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Preparation method of positive electrode material (carbon-coated iron-manganese-lithium phosphate) of lithium ion battery

A carbon-coated lithium iron manganese phosphate and lithium-ion battery technology, which is applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of low battery energy density, limited electrolyte, low working voltage, etc., and reduce the synthesis Effect of cycle and equipment requirements, high reactivity, and increased operating voltage

Inactive Publication Date: 2014-09-10
HEFEI GUOXUAN HIGH TECH POWER ENERGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology describes methods for making certain types of lithiophenium compounds that can be used in secondary cells (referred to also referred to herein interchangeably), specifically LiFeMnPO4. These new compositions have improved properties compared to existing ones due to their unique structure or composition. They exhibit better charge storage capabilities at higher temperatures while maintaining excellent electrical conductivity. Additionally, they provide longer lifetimes during use over multiple cycles through efficient charging and discharging processes.

Problems solved by technology

This patented technical problem addressed in this patents relates to improving the energy content of luminous redox flow secondary cells that use LiFePO_4. Current methods involve modifying or adding certain substances like lanthanoid compounds into these compositions, resulting in lower operational voltages and reduced cell capacities compared to what was previously possible due to their poorer properties than existing ones.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] 1) Preparation of iron and manganese precursors

[0026] Accurately take 3160.8g of potassium permanganate, dissolve it with deionized water, configure it into a 20% potassium permanganate solution, adjust the pH value of the solution with sulfuric acid to <3, take 3600g of battery-grade ferrous oxalate raw material, and dissolve it in the above potassium permanganate solution During the reaction, stir and react. After the reaction is complete, adjust the pH value of the mixed solution to 9 with 25% ammonia water, and slowly stir during the pH value adjustment process. The obtained precipitate is filtered and washed several times before use.

[0027] 2) Preparation of raw material mixed solution

[0028] Weigh 4157.2 g of lithium dihydrogen phosphate according to the calculation of synthesizing 40 mol of lithium iron manganese phosphate, and configure the lithium dihydrogen phosphate and the washed iron-manganese precursor into a suspension with a mass fraction of 30%, ...

Embodiment 2

[0032] 1) Preparation of iron and manganese precursors

[0033] Accurately take 3160.8g of potassium permanganate, dissolve it with deionized water, configure it as a 40% potassium permanganate solution, adjust the pH value of the solution with sulfuric acid to <3, take 3600g of battery-grade ferrous oxalate raw material, and dissolve it in the above potassium permanganate solution During the reaction, stir and react. After the reaction is complete, adjust the pH value of the mixed solution to 9 with 10% ammonia water, and slowly stir during the pH value adjustment process. The obtained precipitate is filtered and washed several times before use.

[0034] 2) Preparation of raw material mixed solution

[0035] Weigh 4080.8 g of lithium acetate and 4600 g of ammonium dihydrogen phosphate according to the calculation of synthesizing 40 mol of lithium iron manganese phosphate, and configure the weighed lithium acetate and ammonium dihydrogen phosphate and the washed iron-manganese...

Embodiment 3

[0039] 1) Preparation of iron and manganese precursors

[0040] Accurately take 3160.8g of potassium permanganate, dissolve it with deionized water, configure it as a 40% potassium permanganate solution, adjust the pH value of the solution with sulfuric acid to <3, take 3600g of battery-grade ferrous oxalate raw material, and dissolve it in the above potassium permanganate solution During the reaction, the reaction was stirred. After the reaction was complete, the pH value of the mixed solution was adjusted to 9 with 20% ammonia water, and the pH value was adjusted slowly while stirring. The obtained precipitate was filtered and washed several times before use.

[0041] 2) Preparation of raw material mixed solution

[0042] Weigh lithium carbonate 1476g and ammonium dihydrogen phosphate 4600g according to the calculation of synthesizing 40mol lithium iron manganese phosphate, and configure the weighed lithium acetate and ammonium dihydrogen phosphate and the washed iron-mangan...

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PUM

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Abstract

The invention discloses a preparation method of a positive electrode material (carbon-coated iron-manganese-lithium phosphate) of a lithium ion battery, and relates to the technical field of preparation of positive electrode materials of lithium ion batteries. The preparation method comprises the following steps: preparing a high-activity iron-manganese precursor mixture by oxidation-reduction reaction, and treating a lithium source, a phosphorus source, a carbon source and the iron-manganese precursor mixture by the steps of mixing, drying, sintering and the like so as to obtain the positive electrode material (carbon-coated iron-manganese-lithium phosphate) of the lithium ion battery. The preparation method has the characteristics of high reaction activity of the synthesized iron-manganese precursor, no need of the grinding procedure in mixing materials, low sintering temperature, short temperature-maintaining time and the like; the prepared positive electrode material (carbon-coated iron-manganese-lithium phosphate) of the lithium ion battery has the advantages that the first discharging capacity is up to 155.2mAh/g when the rate is 0.1C, the discharging capacity is more than 140mAh/g when the rate is 0.2C, so that the good electro-chemical performance and rate performance are shown, and simultaneously, all performance indexes of the material give consideration to the processing performance. Compared with the lithium iron phosphate material, the working voltage of the synthesized material and specific energy of the material are increased, so that the benefit is brought for increasing the specific energy density of a battery core at the later stage.

Description

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Claims

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Application Information

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Owner HEFEI GUOXUAN HIGH TECH POWER ENERGY
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