Materials Science and Engineering Program and Department of Mechanical Engineering, The University of Texas at Austin , Austin, Texas 78712, United States.
Collaborative Innovation Center of Advanced Microstructures, School of Electronic Science and Engineering, Nanjing University , Nanjing 210093, China.
Acc Chem Res. 2017 Jul 18;50(7):1734-1743. doi: 10.1021/acs.accounts.7b00191. Epub 2017 Jun 26.
Conductive polymers have attracted significant interest over the past few decades because they synergize the advantageous features of conventional polymeric materials and organic conductors. With rationally designed nanostructures, conductive polymers can further exhibit exceptional mechanical, electrical, and optical properties because of their confined dimensions at the nanoscale level. Among various nanostructured conductive polymers, conductive polymer gels (CPGs) with synthetically tunable hierarchical 3D network structures show great potential for a wide range of applications, such as bioelectronics, and energy storage/conversion devices owing to their structural features. CPGs retain the properties of nanosized conductive polymers during the assembly of the nanobuilding blocks into a monolithic macroscopic structure while generating structure-derived features from the highly cross-linked network. In this Account, we review our recent progress on the synthesis, properties, and novel applications of dopant cross-linked CPGs. We first describe the synthetic strategies, in which molecules with multiple functional groups are adopted as cross-linkers to cross-link conductive polymer chains into a 3D molecular network. These cross-linking molecules also act as dopants to improve the electrical conductivity of the gel network. The microstructure and physical/chemical properties of CPGs can be tuned by controlling the synthetic conditions such as species of monomers and cross-linkers, reaction temperature, and solvents. By incorporating other functional polymers or particles into the CPG matrix, hybrid gels have been synthesized with tailored structures. These hybrid gel materials retain the functionalities from each component, as well as enable synergic effects to improve mechanical and electrical properties of CPGs. We then introduce the unique structure-derived properties of the CPGs. The network facilitates both electronic and ionic transport owing to the continuous pathways for electrons and hierarchical pores for ion diffusion. CPGs also provide high surface area and solvent compatibility, similar to natural gels. With these improved properties, CPGs have been explored to enable novel conceptual devices in diverse applications from smart electronics and ultrasensitive biosensors, to energy storage and conversion devices. CPGs have also been adopted for developing hybrid materials with multifunctionalities, such as stimuli responsiveness, self-healing properties, and super-repellency to liquid. With synthetically tunable physical/chemical properties, CPGs emerge as a unique material platform to develop novel multifunctional materials that have the potential to impact electronics, energy, and environmental technologies. We hope that this Account promotes further efforts toward synthetic control, fundamental investigation, and application exploration of CPGs.
导电聚合物在过去几十年中引起了极大的关注,因为它们结合了传统聚合物材料和有机导体的优势。通过合理设计的纳米结构,导电聚合物由于在纳米尺度上的受限尺寸,可以进一步表现出优异的机械、电气和光学性能。在各种纳米结构的导电聚合物中,具有合成可调谐的分级 3D 网络结构的导电聚合物凝胶(CPG)由于其结构特征,在生物电子学和能量存储/转换器件等广泛应用中具有很大的潜力。CPG 在将纳米构建块组装成整体宏观结构的同时保留了纳米尺寸导电聚合物的性质,同时从高度交联的网络中产生结构衍生的特征。在本综述中,我们回顾了我们在掺杂交联 CPG 的合成、性质和新颖应用方面的最新进展。我们首先描述了合成策略,其中采用具有多个官能团的分子作为交联剂将导电聚合物链交联成 3D 分子网络。这些交联分子还可以作为掺杂剂来提高凝胶网络的电导率。通过控制合成条件,如单体和交联剂的种类、反应温度和溶剂,可以调节 CPG 的微结构和物理/化学性质。通过将其他功能聚合物或颗粒掺入 CPG 基质中,可以合成具有定制结构的杂化凝胶。这些杂化凝胶材料保留了每个组分的功能,并且能够协同作用,改善 CPG 的机械和电气性能。然后,我们介绍了 CPG 的独特结构衍生性质。由于电子和离子的连续传输途径以及离子扩散的分级孔,网络促进了电子和离子的传输。CPG 还具有高的比表面积和溶剂相容性,类似于天然凝胶。由于这些改进的性质,CPG 已被探索用于从智能电子和超灵敏生物传感器到能量存储和转换器件等各种应用中实现新颖的概念设备。CPG 也已被用于开发具有多功能性的混合材料,例如刺激响应性、自修复性和对液体的超疏油性。具有合成可调物理/化学性质的 CPG 作为一种独特的材料平台出现,用于开发具有潜在影响电子、能源和环境技术的新型多功能材料。我们希望本综述能促进对 CPG 的合成控制、基础研究和应用探索的进一步努力。