Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation and application of a graphene/polyionic liquid-based carbon material

A polyionic liquid, graphene technology, applied in the direction of electrode shape/type, electrolysis components, electrodes, etc., can solve the problem of low catalytic activity

Active Publication Date: 2020-09-29
TONGXIANG BEITE TECH CO LTD
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, current research shows that the catalytic activity of graphene in electrochemical processes such as oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is very low. In order to reduce the electrode overpotential of these reactions, it is often necessary to use Graphene is composited with different materials

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
  • Preparation and application of a graphene/polyionic liquid-based carbon material
  • Preparation and application of a graphene/polyionic liquid-based carbon material
  • Preparation and application of a graphene/polyionic liquid-based carbon material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] The preparation of embodiment 1, GC-6

[0032] Dissolve PCMVImTf2N and GO in an appropriate amount of DMSO at a mass ratio of 6:1, and sonicate for 30 min to form a homogeneous solution; transfer the solution to a petri dish, dry at 80 °C for 4 h, and remove the solvent DMSO by volatilization to obtain Solid composite; soak the dried solid composite in an ammonia solution with a mass concentration of 0.2% for 2 h, take out the solution and dry it naturally to obtain a precursor material; then place the precursor material in a tube furnace, argon As an inert gas, first raise the temperature from room temperature to 300°C for 1 hour at a heating rate of 3°C / min, then raise the temperature from 300°C to 1000°C for 1 hour at a heating rate of 3°C / min; finally cool naturally to room temperature to obtain composite carbon Material GC-6.

[0033] The specific surface area of ​​GC-6 is 588.43 m2g -1 . At a current density of 10 mA cm -2 , the overpotentials were 327mV. In ad...

Embodiment 2

[0034] The preparation of embodiment 2, GC-7

[0035] Dissolve PCMVImTf2N and GO in an appropriate amount of DMSO at a mass ratio of 7:1, and sonicate for 30 min to form a uniform solution; transfer the solution to a petri dish, dry at 80 °C for 4 h, and remove the solvent DMSO by volatilization to obtain Solid composite; soak the dried solid composite in an ammonia solution with a mass concentration of 0.2% for 2 h, take out the solution and dry it naturally to obtain a precursor material; then place the precursor material in a tube furnace, argon As an inert gas, first raise the temperature from room temperature to 300°C for 1 hour at a heating rate of 3°C / min, then raise the temperature from 300°C to 1000°C for 1 hour at a heating rate of 3°C / min; finally cool naturally to room temperature to obtain composite carbon Material GC-7.

[0036] The surface area of ​​GC-7 is 723.61 m2g -1 . At a current density of 10 mA cm -2 , its overpotential is 112 mV. In addition, the T...

Embodiment 3

[0037] The preparation of embodiment 3, GC-8

[0038] Dissolve PCMVImTf2N and GO in an appropriate amount of DMSO at a mass ratio of 8:1, and sonicate for 30 min to form a uniform solution; transfer the solution to a petri dish, dry at 80 °C for 4 h, and remove the solvent DMSO by volatilization to obtain Solid composite; soak the dried solid composite in an ammonia solution with a mass concentration of 0.2% for 2 h, take out the solution and dry it naturally to obtain a precursor material; then place the precursor material in a tube furnace, argon As an inert gas, first raise the temperature from room temperature to 300°C for 1 hour at a heating rate of 3°C / min, then raise the temperature from 300°C to 1000°C for 1 hour at a heating rate of 3°C / min; finally cool naturally to room temperature to obtain composite carbon Material GC-8.

[0039] The specific surface area of ​​GC-8 is 695.12 m2g -1 . At a current density of 10 mA cm -2 , its overpotential is 363 mV. In additi...

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
surface areaaaaaaaaaaa
pore volumeaaaaaaaaaa
Login to View More

Abstract

The invention discloses the preparation of a graphene / polyionic liquid-based carbon material. The material is characterized in that polyionic liquid is taken as a nitrogen source and a sulphur source,the polyionic liquid is compounded with graphene oxide, an electrostatic cross-linking precursor material is obtained after deprotonation is conducted, and a porous GCs carbon material doped with N,Sis obtained by carbonizing. Through characterization tests of TEM, XRD, XPS, BET, Raman and the like, it is discovered that the composite carbon material has extremely high specific surface area reaching 723.61 m<2>g-1, and the material is a mesoporous material. Electrochemical tests show that the carbon material shows excellent catalyzing activities in hydrogen evolution reaction and an oxygen evolution reaction, and therefore the carbon material has excellent application prospect in the hydrogen evolution reaction and the oxygen evolution reaction.

Description

technical field [0001] The invention relates to the preparation of a composite carbon material, in particular to a method for preparing a graphene / polyionic liquid composite carbon material using polyionic liquid (PCMVImTf2N) and graphene oxide (GO) as raw materials, mainly used as a catalyst for electrolysis Water hydrogen production reaction. Background technique [0002] Hydrogen is an abundant, renewable and environmentally friendly clean fuel, which is considered to be an ideal substitute for today's fossil fuels. Among the many hydrogen production methods, hydrogen production by electrolysis of water has attracted the attention of many scholars due to its low cost, simple operation equipment and high purity of hydrogen produced. It is well known that Pt is an efficient electrocatalyst for the hydrogen evolution reaction. However, Pt-based catalysts are still not widely available at present due to their limited storage and high cost. Therefore, the development of ine...

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 Patents(China)
IPC IPC(8): C25B11/06C25B11/12C25B11/03C25B1/04
CPCC25B1/04C25B11/031C25B11/043Y02E60/36
Inventor 熊玉兵宋红红宋鹏飞王荣民
Owner TONGXIANG BEITE TECH CO LTD