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Carbon supported noble metal catalyst and method for preparing same

A precious metal catalyst, catalyst technology, applied in metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, physical/chemical process catalysts, etc. The problem of metal particle diameter in large catalysts can achieve the effect of improving battery performance, easy large-scale preparation, improving catalytic activity and anti-toxicity.

Inactive Publication Date: 2007-07-11
SOUTH CHINA UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0010] However, the above-mentioned preparation method still has defects. Since the stabilizer is closely combined with the metal particles after the reaction, the organic protective layer needs to be removed through high-temperature heat treatment or tedious washing procedures, especially high-temperature heat treatment, which increases the concentration of metal particles in the catalyst. Diameter, resulting in the aggregation of catalyst particles, so that the specific surface area of ​​the catalyst activity is reduced, and the catalytic performance is reduced

Method used

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  • Carbon supported noble metal catalyst and method for preparing same
  • Carbon supported noble metal catalyst and method for preparing same
  • Carbon supported noble metal catalyst and method for preparing same

Examples

Experimental program
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Effect test

Embodiment 1

[0037] (1) H 2 PtCl 6 ·6H 2 O, sodium citrate and Xc-72R carbon black are added together in the mixed solution of ethylene glycol and propylene glycol, the volume ratio of ethylene glycol and propylene glycol is 1:5; Ultrasound at room temperature for 10 minutes. H in the mixed solution 2 PtCl 6 ·6H 2 The mass volume concentration of O is 7g / L; the mass volume concentration of sodium citrate is 5g / L; the mass volume concentration of Xc-72R carbon black suspension is 10g / L.

[0038] (2) To the mixed solution obtained in step (1), add an ethylene glycol solution with a mass concentration of 10% KOH, adjust the pH to 8, and react under normal pressure with nitrogen protection for 4 hours, and the temperature is controlled at 120°C.

[0039] (3) cooling the mixed solution obtained in step (2) to room temperature, adding mass concentration is 10% HNO 3 aqueous solution, adjust the pH value to 1, and ultrasonically vibrate for 10 minutes.

[0040] (4) The mixed solution obtai...

Embodiment 2

[0044] (1) PdCl 2 , disodium edetate, and Xc-72R carbon black are added together to the alcohol reducing agent ethylene glycol and the solvent is a mixed solution of butanediol and water, and the volume ratio of butanediol to water in the solvent is 4: 1; Sonicate at room temperature for 30 minutes, mix PdCl in the solution 2 The mass volume concentration is 5g / L; the mass volume concentration of disodium edetate is 10g / L; the mass volume concentration of Xc-72R carbon black suspension is 10g / L; the volume ratio of reducing agent ethylene glycol to solvent is 1 : 3.

[0045] (2) Adding a butanediol solution of 10% KOH in mass concentration to the mixed solution obtained in step (1), adjusting the pH to 10, reacting in an autoclave for 3 hours, the temperature is controlled at 140° C.

[0046] (3) cooling the mixed solution obtained in step (2) to room temperature, adding mass concentration is 10% HNO 3 aqueous solution, adjust the pH value to 3, and ultrasonically vibrate f...

Embodiment 3

[0051] (1) RuCl 3 ·3H 2 O, sodium oxalate, and Xc-72R carbon black are added together to the mixed solution of propylene glycol and butanediol, the volume ratio of propylene glycol to butanediol is 1:1; ultrasonication at room temperature for 60 minutes, RuCl in the mixed solution 3 ·3H 2 The mass volume concentration of O is 1g / L; the mass volume concentration of sodium oxalate is 40g / L; the mass volume concentration of Xc-72R carbon black suspension is 4g / L.

[0052] (2) To the mixed solution obtained in step (1), add a propylene glycol solution with a mass concentration of 10% KOH to adjust the pH to 12, and react under normal pressure with nitrogen protection for 6 hours, and the temperature is controlled at 140° C.

[0053] (3) cooling the mixed solution obtained in step (2) to room temperature, adding mass concentration is 10% HNO 3 aqueous solution, adjust the pH value to 4, and ultrasonically vibrate for 30 minutes.

[0054] (4) The mixed solution obtained in step ...

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Abstract

The invention relates to a carbon-carrier metal catalyst, wherein the active component is 5-80%; the mol ration of metal atoms is 3:1-1:3; the metal diameter of catalyst is 1-4nm. And the production comprises that: adding active component, complex agent, alcohol reducer and carrier into solvent; functioning ultrasonic wave at room temperature, adding alkali material, adjusting the pH, adding nitrogen gas to protect reflux at normal pressure, or reacting at high-pressure kettle; cooling to room temperature, adding acid, breaking gel via ultrasonic wave; filtering, washing with water until there is no CI-ion detected; vacuum drying; thermally treating at inertia gas; cooling in nitrogen gas to obtain the carbon-carrier metal catalyst. The invention has simple process; the catalyst active component is two-dimension at the surface of carrier; it has small particles, low crystallization degree, high metal utilization, and high catalysis activity.

Description

technical field [0001] The invention belongs to the field of fuel cell catalysts, and specifically refers to a proton exchange membrane fuel cell catalyst, that is, a carbon-supported noble metal catalyst, and a preparation method of the catalyst. Background technique [0002] Fuel cells can directly convert chemical energy into electrical energy, and are recognized as an efficient and clean power generation technology. Among them, direct alcohol fuel cell (DAFC) and proton membrane fuel cell (PEMFC) have become the most adaptable fuel cell types due to their advantages such as low operating temperature, fast start-up, simple structure, and high energy conversion rate. However, the price of these two types of fuel cells is too high, the life is too short, and industrialization is difficult. The development of highly active and anti-poisoning catalysts is the most effective way to solve the above problems and is the key to the commercialization of fuel cells. [0003] The pr...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/89B01J23/38B01J21/18H01M4/92
CPCY02E60/50
Inventor 刘军民廖世军王荣方王宁卡特王润和周琛
Owner SOUTH CHINA UNIV OF TECH
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