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Preparation method of nitrogen-doped porous carbon@cobalt-based catalyst nanocage composite material for lithium-oxygen battery

A nitrogen-doped porous carbon and cobalt-based catalyst technology is applied in fuel cell-type half-cells and secondary battery-type half cells, battery electrodes, nanotechnology, etc., and can solve the problems of low capacity, poor rate, and short cycle life. and other problems, to achieve the effect of high specific capacity, simple preparation process and low cost

Active Publication Date: 2020-07-28
深圳万知达科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The invention provides a method for preparing a nitrogen-doped porous carbon@cobalt-based catalyst nanocage composite material for a lithium-oxygen battery to overcome the problems of low capacity, poor magnification, and short cycle life faced by existing lithium-air batteries. The invention is simple and convenient. Fast, solves the problem of uniform dispersion of catalytically active substances and deposition of solid discharge products leading to passivation of the positive electrode

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Weigh 50 mg of 2-methylimidazole and cobalt nitrate, respectively, and dissolve them in methanol so that their concentrations are both 20 mmol / L. The 2-methylimidazole solution was added dropwise to the metal cobalt salt solution at a rate of 100 mL / min, and then left to stand for 12 hours to form a bulk MOF. The resulting product was centrifuged, washed repeatedly with ethanol, and dried in vacuum at 60°C. Weigh 50mg bulk MOF into 60mmol / L cobalt nitrate / zinc methanol solution, in which the mass ratio of metal cobalt salt and metal zinc salt is 10:90, and the concentration of bulk MOF in the mixed solution is 10mg / mL. The reaction time at 100°C was 6 hours. The resulting product was then centrifuged, washed repeatedly with ethanol and then dried under vacuum at 60 °C to obtain a hollow MOF. Then carbonize at 800°C for 6 hours under nitrogen. Finally, it was activated under air at 300 °C for 4 hours to obtain a three-dimensional nitrogen-doped porous carbon@Co 3 o 4...

Embodiment 2

[0038] Weigh 50 mg of 2-methylimidazole and cobalt nitrate, respectively, and dissolve them in methanol so that their concentrations are both 80 mmol / L. The 2-methylimidazole solution was added dropwise to the metal cobalt salt solution at a rate of 5 mL / min, and then left to stand for 24 hours to form a block MOF. The resulting product was centrifuged, washed repeatedly with ethanol, and dried in vacuum at 60 °C. Weigh 30mg bulk MOF into 80mmol / L cobalt nitrate / zinc methanol solution, in which the mass ratio of metal cobalt salt and metal zinc salt is 90:10, and the concentration of bulk MOF in the mixed solution is 90mg / mL. The reaction time at 100°C was 6 hours. The resulting product was then centrifuged, washed repeatedly with ethanol and then dried under vacuum at 60 °C to obtain a hollow MOF. Then carbonize at 600°C for 6 hours under nitrogen. Finally, it was activated under air at 300 °C for 4 hours to obtain a three-dimensional nitrogen-doped porous carbon@Co 3 o 4...

Embodiment 3

[0041] Weigh 50 mg of 2-methylimidazole and cobalt chloride, respectively, and dissolve them in methanol so that their concentrations are both 40 mmol / L. The 2-methylimidazole solution was added dropwise to the metal cobalt salt solution at a rate of 30 mL / min, and then left to stand for 1 hour to form a block MOF. The resulting product was centrifuged, washed repeatedly with ethanol, and then dried in vacuum at 60 °C. Weigh 20 mg of bulk MOF into 20 mmol / L cobalt chloride / zinc ethanol solution, wherein the mass ratio of metal cobalt salt and metal zinc salt is 50:50, and the concentration of bulk MOF in the mixed solution is 60 mg / mL. The reaction time was 6 hours at 100°C. The resulting product was then centrifuged, washed repeatedly with ethanol and then dried under vacuum at 60 °C to obtain a hollow MOF. Then carbonize at 1000°C for 1 hour under nitrogen. Finally, it was activated under air at 300 °C for 4 hours to obtain a three-dimensional nitrogen-doped porous carbon@...

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Abstract

The invention discloses a preparation method of a nitrogen-doped porous carbon@cobalt-based catalyst nanocage composite material for a lithium-oxygen battery. The method comprises the steps of firstlyweighing 2-methylimidazole and a cobalt metal salt and dissolving into a solvent separately to obtain a 2-methylimidazole solution and a cobalt metal salt solution; dropwise adding the 2-methylimidazole solution into the cobalt metal salt solution, or dropwise adding the 2-methylimidazole solution and the cobalt metal salt solution into an ethanol solvent at the same rate, standing and incubating, centrifugally separating the obtained product, repeatedly washing the product by using ethanol and then drying to obtain a bulk MOF; putting the bulk MOF into a mixed solution of the cobalt metal salt and a zinc metal salt, reacting at 60-150 DEG C for 1-12h, centrifugally separating the obtained product, repeatedly washing the product by using ethanol and then drying to obtain a hollow MOF; carbonizing the prepared hollow MOF in an inert atmosphere; and finally activating powder obtained after carbonization in an air atmosphere to obtain the nitrogen-doped porous carbon@cobalt-based catalyst nanocage composite material for the lithium-oxygen battery.

Description

technical field [0001] The invention relates to the field of new energy materials, in particular to a method for preparing a nitrogen-doped porous carbon@cobalt-based catalyst nanocage composite material for a lithium-oxygen battery. Background technique [0002] As chemical power sources (batteries) are widely used in various fields of human life, the development and utilization of safe, green and efficient secondary batteries has gradually become a global issue. Among them, lithium-air batteries have attracted special attention due to their ultra-high theoretical energy density. Lithium-air batteries have an open system, with metal lithium as the negative electrode and oxygen in the external environment as the positive electrode. The charge and discharge are completed through oxygen reduction reaction and oxygen evolution reaction. Its energy density is about ten times that of conventional lithium-ion batteries, and its light weight and low operating costs make it the most...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/90H01M12/08B82Y30/00B82Y40/00
CPCB82Y30/00B82Y40/00H01M4/9016H01M4/9083H01M12/08Y02E60/10
Inventor 王晓飞张晓侯雪丹郭守武刘毅郑鹏霍京浩张利锋
Owner 深圳万知达科技有限公司