A kind of co-n-c composite catalyst and its preparation method and application

A composite catalyst, co-n-c technology, applied in the field of electrocatalysis, can solve the problems of difficulty in maintaining the stability of catalytic current, unstable graphitized C structure, and reduced catalyst activity, so as to achieve multiple electrochemical reaction active sites and enhance ORR Good dynamics and stability

Inactive Publication Date: 2020-12-22
CENT SOUTH UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] So far, there are many types and methods of non-precious metal catalysts that can be developed. Among them, Co-N-C catalysts have high electrocatalytic activity and excellent anti-toxicity performance, which is a very potential low-cost ORR catalyst. Co and N co-doped carbon material catalysts have been proved to have excellent ORR catalytic activity, but as the reaction progresses, the catalytic activity decreases rapidly, and it is difficult to maintain the stability of the catalytic current. One of the important reasons is that the loss of Co leads to graphitization. The structure of C is unstable and the catalytic activity is reduced

Method used

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  • A kind of co-n-c composite catalyst and its preparation method and application
  • A kind of co-n-c composite catalyst and its preparation method and application
  • A kind of co-n-c composite catalyst and its preparation method and application

Examples

Experimental program
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Effect test

Embodiment 1

[0035] (1) Add 1 g of chitosan to 50 ml of distilled water and stir for 1 hour, add 10 drops of glacial acetic acid to dissolve the chitosan completely;

[0036] (2) Add 0.25g cobalt acetate and 1g urea, stir for 3h, make the cobalt ion fully carry out the chelation reaction with chitosan, and make the urea dissolve completely, move the mixed solution into a hydrothermal kettle with a magnetic stirring device, and the rotating speed is 300rpm , the hydrothermal temperature is 180°C, the reaction time is 8h, and the precursor solution is obtained;

[0037] (3) Add 0.2 g of carbon nanotubes to the precursor solution, stir for 1 h, put all the obtained solution into the liner of the reaction kettle, and put it in a drying oven for hydrothermal reaction. The hydrothermal temperature is 300 ° C, and the reaction time is 12 h. , the obtained product was placed in a freeze-drying box, dried for 72 hours, then put into a tube furnace (Ar gas) for calcining, the heating rate was 5°C / mi...

Embodiment 2

[0040] (1) Add 1 g of chitosan to 50 ml of distilled water and stir for 1 hour, add 10 drops of glacial acetic acid to dissolve the chitosan completely;

[0041] (2) Add 0.25g cobalt acetate and 1g urea, stir for 3h, make the cobalt ion fully carry out the chelation reaction with chitosan, and make the urea dissolve completely, move the mixed solution into a hydrothermal kettle with a magnetic stirring device, and the rotating speed is 300rpm , the hydrothermal temperature is 180°C, the reaction time is 8h, and the precursor solution is obtained;

[0042](3) Place the precursor solution in a freeze-drying oven, dry it for 72 hours, and then put it into a tube furnace (Ar gas) for calcining. The heating rate is 5°C / min. After rising to 900°C, it lasts for 2 hours. After cooling, the product is Sample 2 was obtained by grinding, and the obtained sample was used as a cathode material for an aluminum-air battery. The test method was as in Example 1. The electrochemical performance...

Embodiment 3

[0044] (1) Add 1 g of chitosan to 50 ml of distilled water and stir for 1 hour, add 10 drops of glacial acetic acid to dissolve the chitosan completely;

[0045] (2) Add 1 g of urea, stir for 3 hours to completely dissolve the urea, move the mixed solution into a hydrothermal kettle with a magnetic stirring device, the rotation speed is 300 rpm, the hydrothermal temperature is 180°C, and the reaction time is 8 hours to obtain a precursor solution;

[0046] (3) Add 0.2 g of carbon nanotubes to the precursor solution, stir for 1 h, put all the obtained solution into the liner of the reaction kettle, and put it in a drying oven for hydrothermal reaction. The hydrothermal temperature is 300 ° C, and the reaction time is 12 h. , the obtained product was placed in a freeze-drying box, dried for 72 hours, then put into a tube furnace (Ar gas) for calcining, the heating rate was 5°C / min, and continued for 2h after rising to 900°C, and the product was ground after cooling to obtain Sam...

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Abstract

The invention discloses a Co-N-C composite catalyst. The Co-N-C composite catalyst comprises a Co and N codoped carbon nanoparticle and CNTs (Carbon Nanotube), and the Co and N codoped carbon nanoparticle grows on the surface of the CNTs to form a three-dimensional net structure. The Co-N-C composite catalyst takes chitosan as a carbon source and chitosan and urea as nitrogen sources, the CNTs areadded, the Co-N-C / CNTs composite catalyst is synthesized through an in-situ transformation method, the synergistic effect of the Co-N-C and the CNTs obviously strengthens the ORR dynamics of the Co-N-C, the composite catalyst is applied to an aluminum-air battery cathode material, the limiting current density is up to 5.3 mA cm<-2> and is equivalent to that of a commercial Pt / C electrode (5.2 mAcm<-2>); the Co-N-C nanoparticle grows on the surface of the CNTs to form the three-dimensional net structure, so that the composite catalyst is better in electric conduction and has a large specificsurface area, more electrochemical reaction active sites are achieved, the adsorption of molecular oxygen is promoted, the catalysis is further carried out to reduce the molecular oxygen, then the catalytic activity of the ORR (Oxygen Reduction Reaction) is obviously improved; the process method is simple, the cost is low, the requirement on equipment is not high, and the Co-N-C composite catalystis suitable for large-scale production.

Description

technical field [0001] The invention belongs to the technical field of electrocatalysis, and in particular relates to a Co-N-C composite catalyst and a preparation method and application thereof. Background technique [0002] With the continuous consumption of fossil energy, the continuous increase of energy demand and the enhancement of environmental protection awareness, all countries in the world have turned their attention to new energy sources, and the development of a low-cost, high-performance energy conversion and storage device has become the key. Rechargeable metal-air batteries have attracted widespread attention due to their simple preparation, low cost, excellent safety performance and environmental friendliness. In the field of metal-air batteries, the biggest bottleneck is the cathode material-oxygen reduction (ORR) catalyst. At present, most of the cathode materials of metal-air batteries use precious metals such as platinum carbon, ruthenium, iridium, etc., ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/88H01M4/90H01M12/06
CPCH01M4/8825H01M4/9041H01M12/06
Inventor 史诗伟唐有根蒋金枝李静莎刘德培
Owner CENT SOUTH UNIV
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