A kind of solid polymer electrolyte and preparation method thereof
A technology of solid polymers and electrolytes, which is applied in the manufacture of electrolyte batteries, non-aqueous electrolyte batteries, circuits, etc. It can solve the problems of poor high-current discharge capacity of batteries, slow migration of lithium ions in interface impedance, and affecting battery rate performance.
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[0032] The invention provides a method for preparing a solid polymer electrolyte, comprising the following steps:
[0033] 1) first mixing the lithium salt, polyethylene oxide, auxiliary reagent and acetonitrile to obtain a raw material premix; the auxiliary reagent includes a rigid crosslinking agent and / or a flexible crosslinking agent;
[0034] 2) The raw material premix and the photoinitiator are mixed for the second time and left to stand to obtain a precursor solution;
[0035] 3) The precursor solution is poured on a flat plate, followed by light irradiation and drying to obtain a solid polymer electrolyte.
[0036] In the present invention, lithium salt, polyethylene oxide, auxiliary reagent and acetonitrile are first mixed to obtain a raw material premix. In the present invention, the polyethylene oxide is used as the main material of the solid polymer electrolyte, and its average molecular weight is preferably 400-5,000,000, more preferably 1,000-2,000,000, and most...
Embodiment 1
[0054] 1g of polyethylene oxide with a molar mass of 100000g / mol, 0.5g of the compound shown in formula I-1, 0.5g of tetraethylene glycol dimethyl ether, 0.3824g of lithium bistrifluoromethanesulfonimide and 1mL of anhydrous Acetonitrile was mixed, and stirred at a speed of 300r / min for 12h to obtain a raw material premix;
[0055] The raw material premix and 0.03g of 2-hydroxy-2-methyl-1-phenyl-1-propanone were mixed and heated, stirred at a speed of 300r / min at 50°C for 2h and then left to stand for 1h to obtain a precursor solution;
[0056] At 30°C, 0.5 g of the precursor solution was poured on a polytetrafluoroethylene flat plate using a spatula with a groove depth of 250 μm, and then a polyethylene film was covered on the poured polytetrafluoroethylene flat plate; The polytetrafluoroethylene plate of the ethylene film is irradiated under ultraviolet light for 15 minutes, wherein the wavelength of ultraviolet light is 365nm, and the intensity of ultraviolet light is 150m...
Embodiment 2
[0065] 1g of polyethylene oxide with a molar mass of 100000g / mol, 0.5g of the compound shown in formula I-2, 0.5g of tetraethylene glycol dimethyl ether, 0.3824g of lithium bistrifluoromethanesulfonimide and 1mL of anhydrous Acetonitrile was mixed, and stirred at a speed of 300r / min for 12h to obtain a raw material premix;
[0066] The raw material premix and 0.03g of 2-hydroxy-2-methyl-1-phenyl-1-propanone were mixed, heated, stirred at 300r / min for 2h at 50°C, and left to stand for 1h to obtain the precursor body solution;
[0067] At 30°C, 2 g of the precursor solution was poured on a polytetrafluoroethylene flat plate using a spatula with a groove depth of 250 μm, and then a polyethylene film was covered on the poured polytetrafluoroethylene flat plate; The PTFE plate of the film is irradiated with ultraviolet light for 15 minutes, wherein the wavelength of ultraviolet light is 365nm, and the intensity of ultraviolet light is 150mW / cm 2 After the light irradiation, the p...
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Abstract
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