Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Layer combination controllable carbon material with nano pole of different scale, preparation method and application

A carbon material and nanopore technology, applied in the application field of electrochemical capacitor electrode materials, can solve the problems of low content, poor structure reproducibility, improvement of limiting performance and broadening of application range, etc., to achieve the effect of high-efficiency ion transport capacity

Inactive Publication Date: 2007-10-17
INST OF METAL RESEARCH - CHINESE ACAD OF SCI
View PDF0 Cites 47 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Although traditional chemical / physical activation methods can prepare activated carbon with a certain mesopore content, these mesopores are relatively small in size and relatively low in content, which limits the improvement of its performance and the broadening of its application range.
However, the process using mesoporous or microporous molecular sieves as a template has the disadvantages of long cycle, high cost, and poor structure reproducibility, which is not conducive to large-scale utilization.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Layer combination controllable carbon material with nano pole of different scale, preparation method and application
  • Layer combination controllable carbon material with nano pole of different scale, preparation method and application
  • Layer combination controllable carbon material with nano pole of different scale, preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022]Magnesium acetate and water are mixed and dissolved completely according to the weight ratio of 1:4 to form solution I. Sodium hydroxide, P123 and water are mixed and dissolved completely according to the weight ratio of 1:0.5:30 to form solution II, and then the above two solution systems are stirred and mixed at 20°C, and the weight ratio of magnesium acetate to sodium hydroxide is 1: 1. Under the action of a strong base (NaOH), the magnesium salt forms its hydroxide sol, and the ethanol solution of the alcohol-soluble phenolic resin is added (the weight ratio of the phenolic resin and ethanol is 1: 4), and the mixture of the phenolic resin and the magnesium salt is Adding the weight ratio is 1:1, after the phenolic resin is completely precipitated under the action of water, the solvent water and ethanol are evaporated and removed at 60°C (48 hours), and the phenolic resin / oxide composite material can be obtained, which is carbonized (600 °C, 6 hours, ammonia gas), was...

Embodiment 2

[0027] Nickel nitrate and water are mixed and dissolved completely according to the weight ratio of 1:5 to form solution I. Urea, CTAB and water are completely dissolved in a weight ratio of 1:1:20 to form solution II, and then the above two solution systems are stirred and mixed at 90°C. The weight ratio of nickel nitrate to urea is 1:3, and nickel nitrate is mixed in urea. Form its hydroxide sol under hydrolysis, add the ethanol solution of alcohol-soluble phenolic resin (the weight ratio of phenolic resin and ethanol is 1: 3), the adding weight ratio of phenolic resin and described nickel salt is 1: 1, treat phenolic resin After the resin is completely precipitated under the action of water, the solvent water and ethanol are evaporated and removed at 60°C (48 hours), and the phenolic resin / oxide composite material can be obtained, which is then carbonized (700°C, 6 hours, argon), and used Wash with hydrochloric acid to remove the template, mix the carbonized product and hyd...

Embodiment 3

[0031] Zinc chloride and water were mixed and dissolved completely in a weight ratio of 1:5 to form solution I. Sodium carbonate, Brij30 and water are mixed and dissolved completely according to weight ratio 1: 1: 30 to form solution II, then the above two solution systems are stirred and mixed at 10°C, the weight ratio of zinc chloride and sodium carbonate is 1: 3, Zinc chloride forms its carbonate / oxide composite sol in the double action of carbonate ion and water, adds the ethanol solution of alcohol-soluble phenolic resin (the weight ratio of phenolic resin and ethanol is 1: 6), phenolic resin and described zinc The weight ratio of the salt added is 1:2. After the phenolic resin is completely precipitated under the action of water, the solvent water and ethanol are evaporated and removed at 60°C (48 hours), and the phenolic resin / oxide composite material can be obtained and carbonized (800°C, 5 hours, argon), washed with hydrochloric acid to remove the template, mixed the ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
pore sizeaaaaaaaaaa
pore sizeaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to View More

Abstract

The invention relates to a method for design advanced materials with nano-scaled structure and techniques for preparing same. In particular, the invention relates to a carbon material capable of controllable laminated combination with the nano-holes of variable sizes and preparation and application thereof. The method comprises the steps of: preparing metal oxide sol in the alkali solution system, which is then mixed with an alcohol solution of an alcohol-soluble resin; the oxide sol being used as the template and water being the resin precipitation agent during the process to directly prepare resin / oxide sol composite system. After solvent removal, carbonization, activation and template removal processes, the carbon material with laminated nano-holes combination is prepared which is of controllable micro-holes proportion, controllable medium-holes aperture and proportion, controllable big-holes aperture and propotion and concentrated distribution of medium-holes and big-holes apertures. The carbon material capable of controllable laminated combination with the nano-holes of variable sizes prepared in the invention is characterized in laminated holes structure, excellent ion transfer performances and high electrochemical active specific surface area and the material is expected to be used as high energy density high power density electrochemical capacitor used electrode material.

Description

technical field [0001] The present invention relates to the design method and preparation technology of advanced materials with nanopore structure, specifically a design and preparation method of a new type of carbon material formed by a controllable combination of nanopores of different scales and its application as an electrode material for electrochemical capacitors . Background technique [0002] As an important energy storage element, electrochemical capacitors have attracted wide attention in various fields. However, conventional capacitors only have microfarads or picofarads of capacitance, which is greatly limited in application. It is very urgent to develop a capacitor with larger capacity, which can provide larger energy density and power density at the same time, and can play a role between batteries and traditional capacitors. As an energy storage device, capacitors need to have excellent instantaneous charge and discharge performance and good cycle performance...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C01B31/02
Inventor 成会明王大伟李峰刘敏逯高清
Owner INST OF METAL RESEARCH - CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products