Cited 1 time in
Natural Activation of CuO to CuCl2 as a Cathode Material for Dual-Ion Lithium Metal Batteries
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Li, Siying | - |
| dc.contributor.author | Lee, Jung-Hun | - |
| dc.contributor.author | Hwang, Soo Min | - |
| dc.contributor.author | Yoo, Ji-Beom | - |
| dc.contributor.author | Kim, Hansu | - |
| dc.contributor.author | Kim, Young-Jun | - |
| dc.date.accessioned | 2022-07-06T12:09:22Z | - |
| dc.date.available | 2022-07-06T12:09:22Z | - |
| dc.date.created | 2021-11-22 | - |
| dc.date.issued | 2021-10 | - |
| dc.identifier.issn | 2405-8297 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/140903 | - |
| dc.description.abstract | To meet the rising energy demand for rapidly advancing battery-driven devices, a novel Li/Cl dual-ion battery chemistry based on non-flammable SO2-in-salt electrolyte is receiving significant attention. Herein, we propose a natural-activable CuO hollow nanocube (HNC) cathode material for dual-ion Li metal batteries using SO2-in-salt electrolyte. Natural activation is achieved via spontaneous chlorination of CuO HNCs into an electrochemically active CuCl2 phase upon immersed in a SO2-in-salt electrolyte. The on-site conversion reactions are proposed with the support of thermodynamic calculations; the phase transformations of active materials are confirmed through X-ray diffraction, X-ray photoelectron spectroscopy, and field emission scanning electron microscopy. As a solution to alleviate the volume expansion after chlorination, the HNC structure of CuO allows the resulting CuCl2 cathode material to deliver a reversible capacity up to 262.2 mAh g(-1) (894.2 Wh kgCuO(-1)) with stable cycle performance over 150 cycles. The Li-CuO battery system presented here demonstrates the feasibility of non-flammable, high-energy density Li/Cl dual-ion Li metal batteries as a potential alternative to currently used lithium ion batteries. | - |
| dc.language | 영어 | - |
| dc.language.iso | en | - |
| dc.publisher | ELSEVIER | - |
| dc.title | Natural Activation of CuO to CuCl2 as a Cathode Material for Dual-Ion Lithium Metal Batteries | - |
| dc.type | Article | - |
| dc.contributor.affiliatedAuthor | Kim, Hansu | - |
| dc.identifier.doi | 10.1016/j.ensm.2021.06.022 | - |
| dc.identifier.scopusid | 2-s2.0-85108779981 | - |
| dc.identifier.wosid | 000684950400008 | - |
| dc.identifier.bibliographicCitation | ENERGY STORAGE MATERIALS, v.41, pp.466 - 474 | - |
| dc.relation.isPartOf | ENERGY STORAGE MATERIALS | - |
| dc.citation.title | ENERGY STORAGE MATERIALS | - |
| dc.citation.volume | 41 | - |
| dc.citation.startPage | 466 | - |
| dc.citation.endPage | 474 | - |
| dc.type.rims | ART | - |
| dc.type.docType | Article | - |
| dc.description.journalClass | 1 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | INORGANIC ELECTROLYTE | - |
| dc.subject.keywordPlus | LIALCL4-CENTER-DOT-3SO(2) | - |
| dc.subject.keywordPlus | COPPER | - |
| dc.subject.keywordPlus | CHLORINE | - |
| dc.subject.keywordPlus | CATALYST | - |
| dc.subject.keywordPlus | LIALCL4 | - |
| dc.subject.keywordPlus | ALKALI | - |
| dc.subject.keywordPlus | OXIDES | - |
| dc.subject.keywordPlus | ANODE | - |
| dc.subject.keywordPlus | WATER | - |
| dc.subject.keywordAuthor | non-flammable | - |
| dc.subject.keywordAuthor | dual-ion batteries | - |
| dc.subject.keywordAuthor | CuO | - |
| dc.subject.keywordAuthor | natural activation | - |
| dc.subject.keywordAuthor | Li metal batteries | - |
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