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Vol 61, No 6 (2025)

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Articles

Ions transport properties in polymer gel electrolytes with introduction of ionic liquid for lithium electrochemical systems

Slesarenko N.A., Chernyak A.V., Khatmullina K.G., Yudina A.V., Slesarenko A.A., Chernyaev D.A., Yarmolenko O.V.

Abstract

The study focused on the competitive ionic and molecular transport characteristics of four polymer gel electrolyte compositions synthesized through the radical polymerization of polyethylene glycol diacrylate, incorporating LiBF4 salt, 1-ethyl-3-methylimidazolium tetrafluoroborate, and various organic solvents: dioxolane (DOL), diglyme (G2), tetraglyme (G4), and ethylene carbonate (EC). The aim was to identify a composition with the highest mobility for the Li+ cation. Flexible films of the polymer gel electrolytes were analyzed using differential scanning calorimetry, thermogravimetric analysis, and Fourier transform infrared spectroscopy. The features of ionic and molecular transport were investigated using pulsed field gradient NMR in conjunction with electrochemical impedance spectroscopy. The total conductivity of these systems ranged from 1.8 to 4.1 mS cm–1 at room temperature. Although the composition with EC exhibited high ionic conductivity, the mobility of the Li+ cation at room temperature increased in the following order: Li+(EC)4 < Li+(DOL)4 < Li+(G4) < Li+(G2)2. Calculating the hydrodynamic radius of the lithium cation revealed that for Li+(EC)4 and Li+(DOL)4, the radius decreased with rising temperature; for Li+(G2)2, it remained nearly constant; while for Li+(G4), it exhibited an abnormal increase. This unusual behavior is likely due to the re-solvation of the lithium cation from the polymer matrix into tetraglyme. In assessing the compatibility of the polymer gel electrolytes with metallic lithium, it was found that electrolyte compositions containing tetraglyme, diglyme, and ethylene carbonate show promise for further research and potential application as electrolytes in lithium power sources.

Èlektrohimiâ. 2025;61(6):273-286
pages 273-286 views

Electrochemical behavior of complexes of cobalt and zinc methoxyphenoxyphthalocyanines

Rassolova A.E., Berezina N.M., Bazanov M.I., Maizlish V.E., Tesakova M.V., Parfenyuk V.I.

Abstract

The electrochemical behavior of a number of isomers of methoxyphenoxy derivatives of cobalt phthalocyanine {CoPc[4-(x-OСH3OPh)]4 and CoPc[3-(x-OСH3OPh)]4, where x = 4/, 3/, or 2/} in an aqueous alkaline solution and ZnPc[4-(x-OСH3OPh)]4, where x = 4/, 3/, or 2/ in a CH2Cl2 medium was studied for the first time using cyclic voltammetry. A comparative analysis of the electrochemical behavior and changes in the electrocatalytic activity of cobalt phthalocyanines in the reaction of molecular oxygen electroreduction depending on the functional substitution in the macrocycle molecule is given. It is shown that for the compounds {CoPc[4-(x-OСH3OPh)]4 and CoPc[3-(x-OСH3OPh)]4} the processes of oxidation (Co 2+ ↔ Co3+) and reduction of the central metal ion (Co2+ ↔ Co1+) are recorded, as well as two successive one-electron stages of electroreduction of the phthalocyanine ligand. It is established that the studied cobaltphthalocyanine derivatives are quite effective systems for the process of electroreduction of molecular oxygen. For ZnPc[4-(x-OСH3OPh)]4, where x = 4/, 3/or 2/, the formation of polyphthalocyanine films was detected in the process of electrooxidation of monomers in dichloromethane.
Èlektrohimiâ. 2025;61(6):287-298
pages 287-298 views

Electric Transport Properties of Solid Solution and Composite Samples in the Ba2In2O5–Ba2InNbO6 System with Responce Atmospheric Humidity

Matveev E. ., Kochetova N. ., Alyabisheva I. ., Animitsa I. .

Abstract

Thermal and electrical properties of solid solution and composite samples in the quasi-binary system Ba2In2O5–Ba2InNbO6 were investigated. It was proven that in a humid atmosphere at temperatures below 600°C the samples reversibly interact with water vapor to form proton defects. The hydration process is accompanied by a significant increase in the total electrical conductivity due to the appearance of a contribution from proton transfer. Below 500°C in humid air the samples are predominantly proton conductors. The composite effect of proton electrical conductivity was established.
Èlektrohimiâ. 2025;61(6):299-310
pages 299-310 views