Carbon material for negative electrode of lithium secondary battery, negative electrode of lithium secondary battery, lithium secondary battery and method for producing carbon material for negative electrode of lithium secondary battery
A technology for lithium secondary batteries and carbon materials, applied in battery electrodes, lithium storage batteries, chemical instruments and methods, etc., can solve the problem that the negative electrode active material is difficult to achieve high capacity, achieve excellent charge-discharge cycle characteristics, and inhibit conductivity. The effect of reducing and simplifying the manufacturing process
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Embodiment 1
[0063] 135 parts by mass of novolac (novolak) type phenolic resin (PR-50237 manufactured by Sumitomo Bakelite Co., Ltd.) and 25 parts by mass of hexamethylenetetramine (Mitsubishi Gas Chemical Co., Ltd.), 50 parts by mass of silicon monoxide (average particle diameter: 1.2 μm) was further added, and stirred for 2 hours. After the stirring was completed, the obtained slurry was cured at 200° C. for 5 hours. After the curing treatment, the temperature was raised in a nitrogen atmosphere, and carbonization was performed for 1 hour after reaching 500°C. The obtained carbon material was pulverized until the average particle size reached 11 μm, and the temperature of the carbon material obtained by the pulverization treatment was further raised to 1100° C. and then carbonized for 10 hours to obtain a secondary battery carbon material. For the obtained carbon material, when measured by the following measurement method, the pore volume of 0.25 to 0.45 nm is 0.85 cm 3 / g, 55% by volu...
Embodiment 2
[0102] 135 parts by mass of novolac type phenolic resin (PR-50237 manufactured by Sumitomo Bakelite Co., Ltd.) and 25 parts by mass of hexamethylenetetramine (Mitsubishi Gas Chemical Co., Ltd.) were dissolved in a four-necked flask with 30 parts by mass of acetone added. Co., Ltd.), 30 parts by mass of silicon monoxide (average particle diameter: 3.3 μm) was further added, and stirring was performed for 3 hours. After the stirring, the obtained slurry was cured at 200° C. for 3 hours. After the curing treatment, the temperature was raised in a nitrogen atmosphere, and carbonization was performed for 1 hour after reaching 550°C. The obtained carbon material was pulverized until the average particle size reached 7 μm, and the temperature of the carbon material obtained by the pulverization treatment was further raised to 1150° C. and then carbonized for 10 hours to obtain a carbon material for secondary batteries. The 0.25-0.45nm micropore volume of the obtained carbon material...
Embodiment 3
[0104] 135 parts by mass of novolak-type phenolic resin (PR-50237 manufactured by Sumitomo Bakelite Co., Ltd.) and 25 parts by mass of hexamethylenetetramine (Mitsubishi Gas Chemical Co., Ltd.) were dissolved in a four-necked flask containing 45 parts by mass of acetone. Co., Ltd.), further added 45 parts by mass of silicon monoxide (average particle diameter: 0.7 μm), and stirred for 5 hours. After the stirring, the obtained slurry was cured at 200° C. for 3 hours. After the curing treatment, the temperature was raised in a nitrogen atmosphere, and after reaching 500° C., carbonization was performed for 3 hours. The obtained carbon material was pulverized until the average particle size reached 11 μm, and the temperature of the carbon material obtained by the pulverization treatment was further raised to 1100° C. and then carbonized for 5 hours to obtain a secondary battery carbon material. The resulting carbon material was evaluated in the same manner as in Example 1. As a ...
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