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Preparation method of nanometer lithium titanate covered with double highly-conductive materials

A high-conductivity, lithium titanate technology, applied in nanotechnology, circuits, electrical components, etc., can solve the problems of electrolyte consumption, low first-time Coulombic efficiency, low first-time charge-discharge efficiency, limitations, etc., and achieve superior fast charge-discharge performance , Improve the effect of particle agglomeration and good cycle stability

Inactive Publication Date: 2014-03-26
SHANGHAI NAT ENG RES CENT FORNANOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, most commercial lithium-ion battery anode materials use carbon anode materials, but carbon anode materials have some defects: they react with the electrolyte to form a surface passivation film during the first discharge process, resulting in the consumption of electrolyte and lower initial Coulombic efficiency. Low; the electrode potential of the carbon electrode is similar to that of metal lithium. When the battery is overcharged, metal lithium may still be precipitated on the surface of the carbon electrode, forming dendrites and causing short circuits, causing safety problems, etc.
Carbon materials have some disadvantages: the presence of lithium dendrites; the first charge and discharge efficiency is relatively low; it interacts with the electrolyte to form a solid electrolyte interface film; there is a relatively obvious voltage hysteresis effect; the preparation method is relatively complicated
Compared with carbon anode materials, alloy-type anode materials generally have higher specific capacity, but poor cycle performance, and alloy-type anode materials also solve some safety problems; recently, spinel-type lithium titanate has been used as a The new type of negative electrode material has the advantages of "zero strain", good cycle performance, good charge and discharge platform, no reaction with electrolyte, cheap price, easy preparation, etc., and has gradually become a research hotspot.
However, Li 4 Ti 5 o 12 The conductivity is very low, almost insulating, and the performance at high magnification is poor. If it is used in power vehicles, large energy storage batteries and other fields, it will be greatly restricted.
Therefore, for Li 4 Ti 5 o 12 Due to the disadvantage of poor electrical conductivity of the material, it is particularly important to improve its electrical conductivity and high-rate performance.

Method used

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Experimental program
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Effect test

Embodiment 1

[0028] First, premix 300 ml of ethanol and 30 ml of water according to the volume ratio of 1:0.1 to form a mixed solvent, and then add 15 ml of HNO 3As an inhibitor of the follow-up reaction; the soluble compounds of Li and Ti are compounded according to the molar ratio of Li:Ti=4.2:5, and 25.52g of tetra-n-butyl titanate (analytically pure) is weighed, and 2.33g of carbonic acid Lithium (analytical pure), added to the previous alcohol-water-acid mixture, stirred by a magnetic heating stirrer until completely dissolved; then 20g of ethylenediaminetetraacetic acid and 30g of citric acid were added to the pre-mixed metal ion solution After mixing evenly, add 100 ml of ammonia water dropwise to adjust the pH value to 8, and continue to stir; after the above mixed solution is stirred evenly to form a sol, heat and stir at 80°C until it reaches a gel state; :Sr:Sc:Mn=0.5:0.5:0.1:0.9 molar ratio for batching, weigh 9.48 g lanthanum acetate (analytical pure), 9.69 g strontium nitrate...

Embodiment 2

[0030] According to the volume ratio of 1:0.1, 300 ml of ethanol and 30 ml of water are premixed to form a mixed solvent, and then 15 ml of HCl is added as an inhibitor of the subsequent reaction; the soluble compound of Li and Ti is compounded according to Li:Ti=4.2:5 The molar ratio is carried out batching, and the tetraisopropyl titanate (analytical pure) of 21.31g, the lithium acetate (analytical pure) of 6.43 g are joined in the previous alcohol-water-acid mixture, stirred by a magnetic heating stirrer, Until it is completely dissolved; then add 20 g of ethylenediaminetetraacetic acid and 40 g of citric acid into the premixed metal ion solution, mix well, add 100 ml of ammonia water dropwise to adjust the pH value to 9, and continue stirring; wait for the above mixing After the solution was stirred evenly to form a sol, it was then heated and stirred at 80°C until it reached a gel state; the La, Sr, Sc and Mn compounds were mixed according to the molar ratio of La:Sr:Sc:Mn...

Embodiment 3

[0032] According to the volume ratio of 1:0.2, pre-mix 300 ml of ethanol and 60 ml of water to form a mixed solvent, and then add 30 ml of HNO 3 As an inhibitor of the follow-up reaction; the soluble compounds of Li and Ti are compounded according to the molar ratio of Li:Ti=4.4:5, and 25.52 g of tetra-n-butyl titanate (analytical pure), 4.55 g of nitric acid Lithium (analytically pure), was added to the previous alcohol-water-acid mixture, stirred by a magnetic heating stirrer until it was completely dissolved; then 20 g of ethylenediaminetetraacetic acid and 60 g of citric acid were added to the pre-mixed metal In the ionic solution, after mixing evenly, add 110ml of ammonia water dropwise to adjust the pH value to 7, and continue to stir; after the above mixed solution is stirred evenly to form a sol, heat and stir at 80°C until it is in a gel state; La:Sr:Sc:Mn=0.5:0.5:0.1:0.9 molar ratio for batching, weigh 9.48 g lanthanum oxalate (analytical pure), 5.27 g strontium oxal...

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Abstract

The invention provides a preparation method of nanometer lithium titanate covered with double highly-conductive materials. Through a sol-gel method, a La[0.5]Sr[0.5]Sc[0.1]Mn[0.9]O3 / C-Li4Ti5O12 anode material is prepared by a step of blending a soluble Li compound and a soluble Ti compound according to a molar ratio of Li / Ti=0.8-1.0, adding into an alcohol-water mixed solvent containing a hydrolysis inhibitor, adding a bi-component chelating agent, subjecting the bi-component chelating agent and metal ions to chelation under alkaline conditions, and stirring and heating to form gel; a step of dissolving a La compound, a Sr compound, a Sc compound and a Mn compound into an alcohol-water mixed solvent according to a molar ratio of La: Sr: Sc: Mn=0.5:0.5:0.1:0.9, adding the bi-component chelating agent, subjecting the bi-component chelating agent and metal ions to chelation under alkaline conditions, and stirring to form sol; a step of mixing the gel and the sol and stirring to form co-gel to obtain a sintering precursor; and a step of ball milling and calcining at 900-1150 DEG C for 5-15 h. The lithium titanate prepared by the method has good dispersion effects and excellent electrochemical performance, and the agglomeration phenomenon of nano-powder is improved significantly.

Description

technical field [0001] The invention relates to a method for preparing lithium titanate, a negative electrode material of a lithium ion secondary battery, in particular to a method for preparing lithium titanate coated with double high-conductivity materials by a sol-gel method. Background technique [0002] As a high specific energy chemical power source, lithium-ion secondary batteries have been widely used in mobile communications, notebook computers, video cameras, cameras, portable instruments and other fields, and have rapidly developed into one of the most important secondary batteries at present. Lithium-ion batteries are favored because of their high voltage, high energy density, long cycle life, and low environmental pollution. At present, most commercial lithium-ion battery anode materials use carbon anode materials, but carbon anode materials have some defects: they react with the electrolyte to form a surface passivation film during the first discharge process, ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/485B82Y40/00
CPCY02E60/122B82Y40/00H01M4/366H01M4/485H01M4/624H01M10/0525Y02E60/10
Inventor 张春明吴晓燕黄昭王丹严鹏何丹农
Owner SHANGHAI NAT ENG RES CENT FORNANOTECH
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