In Situ AFM Imaging of Li-O-2 Electrochemical Reaction on Highly Oriented Pyrolytic Graphite with Ether-Based Electrolyte

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dc.contributor.authorWen, Ruiko
dc.contributor.authorHong, Mi Sunko
dc.contributor.authorByon, Hye Ryungko
dc.date.accessioned2016-05-12T03:04:26Z-
dc.date.available2016-05-12T03:04:26Z-
dc.date.created2016-02-17-
dc.date.created2016-02-17-
dc.date.created2016-02-17-
dc.date.issued2013-07-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.135, no.29, pp.10870 - 10876-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/207225-
dc.description.abstractUnderstanding the lithium oxygen (Li-O-2) electrochemical reaction is of importance to improve reaction kinetics, efficiency, and mitigate parasitic reactions, which links to the strategy of enhanced Li-O-2 battery performance. Many in situ and ex situ analyses have been reported to address chemical species of reduction intermediate and products, whereas details of the dynamic Li-O-2 reaction have not as yet been fully unraveled. For this purpose, visual imaging can provide straightforward evidence, formation and decomposition of products, during the Li-O-2 electrochemical reaction. Here, we present real-time and in situ views of the Li-O-2 reaction using electrochemical atomic force microscopy (EC-AFM). Details of the reaction process can be observed at nano-/micrometer scale on a highly oriented pyrolytic graphite (HOPG) electrode with lithium ion-containing tetraglyme, representative of the carbon cathode and ether-based electrolyte extensively employed in the Li-O-2 battery. Upon oxygen reduction reaction (ORR), rapid growth of nanoplates, having axial diameter of hundreds of nanometers, length of micrometers, and similar to 5 nm thickness, at a step edge of HOPG can be observed, which eventually forms a lithium peroxide (Li2O2) film. This Li2O2 film is decomposed during the oxygen evolution reaction (OER), for which the decomposition potential is related to a thickness. There is no evidence of byproduct analyzed by X-ray photoelectron spectroscopy (XPS) after first reduction and oxidation reaction. However, further cycles provide unintended products such as lithium carbonate (Li2CO2), lithium acetate, and fluorine-related species with irregular morphology due to the degradation of HOPG electrode, tetraglyme, and lithium salt. These observations provide the first visualization of Li-O-2 reaction process and morphological information of Li2O2, which can allow one to build strategies to prepare the optimum conditions for the Li-O-2 battery.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectLI-AIR BATTERIES-
dc.subjectLITHIUM-OXYGEN BATTERY-
dc.subjectKINETIC OVERPOTENTIALS-
dc.subjectSPECTROSCOPY-
dc.subjectPERFORMANCE-
dc.subjectCHALLENGES-
dc.subjectSTABILITY-
dc.subjectCATALYSTS-
dc.subjectPRODUCTS-
dc.subjectSOLVENTS-
dc.titleIn Situ AFM Imaging of Li-O-2 Electrochemical Reaction on Highly Oriented Pyrolytic Graphite with Ether-Based Electrolyte-
dc.typeArticle-
dc.identifier.wosid000322432400041-
dc.identifier.scopusid2-s2.0-84880781320-
dc.type.rimsART-
dc.citation.volume135-
dc.citation.issue29-
dc.citation.beginningpage10870-
dc.citation.endingpage10876-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/ja405188g-
dc.contributor.localauthorByon, Hye Ryung-
dc.contributor.nonIdAuthorWen, Rui-
dc.contributor.nonIdAuthorHong, Mi Sun-
dc.type.journalArticleArticle-
dc.subject.keywordPlusLI-AIR BATTERIES-
dc.subject.keywordPlusLITHIUM-OXYGEN BATTERY-
dc.subject.keywordPlusKINETIC OVERPOTENTIALS-
dc.subject.keywordPlusSPECTROSCOPY-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusCHALLENGES-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusPRODUCTS-
dc.subject.keywordPlusSOLVENTS-
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