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A kind of three-dimensional cobalt/carbon nanocomposite catalytic material and its preparation method and application

A carbon nanocomposite and catalytic material technology, applied in the field of three-dimensional cobalt/carbon nanocomposite catalytic materials and its preparation, can solve the problems of slow reduction reaction rate, scarce resources, weak resistance to methanol, etc., and achieve easy industrial production and preparation process Simple, adsorption-promoting effect

Active Publication Date: 2022-05-06
INST OF METAL RESEARCH - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, in the technical achievements at this stage, the reduction reaction rate of oxygen on the negative electrode material in the fuel cell is 6-7 orders of magnitude slower than that on the positive electrode. The development of efficient oxygen reduction catalytic materials directly restricts the development of fuel cell technology. Whether the technology can be further applied to the key scientific and technological issues
[0003] At present, the best oxygen reduction electrocatalytic material is platinum-based material, but platinum-based material is not only expensive and scarce resources, but also the electrocatalytic material of this system has poor stability and weak resistance to methanol
These defects severely restrict the commercialization of platinum-based oxygen reduction electrocatalytic materials and the further application of fuel cell technology.

Method used

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  • A kind of three-dimensional cobalt/carbon nanocomposite catalytic material and its preparation method and application
  • A kind of three-dimensional cobalt/carbon nanocomposite catalytic material and its preparation method and application
  • A kind of three-dimensional cobalt/carbon nanocomposite catalytic material and its preparation method and application

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preparation example Construction

[0030] The preparation process of Co / CoO@N-C catalyst is as follows:

[0031] (1) Preparation of three-dimensional cobalt-based in-situ templates: Take 0.111 g of ammonium fluoride, 0.291 g of cobalt chloride, and 0.3 g of urea in 25-45 ml of deionized water and stir for 30-60 minutes, then place them at 110-130 ° C Keep warm at high temperature for 250-350 minutes, wait for the temperature of the reaction kettle to cool down to room temperature, take out the pink precipitate, centrifuge, wash with water and alcohol for 5-8 times, and finally dry at 50-80°C for 6-8 hours (the The dried powder is heated to 350-450°C at a rate of 3-5°C per minute (, kept for 1-3 hours, and then naturally cooled to room temperature to obtain the three-dimensional cobalt-based in-situ template;

[0032] (2) Preparation of carbon-coated three-dimensional precursor: take 0.1-1 g (preferably 0.2-0.8 g) of the powder obtained in step 1 in 3-100 ml of glucose solution, and keep it warm at 170-190 ° C f...

Embodiment 1

[0040] Take 0.111 g of ammonium fluoride, 0.291 g of cobalt chloride and 0.3 g of urea in 30 ml of deionized water and stir for 40 minutes, then keep it at 120°C for 270 minutes, wait for the reaction kettle to cool down to room temperature, and take out the pink precipitate , centrifuged, washed with water and alcohol for 6 times, and finally dried at 60°C for 7 hours. The dried powder was heated to 400°C at a rate of 4°C per minute, kept for 2 hours, and then naturally cooled to room temperature. A powdery three-dimensional cobalt-based in situ template was obtained, which is a hollow sea urchin-like Co 3 o 4 ; 0.5 g of the obtained three-dimensional cobalt-based in-situ template powder was placed in 40 ml of glucose solution, kept at 180°C for 8 hours, cooled naturally to room temperature, centrifuged, washed with water and ethanol for 6 times, and then dried at 70°C After 10 hours, the carbon-coated three-dimensional precursor was obtained; the obtained carbon-coated thre...

Embodiment 2

[0042] Take 2.22 grams of ammonium fluoride, 5.82 grams of cobalt chloride and 6 grams of urea in 600 milliliters of deionized water and stir for 40 minutes, then keep warm at 120°C for 270 minutes, wait for the reaction kettle to cool down to room temperature, and take out the pink precipitate , centrifuged, washed with water and alcohol for 6 times, and finally dried at 60°C for 7 hours. The dried powder was heated to 400°C at a rate of 4°C per minute, kept for 2 hours, and then naturally cooled to room temperature. Obtain three-dimensional cobalt-based in-situ template powder; put 10 grams of the obtained three-dimensional cobalt-based in-situ template powder in 800 ml of glucose solution, keep it warm at 180°C for 8 hours, naturally cool to room temperature, centrifuge, wash with water and ethanol for 6 After drying for 10 hours at a temperature of 70°C, a carbon-encapsulated three-dimensional precursor was obtained; the obtained carbon-encapsulated three-dimensional precur...

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Abstract

The invention discloses a three-dimensional cobalt / carbon nanocomposite catalytic material and its preparation method and application, belonging to the technical field of energy and nanometer material preparation. Specifically, cobalt oxide with a three-dimensional sea urchin-like structure is used as an in-situ template, combined with a high-temperature nitrogen doping process to prepare high-performance cobalt-carbon nanocomposites. The three-dimensional cobalt / carbon nanocomposite catalytic material exhibits better activity, stability and methanol resistance than commercial platinum-carbon catalysts in alkaline electrolytes, and solves the problem of poor electrical conductivity and active site loss of oxide catalytic materials prepared by conventional methods problems, especially the large-scale production of key electrode materials for high-efficiency and low-cost fuel cells.

Description

technical field [0001] The invention belongs to the technical field of energy and nanometer material preparation, and specifically relates to a three-dimensional cobalt / carbon nanocomposite catalytic material and its preparation method and application. Background technique [0002] The massive exploitation and use of traditional fossil energy has not only caused the depletion of non-renewable energy, but also caused serious pollution to the environment. The main reason is that there are disadvantages in the traditional way of using fossil energy: on the one hand, fuel is usually burned to convert chemical energy into thermal energy or mechanical energy. Limited by the Carnot cycle, the conversion efficiency of this process is only 33-35%, resulting in non-renewable energy. On the other hand, when the fuel is burned, it will produce a large amount of waste water, waste gas, waste residue and other pollutants, causing damage to the ecological environment that is difficult to r...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/90B82Y30/00
CPCH01M4/9083H01M4/9016H01M4/9041B82Y30/00Y02E60/50
Inventor 李琦杨炜沂丁亚军
Owner INST OF METAL RESEARCH - CHINESE ACAD OF SCI