1134results about How to "High charge and discharge capacity" patented technology

An electrode material comprising a particle containing at least one member selected from the particles containing silicon, tin, silicon compound and tin compound, and fibrous carbon. The particle includes: (1) a particle comprising at least one member of a silicon particle, tin particle, particle containing a lithium-ion-intercalatable/releasable silicon compound and particle containing a lithium-ion-intercalatable/releasable tin compound; or (2) a particle comprising a silicon and/or silicon compound-containing carbonaceous material deposited onto at least a portion of the surfaces of a carbon particle having a graphite structure. The lithium secondary battery using the electrode material as a negative electrode has high discharging capacity and is excellent in cycle characteristics and characteristics under a load of large current.

An electrode for lithium batteries, in which a thin film of active material capable of storage and release of lithium, such as a microcrystalline or amorphous silicon thin film, is provided, through an interlayer, on a current collector, the electrode being characterized in that the interlayer comprises a material alloyable with the thin film of active material.

An electrode for a rechargeable lithium battery characterized in that thin films of active material capable of lithium storage and release, i.e., microcrystalline or amorphous silicone thin films are deposited on opposite faces of a plate-form current collector.

Negative active materials including metal nanocrystal composites comprising metal nanocrystals having an average particle diameter of about 20 nm or less and a carbon coating layer are provided. The negative active material includes metal nanocrystals coated by a carbon layer, which decreases the absolute value of the change in volume during charge/discharge and decreases the formation of cracks in the negative active material resulting from a difference in the volume change rate during charge/discharge between metal and carbon. Therefore, high charge/discharge capacities and improved capacity retention capabilities can be obtained.

The invention discloses a manganese/lithium phosphate of lithium iron battery positive pole material and a production method thereof, the technical issue to be solved is to improve electrochemical performances of the positive pole material. The material of the invention includes substrates of manganese/lithium phosphate which are covered by a carbon material covering layer, the lithium covering the manganese/lithium phosphate behind the carbon material covering layer is spherical and has microscopic characteristics of being near spherical, rhombic, tapered, tabular, layered or/and block-shaped as well as of having 0.5-30 mum long and short axles. The production method comprises the following steps of: production of nanometer particles, liquid phase mixed reaction, production of precursor, sintering treatment, covering organic substances. Compared with the prior art, the invention improves the electron conductivity of the manganese/lithium phosphate by covering with carbon liquid phase, the carbon sufficiently covers active materials to efficiently prevent particle aggregation, the invention has the characteristics of about 4V of discharge voltage, high discharge and charge capacitance, excellent circulation stability, high safety, simple process, low cost and little influence on the environment.

A non-aqueous electrolyte to be used in a Li-ion battery includes a lithium salt, a cyclic carbonate, a linear carbonate and an alkyl fluorinated phosphate, of the following general formula

wherein R¹, R² and R³, independently, are selected from the group consisting of straight and branched alkyl groups having 1-5 carbon atoms, and at least one of said alkyl groups is fluorinated, with the locations of said fluorination being at least β-positioned away from the phosphorous of said phosphate, such that said alkyl phosphate has a F/H ratio of at least 0.25, and said electrolyte solution is non-flammable.

The invention relates to a titanium dioxide/graphene nanocomposite material, a preparation method of the nanocomposite material and application of the nanocomposite material in the field of energy source and cleaning environment. The graphene accounts for 1-25wt% and the balance is titanium dioxide. Morphology of the titanium dioxide is a mesoporous structure or a structure with a dominant high energy surface, and titanium dioxide is scattered uniformly on the surface of graphene. According to the invention, by adopting a titanium source and graphene as initial materials, and water or organic solvents as reaction solvents, the nanocomposite material with titanium dioxide with the mesoporous structure or a titanium dioxide nano sheet with the dominant high energy surface compounded with graphene can be obtained through hydrothermal synthesis or a hydrolysis reaction. The invention can be carried out in an aqueous solution system and the crystallinity of the product is high. The composite material can be applied to a cathode material of a power ion battery, has a higher charge-discharge capacity, is excellent in high current charge and discharge, stable in circulating performance, has very good photocatalytic performance and can be used to light degradation of organic pollutants and water photolysis for preparing hydrogen.

The invention relates to a graphene-coated mesoporous metallic oxide, and a preparation method and use thereof. The preparation method for the graphene-coated mesoporous metallic oxide comprises the following steps of: 1) synthesizing mesoporous metallic oxides with different pore passage structures by taking mesoporous silicon dioxides with the different pore passage structures as templates; 2) preparing a graphene oxide by using an oxidation method; 3) absorbing mesoporous metallic oxide particles on the surface of the graphene oxide by using a heterocoagulation method; 4) reducing the graphene oxide into graphene by adding a reducing agent; and 5) performing centrifugal separation, washing and drying. The graphene-coated mesoporous metallic oxide provided by the invention has high electrochemical properties, and can be used as an electrode material of a lithium battery.

The invention relates to a method for synthesizing LiFePO4/C material by chemical vapor deposition supporting the solid phase reaction method, namely, the method for preparing carbon coating lithium iron battery anode material, belonging to the Li-ion battery material preparation art technical field. The characteristics of the method for synthesizing LiFePO4/C materials by solid phase and auxiliary chemical vapor deposition are that auxiliary chemical vapor deposition supporting the solid phase reaction method is adopted to synthesize the carbon coating phosphate lithium iron, namely, the LiFePO4/C material. In the method for synthesizing LiFePO4/C material by chemical vapor deposition supporting the solid phase reaction method, a precursor comprising raw materials of lithium, iron and phosphor is adopted to prepare the carbon coating phosphate lithium iron after being blended, grinded by a globe mill, treated by preheating and calcined as well as vapor deposition. The method for synthesizing LiFePO4/C material by chemical vapor deposition supporting the solid phase reaction method has the advantages that the chemical composition, carbon contents and grain size of LiFePO4 can be controlled effectively; the Li-ion battery anode material prepared has sound conductive performance and can improve the charge-discharge rate and cycling performance of the material.

The invention relates to a multi-stage core and shell structure multi-element material precursor used for an anode material of a lithium ion battery. The molecular formula of the multi-stage core and shell structure multi-element material precursor is (1-x)Li[NiaMnbCo1-a-b][OH]2 x [NimConM1-m-n][OH]2, wherein M=Mn, Al, Mg andTi, the x is larger than or equal to 0.2 and smaller than or equal to 0.9, the a is larger than or equal to 1/3, the b is smaller than or equal to 1/2, the m is larger than or equal to 0.6 and smaller than 1, and the n is larger than or equal to 0 and smaller than or equal to 0.3. A core and shell multi-layered compound structure is adopted, a core of the core and shell multi-layered compound structure is made of a high-nickel-based and high-specific-capacity multi-element material, a shell of the core and shell multi-layered compound structure is made of a high-safety material with the identical nickel and manganese molar content, wherein the high-safety material contains a small quantity of cobalt or does not contain the cobalt, a space between the core and the shell is made of a multi-layered material and is configured according to proportions different from those of the shell and proportions of the core, the proportions of core materials in the multi-layered material from inside to outside are gradually reduced while the proportions of shell materials in the multi-layered material from inside to outside are gradually increased, and accordingly the multi-stage core and shell structure is formed. The multi-stage core and shell structure multi-element material precursor not only has a high specific capacity performance of the core materials, but also has characteristics of high circulatory stability and safety of the shell materials, and is low in large-scale manufacturing cost. The cost is not increased as compared with a homogeneous multi-element material. Besides, repeatability is high, batch stability is good, and the multi-stage core and shell structure multi-element material precursor meets requirements of large-scale commercial application.

The present invention provides a cathode active material that makes possible a high capacity nonaqueous electrolyte secondary battery that has excellent discharge load characteristics that provide both good cycle characteristics and thermal stability. The cathode active material comprises a lithium nickel composite oxide having the compositional formula LiNi_1−aM_aO₂ (where, M is at least one kind of element that is selected from among a transitional metal other than Ni, a group 2 element, and group 13 element, and 0.01≦a≦0.5) to which fine lithium manganese composite oxide particle adhere to the surface thereof. This lithium nickel composite oxide is obtained by adding manganese salt solution to a lithium nickel composite oxide slurry, causing manganese hydroxide that contains lithium to adhere to the surface of the lithium nickel composite oxide particles, and then baking that lithium nickel composite oxide.

A SiCO—Li composite is prepared by causing a reactive silane and/or siloxane having crosslinkable groups to crosslink, sintering the crosslinked product into an inorganic Si—C—O composite, and doping the Si—C—O composite with lithium. When the SiCO—Li composite is used as a negative electrode, a lithium ion secondary cell exhibits good cycle performance, unique discharge characteristics and improved initial efficiency.

A subject is to provide a nonaqueous electrolyte excellent in cycle performances such as capacity retention after cycling, output after cycling, discharge capacity after cycling, and cycle discharge capacity ratio, output characteristics, high-temperature storability, low-temperature discharge characteristics, heavy-current discharge characteristics, high-temperature storability, safety, high capacity, high output, high-current-density cycle performances, compatibility of these performances, etc. Another subject is to provide a nonaqueous-electrolyte secondary battery employing the nonaqueouselectrolyte. The subjects have been accomplished with a nonaqueous electrolyte which contains a monofluorophosphate and/or a difluorophosphate and further contains a compound having a specific chemical structure or specific properties.

This invention relates to a kind of improving method of lithium ionic cell cathode materials. The cathode materials in need of improving are mixed evenly with catalyst which has 0.1úÑ-10úÑ weight percent of cathode materials. The materials are then put into reaction furnace, which uses hydrocarbon as carbon source. The cathode materials are mixed with buffer gas according to 1í†(0-10) volume ratio. Then the mixture are reacted in reaction furnace at 600-1300íµ for 1-900 minutes. A kind of improved composite cathode materials, at the surface of which in-situ grows nanometer carbon fibrin/ carbon tube, are gained. The improved materials have good cell kinetic ability, circulating ability, charge-discharge capacity and consistency with electrolyte.

The invention discloses a film for a graphene/porous nickel oxide composite super capacitor. The invention is characterized in that the film is of a disordered nano porous structure, the aperture range is 10 to 350nm, the thickness of the film is 1 to 5 mu m, and the weight ratio of graphene to nickel oxide is (0.5:100) to (2:100). The method for preparing the film comprises the following steps: dissolving graphite oxide sheets and magnesium nitrate into an isopropanol solution so as to form a positively-charged graphite oxide sheet sol, then carrying out electrophoretic deposition on the obtained sol so as to obtain a graphene film; and through taking the graphene film as a deposition carrier, preparing a three-dimensional porous film for the graphene/porous nickel oxide composite super capacitor by using a chemical bath film-coating method. The porous composite thin film prepared by the method has the advantages of good mechanical capacity and super-capacitance property, high-discharge specific capacitance, high-ratio charge-discharge properties, high cycle life and the like, and has wide application prospects in the fields such as electric automobiles, communication, consumer electronics, signal control and the like.

The invention relates to a flake MoS2/graphene composite aerogel and a preparation method thereof and belongs to the technical field of anode materials of lithium ion batteries. The preparation method comprises the following steps: ultrasonically dispersing a certain quantity of graphene oxide solution into deionized water, adding a certain quantity of water-soluble molybdate and thiourea, then adding 0.1-3mL organic amine solution, taking out a cylindrical product after hydrothermal reaction at the temperature of 160-240 DEG C, freeze-drying, and then carrying out thermal treatment for 2h in the mixed atmosphere of argon and hydrogen at the temperature of 800 DEG C to obtain the flake MoS2/graphene composite aerogel. According to the flake MoS2/graphene composite aerogel and the preparation method thereof disclosed by the invention, thin layers of graphene are connected with one another in a staggering mode to form a three-dimensional ordered conductive network and form micron pore canals, MoS2 is uniformly dispersed on the ultra-large superficial area, and thus, the problems of volume expansion and crushing materials are effectively solved; meanwhile, the structure stability and the cycle performance of the flake MoS2/graphene composite aerogel, serving as the anode material, are improved.

A composite positive electrode material with a core-shell structure for a lithium ion battery consists of a core active material and a shell active material. The core active material is a lithium iron phosphate or a lithium manganate, and the shell active material is a composite lithium iron phosphate with carbon. The carbon is one or more of carbon nanotube, superfine conductive carbon black and amorphous carbon material. The composite positive electrode material includes from 65% to 99% core active material and from 1% to 35% shell active material, based on the total weight of the composite positive electrode material. The composite positive electrode material has stable property and excellent electrochemistry performance. The lithium ion battery made with the material has higher charge-discharge capacity, excellent cycle performance. It can be charged quickly and discharged at high rate. A preparing method for the composite positive electrode material is also provided.