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A kind of activity optimization processing method of platinum nanocrystal catalyst

A treatment method, platinum nanotechnology, applied in the field of platinum nanocrystal catalyst activity optimization treatment, to achieve the effects of large active area, high oxygen reduction activity, and huge market benefits

Inactive Publication Date: 2016-01-20
LIAOCHENG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] However, there is no method to optimize a series of conditions for platinum nanocrystals as a good oxygen reduction catalyst.

Method used

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  • A kind of activity optimization processing method of platinum nanocrystal catalyst
  • A kind of activity optimization processing method of platinum nanocrystal catalyst
  • A kind of activity optimization processing method of platinum nanocrystal catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] Preparation of platinum nanocrystals, the specific preparation process is as follows:

[0047] Reflux 2.5ml ethylene glycol for 5min, add 0.5ml2×10 -3 MAgNO 3 solution, then, add 93.8 μL 0.375M polyvinylpyrrolidone (total 3mL, polyvinylpyrrolidone / platinic acid=12:1) and 46.9 μL 0.0625MH 2 PtCl 6 .6H 2 O (a total of 1.5mL) solution (the solvent is ethylene glycol) was added to the boiling ethylene glycol every 30s within 16min, the final mixture was refluxed for 5min, the product was centrifuged at 5000 rpm for 15min, and the supernatant was Separate, add three times of acetone to the resulting precipitate, then centrifuge at 3000 rpm for 5 min, collect the precipitate, ultrasonically disperse it in 3 ml of ethanol, then add 9 ml of n-hexane and centrifuge at 3000 rpm for 5 min, and finally The precipitate was washed twice in a mixed solvent of ethanol:n-hexane=1:3. Finally, the precipitate was dispersed in 18ml of water and sonicated for 20min. The as-synthesized...

Embodiment 2

[0052] 20%H at different temperatures 2 The 20%PtNCs-CNTs obtained in -80%Ar atmosphere treatment embodiment 1: put the gained 20%PtNCs-CNTs in the quartz boat, put the quartz boat into the quartz tube, then put the quartz tube into the tube furnace, 20%H 2 Heat treatment at different temperatures from 100 °C to 800 °C for 1 h in a -80% Ar atmosphere at a rate of 10 °C / min. The obtained samples were characterized as Figure 1C , D, E, F, G, H, as shown.

[0053] Use the 20% PtNCs-CNTs sample treated in this example to prepare a sample with a Pt concentration of 1 mg / ml, measure 1 ul and drop-coat it on the surface of the glassy carbon electrode, dry it, and drop-coat 0.5 ul of 0.5% nafion solution Fix the sample and use a three-electrode system (the glassy carbon electrode modified by the prepared sample is the working electrode, Pt is the counter electrode, Hg / HgSO 4 electrode as the reference electrode), at H 2 SO 4 and H 2 o 2 The mixed solution was treated for 20mi...

Embodiment 3

[0057] Treat the 20%PtNCs-CNTs prepared in Example 1 in an Ar atmosphere at 300°C: put the resulting 20%PtNCs-CNTs in a quartz boat, put the quartz boat into the quartz tube, and then put the quartz tube into the tube furnace , heated at a rate of 10 °C / min to 300 °C for 1 h in an Ar atmosphere, and its sample characterization is as follows Figure 1I .

[0058] Use the 20% PtNCs-CNTs sample treated in this example and the 20% PtNCs-CNTs sample obtained at the same temperature in Example 2 to prepare a sample with a Pt concentration of 1 mg / ml, and take 1 ul and drop-coat it on the glassy carbon Dry the surface of the electrode, apply 0.5ul of 0.5% nafion solution to fix the sample, and use a three-electrode system (the glassy carbon electrode modified by the prepared sample is the working electrode, Pt is the counter electrode, Hg / HgSO 4 electrode as the reference electrode), at H 2 SO 4 and H 2 o 2 The mixed solution was treated for 20min, and the cyclic voltammetry sca...

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Abstract

The invention relates to a platinum nanocrystal catalyst activity optimizing treatment method. The method comprises the following steps: (1) synthesizing a Pt nanocrystal; (2) adding the Pt nanocrystal into a solvent and performing centrifugal separation purification; (3) adding the purified Pt nanocrystal into a carbon nano-tube and performing ultrasonic mixing, thereby obtaining a carbon nano-tube loaded Pt nanocrystal; and (4) heating the obtained sample in a tubular furnace to 100-800 DEG C, and performing heat treatment for 1 hour under an Ar atmosphere or an H2-Ar mixed atmosphere. The invention provides a new optimizing method for preparing an electrochemical oxygen-reduction catalyst by processing the Pt nanocrystal, i.e., on the basis of the existing crystal, the size of the Pt nanocrystal and the morphology of a crystal surface can be changed via a certain treatment approach, so that the excellent electrochemical catalyst is finally obtained and the activity of the catalyst is enhanced by 1-3 times than that of an untreated catalyst.

Description

technical field [0001] The invention relates to an activity optimization treatment method of a platinum nanocrystal catalyst, so that it can be widely used in the field of electrochemical catalyst oxygen reduction system. Background technique [0002] At present, many research groups have synthesized platinum nanocrystals with different shapes, such as cubes, truncated cubes, or cube-octahedrons, etc. by colloidal methods, which has opened up a new path for catalysts. The catalyst activity depends not only on the particle size but also on the shape of the nanocrystals. However, to obtain effective catalytic properties, the polymer on the nanoparticle surface must be removed first, and many catalytic reactions occur at relatively high temperatures. Therefore, future applications will require heating of the catalyst, and the thermal stability of the nanocrystals involved in the shape change is very necessary for the activity of the catalyst. [0003] For hybrid catalysts, th...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J23/42H01M4/92
CPCY02E60/50
Inventor 蒋秀秀刘继锋
Owner LIAOCHENG UNIV