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dc.contributor.author선양국-
dc.date.accessioned2019-11-20T11:47:44Z-
dc.date.available2019-11-20T11:47:44Z-
dc.date.issued2017-02-
dc.identifier.citationACS APPLIED MATERIALS & INTERFACES, v. 9, no. 5, page. 4352-4361en_US
dc.identifier.issn1944-8244-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsami.6b10974-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/112800-
dc.description.abstractAprotic Li-O-2 battery is an exciting concept. The enormous theoretical energy density and cell assembly simplicity make this technology very appealing. Nevertheless, the instability of the cell components, such as cathode, anode, and electrolyte solution during cycling, does not allow this technology to be fully commercialized. One of the intrinsic challenges facing researchers is the use of lithium metal as an anode in Li-O-2 cells. The high activity toward chemical moieties and lack of control of the dissolution/deposition processes of lithium metal makes this anode material unreliable. The safety issues accompanied by these processes intimidate battery manufacturers. The need for a reliable anode is crucial. In this work we have examined the replacement of metallic lithium anode in Li-O-2 cells with lithiated hard carbon (HC) electrodes. HC anodes have many benefits that are suitable for oxygen reduction in the presence of solvated lithium cations. In contrast to lithium metal, the insertion of lithium cations into the carbon host is much more systematic and safe. In addition, with HC anodes we can use aprotic solvents such as glymes that are suitable for oxygen reduction applications. By contrast, lithium cations fail to intercalate reversibly into ordered carbon such as graphite and soft carbons using ethereal electrolyte solutions, due to detrimental co-intercalation of solvent molecules with Li ions into ordered carbon structures. The hard carbon electrodes were prelithiated prior to being used as anodes in the Li-O-2 rechargeable battery systems. Full cells containing diglyme based solutions and a monolithic carbon cathode were measured by various electrochemical methods. To identify the products and surface films that were formed during cells operation, both the cathodes and anodes were examined ex situ by XRD, FTIR, and electron microscopy. The HC anodes were found to be a suitable material for (Li-ion) O-2 cell. Although there are still many challenges to tackle, this study offers a more practical direction for this promising battery technology and sets up a platform for further systematic optimization of its various components.en_US
dc.description.sponsorshipA.A.F. thanks the Israel Science Foundation (ISF; Grant No. 1469/13) as well as the Ethel and David Resnick Chair in Active Oxygen Chemistry for their kind and generous support. Partial support was obtained also from the ISF in the framework of the INREP project.en_US
dc.language.isoen_USen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectLi-O-2 batteriesen_US
dc.subjectlithium metalen_US
dc.subjecthard carbonen_US
dc.subjectXRDen_US
dc.subjectFTIRen_US
dc.subjectglyme solventsen_US
dc.titleFeasibility of Full (Li-Ion)-O-2 Cells Comprised of Hard Carbon Anodesen_US
dc.typeArticleen_US
dc.relation.no5-
dc.relation.volume9-
dc.identifier.doi10.1021/acsami.6b10974-
dc.relation.page4352-4361-
dc.relation.journalACS APPLIED MATERIALS & INTERFACES-
dc.contributor.googleauthorHirshberg, Daniel-
dc.contributor.googleauthorSharon, Daniel-
dc.contributor.googleauthorDe la Llave, Ezequiel-
dc.contributor.googleauthorAfri, Michal-
dc.contributor.googleauthorFrimer, Aryeh A.-
dc.contributor.googleauthorKwak, Won-Jin-
dc.contributor.googleauthorSun, Yang-Kook-
dc.contributor.googleauthorAurbach, Doron-
dc.relation.code2017001478-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF ENERGY ENGINEERING-
dc.identifier.pidyksun-
dc.identifier.researcherIDB-9157-2013-
dc.identifier.orcidhttp://orcid.org/0000-0002-0117-0170-
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > ENERGY ENGINEERING(에너지공학과) > Articles
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