Covalent design of ionogels: bridging with hydrogels and covalent adaptable networks

IF 3.9 2区 化学 Q2 POLYMER SCIENCE Polymer Chemistry Pub Date : 2025-04-22 Epub Date: 2025-04-16 DOI:10.1039/d5py00217f
Junjia Zhang , Yian Wang , Yinglu Liu , Jérémy Odent , Yukikazu Takeoka
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Abstract

Ionogels are conductive soft matter with ionic liquids as conductive media, exhibiting significant potential as multifunctional materials. Over the past two decades, ionogels have been developed for applications in sensors, actuators, supercapacitors, lithium-ion batteries, adhesives, antifouling coatings, nanotriboelectric generators, thermoelectric devices, etc. To achieve recyclability that is advantageous for various applications, dissociative supramolecular interactions—e.g. electrostatic interactions, hydrogen bonds and π–π stacking—have garnered significant attention in the crosslinking design of ionogels. High-strength ionogels utilizing dissociative supramolecular interactions as a crosslinking mechanism have been synthesized. However, due to the inherently low bond energy and high dynamics of dissociative supramolecular crosslinking, issues such as low thermal stability and insufficient solvent resistance arise, limiting the broader applications of ionogels. To address these challenges, the network structure can be precisely designed, and reversible covalent bonds can be introduced as a crosslinking mechanism to mitigate the trade-off between material durability and dynamic behavior. Several studies provide insights into realizing this approach. For instance, hydrogels, which are also classified as soft materials, can enhance both mechanical strength and deformability by incorporating topological network structures based on organic covalent bonds. Similarly, covalent adaptable networks (CANs), a class of dynamic materials, achieve high thermal stability, solvent resistance, and recyclability by utilizing densely reversible covalent bonds. Hence, we chiefly focus on the critical roles of designing the organic polymer network structures and utilizing reversible covalent bonding to enhance key physical properties of ionogels, including mechanical strength, electrical conductivity, and processability. Last but not least, we discuss the current challenges associated with the design and application of ionogels, while also anticipating potential strategies that leverage superior designs from materials such as hydrogels and CANs to develop innovative ionogels.
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离子凝胶的共价设计:与水凝胶的桥接和共价自适应网络
离子凝胶是以离子液体为导电介质的导电软物质,具有作为多功能材料的巨大潜力。在过去的二十年里,离子凝胶已经发展到传感器、执行器、超级电容器、锂离子电池、粘合剂、防污涂层、纳米摩擦发电机、热电器件等领域。为了实现有利于各种应用的可回收性,解离的超分子相互作用-例如。静电相互作用、氢键和-堆叠在电离胶的交联设计中引起了极大的关注。利用解离超分子相互作用作为交联机制合成了高强度离子凝胶。然而,由于离解超分子交联固有的低键能和高动力学,出现了热稳定性低和耐溶剂性不足等问题,限制了离子凝胶的广泛应用。为了应对这些挑战,可以精确设计网络结构,并引入可逆共价键作为交联机制,以减轻材料耐久性和动态性能之间的权衡。一些研究为实现这一方法提供了见解。例如,水凝胶也被归类为软材料,它可以通过结合基于有机共价键的拓扑网络结构来提高机械强度和变形能力。同样,共价适应性网络(can)是一类动态材料,通过利用密集可逆的共价键,实现了高热稳定性、耐溶剂性和可回收性。因此,我们主要关注设计有机聚合物网络结构和利用可逆共价键来提高电离胶的关键物理性能,包括机械强度,导电性和可加工性的关键作用。最后,我们讨论了当前与电离层设计和应用相关的挑战,同时也预测了利用水凝胶和can等材料的卓越设计来开发创新电离层的潜在策略。
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来源期刊
Polymer Chemistry
Polymer Chemistry POLYMER SCIENCE-
CiteScore
8.60
自引率
8.70%
发文量
535
审稿时长
1.7 months
期刊介绍: Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
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