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dc.contributor.author이윤정-
dc.date.accessioned2022-09-27T04:23:53Z-
dc.date.available2022-09-27T04:23:53Z-
dc.date.issued2020-12-
dc.identifier.citationACS APPLIED ENERGY MATERIALS, v. 3, NO 12, Page. 12575-12583en_US
dc.identifier.issn2574-0962en_US
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsaem.0c02495en_US
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/174110-
dc.description.abstractThe theoretical energy density of lithium-oxygen (Li-O-2) batteries is extremely high, although there are many challenges that must be overcome to achieve high energy density in a manufactured cell. For example, little is known about the properties of one of the key intermediates, lithium superoxide (LiO2), which until recently had not been stabilized in bulk form. In this work, lithium superoxide was deposited onto iridium-reduced graphene oxide (Ir-rGO) cathodes in a Li-O-2 system under a flow of O-2. Lithium peroxide (Li2O2) was subsequently produced on the cathode surface in an inert Ar atmosphere. Based on a detailed analysis of electrochemical impedance spectroscopy data, it was demonstrated experimentally for the first time that the charge transport resistance through LiO2 was much lower than for Li2O2 and correlated with lower LiO2 charge overpotentials. This result indicates that LiO2 has good electronic conductivity and confirms previous theoretical predictions that bulk LiO2 has better charge transport properties than Li2O2. In addition, impedance and other characterization of Li2O2 formation from LiO2 in an Ar atmosphere revealed that when surface-mediated Li2O2 formation occurs, it has a significantly lower discharge potential than when it forms through a solution-phase-mediated process. These significant findings will contribute to the development of Li-O-2 batteries through better understanding of LiO2 properties and formation mechanisms.en_US
dc.description.sponsorshipThis work was supported by the U.S. Department of Energy under Contract DE-AC02-06CH11357 from the Vehicle Technologies Office, Office of Energy Efficiency and Renewable Energy. This work made use of instruments in the Electron Microscopy Core of UIC's Research Resources Center.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectlithium−oxygen battery; lithium superoxide; electrochemical impedance spectroscopy; charge transport; charge overpotential; discharge mechanismen_US
dc.titleCharge Transport Properties of Lithium Superoxide in Li-O2 batteriesen_US
dc.typeArticleen_US
dc.relation.no12-
dc.relation.volume3-
dc.identifier.doi10.1021/acsaem.0c02495en_US
dc.relation.page12575-12583-
dc.relation.journalACS APPLIED ENERGY MATERIALS-
dc.contributor.googleauthorPlunkett, Samuel T.-
dc.contributor.googleauthorWang, Hsien-Hau-
dc.contributor.googleauthorPark, Se Hwan-
dc.contributor.googleauthorLee, Yun Jung-
dc.contributor.googleauthorCabana, Jordi-
dc.contributor.googleauthorAmine, Khalil-
dc.contributor.googleauthorAl-Hallaj, Said-
dc.contributor.googleauthorChaplin, Brian P.-
dc.contributor.googleauthorCurtiss, Larry A.-
dc.relation.code2020047810-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF ENERGY ENGINEERING-
dc.identifier.pidyjlee94-
dc.identifier.researcherIDM-1198-2017-
dc.identifier.orcidhttps://orcid.org/0000-0003-3091-1174-
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COLLEGE OF ENGINEERING[S](공과대학) > ENERGY ENGINEERING(에너지공학과) > Articles
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