Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/20605
Title: Дифузія іонів літію в пористі вуглецеві електродні матеріали згідно методу гальваностатичного переривчастого титрування
Other Titles: Li-ion Diffusion in Porous Carbon Electrode Materials by GITT Method
Authors: Мандзюк, Володимир Ігорович
Mandzyuk, Volodymyr
Іванічок, Наталія Ярославівна
Ivanichok, Natalia
Соломовський, Роман Володимирович
Solomoskyi, Roman
Keywords: Porous carbon material
Lithium ion
Intercalation degree
Diffusion coefficient
Galvanostatic intermittent titration technique
Issue Date: 2024
Publisher: Сумський державний університет
Citation: V.I. Mandzyuk, N.Ya. Ivanichok, R.V. Solomoskyi. Li-ion diffusion in porous carbon electrode materials by GITT method //
Series/Report no.: 16(2);02024
Abstract: The process of diffusion of lithium ions into porous carbon electrode materials obtained by hydrothermal carbonization of plant raw materials at different temperatures was the galvanostatic intermittent titration technique. The diffusion coefficient of lithium ions in the electrode material was calculated and its dependence on the intercalation degree x was analyzed. It was found that with the increase in the carbonation temperature of the raw material, which results in the removal of gaseous aliphatic and then aromatic molecules with low molecular weight, processes of cyclization and aromatization of molecules, as well as intensive carbonization of the raw material, the formation of carbon layers and primary graphite nuclei, the coefficient diffusion increases due to ordering the structure of the porous carbon material and reducing its specific surface area and total pore volume. When the maximum value of the intercalation degree is reached, the diffusion coefficient of lithium ions is 3.6·10 – 12 сm2/s (х = 0.28), 7.9·10 – 12 сm2/s (х = 0.44), and 1.9·10 – 10 сm2/s (х = 0.19) for samples obtained at carbonization temperatures of 600, 750, and 1000 °C, respectively. A comparative analysis of the values of the diffusion coefficient, calculated on the basis of the data of galvanostatic intermittent titration technique and electrochemical impedance spectroscopy, was carried out.
URI: http://hdl.handle.net/123456789/20605
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