Li Qi, Yan Feng, Texter John
Department of Materials Science, School of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, Jiangsu, PR China.
Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, PR China.
Chem Rev. 2024 Apr 10;124(7):3813-3931. doi: 10.1021/acs.chemrev.3c00429. Epub 2024 Mar 21.
The breadth and importance of polymerized ionic liquids (PILs) are steadily expanding, and this review updates advances and trends in syntheses, properties, and applications over the past five to six years. We begin with an historical overview of the genesis and growth of the PIL field as a subset of materials science. The genesis of ionic liquids (ILs) over nano to meso length-scales exhibiting 0D, 1D, 2D, and 3D topologies defines colloidal ionic liquids, CILs, which compose a subclass of PILs and provide a synthetic bridge between IL monomers (ILMs) and micro to macro-scale PIL materials. The second focus of this review addresses design and syntheses of ILMs and their polymerization reactions to yield PILs and PIL-based materials. A burgeoning diversity of ILMs reflects increasing use of nonimidazolium nuclei and an expanding use of step-growth chemistries in synthesizing PIL materials. Radical chain polymerization remains a primary method of making PILs and reflects an increasing use of controlled polymerization methods. Step-growth chemistries used in creating some CILs utilize extensive cross-linking. This cross-linking is enabled by incorporating reactive functionalities in CILs and PILs, and some of these CILs and PILs may be viewed as exotic cross-linking agents. The third part of this update focuses upon some advances in key properties, including molecular weight, thermal properties, rheology, ion transport, self-healing, and stimuli-responsiveness. Glass transitions, critical solution temperatures, and liquidity are key thermal properties that tie to PIL rheology and viscoelasticity. These properties in turn modulate mechanical properties and ion transport, which are foundational in increasing applications of PILs. Cross-linking in gelation and ionogels and reversible step-growth chemistries are essential for self-healing PILs. Stimuli-responsiveness distinguishes PILs from many other classes of polymers, and it emphasizes the importance of segmentally controlling and tuning solvation in CILs and PILs. The fourth part of this review addresses development of applications, and the diverse scope of such applications supports the increasing importance of PILs in materials science. Adhesion applications are supported by ionogel properties, especially cross-linking and solvation tunable interactions with adjacent phases. Antimicrobial and antifouling applications are consequences of the cationic nature of PILs. Similarly, emulsion and dispersion applications rely on tunable solvation of functional groups and on how such groups interact with continuous phases and substrates. Catalysis is another significant application, and this is an historical tie between ILs and PILs. This component also provides a connection to diverse and porous carbon phases templated by PILs that are catalysts or serve as supports for catalysts. Devices, including sensors and actuators, also rely on solvation tuning and stimuli-responsiveness that include photo and electrochemical stimuli. We conclude our view of applications with 3D printing. The largest components of these applications are energy related and include developments for supercapacitors, batteries, fuel cells, and solar cells. We conclude with our vision of how PIL development will evolve over the next decade.
聚合离子液体(PILs)的广度和重要性正在稳步扩大,本综述更新了过去五到六年中合成、性质及应用方面的进展和趋势。我们首先对PIL领域作为材料科学一个子集的起源和发展进行历史概述。纳米到介观长度尺度上呈现0D、1D、2D和3D拓扑结构的离子液体(ILs)的起源定义了胶体离子液体(CILs),它构成了PILs的一个子类,并在IL单体(ILMs)与微观到宏观尺度的PIL材料之间提供了一个合成桥梁。本综述的第二个重点是ILMs的设计与合成及其聚合反应,以生成PILs和基于PIL的材料。ILMs迅速增加的多样性反映出在合成PIL材料时非咪唑鎓核的使用日益增多以及逐步增长化学方法的应用不断扩大。自由基链式聚合仍然是制备PILs的主要方法,这反映出可控聚合方法的使用日益增加。用于制备某些CILs的逐步增长化学方法利用了广泛的交联。通过在CILs和PILs中引入反应性功能实现这种交联,其中一些CILs和PILs可被视为特殊的交联剂。本更新的第三部分聚焦于一些关键性质的进展,包括分子量、热性质、流变学、离子传输、自修复和刺激响应性。玻璃化转变、临界溶解温度和流动性是与PIL流变学和粘弹性相关的关键热性质。这些性质进而调节机械性能和离子传输,这在PILs应用不断增加中起着基础性作用。凝胶化和离子凝胶中的交联以及可逆逐步增长化学方法对于自修复PILs至关重要。刺激响应性使PILs区别于许多其他类别的聚合物,并强调了在CILs和PILs中对溶剂化进行分段控制和调节的重要性。本综述的第四部分讨论了应用的发展,此类应用的广泛范围支持了PILs在材料科学中日益增加的重要性。离子凝胶性质支持了粘附应用,特别是与相邻相的交联和可调节溶剂化相互作用。抗菌和防污应用是PILs阳离子性质的结果。同样,乳液和分散应用依赖于官能团的可调节溶剂化以及这些基团与连续相和底物的相互作用方式。催化是另一个重要应用,这是ILs和PILs之间的历史联系。这一部分还与以PILs为模板的各种多孔碳相建立了联系,这些碳相是催化剂或用作催化剂的载体。包括传感器和致动器在内的器件也依赖于溶剂化调节和刺激响应性,其中包括光和电化学刺激。我们以3D打印结束对应用的阐述。这些应用中最大的部分与能源相关,包括超级电容器、电池、燃料电池和太阳能电池的发展。我们以对PIL未来十年发展的展望作为结尾。