Fuel-cell catalyst with non-platinum core-shell structure and preparation method of fuel-cell catalyst

A fuel cell, shell structure technology, applied in chemical instruments and methods, physical/chemical process catalysts, battery electrodes, etc., can solve the problems of reducing the usage of precious metal Pt, cost, grain size and lack of microstructure, etc., to achieve the preparation method Simple and easy to implement, suitable for large-scale industrial production, and the effect of easy particle size

Inactive Publication Date: 2013-01-30
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is a lack of more precise control over cost, core composition, grain size, and microstructure, especially to further substantially reduce the use of noble metal Pt or replace Pt with other noble metals that are cheaper than Pt while maintaining the original catalytic performance. technical flaw

Method used

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  • Fuel-cell catalyst with non-platinum core-shell structure and preparation method of fuel-cell catalyst
  • Fuel-cell catalyst with non-platinum core-shell structure and preparation method of fuel-cell catalyst
  • Fuel-cell catalyst with non-platinum core-shell structure and preparation method of fuel-cell catalyst

Examples

Experimental program
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Effect test

Embodiment 1

[0021] Example 1: First, 10 mg of activated carbon was dissolved in 6 mL of ethanol solution, ultrasonicated for 30 min, and then a protective gas of argon was introduced and stirred. After 30 min, 9.8 mg of reducing agent sodium borohydride was added, and then 1.67 mL (1 g / 100 mL) of palladium chloride solution was added dropwise, and the stirring was continued for 15 min. After the reaction, filter, wash with ultrapure water for 4 times, and dry under vacuum at 70° C. for 2 hours to obtain carbon-supported palladium nanocrystals Pd / C.

Embodiment 2

[0022] Example 2: First, 15 mg of activated carbon was dissolved in 8 mL of ultrapure water, ultrasonicated for 40 min, and then a protective gas of argon was introduced and stirred. After 50 minutes, add 10 mg of reducing agent sodium borohydride, and then add 2 mL of ferrous chloride aqueous solution (0.09 M) dropwise. After 15 minutes of reaction, add 0.64 mL of palladium chloride aqueous solution (1 g / 100 mL) dropwise for displacement reaction, and continue stirring for 20 minutes. After the reaction, filter, wash with ultrapure water 4 times, and dry under vacuum at 60°C for 3 hours to obtain a non-platinum core-shell catalyst FePd / C with nanocrystalline iron Fe as the core and thin-layer nanocrystalline palladium Pd as the shell. .

Embodiment 3

[0023] Example 3: First, 12 mg of activated carbon was dissolved in 7 mL of ultrapure water, ultrasonicated for 45 min, and then a protective gas of nitrogen was introduced and stirred. After 50 minutes, 11 mg of reducing agent sodium borohydride was added, and then 2 mL of ferrous sulfate aqueous solution (0.09 M) was added dropwise. After reacting for 15 minutes, 0.6 mL of palladium chloride aqueous solution (1 g / 100 mL) was added dropwise for displacement reaction, and stirring was continued for 20 minutes. After the reaction, filter, wash 5 times with ultrapure water, and dry under vacuum at 50°C for 3 hours to obtain a non-platinum core-shell catalyst FePd / C with nanocrystalline iron Fe as the core and thin-layer nanocrystalline palladium Pd as the shell. .

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Abstract

The invention provides a fuel-cell catalyst with a non-platinum core-shell structure and a preparation method of the fuel-cell catalyst, and relates to a fuel-cell catalyst. A carrier of the catalyst is activated carbon, the active ingredient of the carrier is Fe-coated Pd, the molar ratio of nanocrystalline iron of the active ingredient Fe-coated Pd to palladium of the active ingredient Fe-coated Pd is 5:1, and the active ingredient Fe-coated Pd accounts for 40%-50% of the total mass of the fuel-cell catalyst with the non-platinum core-shell structure. The preparation method comprises the followings steps of: dissolving the activated carbon into water; performing ultrasonic treatment on the mixture; leading shielding gas in the mixture; adding reducing agents in the mixture; then adding a ferric salt aqueous solution in the mixture; reacting and then adding a palladium chloride aqueous solution in the mixture to perform replacement reaction; and filtering, washing and drying the mixture after the replacement reaction so as to obtain a product. The electrocatalytic activity of the catalyst is 10.63 times that of the traditional carbon load palladium nanocrystal Pd / C catalyst, and is 23.05 times that of a commercial Pt / C catalyst. The cost is low, the preparation method is simple and practicable, the particle size of the catalyst is easy to control, and the fuel-cell catalyst is suitable for large-scale industrial production.

Description

technical field [0001] The invention relates to a fuel cell catalyst, in particular to a fuel cell catalyst with a non-platinum core-shell structure and a preparation method thereof. Background technique [0002] Energy production and consumption are related to global climate change. Currently, 80% of energy consumption relies on fossil fuels—coal and oil. However, the traditional energy consumption has the following disadvantages: coal and oil are non-renewable resources and will be used up quickly; because the energy conversion of traditional heat engines is limited by the Carnot cycle, the utilization rate of combustion relative to energy is very low; a large number of fossils A large amount of carbon dioxide and CO produced by the combustion of fuel x , NO x pollutants, causing serious environmental problems such as the greenhouse effect and acid rain. The traditional energy structure and low utilization rate cannot meet the needs of efficient, clean, economical and ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/92B01J23/89
CPCY02E60/50
Inventor 陈秉辉廖梦垠陈国钦李云华尤桂荣郑进保
Owner XIAMEN UNIV
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