Fuel cell oxygen reduction catalyst with high performance and low pt loading and preparation method thereof
A fuel cell, high-performance technology, applied to battery electrodes, circuits, electrical components, etc., can solve the problems of high raw material prices, low utilization rate of precious metals, complicated preparation methods, etc., and achieve easy operation, excellent electrochemical performance, and production short cycle effect
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Embodiment 1
[0041] (1) Add 0.316g of ellagic acid and 0.46g of zinc acetate dihydrate into a beaker containing 50mL of N-methylpyrrolidone, ultrasonicate for 30min, stir for 60min, centrifuge and dry at 55°C to obtain 0.53g of product, the prepared carrier Labeled Zn-MOF.
[0042] (2) Weigh 530 mg of Zn-MOF prepared in step (1), add it into a beaker containing 100 mL of ethanol, and add chloroplatinic acid hexahydrate (13 mg of chloroplatinic acid hexahydrate) containing 5 mg of platinum at the same time, after ultrasonication for 30 min Stir for 5h, dry by rotary evaporation at 65°C, then place the product in a quartz boat and place it in a tube furnace under argon hydrogen (Ar:H 2 =9:1) Calcination at 950°C for 60min in a mixed atmosphere, tube furnace at room temperature at 5°Cmin -1The heating rate is raised to 950°C, and the prepared catalyst is marked as PtZn / C, wherein the mass percentage of platinum in the catalyst is 5%, and the catalyst is analyzed by TEM and SEM (such as Fig...
Embodiment 2
[0052] (1) Add 0.316g of ellagic acid and 0.46g of zinc acetate dihydrate into a beaker containing 50mL of N-methylpyrrolidone, ultrasonicate for 30min, stir for 60min, centrifuge and dry at 55°C to obtain 0.53g of product, the prepared carrier Labeled Zn-MOF.
[0053] (2) Weigh 530 mg of Zn-MOF prepared in step (1), add it into a beaker containing 100 mL of ethanol, and add different masses of chloroplatinic acid hexahydrate (according to the mass percentage of Pt in the catalyst is 2.8 %, 4.0%, and 6.0% were added with chloroplatinic acid hexahydrate), stirred for 5 h after ultrasonication for 30 min, and dried by rotary evaporation at 65 ° C. Then, the product was added to a quartz boat and placed in a tube furnace. Ar: H 2 =9:1) Calcination at 950°C for 60min in a mixed atmosphere, tube furnace at room temperature at 5°Cmin -1 The heating rate is increased to 950°C, and the prepared catalyst is marked as PtZn / C-x%.
[0054] (3) Add 50 μL of Aldrich’s Nafion solution wit...
Embodiment 3
[0056] (1) Add 0.316g of ellagic acid and 0.46g of zinc acetate dihydrate into a beaker containing 50mL of N-methylpyrrolidone, ultrasonicate for 30min, stir for 60min, centrifuge and dry at 55°C to obtain 0.53g of product, the prepared carrier Labeled Zn-MOF.
[0057] (2) Weigh 530 mg of Zn-MOF prepared in step (1), and then place the product in a quartz boat and place it in a tube furnace under argon hydrogen (Ar:H 2 =9:1) Calcination at 950°C for 60min in a mixed atmosphere, tube furnace at room temperature at 5°Cmin -1 The heating rate was increased to 950°C, and the prepared catalyst was labeled as MOF-C.
[0058] (3) Add 50 μL of Nafion solution with a mass fraction of 5% produced by Aldrich to a beaker containing 950 μL of ethanol solution, then add 5 mg of the MOF-C catalyst prepared in step (2), and disperse it ultrasonically for 30 minutes to obtain a mixed solution ; 18 μ L of the above solution was drip-coated on a glassy carbon electrode, and after drying at roo...
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