Self-assembled pd-cu bimetallic multi-dendritic nanocrystalline catalyst and its preparation and use
A bimetallic and catalyst technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, nanotechnology, etc., can solve problems such as no clear physical mechanism, achieve mild preparation conditions and simple method , the effect of convenient operation
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Embodiment 1
[0017] Embodiment 1: multi-dendritic palladium-copper bimetallic nanocrystal catalyst Pd 12.1 The preparation method of Cu
[0018] First, add 1.7mg copper chloride dihydrate, 87mg sodium dodecylbenzenesulfonate, and 352.2mg ascorbic acid into a 15ml wall-thick pressure-resistant bottle, add water to dissolve completely, and the total volume is 5mL. Then transfer to an 80°C oil bath and heat for 18h. After the reaction is completed, cool to room temperature, ultrasonicate for 5min to form a uniform copper sol, add 24mg of potassium bromide, stir for 5min, then transfer to a constant temperature water bath at 15°C, and use 0.043L / h Injection speed 5 mL of 10 mmol / L chloropalladium acid (containing 44.3 mg of palladium chloride and 1.25 mmol of aqueous hydrochloric acid) was added to the copper sol. After reacting for 2 hours, wash 3 times with a mixed solution of water and ethanol, and dry for later use.
Embodiment 2
[0019] Embodiment 2: Reaction steps of ethanol electrocatalytic oxidation
[0020] Preparation of electrodes: Electrochemical tests were performed in a three-electrode glass electrolytic cell. The working electrode is to drop the dispersed liquid of the catalyst in ultrapure water on the glassy carbon electrode (glassy carbon electrode, diameter 6mm, glassy carbon surface 3mm, area 0.07cm 2 ), dry naturally, drop 0.02% Nafion solution onto the surface of the catalyst, and dry it. The platinum wire is the counter electrode, and the reference electrode is Ag / AgCl.
[0021] Electrochemical performance test: at N 2 Cyclic voltammetry scanning was carried out in a saturated 1M NaOH solution with a scanning speed of 50mV·s -1 , the scanning range is -0.9 ~ 0.5V, after the curve is stable, the electrochemical active area is calculated. after N 2 Ethanol electrooxidation performance test was carried out in a saturated 1M EtOH+1M KOH solution, and the scanning speed was 50mV s -1 ...
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