Self-healable triboelectric nanogenerators based on ionic poly(hindered urea) network materials cross-linked with fluorinated block copolymers
- Authors
- Nellepalli, Pothanagandhi; Patel, Twinkal; Kim, Minsoo P.; Park, Junyoung; Ye, Zhibin; Jung, Hyun Wook; Ko, Hyunhyub; Oh, Jung Kwon
- Issue Date
- 26-7월-2022
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- POLYMER CHEMISTRY, v.13, no.29, pp.4343 - 4351
- Indexed
- SCIE
SCOPUS
- Journal Title
- POLYMER CHEMISTRY
- Volume
- 13
- Number
- 29
- Start Page
- 4343
- End Page
- 4351
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/142893
- DOI
- 10.1039/d2py00252c
- ISSN
- 1759-9954
- Abstract
- The triboelectric nanogenerator (TENG) has been anticipated as a cost-effective energy harvesting device that can convert mechanical energies to electricity. Further to the modification of structural and functional properties of triboelectric materials, an integration of self-healability has been explored as an advanced platform for the development of multifunctional TENGs due to their improved lifetime and function. In this study, we demonstrate the versatility of a reactive block copolymer approach that allows for the fabrication of ionic poly(hindered urea)-based covalent adaptive networks having pendant fluorinated species formulated with ionic liquid as effective self-healable triboelectric materials. The reactive block copolymer is well-defined, designed with a dynamic t-butylamino block for self-healability and a dielectric fluorinated block for improved triboelectric output, and used as a multifunctional crosslinker. Fabricated by two-step polyaddition in combination with physical blending with ionic liquid, the formed ionic fluorinated poly(hindered urea) networks crosslinked with reactive block copolymer have enhanced TENG outputs while retaining good self-healing and mechanical strength. Promisingly, their recovery of triboelectric performance is greater than 90% upon the repair of damaged surfaces. This work demonstrates the versatility of the new reactive block copolymer approach to fabricate dynamic PHU networks exhibiting desired properties useful for advanced self-healable-TENG-based energy harvesting devices and electronics.
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