Preparation method and application of precious metal electrocatalyst
An electrocatalyst and precious metal technology, applied in the field of precious metal electrocatalyst preparation, can solve the problems of easy growth and aggregation of platinum particles, increase production cost, complex synthesis steps, etc., and achieve a wide range of carrier selection, high oxygen reduction activity, and simple operation. Effect
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Embodiment 1
[0028] Add carbon nanotubes (23.5mg) and ammonia water (7.659mL, 100mM) to deionized water (39mL), add chloroplatinic acid (5.73mL, 20mM) solution, add chloropalladium acid (1.91mL, 20mM) solution, Add chloroauric acid (0.0191mL, 20mM) solution, sonicate for 30min, condense and reflux at 75°C for 2h, let it stand for precipitation, remove the supernatant, and then add NaBH 4 (7.659mL, 150mM) solution, stirred for 0.5h, the resulting precipitate was washed with deionized water until neutral, and dried under vacuum at 65°C. Heat treatment at 200°C for 2h under argon atmosphere.
Embodiment 2
[0030] Add carbon nanotubes (25mg) and ammonia water (7.659mL, 100mM) into deionized water (31mL), add chloroplatinic acid (19.225mL, 20mM) solution, sonicate for 30min, reflux at 75°C for 1h, let stand to precipitate, Remove supernatant, then add KBH 4 (19.225 mL, 150 mM) solution, stirred for 1 h, washed the obtained precipitate with deionized water until neutral, and dried in vacuum at 65 °C. Heat treatment at 200°C for 2h under argon atmosphere.
Embodiment 3
[0032] Graphene (23.5mg) and ammonia water (7.659mL, 100mM) were added in deionized water (39mL), chloroplatinic acid (5.73mL, 20mM) solution was added, chlororhodium acid (1.91mL, 20mM) solution was added, ultrasonic 30min, reflux at 75°C for 2h, set aside for precipitation, remove the supernatant, then add NaBH 4 (7.659mL, 150mM) solution, stirred for 1h, the resulting precipitate was washed with deionized water until neutral, and dried under vacuum at 65°C. Heat treatment at 200°C for 2h under argon atmosphere.
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