Disclosed herein are a secondary battery configured to be prevented from catching fire or exploding in a critical situation such as overcharging and a method of preventing the secondary battery from catching fire or exploding. Since a separator including a low melting point material is used, a short circuit in the battery occurs when the battery is abnormally heated, and the resistance of an electrode is increased when the temperature of the battery increases to a predetermined temperature or higher. As a result, a positive temperature coefficient (PTC) material is operated at a stable State of Charge (SoC). Consequently, it is possible to prevent the occurrence of a thermal runaway phenomenon of the battery.

A method for producing an electrode for a storage device for storing electrical energy is provided. A main body of the electrode is coated with at least one active material for storing electrical energy. A mixture, which includes the active material and fibers, is provided. The main body is coated with the mixture, which is free of a solvent that receives the fibers and escapes at least predominantly from the mixture after coating of the main body. By coating the main body with the mixture, a coating which includes the active material and the fibers is formed on the main body from the mixture.

An electropositive metal electrode coated by an ion-selective conformable polymer provides the negative electrode and the solid-state electrolyte for a rechargeable bi-electrolyte displacement battery that further includes a molten salt electrolyte having a melting temperature below 140° C. interposed between the conformable polymer coating and a positive electrode. Suitable electropositive metals include lithium, sodium, magnesium, and aluminum and the molten salt incorporates a soluble salt of the metal of the negative electrode. Positive electrodes may incorporate metals including Fe, Ni, Bi, Pb, Zn, Sn, and Cu, and thanks to the ion-selective conformable solid-state electrolyte the molten salt is able to incorporate a soluble salt of the metal of the positive electrode. The conformable polymer-coated electropositive metal electrode may be manufactured by a process involving electroplating electropositive metal through a conformable polymer-coated conductive substrate. The conformable polymer-coated conductive substrate may be prepared by coating the conductive substrate in a conformable polymer solution followed by evaporating the solvent. Alternatively, an electropositive metal electrode may be coated directly with the conformable polymer.

A method of manufacturing an all-solid-state battery electrode, an all-solid-state battery electrode manufactured by the method, and an all-solid-state battery including the electrode are disclosed. In the method, a specific type of binder included in the electrode is prepared in a fiber form by applying pressure to the binder under specific conditions, so that the fiber-form binder thus prepared has an average fineness that satisfies a specific range. Therefore, the all-solid-state battery including the electrode has an advantage of having high capacity even in the case of electrode thickening for high loading.

In conventional arts, it is impossible to form a good solid-solid interface in cathode mixture layers of all-solid-state batteries, which significantly deteriorates resistance of the all-solid-state battery after the charge/discharge cycle, which is problematic. A cathode slurry is produced by a method including: a first step of dispersing a conductive additive constituted of carbon in a solvent to obtain a first slurry; a second step of dispersing a sulfide solid electrolyte in the first slurry to obtain a second slurry; and a third step of dispersing a cathode active material in the second slurry to obtain a third slurry, to be used to form a cathode mixture layer. This may suppress agglomeration of the cathode active material as using the conductive additive as a core, and may lower the proportion of agglomerate present in the cathode mixture layer. As a result, a good solid-solid interface may be formed in the cathode mixture layer of the all-solid-state battery, and the resistance increase of the all-solid-state battery after the charge/discharge cycle may be suppressed.

Systems and methods utilizing water soluble (aqueous) PAA-based polymer binders for silicon-dominant anodes may include an electrode coating layer on a current collector, where the electrode coating layer is formed from silicon and a pyrolyzed water soluble PAA-based polymer blend, wherein the water soluble PAA-based polymer blend comprises PAA and one or more additional water-soluble polymer components. The electrode coating layer may include more than 70% silicon and the anode may be in a lithium ion battery.

A lithium-ion battery and an apparatus containing the same are provided. In some embodiments, the lithium-ion battery includes: a positive electrode plate including a positive electrode current collector and a positive electrode active substance layer; and an electrolyte including a non-aqueous organic solvent. A low-swelling adhesive layer and an oily adhesive layer are sequentially arranged between the positive electrode current collector and the positive electrode active substance layer; the low-swelling adhesive layer includes a low-swelling binder, and the oily adhesive layer includes a first binder, where a solubility parameter SP.sub.1 of the low-swelling binder is less than a solubility parameter SP.sub.2 of the first binder.

The present invention relates to a negative electrode which includes a negative electrode current collector, and a negative electrode active material layer formed on the negative electrode current collector, wherein the negative electrode active material layer includes a silicon-based active material and a carbon-based active material, wherein a ratio of an average particle diameter (D.sub.50) of the carbon-based active material to an average particle diameter (D.sub.50) of the silicon-based active material is in a range of 2 to 8, and a porosity of the negative electrode is in a range of 48% to 62%.

A preparation method of a cathode slurry and a battery are provided. The preparation method includes: S1, mixing materials containing a plasticizer and an additive to form a premixed slurry A; and S2, mixing a styrene-butadiene rubber emulsion with the premixed slurry A. The plasticizer includes a first functional group including at least one of a hydroxyl group, a carbonate group, and a ketone group. The additive includes a second functional group including at least one of a carboxyl group, a nitrile group, and an amide group.

A preparation method of fluorocarbon-coated VSe.sub.2 composite (VSe.sub.2@CF) anode electrode material, including: weighting and dissolving an acetylacetone oxovanadium (VO(acac).sub.2) and a selenium dioxide in a solvent to prepare a first solution with a concentration of 0.5-2 mol/L, and stirring the first solution for 0.5 h to obtain a dark green solution; adding the dark green solution with an organic acid to obtain a second solution; transferring the second solution to a polytetrafluoroethylene-lined high-pressure hydrothermal reactor, and holding at a heat insulation temperature for 15-30 h to obtain a third solution; after the third solution is cooled, suction filtering the cooled third solution, and washing the filtered third solution repeatedly to obtain a precipitate; drying the precipitate to obtain a black powder; co-mixing a citric acid solution with the black powder, stirring, ball milling, and drying; and heating up, holding, and finally cooling naturally to room temperature under inert atmosphere.