Based on the Second Virial Coefficient(A2)to Study Effect of the Synergistic Action of Solvent and External Electric Field on the Solution Behavior and Film's Condensed State Structure

• 作者: Ya-Nan Guo Hao Zhang Bin Liu Dan Lu
• 来源期刊: 高分子科学（英文版）
• 年，卷（期）: 2022,（5）
• 所属期刊栏目: RESEARCH ARTICLES
• 页码范围: 478-490
• 页数: 13页
• 语种: 英文

摘要

The solventnatures are crucial to deeply reveal solution behavior of macromolecular chains,physical essence of condensed state structures formation of the film as well as the photoelectronic devices performance.Based on the second virial coefficient(A2),effect of the synergistic action of solvents and external electric field on both solution behavior and the film's condensed state structure for the semi-rigid conjugated polymer,poly[2-methoxy-5-(2'-ethylhexoxy)-1,4-phenylvinylene](MEH-PPV)was investigated by dynamic/static light scattering,photoluminescence spectroscopy and transmission electron microscopy,etc.It was found that although the MEH-PPV solutions with different solvents(toluene,chlorobenzene,chloroform and tetrahydrofuran)all could generate a response to the external electric field,the degree of response varied significantly with the change of solvent nature.Furthermore,ordered degree of the film from the solutions was also obviously different.The essential reason for this responsive difference was firstly revealed in the research,which actually depended on the degree of interaction between the solute and solvent,and this degree of interaction could be quantitatively described by the second virial coefficient(A2).The bigger the A2,the stronger the interaction between solvent and solute in the solution,and the stronger the response to the external electric field.Further,under the induction of external electric field,chains aggregations with different sizes were formed accompanied by large-scale chains ordered structure in the solution.This ordered structure not only can effectively transfer to film prepared by the precursor solution but also is beneficial to enhance the carrier mobility and device efficiency of the photoelectronic film.