Preparation method of carbon foam with high electrochemical performances
A carbon foam and electrochemical technology, applied in the field of carbon foam preparation, can solve the problems of low electrical conductivity and unsatisfactory electrochemical performance, and achieve the effects of improving electrical conductivity, good charge-discharge cycle performance, and improving wetting performance
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Embodiment 1
[0015] According to phenol: formaldehyde: sodium metavanadate: EO 20 PO 70 EO 20 : sodium hydroxide: absolute ethanol = 1: 1: 0.01: 1: 0.01: 100 by weight, and mixed uniformly to obtain a carbon foam precursor solution. The obtained carbon foam precursor solution was placed in an environment of 15° C. to completely evaporate the solvent to obtain a solid carbon foam precursor. The obtained solid carbon foam precursor was cured at 100°C for 24h, and then carbonized at 600°C for 10h under the protection of a nitrogen atmosphere at a heating rate of 1°C / min to obtain a carbon foam. EO 20 PO 70 EO 20 It is a reagent-grade product purchased from Sigma-Aldrich Company of the United States, and other raw materials are commercially available.
[0016] Take the above-mentioned carbon foam by mass ratio: 12wt% polytetrafluoroethylene emulsion (purchased from Shanghai Sanaifu New Material Co., Ltd.): dehydrated alcohol=90:10:50, after mixing evenly, dry under the infrared lamp , t...
Embodiment 2
[0019] According to phenol: formaldehyde: sodium metavanadate: EO 20 PO 70 EO 20 : sodium hydroxide: absolute ethanol = 1: 4: 0.03: 2: 0.03: 100 mass ratio ratio weighed, mixed evenly to obtain a carbon foam precursor solution. The obtained carbon foam precursor solution was placed in an environment of 30° C. to evaporate the solvent to obtain a solid carbon foam precursor. The obtained solid carbon foam precursor was cured at 100°C for 12 hours, and then carbonized at 700°C for 5 hours at a rate of 30°C / min under the protection of a nitrogen atmosphere to obtain a carbon foam.
[0020] According to the method of Example 1, the carbon foam was used to make an electrode, and assembled into an electrochemical capacitor in a 7mol / L KOH solution. Under the condition that the current density is 100mA / g, the mass specific capacitance of the carbon foam material is increased by more than 5% compared with the carbon foam without vanadate; The mass specific capacitance of the carbo...
Embodiment 3
[0022] According to phenol: formaldehyde: sodium metavanadate: EO 106 PO 70 EO 106 : sodium hydroxide: absolute ethanol = 1: 0.6: 0.05: 2: 0.05: 100 mass ratio ratio weighed, mixed evenly to obtain a carbon foam precursor solution. The obtained carbon foam precursor solution was placed in an environment of 30° C. to evaporate the solvent to obtain a solid carbon foam precursor. The obtained solid carbon foam precursor was cured at 100°C for 12h, and then carbonized at 950°C for 3h at a rate of 60°C / min under the protection of a nitrogen atmosphere to obtain a carbon foam.
[0023] EO 106 PO 70 EO 106 It is a reagent-grade product purchased from Sigma-Aldrich Company of the United States, and other raw materials are commercially available.
[0024] According to the method of Example 1, the electrode made of this carbon foam was assembled into an electrochemical capacitor in a 7mol / L KOH solution. Under the condition that the current density is 100mA / g, the mass specific ...
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