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Porous carbon self-reduction preparation method of porous carbon loaded small-size precious metal nanoparticle composite material

A technology of metal nanoparticles and composite materials, which is applied in the field of nanomaterial preparation and electrocatalysis, can solve the problems of unreduced cost, complicated preparation steps, cumbersome preparation process, etc., and achieve excellent catalytic activity, high-efficiency catalytic activity, and simple synthesis method Effect

Active Publication Date: 2021-04-27
INST OF CHEM CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the methods for preparing high-efficiency noble metal electrocatalytic hydrogen evolution catalysts include: 1) increasing the effective area of ​​the catalyst, usually by designing special morphology (hierarchical structure, porous structure, etc.) to increase the contact area between the electrode and the electrode solution, but the metal loading of this method 2) Alloying with non-precious metals, introducing the second or third alloy through high temperature methods such as hydrothermal and calcination, the preparation steps are generally more complicated and energy consumption is high; 3) Find or prepare suitable Carrier: generally choose a material with good conductivity, many surface functional groups, and a large specific surface area as the carrier
[0005] There are various forms of carriers. At present, carbon materials are widely used, such as carbon nanotubes, graphene oxide, graphyne, etc. These carriers usually have cumbersome preparation processes and low cost performance.

Method used

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  • Porous carbon self-reduction preparation method of porous carbon loaded small-size precious metal nanoparticle composite material
  • Porous carbon self-reduction preparation method of porous carbon loaded small-size precious metal nanoparticle composite material
  • Porous carbon self-reduction preparation method of porous carbon loaded small-size precious metal nanoparticle composite material

Examples

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Embodiment 1-9

[0058] Examples 1-9: Preparation of porous carbon-supported small-sized noble metal nanoparticle composites

Embodiment 1

[0059] Example 1 Preparation of porous carbon-supported small-sized ruthenium nanoparticle composites

[0060] The small-sized ruthenium nanoparticle composite material supported by porous carbon is prepared according to the following steps:

[0061] (1) Using potassium citrate as a carbon source, calcining at 800° C. for 1 hour, acid soaking, washing, and drying to obtain the porous carbon material; the average pore diameter is 2.33 nanometers, and the specific surface area is 2208 square meters per gram.

[0062] (2) Add 40 mg of the above-mentioned porous carbon as a carrier to 25 ml of water, and ultrasonically disperse evenly;

[0063] (3) 0.2 millimoles of ruthenium trichloride hydrate was dissolved in 25 milliliters of water, and ultrasonically dispersed evenly;

[0064] (4) Add the porous carbon dispersion prepared in (1) to the ruthenium metal salt solution prepared in (2), stir at room temperature (25° C.) for 12 hours to complete the self-reduction reaction of th...

Embodiment 2

[0065] Example 2 Preparation of porous carbon-supported small-sized iridium nanoparticles composites

[0066] The porous carbon-supported small-sized iridium nanoparticle composite material was prepared according to the same method as in Example 1, except that the noble metal salt was replaced with iridium trichloride hydrate to obtain a porous carbon-supported small-sized iridium metal nanoparticle composite material.

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Abstract

The invention discloses a porous carbon loaded small-size precious metal nanoparticle composite material, and a porous carbon self-reduction preparation method and application of the composite material. An aqueous solution containing porous carbon and a metal salt is stirred, a self-reduction reaction is conducted on the metal salt under the action of the porous carbon in a stirring adsorption process, the metal nanoparticles obtained by reduction are loaded on porous carbon, and aftertreatment is conducted to obtain the porous carbon loaded metal nanoparticle composite material. The reduction potential of the porous carbon is lower than the reduction potential of the metal. Porous carbon which is low in price, easy to obtain, large in specific surface area, good in electrical conductivity, low in reduction potential and rich in surface functional groups is adopted as a self-reducing agent and a carrier, and the small-size precious metal nanoparticle composite porous carbon material high in dispersity is synthesized. Compared with other synthesis methods, the method has the advantages of effective reduction of the cost, simplicity, clear product, and facilitation of large-scale production; and the composite material obtained by the invention has excellent electrocatalytic hydrogen evolution and hydrogen oxidation reaction activity.

Description

technical field [0001] The invention belongs to the technical field of nanomaterial preparation and electrocatalysis, and in particular relates to a porous carbon-loaded small-sized noble metal nanoparticle composite material, a porous carbon self-reduction preparation method and application thereof. Background technique [0002] In order to reduce the environmental pollution caused by our high consumption of non-renewable fossil fuels, the development of clean and sustainable energy and its storage technology has received more and more attention in recent years. Among them, hydrogen has the highest energy density among all chemical fuels (142MJ kg -1 ), considered to be the ultimate clean energy. Among all kinds of fuel cells, hydroxide exchange membrane fuel cells (HEMFCs) have attracted much attention due to their high energy conversion efficiency, high power density, and good environmental compatibility. With water as the medium, the hydrogen evolution reaction (HER) a...

Claims

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Application Information

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IPC IPC(8): B01J23/46B01J35/10
CPCB01J23/462B01J23/468B01J23/464B01J35/394B01J35/33B01J35/60
Inventor 胡劲松明媚张云
Owner INST OF CHEM CHINESE ACAD OF SCI
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