the chain connectivity of polymerized monomers, the compressibility of the liquid mixtures under electrostriction, the permanent and induced dipole moments of monomers, and the resultant dielectric contrast among species. In our coarse-grained model, dipoles are attached to the monomers and allowed to rotate freely in response to electrostatic fields. We demonstrate that a strong electrostatic field near an ion reorganizes dipolar monomers, resulting in nonmonotonic changes in the volume fraction profile and the dielectric function of the polymers with respect to those of simple liquid mixtures. For the parameter sets used, the spatial variations near an ion can be in the range of 1 nm or larger, producing significant differences in the solvation energy among simple liquid mixtures, polymer blends, and block copolymers. The solvation energy of an ion depends substantially on the chain length in block copolymers; thus, our theory predicts the preferential solvation of ions arising from differences in chain length.