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High-Voltage Symmetric Nonaqueous Redox Flow Battery Based on Modularly Tunable [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn) Cluster Compounds with Multielectron Storage Capability

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dc.contributor.authorChoi, Suhyuk-
dc.contributor.authorJeon, Hyeri-
dc.contributor.authorKim, Youngsam-
dc.contributor.authorKang, Philjae-
dc.contributor.authorSim, Eunji-
dc.contributor.authorHong, Seungwoo-
dc.contributor.authorAhn, Hyun S.-
dc.date.accessioned2023-11-08T07:50:21Z-
dc.date.available2023-11-08T07:50:21Z-
dc.date.issued2022-11-
dc.identifier.issn2639-4979-
dc.identifier.issn2639-4979-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/152340-
dc.description.abstractRedox flow batteries (RFBs) provide an attractive solution for large-scale energy buffering and storage. This report describes the development of nonaqueous RFBs based on trimetallic coordination cluster compounds: [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn). The all-ruthenium complex exhibited stable battery cycles in anolyte-catholyte symmetric operation, with rarely observed multielectron storage in a single molecule. Moreover, the complex holds modularly tunable synthetic handles for systematic improvements in solubility and redox potentials. An optimized battery stack containing [Ru3(μ3-O)(CH3CO2)6(py)3]+ anolyte and [Ru2Co(μ3-O)(CH3CO2)6(py)3] catholyte yielded stable cycles with a discharge voltage of 2.4 V, comparable to the state-of-the-art nonaqueous RFBs. Explanation for the exceptional stability of the charged states and prediction of systematic tunability of the redox potentials of the cluster compounds were assisted by DFT calculations. © 2022 American Chemical Society.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleHigh-Voltage Symmetric Nonaqueous Redox Flow Battery Based on Modularly Tunable [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn) Cluster Compounds with Multielectron Storage Capability-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsmaterialslett.2c00718-
dc.identifier.scopusid2-s2.0-85139411330-
dc.identifier.wosid000883619500001-
dc.identifier.bibliographicCitationACS Materials Letters, v.4, no.11, pp 2159 - 2165-
dc.citation.titleACS Materials Letters-
dc.citation.volume4-
dc.citation.number11-
dc.citation.startPage2159-
dc.citation.endPage2165-
dc.type.docTypeArticle in Press-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusELECTRICAL ENERGY-STORAGE-
dc.subject.keywordPlusRUTHENIUM COMPLEX-
dc.subject.keywordPlusACETATE CLUSTERS-
dc.subject.keywordPlusPOTENTIALS-
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