Pre-lithiated negative electrodes, secondary batteries including same, and methods for their manufacture
A secondary battery and pre-lithiation technology, which is applied in the field of secondary battery and the manufacture of the secondary battery, can solve the problems of metal lithium efficiency and lithium dendrite problem that have not been completely solved
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example 1
[0081] First, according to the conventional method, the graphite negative electrode active material is coated on the surface of the copper current collector, and the surface capacity is 3mAh / cm 2 .
[0082] Next prepare the reaction buffer layer. 0.98 g of polyvinylidene fluoride (PVDF) was added to 9 g of N-methylpyrrolidone (NMP) solution, and stirred in a stirrer at a speed of 1000 rpm for 30 min. After the PVDF was completely dissolved, 0.02 g of ketjen carbon (KB) was added, and stirring was continued at 800 rpm for 100 min to prepare a uniform reaction buffer layer slurry. Next, the slurry was coated on the surface of the negative electrode active layer with a 50 μm doctor blade, and then baked in a drying oven at 55° C. for 24 h. It was made into a pole piece with a diameter of 14 mm, and placed in a vacuum oven at 120° C. for 6 hours.
[0083] Then, in a specific environment such as a glove box, assemble a secondary battery in the order of metal, separator, lithium-...
example 2
[0091] First, according to the conventional method, the mixed negative electrode active material of silicon oxide and graphite is coated on the surface of the copper current collector. The capacity of this material is 600mAh / g, and the surface capacity of the coating is 3mAh / cm 2 .
[0092] Next prepare the reaction buffer layer. 0.99 g of polyacrylonitrile (PAN) was added to 9 g of N-methylpyrrolidone (NMP) solution, and stirred in a stirrer at a speed of 1000 rpm for 30 min. After the PAN is completely dissolved, add 0.01 g of acetylene black and continue to stir at 800 rpm for 100 min to prepare a uniform reaction buffer layer slurry. Next, the slurry was coated on the surface of the negative electrode active layer with a 50 μm doctor blade, and then baked in a drying oven at 55° C. for 24 h. It was made into a pole piece with a diameter of 14 mm, and placed in a vacuum oven at 120° C. for 6 hours.
[0093] Then, in a specific environment such as a glove box, assemble a ...
example 3-30
[0100]Examples 3-30 are examples of reaction buffer layers used with negative active materials according to some embodiments of the present invention. As previously mentioned, the reaction buffer layer includes a polymer and an electron conductor, and the electron conductor described herein encompasses mixed electron-ion conductors.
[0101] The polymer included in the reaction buffer layer can be selected from the following: polymer 1, polyvinylidene chloride (PVDF); polymer 2, polyvinylidene chloride-hexafluoropropylene (PVDF-HFP); polymer 3, polytetrafluoroethylene Polymer 4, polyethylene oxide; Polymer 5, polyester; Polymer 6, polyamide; Polymer 7, polymethyl methacrylate; Polymer 8, polycarbonate; Polymer 9 , carboxymethylcellulose; polymer 10, styrene-butadiene copolymer; polymer 11, polyacrylonitrile; polymer 12, sodium carboxymethylcellulose, polymer 13, sodium carboxymethylcellulose: Styrene-butadiene rubber = 1:1; polymer 14, polyacrylic acid; polymer 15, lithium po...
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