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      Controllable synthesis and structural design of novel all-organic polymers toward high energy storage dielectrics

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          Abstract

          As the core unit of energy storage equipment, high voltage pulse capacitor plays an indispensable role in the field of electric power system and electromagnetic energy related equipment. The mostly utilized polymer materials are metallized polymer thin films, which are represented by biaxially oriented polypropylene (BOPP) films, possessing the advantages including low cost, high breakdown strength, excellent processing ability, and self-healing performance. However, the low dielectric constant ( ε r < 3) of traditional BOPP films makes it impossible to meet the demand for increased high energy density. Controlled/living radical polymerization (CRP) and related techniques have become a powerful approach to tailor the chemical and physical properties of materials and have given rise to great advances in tuning the properties of polymer dielectrics. Although organic-inorganic composite dielectrics have received much attention in previous studies, all-organic polymer dielectrics have been proven to be the most promising choice because of its light weight and easy large-scale continuous processing. In this short review, we begin with some basic theory of polymer dielectrics and some theoretical considerations for the rational design of dielectric polymers with high performance. In the guidance of these theoretical considerations, we review recent progress toward all-organic polymer dielectrics based on two major approaches, one is to control the polymer chain structure, containing microscopic main-chain and side-chain structures, by the method of CRP and the other is macroscopic structure design of all-organic polymer dielectric films. And various chemistry and compositions are discussed within each approach.

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          Polymer brushes via surface-initiated controlled radical polymerization: synthesis, characterization, properties, and applications.

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            Recent Progress on Ferroelectric Polymer-Based Nanocomposites for High Energy Density Capacitors: Synthesis, Dielectric Properties, and Future Aspects.

            Dielectric polymer nanocomposites are rapidly emerging as novel materials for a number of advanced engineering applications. In this Review, we present a comprehensive review of the use of ferroelectric polymers, especially PVDF and PVDF-based copolymers/blends as potential components in dielectric nanocomposite materials for high energy density capacitor applications. Various parameters like dielectric constant, dielectric loss, breakdown strength, energy density, and flexibility of the polymer nanocomposites have been thoroughly investigated. Fillers with different shapes have been found to cause significant variation in the physical and electrical properties. Generally, one-dimensional and two-dimensional nanofillers with large aspect ratios provide enhanced flexibility versus zero-dimensional fillers. Surface modification of nanomaterials as well as polymers adds flavor to the dielectric properties of the resulting nanocomposites. Nowadays, three-phase nanocomposites with either combination of fillers or polymer matrix help in further improving the dielectric properties as compared to two-phase nanocomposites. Recent research has been focused on altering the dielectric properties of different materials while also maintaining their superior flexibility. Flexible polymer nanocomposites are the best candidates for application in various fields. However, certain challenges still present, which can be solved only by extensive research in this field.
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              Reversible-deactivation radical polymerization (Controlled/living radical polymerization): From discovery to materials design and applications

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                Author and article information

                Contributors
                Journal
                Front Chem
                Front Chem
                Front. Chem.
                Frontiers in Chemistry
                Frontiers Media S.A.
                2296-2646
                17 August 2022
                2022
                : 10
                : 979926
                Affiliations
                [1] 1 Xi’an Key Laboratory of Sustainable Energy Materials Chemistry , Department of Applied Chemistry , School of Chemistry , Xi’an Jiaotong University , Xi’an, Shaanxi, China
                [2] 2 Xi’an Jiaotong University Suzhou Academy , Suzhou, Jiangsu, China
                Author notes

                Edited by: Minghua Chen, Harbin University of Science and Technology, China

                Reviewed by: Xiaoxu Liu, Shaanxi University of Science and Technology, China

                Yunhe Zhang, Jilin University, China

                *Correspondence: Zhicheng Zhang, zhichengzhang@ 123456mail.xjtu.edu.cn

                This article was submitted to Polymer Chemistry, a section of the journal Frontiers in Chemistry

                Article
                979926
                10.3389/fchem.2022.979926
                9428677
                76c9a0bf-84f5-4765-8e6d-a5ab1fafef70
                Copyright © 2022 Gong, Ji, Cheng, Xiong, Zhang and Zhang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 28 June 2022
                : 20 July 2022
                Funding
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Categories
                Chemistry
                Review

                dielectric capacitors,all-organic polymer dielectric,controlled/living radical polymerization,dipole regulation,multilayer structure

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