Method for preparing carbon hollow sphere composite material with low platinum loading capacity, product and application
A technology of carbon hollow spheres and composite materials, which is applied in the direction of electrical components, battery electrodes, circuits, etc., and can solve problems such as unrealistic applications, unsatisfactory performance, and reduced catalyst activity.
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Embodiment 1
[0020] (1) According to the improved existing technology (Wei Wu, Wei Zhang, Yu Long, et al, Journal of Colloidand Interface Science 531 (2018) 642–653), prepare nickel-cobalt-doped polydopamine-coated silica Ball (PDA-Co 3 Ni 1 @SiO 2 ):
[0021] First, prepare silica balls with a diameter of 360 – 380 nm, that is, under constant stirring, slowly add 20 mL of ethyl orthosilicate to the mixture of 250 mL of ethanol, 100 mL of water and 13 mL of ammonia (containing 25wt ammonia). %) in the mixed solution, after the addition is complete, continue to stir at a constant speed for 3 hours, the resulting solid is centrifuged, and washed with water and ethanol 3 times each, 50 o Vacuum drying at C for 24 hours to obtain silica balls;
[0022] Next, ultrasonically disperse 1 g of the above silica balls in 2000 mL of water to form a uniform dispersion; then add 0.1 g of NiCl 2 ×6H 2 O and 0.3 g CoCl 2 ×6H 2 O, continue sonication, after complete dissolution, add 1 g of dopamine, continue so...
Embodiment 2
[0032] Steps (1) and (2) are the same as steps (1) and (2) of Example 1, respectively.
[0033] (3) Add 500 mg of the above rGO / Co 3 Ni 1 / C-N@SiO 2 The solid was mixed with 50 mL of absolute ethanol, sonicated to make the solid uniformly dispersed, and then 25 mg of chloroplatinic acid (H 2 PtCl 6 ×6H 2 O), after ultrasonic treatment of the obtained mixture for 4 hours, the ethanol was evaporated and dried in vacuum at room temperature, and the obtained solid was recorded as the nano-platinum precursor.
[0034] Steps (4), (5), (6), and (7) are the same as steps (4), (5), (6), and (7) of Embodiment 1, respectively.
[0035] The test results are listed in the table below:
[0036]
Embodiment 3
[0038] Steps (1) and (2) are the same as steps (1) and (2) of Example 1, respectively.
[0039] (3) Add 500 mg of the above rGO / Co 3 Ni 1 / C-N@SiO 2 The solid was mixed with 50 mL of absolute ethanol, sonicated to make the solid uniformly dispersed, and then 50 mg of chloroplatinic acid (H 2 PtCl 6 ×6H 2 O). After ultrasonic treatment of the obtained mixture for 4 hours, the ethanol was evaporated and dried under vacuum at room temperature. The obtained solid was recorded as the nano-platinum precursor.
[0040] Steps (4), (5), (6), and (7) are the same as steps (4), (5), (6), and (7) of Embodiment 1, respectively.
[0041] The test results are listed in the table below:
[0042]
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