Cd|KOH|NiOOH

Zn|NH4CI|MnO2

Li|LiClO4|MnO2

Pb|H2SO4|PbO2

H2|KOH|O2

Lithium electrochemical systems

Properties of LiFePO4-based cathode material with additions of conducting polymer for Li–ion batteries

In this study, the electrochemical behavior and properties of the novel LiFePO4-based composite cathode material with a water-soluble binder LA-133 and a conductive polymer PEDOT:PSS (poly-3,4-ethylenedioxythiophene: polystyrenesulfonate) as an aqueous dispersion were studied. Using the conductive polymer in combination with a water-soluble binder LA-133 allows to reduce the proportion of electrochemically inactive components (up to 10\%) and thus to increase its specific capacity for a given weight of the active material.

Study of influence of structural parameters of cathode materials of \alpha -NaFeO2 type on electrochemical characteristics of positive electrode of lithium-ion battery

The relationship between the structural parameters of layered materials such as \alpha -NaFeO2 used as positive electrode materials of lithium-ion battery, and electrochemical characteristics were investigated. The dependence of charge transfer resistance on the ratio of cobalt to lithium mole fractions in layered oxides was studied.

Influence of additives of EMIBF4 and BMIBF4 ionic liquids on the properties of network polymer electrolytes for lithium power sources

The effect of 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF4) and 1-butyl-3-methylimidazolium tetrafluoroborate (BMIBF4) ionic liquids on the properties of the polymer electrolyte based on polyethylene glycol diacrylate (PEG-DA) and LiBF4 salt was studied. Research was carried out by spray-mass spectroscopy, differential scanning calorimetry, and electrochemical impedance spectroscopy technique in the temperature range from -40 to 120 °C.

On the use of ferrous oxalate FeC2O4-2H2O for the synthesis of electrode material LiFePO4

The review summarizes literature data on the thermal decomposition of ferrous oxalate with the formation of Fe, FeO, Fe2O3, Fe3O4, Fe3C, and other products. Historical evolution of views on the ways and mechanisms of oxalate thermolysis is traced. The current state of the art is analyzed from the perspective of FeC2O4·2Н2O0 compound for the synthesis of lithium iron phosphate LiFePO4, which is a promising cathode material for lithium-ion batteries.

On determination of the mechanism of the processes proceeding at syntesis of electrode material LiFePO4

The methods for the synthesis of lithium iron phosphate LiFePO4 with olivine structure have been developed. New materials based on lithium iron phosphate, including doped with metals, the «LiFePO4 + carbon» composites obtained by pyrolysis of organic compounds have been synthesized. Crystallographic characterization of the synthesized materials was carried out; their electrochemical characteristics of the extraction and intercalation of lithium have been identified. A correlation between the crystallographic and electrochemical characteristics of the materials was found. It was confirmed that an effective way to improve the electrical conductivity of LiFePO4 is to create a carbon shell of the products of pyrolysis of organic compounds on the material's particles surface. A correlation of electrical conductivity and temperature of synthesis of the material was determined. The sequence of chemical interaction between precursors for the synthesis of LiFePO4 is defined; the mechanism of solid-phase interaction is described.

Negative electrodes based on regular structured porous silicon for lithium-ion batteries

Silicon electrodes with regular porous structure were prepared by the photoelectrochemical etching of single-crystal n-type silicon wafers, followed by the removal of the substrate. Electrodes with pores having circular and square section were studied. The porosity was increased via additional oxidation with the subsequent etching of oxide. The electrochemical characteristics of anodes were found to depend on porosity, electrodes with porosity 60-70% possessing maximal capacity for lithium reversible insertion. Electrodes thus prepared feature much higher capacity per area unit (up to 25 mA·h/cm2) than usual thin-film electrodes (about 1 mA·h/cm2).

Corrosion and Еlectrochemical Behaviour of Magnesium and Magnesium-Lithium Alloys in Phosphoric Acid Media

The corrosion and electrochemical behavior of magnesium and the MA 21 magnesium-lithium alloys in solutions of moderately acidic phosphates with various additives was studied. The inhibiting effect of nitrate and fluoride ions on the anode dissolution of these objects was revealed. Features of the electrochemical dissolution of magnesium and the magnesium-lithium alloys in nitrate phosphate solutions with fluoride ions caused by their activation-passivation competition have been noted. Distinctive features of the electrochemical behavior of the magnesium-lithium alloys in comparison with pure magnesium in nitrate phosphate fluoride solutions due to their structural and phase specifics have been established.

Searching for Optimal Electrolyte Compo-sitions for Chemical Sources of the Current and Heat- Accumulating Materials on the Ba-sis of Li,K||F,Cl,VO3,MoO4 Five-component Resiprocal System

In modem technological processes increase used molten multicomponent solt mixtures. Determination of the composition and melting temperature are important in application of the compositions, identification of patterns processes occurring during melting and solidification of alloys, as well as the phases in equilibrium at a given thermodynamic conditions, possibly in the study of phase diagrams. In this paper we propose a graphical method of calculation and choice of salt composition on the basis of the study five-component reciprocal system Li,K||F,Cl,VO3,MoO4 for use as electrolytes and heat storage materials.

Spectral Analysis of Nonharmonic and Polyharmonic Responses of an Electrochemical Object at Impedance Measurements

Possibilities for increasing efficiency of impedance spectral measurements are investigated. It is shown that for determination of linear electrochemical impedance a linearly changing input signal is preferable, and for the quantitative estimation of non-linearity of electrochemical impedance as an input signal it is expedient to use the cosine electric beats. The constructive diagrams of generators of such signals are offered.

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