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Designing Redox-Stable Cobalt–Polypyridyl Complexes for Redox Flow Batteries: Spin-Crossover Delocalizes Excess Charge

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dc.contributor.authorChunzhen Yang-
dc.contributor.authorGeorgios Nikiforidis-
dc.contributor.authorJi Young Park-
dc.contributor.authorJonghoon Choi-
dc.contributor.authorYong Luo-
dc.contributor.authorLiang Zhang-
dc.contributor.authorShi-Cheng Wang-
dc.contributor.authorYi-Tsu Chan,-
dc.contributor.authorJihun Lim-
dc.contributor.authorZhaomin Hou-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorYunho Lee-
dc.contributor.authorHye Ryung Byon-
dc.date.available2018-07-18T02:07:09Z-
dc.date.created2018-06-26-
dc.date.issued2018-05-
dc.identifier.issn1614-6832-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4712-
dc.description.abstractRedox-active organometallic molecules offer a promising avenue for increasing the energy density and cycling stability of redox flow batteries. The molecular properties change dramatically as the ligands are functionalized and these variations allow for improving the solubility and controlling the redox potentials to optimize their performance when used as electrolytes. Unfortunately, it has been difficult to predict and design the stability of redox-active molecules to enhance cyclability in a rational manner, in part because the relationship between electronic structure and redox behavior has been neither fully understood nor systematically explored. In this work, rational strategies for exploiting two common principles in organometallic chemistry for enhancing the robustness of pseudo-octahedral cobalt–polypyridyl complexes are developed. Namely, the spin-crossover between low and high-spin states and the chelation effect emerging from replacing three bidentate ligands with two tridentate analogues. Quantum chemical models are used to conceptualize the approach and make predictions that are tested against experiments by preparing prototype Co-complexes and profiling them as catholytes and anolytes. In good agreement with the conceptual predictions, very stable cycling performance over 600 cycles is found. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectcatholytes-
dc.subjectchelation effects-
dc.subjectredox flow batteries-
dc.subjectredox organic molecules-
dc.subjectspin-crossover-
dc.titleDesigning Redox-Stable Cobalt–Polypyridyl Complexes for Redox Flow Batteries: Spin-Crossover Delocalizes Excess Charge-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000435713600018-
dc.identifier.scopusid2-s2.0-85047821848-
dc.identifier.rimsid63884ko
dc.contributor.affiliatedAuthorJi Young Park-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.identifier.doi10.1002/aenm.201702897-
dc.identifier.bibliographicCitationADVANCED ENERGY MATERIALS, v.8, no.14, pp.1702897-
dc.citation.titleADVANCED ENERGY MATERIALS-
dc.citation.volume8-
dc.citation.number14-
dc.citation.startPage1702897-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthorcatholytes-
dc.subject.keywordAuthorchelation effects-
dc.subject.keywordAuthorredox flow batteries-
dc.subject.keywordAuthorredox organic molecules-
dc.subject.keywordAuthorspin-crossover-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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