A high-performance carbon paper-based electrode negative electrode composite material and its preparation method and application
A composite material and base electrode technology, applied in battery electrodes, circuits, electrical components, etc., can solve the problems of poor cycle stability, unenvironmentally friendly preparation process, low rate performance, etc., and achieve excellent charge-discharge performance, good cycle stability, good repeatability
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Embodiment 1
[0033] The hydroxylated carbon paper is prepared by ultrasonicating the carbon paper through a mixed solution of concentrated sulfuric acid / concentrated nitric acid (3 / 1 volume ratio) at 60°C for 1 hour.
[0034] Disperse 0.2g of Si powder in 10mL of 0.5% acetic acid aqueous solution, sonicate evenly, add 0.05g of P123, 0.3g of polystyrene balls, and continue to sonicate for 15min. The chitosan with a viscosity of 168cps was configured into 3.5% chitosan gel (containing 0.5% acetic acid). Take out 10g of chitosan gel and disperse it in the solution obtained by ultrasound, and stir it ultrasonically for 20 minutes; stir the solution under heating until viscous, apply it on hydroxylated carbon paper, and dry it in vacuum at 700°C 3h Ar gas sintering.
[0035] The sintered electrode is used as the negative electrode material of the lithium ion electrode, placed in the 2025 battery case, with the lithium sheet as the counter electrode, the polyethylene film as the separator, and ...
Embodiment 2
[0039] The hydroxylated carbon paper is prepared by ultrasonicating the carbon paper through a mixed solution of concentrated sulfuric acid / concentrated nitric acid (3 / 1 volume ratio) at 60°C for 1 hour.
[0040] Disperse 0.2g of Sn powder in 10mL of 1% acetic acid aqueous solution, sonicate for 20min, add 0.4g of F127, add 0.1g of polystyrene balls, and continue to sonicate for 15min. The chitosan with a viscosity of 500cps was configured into 3.5% chitosan gel (containing 1% acetic acid). Take out 5.8 g of chitosan gel and disperse it in the solution obtained by the above-mentioned ultrasound, and stir it ultrasonically for 20 minutes; stir the solution under heating until it becomes viscous, apply it on the hydroxylated carbon paper, and dry it in vacuum at 500 Degree 6h Ar gas sintering.
[0041] The obtained composite material is detected by SEM and TEM, and the structure of the material obtained in Example 1 is basically similar.
[0042] The sintered electrode is used...
Embodiment 3
[0044] The hydroxylated carbon paper is prepared by ultrasonicating the carbon paper through a mixed solution of concentrated sulfuric acid / concentrated nitric acid (3 / 1 volume ratio) at 60°C for 1 hour.
[0045] Disperse 0.2g of zinc manganate powder in 10mL of 0.5% aqueous acetic acid solution, ultrasonicate for 20min, add 0.2g of P123, add 0.2g of polystyrene balls, and continue ultrasonicating for 15min. Chitosan with a viscosity of 50 cps. was configured into 3.5% chitosan gel (containing 0.5% acetic acid). Take out 15g of chitosan gel and disperse it in the solution obtained by ultrasound, and stir it ultrasonically for 20 minutes; stir the solution under heating until viscous, apply it on hydroxylated carbon paper, and dry it in vacuum at 600°C 3h Ar gas sintering.
[0046] The obtained composite material is detected by SEM and TEM, and the structure of the material obtained in Example 1 is basically similar.
[0047] The sintered electrode is used as the negative ele...
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