Lithium ion secondary battery and negative electrode piece of lithium ion secondary battery
A secondary battery and negative electrode technology, applied in the direction of secondary batteries, battery electrodes, non-aqueous electrolyte battery electrodes, etc., can solve the problems of poor battery cycle performance, battery polarization, large irreversible capacity loss, etc., and achieve high temperature Improved storage performance and charge-discharge rate performance, improved first-time charge-discharge efficiency, and improved ion-conducting performance
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Embodiment 1
[0034] Preparation of adhesive: After replacing the air in a three-necked glass flask with an inner volume of 2L with nitrogen, 364g of butyl acrylate, 150g of polyethylene glycol methyl ether acrylate (weight average molecular weight 480), polyethylene glycol Add 2 g of diacrylate (weight average molecular weight 600) into the flask; dissolve 0.2 g of azobisisobutyronitrile (AIBN) in 900 g of deionized water, add it to the above flask, and detect the content of acrylic acid by gas chromatography at the same time; polymerize After 20 hours at 50°C, the polymer was separated by decantation, vacuum-dried at normal temperature for 24 hours, and then vacuum-dried at 100°C for 10 hours to obtain 280 g of a polymer. The number average molecular weight of the polymer was measured to be 150,000, and the dispersion coefficient was 1.6.
[0035] Preparation of negative electrode sheet: Dissolve the polymer prepared above in deionized water, add carbon-coated Si powder used as negative e...
Embodiment 2
[0038] Preparation of adhesive: After replacing the air in a three-necked glass flask with an inner volume of 2L with nitrogen, 56g of methyl acrylate, 108g of polyethylene glycol methyl ether methacrylate (weight average molecular weight 480), polyethylene glycol 36g of diol dimethacrylate (weight average molecular weight 600) was added to the flask; 20g of benzoyl peroxide (BPO) was dissolved in DMF (1000g), and added to the above flask, and the concentration of methyl acrylate was detected by gas chromatography. Content: After the polymerization reaction was carried out at 100° C. for 16 hours, the polymer was separated by decantation, vacuum-dried at room temperature for 24 hours, and then vacuum-dried at 100° C. for 10 hours to obtain 196 grams of polymer. The number average molecular weight of the polymer was measured to be 350,000, and the dispersion coefficient was 1.5.
[0039] Preparation of negative electrode sheet: Dissolve the polymer prepared above in deionized w...
Embodiment 3
[0042] Preparation of adhesive: After replacing the air in a three-neck glass flask with an inner volume of 2L with nitrogen, add 67g of methyl methacrylate and 37g of polyethylenediamine dimethylacrylamide (weight average molecular weight 500) into the flask Medium; 1 g of azobisisoheptanonitrile (ABVN) was dissolved in 1000 g of DMF, and added to the above-mentioned flask, and the content of methyl methacrylate was detected by gas chromatography; after the polymerization reaction was carried out at 70 ° C for 40 hours, it was decanted The polymer was isolated, vacuum-dried at normal temperature for 24 hours, and then vacuum-dried at 80° C. for 10 hours to obtain 82 g of polymer. The number average molecular weight of the polymer was measured to be 500,000, and the dispersion coefficient was 1.7.
[0043] Preparation of negative electrode sheet: Dissolve the polymer prepared above in deionized water, add carbon-coated Si powder used as negative electrode active material and a...
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