Preparation method of oxygen reduction catalyst
A catalyst and nano-silicon dioxide technology, applied in electrical components, battery electrodes, circuits, etc., can solve the problems of low crustal reserves of platinum group metals, poor resistance to methanol poisoning, poor discharge performance, etc., and achieve high oxygen reduction catalytic activity And stability, high yield, good reproducibility
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Embodiment 1
[0035]The method for preparing a monoatomic copper oxygen reduction catalyst has the following preparation steps:
[0036]Step 1. Dissolve 1000 mg of glucosamine hydrochloride and 170.48 mg of copper chloride dihydrate in 10 ml of water to fully dissolve;
[0037]Step 2: Dissolve 1028.04 mg of nano-silica in it, and stir thoroughly to form a uniform suspension;
[0038]Step 3: Perform low-temperature freeze-drying of the suspension and select minus 5 to minus 10 degrees for freeze drying;
[0039]Step 4. After lyophilization, the product is pyrolyzed in an argon atmosphere at 900 degrees Celsius for 2 hours, and the temperature rises from room temperature to 900 degrees Celsius per minute for heat preservation pyrolysis;
[0040]Step 5. Put the pyrolyzed product in 2 moles per liter of sodium hydroxide aqueous solution at 80 degrees Celsius for 6 hours to remove nano-silica;
[0041]Step 6, washing and drying to obtain a monoatomic copper oxygen reduction catalyst.
Embodiment 2
[0043]The preparation process is basically the same as that of Example 1, and the difference is only: in step 4, the pyrolysis temperature is 800 degrees Celsius.
Embodiment 3
[0045]The preparation process is basically the same as that of Example 1, with the only difference being: in step 4, the pyrolysis temperature is 1000 degrees Celsius.
[0046]The prepared catalyst was characterized as follows. As attachedfigure 1 with2As shown, the monoatomic copper oxygen reduction catalyst sample prepared by the present invention has a cotton-like porous structure,figure 2 The inset is a selected area electron diffraction photograph of this area. It can be seen that the catalyst sample has a nanoporous structure with a pore size of 20±2 nanometers. Selected area electron diffraction is a typical amorphous form without any crystalline diffraction spots, indicating the sample The medium metal is dispersed and there is no bulk metal phase.image 3 The XRD diffraction pattern of the sample was obtained by the Rigaku MiniFlex600 X-ray diffractometer, and the scanning speed was 2° / min. It can be seen from the figure that there is only one carbon diffraction peak in the sam...
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