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Lithium ion battery positive electrode material lithium iron manganese phosphate and liquid phase preparation method thereof

A lithium-ion battery, lithium iron manganese phosphate technology, applied in battery electrodes, circuits, electrical components, etc., can solve problems such as structural instability, and achieve the effects of reducing battery costs, high discharge voltage platform, and simple operation

Inactive Publication Date: 2015-04-29
SHANDONG GOLDENCELL ELECTRONICS TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The purpose of the present invention is to provide a lithium-ion battery capable of improving the electronic conductivity of lithium manganese phosphate positive electrode material, solving the problem of structural instability in lithium manganese phosphate due to the ginger-Taylor effect of manganese element, and improving the discharge specific capacity and rate performance Cathode material lithium iron manganese phosphate;

Method used

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  • Lithium ion battery positive electrode material lithium iron manganese phosphate and liquid phase preparation method thereof
  • Lithium ion battery positive electrode material lithium iron manganese phosphate and liquid phase preparation method thereof

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preparation example Construction

[0023] A liquid phase preparation method of lithium iron manganese phosphate lithium ion battery cathode material, characterized in that: the steps are as follows: (1) synthesis of precursor: iron salt weighed according to molar ratio 1-x:x:1.0-2.0, Manganese salt, oxalate, iron salt, manganese salt and antioxidant are made into solution A, oxalate is made into solution B, and ammonia water is made into solution C; measure B solution as the bottom liquid and pour it into a four-neck flask; A and solution C are added dropwise in parallel, after solution A and solution C are added dropwise, stir for 10-60min, then dropwise add solution B; stir and age for 3-6h, then stand and age for 10-15h; filter, wash, After vacuum drying at 50°C, the ferromanganese oxalate precipitation precursor was obtained;

[0024] (2) Ingredients: Weigh 10-15% of the carbon source, add it to a ball mill tank, dissolve it in a quantitative solvent, then add lithium source, precursor, and phosphorus sourc...

Embodiment 1

[0035] Weigh a certain amount of ferrous sulfate, manganese sulfate, and ascorbic acid in a molar ratio of 1:1:0.1 and dissolve them in 60ml of distilled water to make a 1M solution A; Take 200mL of distilled water as solution B; measure 45mL of 2M ammonia solution as solution C; take 67mL of B solution and pour it into a four-necked flask as the bottom solution, and drop solution A and solution C into the four-necked flask in parallel, and control the dripping Acceleration is 5 seconds / drop, after the dropwise addition, stir for 10 minutes, then add solution B dropwise, control the dropping speed to 3 seconds / drop, stir for 4 hours after the dropwise addition, let stand and age for 15 hours, suction filter, wash, 50 ℃ Vacuum-dried to obtain the oxalate co-precipitation precursor, the specific morphology is shown in the scanning electron microscope image, see the attached figure 1 ;According to the molar ratio of lithium source: precursor: phosphorus source: carbon source = 1....

Embodiment 2

[0038] Weigh a certain amount of ferrous chloride, manganous acetate, and ascorbic acid in a molar ratio of 3:2:0.1 and dissolve them in 60ml of distilled water to make a 1M solution A; Dissolve ammonium in 200mL of distilled water as solution B; measure 45mL of 2M ammonia solution as solution C; take 67mL of solution B and pour it into a four-necked flask as the bottom solution, and pour solution A and solution C into the four-necked flask in parallel, Control the rate of addition to be 5 seconds / drop, complete the dropwise addition and stir for 10 min, then add solution B dropwise, control the rate of addition to be 3 seconds / drop, stir for 4 hours after the completion of the dropwise addition, leave to stand for aging for 15 hours, suction filtration, washing, Vacuum drying at 50°C to obtain the oxalate co-precipitation precursor; according to the molar ratio of lithium source: precursor: phosphorus source: carbon source = 1.03:1:1:0.12, weigh the oxalate co-precipitation pr...

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Abstract

The invention discloses a lithium ion battery positive electrode material lithium iron manganese phosphate which has a general chemical formula of LiFe1-xMnxPO4, wherein x is equal to 0.2-0.8. The liquid phase preparation method of the lithium ion battery positive electrode material lithium iron manganese phosphate comprises the following steps: synthesizing a precursor, namely weighing an iron salt, a manganese salt and oxalate according to a molar ratio, preparing a solution A from the iron salt, the manganese salt and an antioxidant, preparing the oxalate into a solution B, and preparing ammonia water into a solution C; measuring the solution B to serve as a base solution; simultaneously dripping the solution A and the solution C, and dripping the solution B; filtering, washing and performing vacuum drying, thereby obtaining an iron manganese oxalate precipitate precursor; dosing, namely weighing a carbon source, adding a lithium source, the precursor and a phosphorus source, mixing and performing ball-milling; compounding, namely adding the mixed materials into a compounding furnace, and treating the materials for calcining; and sintering, namely controlling the temperature rise rate, and performing furnace cooling on the compounded precursor powder to room temperature under the protection of inert gas atmosphere, thereby obtaining the carbon-coated lithium iron manganese phosphate positive electrode material.

Description

technical field [0001] The invention relates to a battery positive electrode material and a preparation method thereof in the field of materials, in particular to a lithium iron manganese battery positive electrode material lithium iron manganese phosphate and a liquid phase preparation method thereof. Background technique [0002] Now, lithium-ion batteries have been widely used in portable electric devices, and are gradually developing towards large-scale electric devices. However, high cost, safety issues, and toxicity have become the main obstacles for the current lithium-ion batteries to be used in electric vehicles or large-scale electrostatic energy storage systems, especially lithium-cobalt-based oxide cathode materials. Cathode material LiMPO 4 (M=Fe, Mn, Ni, Co) series materials have been recognized by researchers because of their environmental friendliness, high thermal stability, relatively high energy density and abundant resources, and they believe that polya...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/58H01M4/136H01M4/1397
CPCH01M4/136H01M4/1397H01M4/5825Y02E60/10
Inventor 关成善宗继月孟博赵玲
Owner SHANDONG GOLDENCELL ELECTRONICS TECH
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