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Dynamic and Reprocessable Fluorinated Poly(hindered urea) Network Materials Containing Ionic Liquids to Enhance Triboelectric Performance

Authors
Nellepalli, PothanagandhiKim, Minsoo P.Park, JunyoungNoh, Seung ManYe, ZhibinJung, Hyun WookKo, HyunhyubOh, Jung Kwon
Issue Date
20-4월-2022
Publisher
AMER CHEMICAL SOC
Keywords
dynamic/reversible chemistries; poly(hindered urea); fluorinated polymer network; triboelectric nanogenerator; ionic liquids; self-healability; reprocessability
Citation
ACS APPLIED MATERIALS & INTERFACES, v.14, no.15, pp.17806 - 17817
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
14
Number
15
Start Page
17806
End Page
17817
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/142283
DOI
10.1021/acsami.2c01963
ISSN
1944-8244
Abstract
Triboelectric nanogenerators (TENGs), a newly developed energy harvesting device that converts surrounding environmental mechanical stimuli into electricity, have been significantly explored as an ideal long-term power source for electrical devices. Despite recent advances, the development of advanced TENG devices with sufficient outputs to sustainably power electronic devices and rapid self-healability under mild conditions to improve their lifetime and function is highly demanded. Here, we report a robust self-healable and reprocessable TENG fabricated with a covalent adaptive network based on mechanically strong fluorinated poly(hindered urea) (F-PHU) integrated with ionic liquid as an efficient dielectric material to improve its triboelectric efficiency and self-healing capability simultaneously. The synthesis and integration of a well-defined reactive copolymer having both pendant fluorinated and t-butylamino bulky groups are the key to fabricate robust F-PHU networks containing fluorinated dangling chains that can interact with ionic liquids to induce ionic polarization, which raises the dielectric constant and thus increases triboelectric performance. They also are cross-linked with dynamic bulky urea linkages for rapid self-healability and high reprocessability through their reversible exchange reactions at moderate temperatures. The developed ionic F-PHU materials exhibit a high TENG output performance (power density of 173.0 mW/m(2)) as well as high TENG output recovery upon repairing their surface damages. This work demonstrates that such a synergistic design of triboelectric ionic F-PHU materials could have great potential for applications requiring high-performance and long-lasting energy harvesting.
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