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A kind of porous carbon electrode material supporting metal oxide and preparation method thereof

A porous carbon electrode, metal-loaded technology, applied in chemical instruments and methods, carbon compounds, non-metallic elements, etc., can solve the problems of low energy density of activated carbon-based supercapacitors, affecting the performance of electrode materials, limited specific capacitance, etc., and achieve stability. Cycling performance, increasing storage, increasing the effect of specific capacitance

Active Publication Date: 2022-05-31
HAINAN UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When the specific surface area of ​​the activated carbon material used is not high, the specific capacitance it can contribute is extremely limited, making the energy density of activated carbon-based supercapacitors low
In addition, the surface modification of general activated carbon materials is difficult to achieve uniform loading, and it is easy to agglomerate, which greatly affects the performance of electrode materials.

Method used

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  • A kind of porous carbon electrode material supporting metal oxide and preparation method thereof
  • A kind of porous carbon electrode material supporting metal oxide and preparation method thereof
  • A kind of porous carbon electrode material supporting metal oxide and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] A. Place 8g of activated carbon powder in a hydrochloric acid solution with a concentration of 10% by volume, and the mass-volume ratio kg / L of activated carbon to hydrochloric acid solution is 1:200; and heat under reflux at 25-50°C for 5h, and filter the precipitate obtained by suction. drying;

[0030] B, the material obtained in step A is washed with deionized water at 25°C for 12h, and the mass-volume ratio kg / L of the material and deionized water is 1:500; the precipitate obtained by suction filtration is dried and repeated 3 times to obtain activated carbon material;

[0031] C, the activated carbon material obtained in step B is placed in a suction filter bottle, and the 0.03M FeCl is mixed with a burette 3 10ml of the aqueous solution was slowly dropped into a suction filter bottle under vacuum and kept shaking to obtain a mixture in a paste state, then ultrasonically immersed at 60°C for 1h, then dried at 120°C under vacuum for 5h, and finally placed in a tub...

Embodiment 2

[0034] A. Place 8g of activated carbon powder in a hydrochloric acid solution with a concentration of 10% by volume, and the mass-volume ratio kg / L of activated carbon to hydrochloric acid solution is 1:200; and heat under reflux at 25-50°C for 5h, and filter the precipitate obtained by suction. drying;

[0035] B, the material obtained in step A is washed with deionized water at 25°C for 12h, and the mass-volume ratio kg / L of the material and deionized water is 1:500; the precipitate obtained by suction filtration is dried and repeated 3 times to obtain activated carbon material;

[0036] C, the activated carbon material obtained in step B is placed in a suction filter bottle, and 0.05M FeCl is mixed with a burette 3 10ml of the aqueous solution was slowly dropped into a suction filter bottle under vacuum and kept shaking to obtain a mixture in a paste state, then ultrasonically immersed at 60°C for 1h, then dried at 120°C under vacuum for 5h, and finally placed in a tube fu...

Embodiment 3

[0039] A. Place 8g of activated carbon powder in a hydrochloric acid solution with a concentration of 10% by volume, and the mass-volume ratio kg / L of activated carbon to hydrochloric acid solution is 1:200; and heat under reflux at 25-50°C for 5h, and filter the precipitate obtained by suction. drying;

[0040]B, the material obtained in step A is washed with deionized water at 25°C for 12h, and the mass-volume ratio kg / L of the material and deionized water is 1:500; the precipitate obtained by suction filtration is dried and repeated 3 times to obtain activated carbon material;

[0041] C, the activated carbon material obtained in step B is placed in a suction filter bottle, and 0.1M FeCl is mixed with a burette 3 10ml of the aqueous solution was slowly dropped into a suction filter bottle under vacuum and kept shaking to obtain a mixture in a paste state, then ultrasonically immersed at 60°C for 1h, then dried at 120°C under vacuum for 5h, and finally placed in a tube furn...

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Abstract

The invention provides a porous carbon electrode material loaded with metal oxides and a preparation method thereof, comprising the following steps: A. placing activated carbon powder in a hydrochloric acid solution with a volume concentration of 8-10%, and heating and refluxing for 4-6h, and pumping The precipitate obtained by filtering is dried; B, the material obtained in step A is stirred and washed with deionized water, and the precipitate obtained by suction filtration is dried to obtain an activated carbon material; C, the activated carbon material obtained in step B is placed in a container In the method, metal ion modification is carried out by vacuum vibration equal volume impregnation method, and 0.03~0.1mol / LFeCl is mixed with a burette 3 The aqueous solution was dripped in a vacuum state and kept shaking to obtain a paste state mixture, then ultrasonicated at 25-60°C for 1-3h, then dried under vacuum at 110-120°C for 5-8h, and finally in the tube The temperature was raised to 400-450°C for 2-4 hours in a type furnace, and the sintering atmosphere was an inert atmosphere to obtain the target material. The electrode prepared by the invention improves the energy storage of the supercapacitor without changing the surface structure of the original activated carbon basically.

Description

technical field [0001] The invention relates to the field of preparation of supercapacitor electrode materials, in particular to a metal oxide-supported porous carbon electrode material and a preparation method thereof. Background technique [0002] The energy storage of traditional activated carbon-based supercapacitors is mostly limited by the electric double layer theory. According to the electric double layer theory, the specific capacity of activated carbon material is proportional to its specific surface area, that is, the larger the specific surface area, the larger the specific capacity. When the specific surface area of ​​the activated carbon material used is not high, the specific capacitance it can contribute is extremely limited, so that the energy density of the activated carbon-based supercapacitor is also low. In addition, the surface modification of general activated carbon materials is difficult to achieve uniform loading, and it is easy to produce agglomer...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01G11/86H01G11/24H01G11/26H01G11/32H01G11/46C01B32/354
CPCH01G11/86H01G11/24H01G11/26H01G11/32H01G11/46C01B32/354Y02E60/13
Inventor 陈永杜玉婷
Owner HAINAN UNIVERSITY
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