File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

조재필

Cho, Jaephil
Nano Energy Storage Material Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 262 -
dc.citation.startPage 255 -
dc.citation.title NANO ENERGY -
dc.citation.volume 32 -
dc.contributor.author Song. Woo-Jin -
dc.contributor.author Joo, Se Hun -
dc.contributor.author Kim, Do Hyeong -
dc.contributor.author Hwang, Chihyun -
dc.contributor.author Jung, Gwan Yeong -
dc.contributor.author Bae, Soohyeon -
dc.contributor.author Son, Yeonguk -
dc.contributor.author Cho, Jaephil -
dc.contributor.author Song, Hyun-Kon -
dc.contributor.author Kwak, Sang Kyu -
dc.contributor.author Park, Soojin -
dc.contributor.author Kang, Seok Ju -
dc.date.accessioned 2023-12-21T22:40:43Z -
dc.date.available 2023-12-21T22:40:43Z -
dc.date.created 2017-01-19 -
dc.date.issued 2017-02 -
dc.description.abstract An interesting and effective route for improving battery performance using ferroelectric poly(vinylidene difluoride) (PVDF) polymer as a binder material is demonstrated in this work. A ferroelectric PVDF phase developed under the appropriate thermal annealing process enables generation of suitable polarization on active materials during the discharge and charge process, giving rise to longer capacity with lower overpotential at a high current rate. Electrochemical analysis including in situ galvanostatic electrochemical impedance spectroscopy and a galvanostatic intermittent titration measurement revealed that the ferroelectric binder effectively reduced Li-ion diffusion resistance and supported fast migration in the vicinity of active electrodes. Computational results further support that the binding affinity of the ferroelectric PVDF surface is much higher than that of the paraelectric PVDF, confirmed by ideally formed ferroelectric and paraelectric PVDF conformations with Li-ions. Furthermore, we consistently achieved high Li-ion battery (LIB) performance in full cell architecture consisting of a LTO/separator/LFP with a ferroelectric PVDF binder in the anode and cathode materials, revealing that the polarization field is important for fabricating high-performance LIBs, potentially opening a new design concept for binder materials. -
dc.identifier.bibliographicCitation NANO ENERGY, v.32, pp.255 - 262 -
dc.identifier.doi 10.1016/j.nanoen.2016.12.037 -
dc.identifier.issn 2211-2855 -
dc.identifier.scopusid 2-s2.0-85007578681 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/21207 -
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S2211285516306000 -
dc.identifier.wosid 000397003700031 -
dc.language 영어 -
dc.publisher Elsevier BV -
dc.title Significance of ferroelectric polarization in poly (vinylidene difluoride) binder for high-rate Li-ion diffusion -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary; Physics, Applied -
dc.relation.journalResearchArea Chemistry; Science & Technology - Other Topics; Materials Science; Physics -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Li-ion battery -
dc.subject.keywordAuthor Polymeric binder -
dc.subject.keywordAuthor Ferroelectric -
dc.subject.keywordAuthor PVDF -
dc.subject.keywordAuthor High current rate -
dc.subject.keywordPlus ELECTRICAL ENERGY-STORAGE -
dc.subject.keywordPlus LONG CYCLE LIFE -
dc.subject.keywordPlus LITHIUM BATTERIES -
dc.subject.keywordPlus POLY(VINYLIDENE FLUORIDE) -
dc.subject.keywordPlus CATHODE MATERIALS -
dc.subject.keywordPlus SILICON -
dc.subject.keywordPlus ANODES -
dc.subject.keywordPlus CHALLENGES -
dc.subject.keywordPlus CAPACITY -
dc.subject.keywordPlus SURFACE -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.