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A kind of preparation method of three-dimensional graphene macrobody

A macroscopic, graphene-based technology, applied in ceramic products, other household appliances, hybrid capacitor electrodes, etc., can solve the problem of reducing the specific surface area of ​​materials, achieve the effect of increasing specific capacity, high conductivity, and improving electrochemical performance

Active Publication Date: 2021-08-06
GLOBAL ENERGY INTERCONNECTION RES INST CO LTD +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the three-dimensional graphene prepared by the existing redox method is prone to agglomeration and stacking due to the π-π interaction, van der Waals force and hydrophobicity, which not only inhibits the infiltration of the electrolyte and ion diffusion, but also significantly reduces the material loss. specific surface area

Method used

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  • A kind of preparation method of three-dimensional graphene macrobody
  • A kind of preparation method of three-dimensional graphene macrobody

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Take 100ml concentration is 3mg mL -1 Graphene oxide aqueous solution; Press graphene oxide and nickel salt mass ratio 1:30, take by weighing 9g nickel acetate; Press graphene oxide, Zn(NO 3 ) 2 ·6H 2 The mass ratio of O and 2-methylimidazole is 1:30:80, and 9g Zn(NO 3 ) 2 ·6H 2 O and 24g 2-methylimidazole; graphene oxide solution, nickel salt and Zn(NO 3 ) 2 ·6H 2 O was prepared in proportion and then ultrasonically treated for 2h, then added 2-methylimidazole, and stirred for 15min to obtain a mixed solution; then heated at 100°C for 5h to obtain a graphene hydrogel; the obtained graphene hydrogel was subjected to After freeze-drying, the three-dimensional graphene macroscopic body was obtained, and then reacted at 1000 ° C for 5 h under nitrogen atmosphere, and then the reaction product was mixed with 0.1 mol L -1 After immersing in nitric acid for 1-10 hours, it was repeatedly washed with deionized water and dried to obtain a composite macroscopic body of gr...

Embodiment 2

[0038] Take 100ml concentration as 5mg mL -1 Graphene oxide aqueous solution; Press graphene oxide and nickel salt mass ratio 1:10, take by weighing 5g nickel acetate; Press graphene oxide, Zn(NO 3 ) 2 ·6H 2 The mass ratio of O and 2-methylimidazole is 1:50:100, and 25g Zn (NO 3 ) 2 ·6H 2 O and 50g 2-methylimidazole; graphene oxide solution, nickel salt and Zn(NO 3 ) 2 ·6H 2 O was prepared in proportion and then ultrasonically treated for 2 hours, then added 2-methylimidazole, and stirred for 20 minutes to obtain a mixed solution; heated at 80° C. for 0.5 hours to obtain a graphene hydrogel; the obtained graphene hydrogel was subjected to After freeze-drying, the three-dimensional graphene macroscopic body was obtained, and then reacted at 800 ° C for 1 h under nitrogen atmosphere, and then the reaction product was mixed with 0.1 mol L -1After soaking in nitric acid for 8 hours, it was repeatedly washed with deionized water and dried to obtain a composite macroscopic b...

Embodiment 3

[0040] Take 100ml concentration as 0.1mg mL -1 Graphene oxide aqueous solution; by graphene oxide and nickel salt mass ratio 1:50, take by weighing 0.5g nickel acetate; by graphene oxide, Zn(NO 3 ) 2 ·6H 2 The mass ratio of O and 2-methylimidazole is 1:10:20, and 0.1g Zn(NO 3 ) 2 ·6H 2 O and 0.2g 2-methylimidazole; the graphene oxide solution, nickel salt and Zn(NO 3 ) 2 ·6H 2 O was prepared in proportion and then ultrasonically treated for 1 h, then added 2-methylimidazole, and stirred for 15 min to obtain a mixed solution; heated at 120°C for 1 h to obtain a graphene hydrogel; the obtained graphene hydrogel was frozen After drying, the three-dimensional graphene macroscopic body was obtained, and then reacted at 650 ° C for 5 h under nitrogen atmosphere, and then the reaction product was mixed with 0.1 mol L -1 Hydrochloric acid dipping for 7 hours, repeated washing with deionized water, and drying to obtain graphene and carbon nanotube composite macroscopic body.

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Abstract

The invention provides a method for preparing a three-dimensional graphene macroscopic body. The invention uses hydrothermal self-assembly to construct a three-dimensional macroscopic body, and at the same time synthesizes MOFs in situ between the layered structures of the graphene macroscopic body. The three-dimensional macroscopic body with hierarchical porous structure prepared by the present application not only has a high specific surface area, but also facilitates the diffusion and transmission of electrolyte ions, and the internal crosslinking structure constructed by graphene and carbon nanotubes acts as a conductive network to facilitate the transmission of electrons, effectively reducing the Interface resistance, while improving the specific capacity, rate and cycle performance of supercapacitors. The graphene-based macroscopic body prepared by the invention has stable structure, high specific surface area and high conductivity, and can be applied in supercapacitors. The preparation method of the invention has simple process, easy control of the reaction process, less investment in equipment, does not need to be carried out under vacuum and high pressure conditions, and can realize large-scale production.

Description

technical field [0001] The invention relates to a graphene for a supercapacitor, in particular to a method for preparing a composite three-dimensional macroscopic body of graphene and carbon nanotubes with a porous structure for a capacitor. Background technique [0002] Supercapacitors have the characteristics of high power density, fast charging and discharging, long cycle life of millions of times, and safety and reliability. They have broad application prospects in the fields of rail transportation, national defense, and aerospace. However, the disadvantage of low energy density of supercapacitors restricts its rapid development. For example, the energy density of commercial activated carbon supercapacitors is only 5-7Wh kg -1 . Therefore, in order to meet the growing demand for supercapacitors, it is one of the development trends in the field of new energy to develop lightweight supercapacitors with high energy density, power density and good cycle stability. [0003]...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C04B38/00C04B35/52C04B35/624H01G11/32H01G11/26
CPCC04B35/52C04B35/624C04B38/00C04B2235/422C04B2235/425C04B2235/96H01G11/26H01G11/32Y02E60/13
Inventor 徐丽刘双宇陈新韩钰盛鹏刘海镇赵广耀王博
Owner GLOBAL ENERGY INTERCONNECTION RES INST CO LTD