High-potential lithium ion battery cathode material LiNi<0.5-x>MxMn<1.5-y>SiyO4 and preparation method thereof

A technology for lithium-ion batteries and positive electrode materials, applied in battery electrodes, secondary batteries, circuits, etc., can solve problems such as poor electrochemical cycle performance, and achieve poor stability, easy operation, and easy bulk phase doping Effect

Active Publication Date: 2018-11-13
UNIV OF ELECTRONICS SCI & TECH OF CHINA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The object of the present invention is to aim at lithium-ion battery cathode material spinel type lithium nickel manganese oxide (LiNi 0.5 mn 1.5 o 4 ) has the disadvantage of poor electrochemical cycle performance at high potentials, and provides a bulk composite doped modified spinel lithium-ion battery positive electrode material LiNi 0.5-x m x mn 1.5-y Si y o 4 And preparation method thereof, wherein M=Mg, Zn, Cu, V, 0

Method used

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  • High-potential lithium ion battery cathode material LiNi&lt;0.5-x&gt;MxMn&lt;1.5-y&gt;SiyO4 and preparation method thereof
  • High-potential lithium ion battery cathode material LiNi&lt;0.5-x&gt;MxMn&lt;1.5-y&gt;SiyO4 and preparation method thereof
  • High-potential lithium ion battery cathode material LiNi&lt;0.5-x&gt;MxMn&lt;1.5-y&gt;SiyO4 and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Dissolve 0.0315mol (1.3217g) lithium hydroxide and 0.0394mol complexing agent (citric acid + triethanolamine + PEG) in an appropriate amount of deionized water, and stir in a 50°C water bath to make it completely dissolved to obtain solution A; Dissolve 0.0441mol (10.8085g) manganese acetate, 0.0141mol (3.5089g) nickel acetate and 0.0009mol (0.2308g) magnesium nitrate in deionized water to prepare mixed salt solution B; add 0.0009mol (0.1875g) ethyl orthosilicate Disperse the ester in an appropriate amount of absolute ethanol to obtain an ethanol solution C of ethyl orthosilicate.

[0038] Add mixed salt solution B and ethyl orthosilicate ethanol solution C to solution A slowly and dropwise at the same time, with constant stirring, adjust the pH to 7 with ammonia water, stir for 30 minutes and then raise the temperature to 80°C, and continue stirring until green Then, the green gel obtained is dried in a blast drying oven at 110°C for 24 hours to obtain a dry gel, and the ...

Embodiment 2

[0041] Dissolve 0.0315mol (1.3217g) lithium hydroxide and 0.0394mol complexing agent (citric acid + triethanolamine + PEG) in an appropriate amount of deionized water, and stir in a 50°C water bath to completely dissolve to obtain solution A; Dissolve 0.0441mol (10.8085g) manganese acetate, 0.0141mol (3.5089g) nickel acetate and 0.0009mol (0.2308g) magnesium nitrate in deionized water to prepare mixed salt solution B; add 0.0009mol (0.1875g) ethyl orthosilicate The ester is dispersed in an appropriate amount of absolute ethanol to obtain an ethanol solution C of ethyl orthosilicate.

[0042] Add mixed salt solution B and ethyl orthosilicate ethanol solution C slowly and dropwise to solution A at the same time, with constant stirring, adjust the pH to 7 with ammonia water, stir for 30 minutes and then raise the temperature to 80°C, and continue stirring until green Gel; then dry the obtained green gel in a blast drying oven at 110°C for 24 hours to obtain a dry gel, and put the dr...

Embodiment 3

[0045] Dissolve 0.0315mol (1.3217g) lithium hydroxide and 0.0394mol complexing agent (citric acid + triethanolamine + PEG) in an appropriate amount of deionized water, and stir in a 50°C water bath to make it completely dissolved to obtain solution A; Dissolve 0.0441mol (10.8085g) manganese acetate, 0.0141mol (3.5089g) nickel acetate and 0.0009mol (0.00702g) ammonium metavanadate in an appropriate amount of deionized water to obtain suspension B; add 0.0009mol (0.1875g) ortho silicon Ethyl acid was dispersed in an appropriate amount of absolute ethanol to obtain an ethanol solution C of ethyl orthosilicate.

[0046] Add the B suspension and the ethyl orthosilicate alcohol solution C dropwise to the A solution at the same time, and heat it in a water bath at 50°C with constant stirring, adjust the pH to 7 with ammonia water, and stir until the mixture becomes clear. Afterwards, the water bath was heated to 80°C, and stirring was continued to evaporate the water until a green gel f...

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Abstract

The invention belongs to the field of lithium ion batteries, and specifically provides a high-potential lithium ion battery cathode material LiNi<0.5-x>MxMn<1.5-y>SiyO4 and a preparation method thereof, wherein M is Mg, Zn, Cu and V, x is greater than 0 and smaller than or equal to 0.1, y is greater than 0 and smaller than or equal to 0.2, so that the defect that electrochemical circulating performance is poor when the LiNi0.5Mn1.5O4 is under high potential is overcome. An element Si is adopted to replace part of an element Mn, and metal M is adopted to replace part of an element Ni, so that the lithium ion battery cathode material LiNi<0.5-x>MxMn<1.5-y>SiyO4 has relatively high working voltage, relatively high energy density and excellent circulating stable performance after bulk-phase cooperative doping is realized, and therefore, large-multiplying-power charging and discharging needs can be met; and moreover, a mixed complexing agent is adopted to improve a sol-gel preparation process; the prepared product is high in purity, is high in chemical uniformity, is high in crystallization quality, is fine and uniform in product particles, is excellent in electrochemical performance, is low in manufacturing cost, and is suitable for large-scale industrial production.

Description

Technical field [0001] The invention belongs to the field of lithium-ion batteries, and relates to a lithium-ion battery anode material and a preparation method thereof, and specifically is a lithium-ion battery anode material LiNi 0.5-x M x Mn 1.5-y Si y O 4 And its preparation method, where M=Mg, Zn, Cu, V and other metal elements, 0 <x≤0.1,0 <y≤0.2. Background technique [0002] With the two major issues of energy crisis and environmental pollution becoming increasingly prominent, the development and utilization of clean and renewable new energy has become an important measure to solve these two major issues. In recent years, new energy electric vehicles have developed rapidly. It replaces fossil fuels with clean electric energy, which will undoubtedly reduce the burden on the environment, while the rapid development of electric vehicles depends on the development of battery technology. Lithium-ion battery is a rechargeable secondary battery. Because of its high energy d...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/505H01M4/525H01M4/485H01M4/62H01M10/0525
CPCH01M4/362H01M4/485H01M4/505H01M4/525H01M4/62H01M4/624H01M10/0525Y02E60/10
Inventor 刘兴泉舒小会赵红远张美玲胡友作谭铭刘珊珊冉淇文李浩
Owner UNIV OF ELECTRONICS SCI & TECH OF CHINA
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