High Energy Density Cathode Materials for Lithium Ion Batteries

Inactive Publication Date: 2012-01-05
UNIV OF FLORIDA RES FOUNDATION INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0013]Advantageously, the compounds, materials, batteries, and methods of the present invention can provide increased energy density to meet the increasing demands for power for portable devices.

Problems solved by technology

In lithium-ion batteries, the cathode is typically the most expensive active component.
Moreover, the cathode often limits the charge/discharge rate of the battery system.
However, LiCoO2 can be costly because cobalt is an expensive material.
The crystal structure of LiNiO2 can change during charging/discharging cycles, which can lead to deterioration of the cathode.
Thus, the use of this material for a cathode can have significant drawbacks.

Method used

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  • High Energy Density Cathode Materials for Lithium Ion Batteries
  • High Energy Density Cathode Materials for Lithium Ion Batteries
  • High Energy Density Cathode Materials for Lithium Ion Batteries

Examples

Experimental program
Comparison scheme
Effect test

Example

Example 1

[0081]Sol solutions were prepared from stoichiometric mixtures of Li(CH3COO).2H2O, Ni(CH3COO)).4H2O, and Mn(CH3COO)2.4H2O in distilled water. The solution was then added dropwise to a continuously stirred aqueous solution of citric acid. The pH of the mixed solution was adjusted by adding ammonium hydroxide solution. The solution was then heated at a temperature of about 75° C. overnight. A transparent gel was obtained. The resulting gel precursors were decomposed at a temperature of about 400° C. for about 10 hours in air and then calcined at a temperature of about 800° C. for about 10 hours.

Example

Example 2

[0082]Sol solutions were prepared from stoichiometric mixtures of Li(CH3COO).2H2O, Ni(CH3COO)2.4H2O, and Mn(CH3COO)2.4H2O in distilled water. Chromium acetate was added to the distilled water according to the stoichiometry. The solution was then added dropwise to a continuously stirred aqueous solution of citric acid. The pH of the mixed solution was adjusted by adding ammonium hydroxide solution. The solution was then heated at a temperature of about 75° C. overnight. A transparent gel was obtained. The resulting gel precursors were decomposed at a temperature of about 400° C. for about 10 hours in air and then calcined at a temperature of about 800° C. for about 10 hours to produce a compound of the form Li2CrxNi0.5-x-yMn1.5+yO4.

Example

Example 3

[0083]Sol solutions were prepared from stoichiometric mixtures of Li(CH3COO).2H2O, Ni(CH3COO)2.4H2O, and Mn(CH3COO)2.4H2O in distilled water. Copper acetate was added to the distilled water according to the stoichiometry. The solution was then added dropwise to a continuously stirred aqueous solution of citric acid. The pH of the mixed solution was adjusted by adding ammonium hydroxide solution. The solution was then heated at a temperature of about 75° C. overnight. A transparent gel was obtained. The resulting gel precursors were decomposed at a temperature of about 400° C. for about 10 hours in air and then calcined at a temperature of about 800° C. for about 10 hours to produce a compound of the form Li2CuxNi0.5-x-yMn1.5+yO4.

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Abstract

Compounds and materials for improved cathodes are provided. A compound of the present invention can be of the general form Li2MxNi0.5-x-yMn1.5+yO4, where M is a transition metal. The compounds and materials of the present invention can be used as a cathode for a battery, such as a lithium ion battery. The compounds and materials of the present invention provide high energy and power density at low cost.

Description

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Claims

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Application Information

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Owner UNIV OF FLORIDA RES FOUNDATION INC
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