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Preparation method for high-capacity nanometer organic positive electrode material

A nano-organic and cathode material technology, which is applied in the direction of nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the problems of unfavorable cathode material performance, reduced electrode capacity, and difficulty in dissolution, so as to improve the dissolution rate and electrical conductivity, long cycle life, and low dissolution rate

Inactive Publication Date: 2017-07-04
OPTIMUM BATTERY CO LTD
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Problems solved by technology

At present, widely used inorganic cathode materials generally have defects such as limited capacity improvement, high energy consumption in the production process, potential safety hazards, and high costs.
Traditional inorganic materials also have the following disadvantages: the actual available specific capacity does not exceed 200mAh / g, and the room for improvement is very limited. They all use non-renewable mineral deposits as raw materials, and mining them at the same time consumes a lot of energy, which does not meet the requirements of sustainable development.
However, organic compound cathode materials have problems such as difficulty in dissolving in the electrolyte and low conductivity.
[0005] At present, the existing research on oxygen-containing organic compound cathode materials has carried out many improvement measures from the addition of conductive agents, lithium / sodium salination of carbonyl compounds, polymerization process of carbonyl compounds, etc., and achieved certain results, but there are still The following problems: ①Although the addition of conductive agent improves the solubility and conductivity to a certain extent, it will cause a significant decrease in electrode capacity; ②Although the lithium salinization measure can reduce the solubility, it will introduce additional non-electrochemical Active Li + -O - functional group, leading to a decrease in specific capacity, and the functional group Li + -O - The electron-donating effect of the corresponding small molecule conjugated carbonyl compound reduces the redox potential of the corresponding small molecule conjugated carbonyl compound, which is not conducive to the performance of the positive electrode material; ③Although the polymerization process can effectively reduce the solubility, it will introduce components without chemical activity (such as coupling Unit) leads to a decrease in specific capacity, and the low conductivity of the polymer and the large charge repulsion between the monomers cause a slower ion / electron transport rate, while the swelling of the polymer and its own aggregation during charge and discharge The state structure will also affect the diffusion and migration rate of lithium ions

Method used

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  • Preparation method for high-capacity nanometer organic positive electrode material
  • Preparation method for high-capacity nanometer organic positive electrode material
  • Preparation method for high-capacity nanometer organic positive electrode material

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preparation example Construction

[0020] The invention provides a method for preparing a high-capacity nanometer organic positive electrode material, comprising the following steps:

[0021] Step 1: Put trimellitic anhydride, urea, nickel chloride hexahydrate and ammonium molybdate into a mortar and mix evenly, heat and dry in an oven, cool and grind, then add a saturated solution of hydrochloric acid / sodium chloride , heated to a slight boil, cooled, filtered, and dried.

[0022] Step 2: add the dried product after synthesis into sodium hydroxide solution to heat, cool the solution, mix it with deionized water, adjust the pH with hydrochloric acid solution, and filter and separate the product after complete precipitation.

[0023] Step 3: Wash the product obtained in Step 2 with deionized water and methanol several times, and then put it into a vacuum box for evaporation to remove a small amount of residual low-boiling impurities, and finally obtain a carboxyl-substituted phthalocyanine compound.

[0024] St...

Embodiment 1

[0027] Step 1: Put trimellitic anhydride, urea, nickel chloride hexahydrate and ammonium molybdate into a mortar with a mass ratio of 28:50:20:2, mix evenly, transfer to a beaker, and heat in an oven to 120°C and keep it for 1h (hour), until no more bubbles appear inside the beaker, then set the oven temperature to 150°C for constant temperature reaction for 4h, after cooling, crush the obtained black solid and add it to 3000mL of 1.0mol / L hydrochloric acid / In a saturated solution of sodium chloride, after boiling slightly, cool, filter, and dry.

[0028] Step 2: Add the dried product after synthesis into 3000mL of sodium hydroxide solution and heat to 110°C, react at this temperature until no ammonia gas is released; cool the solution, pour it into 5000mL of deionized water, and use 5.5mol / L hydrochloric acid solution to adjust the pH=3.0, let stand for 24 hours, and filter and separate after the product is completely precipitated.

[0029] Step 3: Wash the product obtaine...

Embodiment 2

[0032] Step 1: Put trimellitic anhydride, urea, nickel chloride hexahydrate and ammonium molybdate into a mortar with a mass ratio of 28:50:20:2, mix evenly, transfer to a beaker, and heat in an oven to 120°C and keep it for 1h until there are no more bubbles in the beaker, then set the temperature of the incubator to 150°C for a constant temperature reaction for 4h, after cooling, crush the obtained black solid and add it to 3000mL of 1.0mol / L hydrochloric acid / chlorination Saturated solution of sodium, after boiling slightly, cool, filter and dry.

[0033] Step 2: Add the dried product after synthesis into 3000mL of sodium hydroxide solution and heat to 110°C, react at this temperature until no ammonia gas is released; cool the solution, pour it into 5000mL of deionized water, and use 5.5mol / L hydrochloric acid solution to adjust the pH=3.0, let stand for 24 hours, and filter and separate after the product is completely precipitated.

[0034] Step 3: Wash the product obtai...

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Abstract

Disclosed is a preparation method for a high-capacity nanometer organic positive electrode material. The preparation method comprises the steps of 1, putting trimellitic anhydride, urea, nickel chloride hexahydrate and ammonium molybdate into a mortar to be mixed uniformly, putting the mixture into a drying oven to be dried, performing cooling and crushing and then adding a saturated solution of hydrochloric acid / sodium chloride, heating until reaching a slight boiling state, and then performing cooling, filtering and drying; 2, putting the synthesized and dried product into a sodium hydroxide solution to be heated, and then cooling the solution, mixing with deionized water, and adjusting pH by a hydrochloric acid solution, and after the product is fully precipitated, performing separation by filtering; 3, washing the product obtained in the step 2 by deionized water and methyl alcohol for many times, and then putting into a vacuum box to be subjected to evaporation to remove a little residual low-boiling-point impurity to finally obtain a carboxyl substituted phthalocyanine compound; and 4, mixing phthalocyanine active material and a conductive agent I2 based on a certain proportion and then putting into a ball grinding mill to be subjected to ball grinding, adding a mixed glue solution into the ball-grinded and sieved powder and performing ball grinding again; and coating an aluminum foil with a slurry solution to obtain the positive electrode material.

Description

[0001] 【Technical field】 [0002] The invention relates to the technical field of lithium batteries, in particular to a method for preparing a high-capacity nanometer organic cathode material. [0003] 【Background technique】 [0004] With the rapid development of energy storage power supply and electric vehicles, the development of lithium-ion batteries with high energy density has become one of the focuses of research. The improvement of the performance of lithium-ion batteries largely depends on the characteristics of the cathode material. At present, the widely used inorganic cathode materials generally have defects such as limited capacity improvement, high energy consumption in the production process, potential safety hazards, and high costs. Traditional inorganic materials also have the following disadvantages: the actual available specific capacity does not exceed 200mAh / g, and the room for improvement is very limited. They all use non-renewable mineral deposits as raw ...

Claims

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Application Information

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IPC IPC(8): H01M4/60H01M4/139B82Y40/00B82Y30/00
CPCB82Y30/00B82Y40/00H01M4/139H01M4/60Y02E60/10
Inventor 陈鹏邓昌源钱龙许浩巴静
Owner OPTIMUM BATTERY CO LTD
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