Positive active material for rechargeable lithium batteries and method of preparing the same
a rechargeable lithium battery and active material technology, applied in the direction of nickel compounds, cell components, sustainable manufacturing/processing, etc., can solve the problems of difficult preparation in the desired structure, low capability of manganese-based materials, and high cost, so as to improve cycle life and power capacity , the effect of good voltage performan
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example 1
[0070]A 1% ethanol suspension of tetraethylorthosilicate was prepared by diluting 98% tetraethylorthosilicate (available from Aldrich Co.) suspension with ethanol. A 1% Al-isopropoxide ethanol suspension was prepared by dissolving Al-isopropoxide powders in ethanol.
[0071]The tetraethylorthosilicate ethanol suspension was mixed with the Al-isopropoxide ethanol suspension in equal volume ratios to provide a coating liquid having ½% Al and ½% Si.
[0072]100 g of LiCoO2 powder (available from UMKorea) was added to 40 ml of the coating liquid followed by mixing for about 10 minutes in an agitator to coat the LiCoO2 powder with the suspension. The resultant product was allowed to stand for 30 minutes, rendering separation of a solid fraction and a suspension fraction, then a solid phase material was obtained by removing the suspension fraction. The obtained solid phase material was dried at 100° C. for 10 hours, and an Al and Si-included hydroxide layer was formed on the surface of the LiCo...
example 2
[0074]A coin-type cell was fabricated by the same procedure as in Example 1, except that a 10% tetraethylorthosilicate suspension was mixed with a 10% Al-isopropoxide suspension to provide a coating liquid including 5% Al and 5% Si. The drying process was performed at 50° C. for 10 hours.
example 3
[0075]A coin-type cell was fabricated by the same procedure as in Example 1, except that a 2% tetraethylorthosilicate suspension was mixed with a 10% Al-isopropoxide suspension to provide a coating liquid including 5% Al and 1% Si. The drying process was performed at 85° C. for 10 hours.
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