Poly(ionic liquid)‐Based Energy and Electronic Devices

Guo, Jiangna; Sun, Zhe; Zhou, Yingjie; Yan, Feng

doi:10.1002/cjoc.202100820

Cited by 19 publications

(11 citation statements)

References 65 publications

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“…Table 1 highlights a variety of reviews focusing on applications of PILs in energy materials, devices, and biomedical materials. 29,33,38,[43][44][45]56,59,62 The types of the applications we discuss here are summarized in Figure 28.…”

Section: Applicationsmentioning

confidence: 99%

Polymerized and Colloidal Ionic Liquids─Syntheses and Applications

Li,

Yan,

Texter

2024

Chem. Rev.

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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 lengthscales 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 macroscale 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 crosslinking 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 stimuliresponsiveness that include photo and electrochemical stimuli. We conclude our view of applications with 3D printi...

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Section: Applicationsmentioning

confidence: 99%

Polymerized and Colloidal Ionic Liquids─Syntheses and Applications

Li,

Yan,

Texter

2024

Chem. Rev.

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“…4a), leading to volatilization loss and electrode corrosion. 197 Tuning the molten salt electrolyte component can form a tenacious and compact Li nickel oxide nano-scale particle layer on the surface of the nickel electrode to retard corrosion, 198 yet the molten salt electrolyte and electrode materials are severely constrained. Furthermore, molten salt electrolytes can not only dissolve metal oxides to form the active materials, 199 but also interact with metals to form metal fog during cycling charge and discharge.…”

Section: Current Progress Of Sem-containing Ht-msbsmentioning

confidence: 99%

Solid electrolyte membrane-containing rechargeable high-temperature molten salt electrolyte-based batteries

Wang

Cheng

2023

Sustainable Energy Fuels

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“…[ 1‐6 ] Lithium‐ion batteries (LIBs) are one of the most promising candidates for stretchable power sources owing to their advantages of high energy density, low self‐discharge, and long‐term stability. [ 7‐20 ] As the electrolyte is one of the key components in LIBs, intrinsically stretchable polymer electrolytes (PEs) with satisfactory mechanical robustness are highly required for the fabrication of stretchable LIBs. [ 21‐28 ] From the perspective of practical applications, the stretchable PEs are expected to endow the stretchable LIBs with fast charging capability to minimize the charging time of wearable devices.…”

Section: Background and Originality Contentmentioning

confidence: 99%

Highly Stretchable and Elastic Polymer Electrolytes with High Ionic Conductivity and Li‐Ion Transference Number for High‐Rate Lithium Batteries

Guo

Liu

2022

Chin. J. Chem.

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Comprehensive SummaryThe ever‐growing demand for wearable electronics drives the development of stretchable lithium‐ion batteries (LIBs) with fast charging capability, in which stretchable polymer electrolytes (PEs) with high ionic conductivity and lithium‐ion transference numbers () are highly desirable. Herein, we report a highly stretchable and elastic PE with high ionic conductivity and , which is applicable in high‐rate and stretchable LIBs. The PE was fabricated by incorporating polyethylene glycol (PEG) and lithium salts into polyurethane networks, wherein α‐cyclodextrin (α‐CD) acts as the cross‐linker. The PEG chains are cross‐linked by covalent and noncovalent bonds, and some PEG chains enter into the cavity of α‐CD to form PEG/α‐CD inclusions. These structural features effectively suppress crystallization of the PEG chains, hinder movement of the counterions of Li+, and endow PE with satisfactory mechanical robustness. The PE with a tensile strength (0.61 MPa) exhibits a large strain at break (840%) and excellent elasticity, possessing a high ionic conductivity (5.0 × 10–4 S·cm–1) and a high (0.52). The Li‖LiFePO4 battery assembled with the PE delivers a high capacity of 75 mAh·g–1 even at the high rate of 16 C. The battery can be stably cycled for 300 and 200 cycles at 1 C and 4 C, respectively.

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Poly(ionic liquid)‐Based Energy and Electronic Devices

Cited by 19 publications

References 65 publications

Polymerized and Colloidal Ionic Liquids─Syntheses and Applications

Polymerized and Colloidal Ionic Liquids─Syntheses and Applications

Solid electrolyte membrane-containing rechargeable high-temperature molten salt electrolyte-based batteries

Highly Stretchable and Elastic Polymer Electrolytes with High Ionic Conductivity and Li‐Ion Transference Number for High‐Rate Lithium Batteries

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