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Anisotropic Li+ ion conductivity in a large single crystal of a Co(III) coordination complex

Authors
Kim, Saet ByeolKim, Jeung YoonJeong, Nak CheonOk, Kang Min
Issue Date
Jan-2017
Publisher
ROYAL SOC CHEMISTRY
Citation
INORGANIC CHEMISTRY FRONTIERS, v.4, no.1, pp 79 - 83
Pages
5
Journal Title
INORGANIC CHEMISTRY FRONTIERS
Volume
4
Number
1
Start Page
79
End Page
83
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/4923
DOI
10.1039/c6qi00314a
ISSN
2052-1553
2052-1553
Abstract
Large single crystals of a novel lithium cobalt coordination compound, LiCo(NC5H3(CO2)(2))(2)(H2O)(2.125) [LiCo(PDC)(2)] were grown via a hydrothermal reaction in high yield. The electrochemical impedance spectroscopy (EIS) data measured on a large single crystal of LiCo(PDC)(2) revealed very interesting anisotropic Li+ ion conductivity. The redox potential for Co3+/Co4+ observed at ca. 200 mV in the cyclic voltammogram was consistent with the electric potential where the ionic conductivity occurred. Detailed structural analysis on a series of stoichiometrically equivalent cobalt coordination compounds, ACo(PDC)(2) (A = Na+, K+, and H3O+), indicated that the presence of ion channels as well as a suitable cation size is critical for the anisotropic ionic conductivity.
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