VOx (at) C three-dimensional interconnection structure material with adjustable oxidation state as well as preparation method and application of VOx (at) C three-dimensional interconnection structure material
A technology of three-dimensional interconnection and structural materials, applied in the preparation/purification of carbon, vanadium oxide, hybrid/electric double layer capacitor manufacturing, etc., can solve the problems of poor stability and low conductivity, and achieve low cost and high specific capacitance , Easy to operate and controllable effect
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[0043] The invention provides a VO with adjustable oxidation state x @C Preparation method of three-dimensional interconnected structure material composed of irregular nanoparticles. The prepared method includes the assistance of biomass chitosan, combined with solvothermal and high temperature annealing methods, successfully prepared a VO x A three-dimensional interconnected structure material composed of @C irregular nanoparticles, and as a supercapacitor positive and negative electrode material, has a high specific capacitance.
[0044] In the above technical scheme, in order to prove that V 2 o 5 @C-3 has excellent specific capacitance performance when used as a positive electrode material for supercapacitors. Preferably, the synthesized V 2 o5 -1 material is used as positive electrode material in supercapacitor for comparison.
[0045] In the above technical scheme, in order to prove that V 2 o 5 @C-3 has excellent specific capacitance performance when used as a po...
Embodiment 1
[0051] 1. Preparation of VO x Precursor:
[0052] (1) Configuration solution: 200mg ammonium metavanadate (NH 4 VO 3 ) was dissolved in 2mL of glacial acetic acid and deionized water mixed solution (V 1 :V 2 =1:40), through the oil bath method, the temperature is 60°C, and the time is 3h, to obtain a homogeneous solution.
[0053] (2) Transfer the above solution to a Teflon-coated reaction kettle, put it into an oven for reaction, the reaction temperature is 180° C., and the reaction time is 12 hours.
[0054] (3) Post-reaction treatment: After washing and centrifuging the precipitate obtained in step (2), put it in a vacuum drying oven at 50-70°C and dry it to constant weight to obtain VO x Precursor.
[0055] 2. High temperature annealing forms large flake V 2 o 5 :
[0056] (1) High temperature annealing: the obtained VO x The precursor product was transferred to a tube furnace, fed with nitrogen, and annealed at 400 °C for 2 h to form V 2 o 5 , denoted as V 2 ...
Embodiment 2
[0062] 1. Preparation of VO x @C Precursor:
[0063] (1) Configuration solution: a certain quality of chitosan (50mg) was dissolved in 2mL of glacial acetic acid and deionized water mixed solution (V 1 :V 2 =0.5:20), stirred evenly, recorded as A solution. Then 200mg ammonium metavanadate (NH 4 VO 3 ) was dissolved in 20mL deionized water, stirred evenly, and recorded as solution B. Then transfer solution A to solution B, and heat it in an oil bath at 60°C for 3 hours to obtain a homogeneous solution.
[0064] (2) Reaction preparation: transfer the above solution into a Teflon-coated reaction kettle, put it into an oven for reaction, the reaction temperature is 180° C., and the reaction time is 12 hours.
[0065] (3) Post-reaction treatment: After washing and centrifuging the black precipitate obtained in step (2), put it in a vacuum drying oven at 50-70°C and dry it to constant weight to obtain VO x @C Precursor.
[0066] 2. High temperature annealing to form V 2 o ...
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