4.2 Article

Electrochemical Rubidium Storage Behavior of Graphite in Ionic Liquid Electrolyte

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ELECTROCHEMISTRY
卷 91, 期 1, 页码 -

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ELECTROCHEMICAL SOC JAPAN
DOI: 10.5796/electrochemistry.22-00122

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Rubidium-ion Battery; Ionic Liquid; Negative Electrode; Graphite

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In this study, a novel rubidium-ion battery was developed using an ionic liquid electrolyte and natural graphite as the negative electrode material at room temperature. The X-ray diffraction technique was employed to investigate the electrochemical phase evolution behavior of rubidium-graphite intercalation compounds. The graphite negative electrode exhibited an initial discharge capacity of 216 mAh g-1 at 0.05 C rate and retained capacities of around 180 mAh g-1 even after 50 cycles at 0.5 C rate.
Electrochemical intercalation behaviors of alkali metals into graphite have been vigorously studied in academic and industrial fields, whereas their mechanisms are still unclarified. In this study, we report a novel rubidium-ion battery utilizing an ionic liquid electrolyte and natural graphite as the negative electrode material operating at room temperature. The electrochemical phase evolution behavior of rubidium-graphite intercalation compounds was elucidated using X-ray diffraction. The graphite negative electrode exhibited an initial discharge capacity of 216 mAh g-1 at 0.05 C rate, and retained its capacities of around 180 mAh g-1 even at 0.5 C rate for 50 cycles. Electrochemical Rb-GIC formation Rb+ Graphite electrode Intercalation Deintercalation Rb[FTA]-[C4C1pyrr][FTA] ionic liquid Graphite RbC8 Intensity RbC8 RbC24 Gr RbC24 RbC8 10 20 30 40 2 theta / deg. (Cu-K alpha) Pristine (Graphite) Charging Full-charged (RbC8) Discharging (c) The Author(s) 2022. Published by ECSJ. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (CC BY-NC-SA, http://creativecommons.org/licenses/by-nc-sa/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium by share-alike, provided the original work is properly cited. For permission for commercial reuse, please email to the corresponding author. [DOI: 10.5796/electrochemistry.22-00122].

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