Cited 3 time in
Dielectric Polarization of a High-Energy Density Graphite Anode and Its Physicochemical Effect on Li-Ion Batteries
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Park, Hyunjung | - |
| dc.contributor.author | Shin, Donghyeok | - |
| dc.contributor.author | Paik, Ungyu | - |
| dc.contributor.author | Song, Taeseup | - |
| dc.date.accessioned | 2021-07-30T05:31:54Z | - |
| dc.date.available | 2021-07-30T05:31:54Z | - |
| dc.date.issued | 2017-11 | - |
| dc.identifier.issn | 0888-5885 | - |
| dc.identifier.issn | 1520-5045 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/5362 | - |
| dc.description.abstract | The high energy density graphite anode for the commercial LIBs has critical problems on Li+-ion kinetics due to decreases both in electrode porosity and electrolyte permeability. To overcome issues, interfaces of graphite particles in the anode are polarized using poly(vinylidene fluoride)-hexafluoropropylene (PVDF-HFP) with the high dielectric constant (ε = 8.4), high solubility with lithium salt, and ability to trap a large amount of liquid electrolyte. The PVDF-HFP treatment promoted electrolyte permeability into the graphite electrode with a high mass loading of 13.8 mg cm–2 and a density of 1.7 g cc–1 (a current density over 5 mA cm–2) which particularly leads to an improvement of capacity retention from 77% of a bare electrode to 95% over 40 cycles. These achievements were attributed not only to the enhancement of the lithium-ion kinetics but also to the stable formation of a solid electrolyte interface (SEI) layer on the graphite surface. | - |
| dc.format.extent | 7 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | Dielectric Polarization of a High-Energy Density Graphite Anode and Its Physicochemical Effect on Li-Ion Batteries | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acs.iecr.7b03797 | - |
| dc.identifier.scopusid | 2-s2.0-85035313996 | - |
| dc.identifier.wosid | 000416499900027 | - |
| dc.identifier.bibliographicCitation | Industrial & Engineering Chemistry Research, v.56, no.46, pp 13776 - 13782 | - |
| dc.citation.title | Industrial & Engineering Chemistry Research | - |
| dc.citation.volume | 56 | - |
| dc.citation.number | 46 | - |
| dc.citation.startPage | 13776 | - |
| dc.citation.endPage | 13782 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Engineering | - |
| dc.relation.journalWebOfScienceCategory | Engineering, Chemical | - |
| dc.subject.keywordPlus | LAYERED OXIDE CATHODES | - |
| dc.subject.keywordPlus | POLYMER ELECTROLYTES | - |
| dc.subject.keywordPlus | HIGH-CAPACITY | - |
| dc.subject.keywordPlus | LITHIUM | - |
| dc.subject.keywordPlus | PERFORMANCE | - |
| dc.subject.keywordPlus | SURFACE | - |
| dc.subject.keywordPlus | ELECTRODES | - |
| dc.subject.keywordPlus | POWER | - |
| dc.subject.keywordAuthor | Anodes | - |
| dc.subject.keywordAuthor | Electric batteries | - |
| dc.subject.keywordAuthor | Electrodes | - |
| dc.subject.keywordAuthor | Electrolytes | - |
| dc.subject.keywordAuthor | Fluorine compounds | - |
| dc.subject.keywordAuthor | Graphite | - |
| dc.subject.keywordAuthor | Graphite electrodes | - |
| dc.subject.keywordAuthor | Ions | - |
| dc.subject.keywordAuthor | Lithium | - |
| dc.subject.keywordAuthor | Solid electrolytes | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/acs.iecr.7b03797 | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1366
COPYRIGHT © 2024 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.
