Surface modification method of catalyst used for fuel cells
A technology of fuel cells and catalysts, applied in battery electrodes, circuits, electrical components, etc., can solve the problems of reduced electrochemical active area, increased overpotential, platinum nanoparticle poisoning, etc., to facilitate large-scale production and simple method Effect
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Embodiment 1
[0027] 1. Take 600 μL of 120.0 mM HO 2 PtCl 6 The aqueous solution was placed in a three-necked flask, and 55.0 mg of cetyltrimethylammonium bromide, 60.0 mg of ascorbic acid, and 60.0 ml of deionized water were added, and stirred to make the solution evenly mixed.
[0028] 2. Transfer the above solution to an oil bath at 100° C., heat and stir for 3 hours, add 5.3 mg of silver nitrate, react in an oil bath at 100° C. for 2 hours, and cool to room temperature.
[0029] 3. Add 50.0 mg of XC72 to the above solution, ultrasonically disperse it evenly, stir at room temperature for 12 hours, centrifuge, wash and dry.
[0030] 4. Mix 5 mg of the above catalyst with 2.5 ml of isopropanol and 20 μL of 5% Nafion aqueous solution, ultrasonically disperse the catalyst and Nafion in isopropanol evenly, take 6 μL of the suspension and apply it to a glassy carbon electrode, and use it as a working solution in a three-electrode system electrode, a platinum sheet as the counter electrode, a...
Embodiment 2 5
[0039] The steps are the same as in Example 1, except that the quality of silver nitrate added is 1.1 mg, 2.2 mg, 3.5 mg, and 11.0 mg, respectively, which are recorded as Pt 10 Ag 1 C. Pt 5 Ag 1 C. Pt 3 Ag 1 C. Pt 1 Ag 1 c.
[0040] Figure 6 for Pt 1 Ag 1 TEM image of C.
[0041] Figure 7 for Pt 10 Ag 1 C. Pt 5 Ag 1 C. Pt 3 Ag 1 C. Pt 2 Ag 1 C and Pt 1 Ag 1 XRD pattern of C before electrochemical treatment.
Embodiment 6
[0043] 1. Take 600 μL of 120.0 mM K 2 PtCl 4 The aqueous solution was placed in a three-necked flask, and 55.0 mg of cetyltrimethylammonium chloride, 60.0 mg of ascorbic acid, and 60.0 ml of deionized water were added, and stirred to make the solution evenly mixed.
[0044] 2. Transfer the above solution to an oil bath at 80°C, heat and stir for 3 hours, add 5.2mg CuSO 4 , reacted in an oil bath at 80°C for 2 hours, and cooled to room temperature.
[0045] 3. Add 50 mg of XC72 to the above solution, ultrasonically disperse it evenly, stir at room temperature for 12 hours, centrifuge, wash and dry.
[0046] 4. Mix 5.0 mg of the above catalyst with 2.5 ml of isopropanol and 20 μL of 5% Nafion aqueous solution, ultrasonically disperse the catalyst and Nafion in isopropanol evenly, take 6 μL of the suspension and apply it to a glassy carbon electrode, and use it as a three-electrode system Working electrode, platinum sheet as counter electrode, saturated calomel electrode as re...
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