自修复聚合物是新型仿生智能材料，可修复传统材料缺陷并延长其寿命。导电功能化对拓展其电子学应用具有重要意义，是亟待探索的交叉领域。本项目拟将本征自修复功能引入本征导电聚（3,4-乙撑二氧噻吩）及其衍生物（PEDOTs），利用可逆动态氢键和共价键（Diels–Alder 反应）结合的超分子聚合物，构建系列兼具热驱动并可多次结构自修复、导电和力学性能等协同恢复的复合物。拟以EDOTs单体结构的设计与合成，超分子前驱体的选择和Diels–Alder聚合为基础，采用化学氧化或电化学聚合策略实现目标复合物及其薄膜的构建。研究复合材料的热动力学，探明复合材料的结构和功能协同自修复机制，重点建立PEDOTs/超分子自修复导电聚合物的构建方法学，研究其电学性能及在新型绿色能源（如热电）及新型节能技术（如电致变色）方面的应用，揭示材料结构与器件性能的关联，推动自修复材料功能化和PEDOTs柔性智能化的发展。

Self-healing polymers are a new type of biomimetic smart material, and can repair the defects and extend the life of traditional materials. Conductive functionalization is of significance for expanding the application of self-healing polymers in electronics. This is an interdisciplinary science that needs to be explored urgently. This project intends to introduce the intrinsic self-healing function to the intrinsically conducting polymers, poly(3,4-ethylenedioxythiophene) and its derivatives (PEDOTs). With the help of supramolecular polymers that with the dual roles of non-covalent hydrogen bonding and reversible covalent bonding induced by Diels–Alder reaction, a series of composites will be fabricated which exhibit thermally-driven multiple self-healing performance, and synergistic recovery of conductive and mechanical properties. This research will begin with the design and synthesis of monomeric structures of EDOTs and the selection and polymerization of supramolecular precursors for Diels–Alder reaction. Then, the chemical oxidation or electrochemical polymerization strategy will be utilized to achieve target composits and their thin films. The thermodynamics of the composites will be investigated, and the synergistic self-healing mechanism of the structure and function of the composites will be explored. The critical object is to establish the method to build PEDOTs/Supramolecular self-healing conductive polymers. Further, their electrical properties and filmy applications for novel green energy (i.e., thermoelectrisity) and novel energy-saving technology (i.e., electrochromics) will be researched, and then the relationship between material structure and device performance will be revealed. It is believed that this work will promote the functionalization of self-healing materials and the flexible and intelligent development of conducting polymers.