A decomposition reaction of an electrolyte solution and the like caused as a side reaction of charge and discharge is minimized in repeated charge and discharge of a lithium ion battery or a lithium ion capacitor, and thus the lithium ion battery or the lithium ion capacitor can have long-term cycle performance. A negative electrode for a power storage device includes a negative electrode current collector and a negative electrode active material layer which includes a plurality of particles of a negative electrode active material. Each of the particles of the negative electrode active material has an inorganic compound film containing a first inorganic compound on part of its surface. The negative electrode active material layer has a film in contact with an exposed part of the negative electrode active material and part of the inorganic compound film. The film contains an organic compound and a second inorganic compound.

Negative electrode for power storage device and power storage device

The invention relates to a preparation method of a silicon/graphene nanocomposite material for a cathode of a lithium ion battery, which comprises the steps of: preparing oxidized graphite; preparing a silica/ graphene nanocomposite material under the existence of a surfactant; then preparing the silicon/graphene nanocomposite material for the cathode of the lithium ion battery through the magnesiothermic reduction reaction. Compared with the prior art, the graphene in the composite material, prepared by the invention, can better inhibit volumetric expansion of silicon material in the insertion and separation process of lithium ions so as to improve the circulating performance of the composite material greatly, so that the volume of the material after 30 circulations under the current of 200mA/g is still maintained to be above 1100mAh/g.

Preparation method of silicon/graphene nanocomposite material for cathode of lithium ion battery

Electrode composite material of lithium secondary battery and preparation method thereof

The invention relates to a lithium iron phosphate intercalated composite material, a preparation method thereof and a lithium ion battery adopting the multi-layer graphene/lithium iron phosphate intercalated composite material as an anode material. In the prior art, the electronic conductivity of the lithium iron phosphate material is poor, high-rate charging/discharging capacity of the lithium ion battery adopting the lithium iron phosphate material as the anode material is poor. The purpose of the present invention is to solve the problems in the prior art, and improve the rapid charging capacity of the power lithium ion battery so as to meet the requirements of the pure electrocar. The composite material is prepared through the following steps that: a rheological phase reaction method is adopted for multi-layer graphene, a trivalent iron salt, a phosphorus compound, a lithium compound and carbon source of small organic molecule to obtain a composite precursor, then the precursor is sintered to obtain the multi-layer graphene/lithium iron phosphate intercalated composite material. The anode slurry of the lithium ion battery anode plate comprises the composite material, a conductive agent and polyvinylidene difluoride. The composite material is an intercalated structure, wherein the lithium iron phosphate particles are intercalated between the multi-layer graphene to form the intercalated structure. The trivalent iron salt is adopted as the raw material, such that the cost is reduced. The lithium ion battery has good charging/discharging cycle performance, wherein the specific capacity is more than 60 mA.h.g at the rate of 20C.

Multi-layer graphene/lithium iron phosphate intercalated composite material, preparation method thereof, and lithium ion battery adopting multi-layer grapheme/lithium iron phosphate intercalated composite material as anode material

The invention aims at providing a preparation method for rapidly obtaining graphene in large quantities On the basis of obtaining graphite oxides, the molecular thermodynamic movement of groups such as hydroxyl groups (-OH), carboxylic groups (-COOH) and the like which are generated on the surfaces of graphite oxide layers through oxidization can be induced and stimulated through microwave treatment so as to produce a momentary unsteady state, so that Van der Waals binding force between graphite layers is damaged, and graphene can be rapidly obtained in large quantities The graphite oxides are obtained through the oxidization of metal salt such as potassium permanganate, potassium dichromate and the like as well as strong protonic acid such as concentrated sulphuric acid, concentrated nitric acid and the like, and then microwave irradiation is carried out under the conditions that the power ranges from 2 to 10 kW, the vacuum pressure ranges from 001 to 006 MPa and so on, so that microwave cleavage of the graphite oxides can be accomplished within 2 to 10 seconds, and graphene with less than ten layers can be obtained rapidly in large quantities The preparation method can also control the layer number or the thickness of graphene products by controlling the concentration and the oxidation time of oxidizing mediums as well as the power, the degree of vacuum and the like of the microwave irradiation

Method for rapidly preparing graphene in large quantities by utilizing graphite oxides

The invention discloses a method for preparing and purifying graphene by microwave radiation under vacuum. The method for preparing graphene is as follows: placing graphite oxide in a reactor, radiating the graphite oxide by microwaves under vacuum, and obtaining the graphene by heating and cleavage of the graphite oxide. The method for purifying graphene is as follows: placing graphene with low purity in a reactor, irradiating the graphite oxide by microwaves under vacuum, and obtaining the graphene with higher purity after impure graphene is subjected to heating and cleavage. The method is implemented under the vacuum condition, thus being favor to preventing the generated graphene from being oxidized by oxygen in the reactor, reducing the cleavage resistance of the graphite oxide, and ensuring the safety in the operation process, and the method also has the advantages of high production efficiency, low production cost, safe operation process, high product purity and the like, and can be used as one of the methods for preparing and purifying graphene massively.

Method for preparing and purifying graphene by microwave radiation under vacuum

The invention relates to a preparation method of a silicon/graphene laminar composite material for lithium ion battery cathode. The composite material adopts a laminar sandwich structure, silicon nano-particles are dispersed on each lamina of the grapheme, the laminas of the grapheme are separated from one another by the silicon nano-particles and the edges of the laminas are in lapped joint so as to constitute a laminar conductive network structure. The preparation method thereof comprises the steps of: formulating anhydrous silicon tetrachloride, surface active agent, sodium naphthalene and graphite oxide to tetrahydrofuran solution, adding the tetrahydrofuran solution into a reactor for reaction in vacuum at the temperature ranging from 380 to 400 DEG C, filtering the reactant to result in the product, and then washing, drying and heating the product to obtain the silicon/grapheme composite material. The preparation method of the invention has the advantages of simple preparation process and great easiness for industrial production; and the silicon/graphene laminar composite material prepared according to the method includes excellent conductivity, power performance, electrochemical activity and cycle stability, and is particularly suitable for manufacturing lithium ion battery cathode.

Silicon/graphene laminar composite material for lithium ion battery cathode and preparation method thereof

The invention discloses a positive pole material of a lithium ion battery with a nanometer structure and a preparation method thereof. The positive pole material is in a particle type core-shell structure, a core material consists of nanometer lithium iron phosphate, lithium vanadium phosphate or cobalt lithium oxide and graphene, and a shell material is porous carbon. The preparation method comprises the following steps of: taking lithium acetate, lithium oxalate, ammonium dihydrogen phosphate, ammonia metavanadate, phosphoric acid, lithium nitrate, cobalt nitrate and graphite oxide as raw materials, adopting a sol-gel method or a ball milling method to prepare a mixture, presintering the mixture in vacuum to obtain the core material, and mixing, grinding and calcining the core material with an organic carbon source to obtain the positive pole material with the particle type core-shell structure. The positive pole material has the advantages of good conductivity, good circulating performance, high capacity, small and uniform particle size, and simple preparation process and is easy for industrialized production.

Positive pole material of lithium ion battery with nanometer structure and preparation method thereof

Lithium ion battery using graphite having multiphase structure as negative pole material

The utility model discloses an electric core structure of a lithium-ion power battery soft-packaged by anisotropic lugs The electric core structure comprises wound cores, a positive pole lug, a negative pole lug and films, wherein each wound core is formed by lamination, arrangement and winding of a positive pole piece, a negative pole piece and a diaphragm, at least two wound cores are stacked together, the films are attached on the positive pole lug and the negative pole lug, and the positive pole lug and the negative pole lug are respectively positioned at the two opposite ends of the wound cores According to the electric core structure of the lithium-ion power battery soft-packaged by the anisotropic lugs, disclosed by the utility model, an electric core is formed by stacking the multiple wound cores, so that the internal resistance of the battery is reduced; simultaneously, the positive pole lug and the negative pole lug are separately arranged at the two opposite ends of the wound cores, so that the problem of difficulty in top sealing of the multiple lugs is solved; and furthermore, the problems that the battery is prone to short circuit and overheating is caused when current is too high are avoided and relieved respectively

Electric core structure of lithium-ion power battery soft-packaged by anisotropic lugs

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