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Elucidating metal and ligand redox activities of a copper-benzoquinoid coordination polymer as the cathode for lithium-ion batteries

Journal Article · · Journal of Materials Chemistry. A
DOI:https://doi.org/10.1039/c9ta05244e· OSTI ID:1777812
A novel redox-active quinone-based organic building block 1,4-dicyano-2,3,5,6-tetrahydroxybenzene (LH4) has been synthesized and used as a bridging ligand to form a new 1D copper-benzoquinoid coordination polymer [CuL(DMF)2]n. The compound is able to deliver an initial capacity as high as 268 mA h g-1 at 30 mA g-1 (~C/2.5) when used as the cathode in Li batteries. Ex situ XPS and FT-IR reveal the involvement of both Cu and organic moieties in the multi-electron redox reaction. Cu K-edge XANES and EXAFS measurements confirm the change in the oxidation state and coordination environment of Cu during the discharge–charge process. In situ generated metallic nanoparticles have been observed by TEM. The obtained mechanistic understanding of the metal–organic electrode materials for Li-based batteries may pave the way for the design of next-generation energy-storage systems.
Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE; USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1777812
Alternate ID(s):
OSTI ID: 1557902
Journal Information:
Journal of Materials Chemistry. A, Journal Name: Journal of Materials Chemistry. A Journal Issue: 41 Vol. 7; ISSN 2050-7488
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English

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2D-metal–organic coordination polymers of lanthanides (La( iii ), Pr( iii ) and Nd( iii )) with redox-active dioxolene bridging ligands journal January 2020


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