Preparation method of zinc selenide/carbon fiber energy storage material and application thereof
A technology of energy storage materials and carbon fibers, applied in electrochemical generators, electrical components, battery electrodes, etc., can solve problems such as poor cycle stability and poor rate performance, achieve low production costs, increase transfer rates, and have good application prospects Effect
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Embodiment 1
[0024] A kind of preparation method of zinc / selenium oxide energy storage material, it comprises the steps:
[0025] Dissolve zinc oxalate and polyacrylonitrile in N,N-dimethylformamide. The concentration of zinc oxalate in the solution is 0.4mol / L, and the total mass ratio of polyacrylonitrile to the solution is 0.08:1. The dissolution condition was stirring in a water bath at 60°C for 30 minutes. Precursor fibers were prepared by electrospinning with a voltage of 13kV and a distance of 20cm between the nozzle and the receiver. Then, the mass ratio of the precursor fiber and selenium powder is 3:1, and the temperature is raised to 650°C under vacuum at a heating rate of 10°C / min, and maintained at 650°C, and the calcination time is 120min. After cooling, it is ground and sieved The energy storage material is obtained.
Embodiment 2
[0027] Dissolve zinc oxalate and polyacrylonitrile in N,N-dimethylformamide. The concentration of zinc oxalate in the solution is 0.3mol / L, and the total mass ratio of polyacrylonitrile to the solution is 0.1:1. The dissolution condition was stirring in a water bath at 60°C for 30 minutes. Precursor fibers were prepared by electrospinning with a voltage of 13kV and a distance of 20cm between the nozzle and the receiver. Then, the mass ratio of the precursor fiber and selenium powder is 3:1, and the temperature is raised to 650°C under vacuum at a heating rate of 10°C / min, and maintained at 650°C, and the calcination time is 90min. After cooling, it is ground and sieved The energy storage material is obtained.
Embodiment 3
[0029] Dissolve zinc oxalate and polyacrylonitrile in N,N-dimethylformamide. The concentration of zinc oxalate in the solution is 0.4mol / L, and the total mass ratio of polyacrylonitrile to the solution is 0.08:1. The dissolution condition was stirring in a water bath at 60°C for 30 minutes. Precursor fibers were prepared by electrospinning with a voltage of 15kV and a distance of 15cm between the nozzle and the receiver. Then, the mass ratio of the precursor fiber and selenium powder is 3:1, and the temperature is raised to 650°C under vacuum at a heating rate of 10°C / min, and maintained at 650°C, and the calcination time is 120min. After cooling, it is ground and sieved The energy storage material is obtained.
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