Preparation method of platinum nanoparticle electrocatalyst based on metal cluster approach
A technology of electrocatalyst and cluster compound is applied in the field of preparing platinum nano electrocatalyst, which can solve the problems of limited commercial development, catalyst poisoning, high polarization overpotential, etc.
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example 1
[0013] Example 1, the preparation of carbon-supported Pt (60wt.%) / C catalyst
[0014] 1. Weigh 159.7mg of Na 2 PtCl 6 6H 2 The anhydrous sodium acetate of O (metal platinum content 31.3%) and 170.0mg joins in the methyl alcohol of 30ml, Na 2 PtCl 6 6H 2 The concentration of O was 5.3 mg / ml. First pass high-purity nitrogen gas for 15 minutes to remove the air in the solution, then react in a CO atmosphere at 50°C for 20 minutes, and then react at room temperature and in a CO atmosphere for 24 hours to obtain a blue-green platinum cluster solution (group point A).
[0015] 2. Add 33.3 mg of Vulcan XC-72R activated carbon to the obtained component A under nitrogen protection, stir for 6 hours, evaporate methanol to dryness in a nitrogen atmosphere at 60°C, and cool to room temperature (component B).
[0016] 3. The component (B) is filtered, washed repeatedly, and tested with silver nitrate until there is no chloride ion, and then dried in nitrogen at 110° C. to obtain t...
example 2
[0018] The preparation of the nano-platinum catalyst of example 2 unsupported
[0019] 1. Weigh 159.7mg of Na 2 PtCl 6 6H 2 The anhydrous sodium acetate of O (metal platinum content 31.3%) and 170.0mg joins in the methyl alcohol of 30ml, Na 2 PtCl 6 6H 2 The concentration of O was 5.3 mg / ml. First pass high-purity nitrogen gas for 15 minutes to remove the air in the solution, then react in a CO atmosphere at 50°C for 60 minutes, and then react in a CO atmosphere at room temperature for 24 hours to obtain a blue-green platinum cluster solution (component A).
[0020] 2. Add 20 ml of a pre-prepared aqueous solution containing 3% sodium dodecylbenzenesulfonate to the obtained solution under the protection of nitrogen, stir continuously for 6 hours, and then cool to room temperature (component B).
[0021] 3. The component (B) is filtered, washed repeatedly, and tested with silver nitrate until there is no chloride ion, and then dried in nitrogen at 110° C. to obtain the fi...
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