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Non-aqueous electrolyte secondary battery

a secondary battery, non-aqueous electrolyte technology, applied in the direction of active material electrodes, non-aqueous electrolyte accumulator electrodes, cell components, etc., can solve the problems of cycle performance deterioration, and achieve the effect of reducing the expansion/contraction of silicon during charge/discharge and improving cycle performan

Inactive Publication Date: 2012-01-26
GS YUASA INT LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0011]According to the present invention, the said negative active material contains the composite particle (C), in which the silicon-containing particle (A) and the electronic conductive additive (B) are contained, and the carbon material (D), and hence the cycle life improves. The reasons for this have not been determined yet clearly; however, it is very likely that the presence of the electronic conductive additive (B) and the carbon material (D) causes the enhancement of the contact conductivity between the silicon-containing particle (A) and between the composite particle (C), respectively.
[0012]In addition, the weight of the electronic conductive additive (B) falls within the range of 0.5 wt. % to 60 wt. % to the weight of the composite particle (C), and hence the discharge capacity and the cycle performance improve. If the weight of the electronic conductive additive (B) is less than 0.5 wt. % to the weight of the composite particle (C), the amount of the electronic conductive additive (B) becomes insufficient to the amount of the silicon-containing particle (A), so that inadequate electronic conductivity causes the deterioration of the cycle performance. Meanwhile, if the weight of the electronic conductive additive (B) is greater than 60 wt. %, the discharge capacity per active material weight is reduced and, consequently, the battery discharge capacity becomes small.
[0014]According to the invention of claim 2, the silicon-containing particle (A) has a content of carbon, and hence the contact conductivity of silicon becomes better and this results in improvement in the cycle life. In addition, the composite particle (C) is configured by coating the silicon-containing particle (A) with the electronic conductive additive (B), and hence the cycle life improves. It is believed that the reason for this may be that since the particle (A) is coated with the electronic conductive additive (B), even when the active material is pulverized due to the active material expansion / contraction that occurs during charge / discharge, the deterioration of the contact conductivity is prevented.
[0016]According to the invention of claim 3, the proportion of the weight of the composite particle (C) to the total weight of the composite particle (C) and the carbon material (D) falls within the range of 60 wt. % to 99.5 wt. %, and hence the discharge capacity and the cycle life improve. If the proportion of the weight of the composite particle (C) to the total weight of the composite particle (C) and the carbon material (D) is less than 60 wt. %, the negative active material becomes insufficient, so that the discharge capacity decreases. If the proportion of the weight of the composite particle (C) is greater than 99.5 wt. %, the contact conductivity between the active material deteriorates, so that the cycle life is reduced.
[0023]In addition, carbon is contained in the composite particle (C), and hence the cycle life improves. The reason for this is that even when silicon or SiOx is pulverized during charge / discharge, a conductive pathway is kept by carbon, so that a decrease in the current collection efficiency can be inhibited.
[0025]According to the invention of claim 7, the composite particle (C) has a content of carbon and when measured at a temperature rising rate of 10±2° C. / min by thermogravimetry, it exhibits two stages of weight loss in the range of 30 to 1000° C., and hence the cycle performance is improved. The reasons for this can be explained as follows. Weight loss hardly occurs to silicon at a temperature range of 30 to 1000° C.; therefore, it is carbon that causes weight loss in such a temperature range. Carbon, depending on the different properties, will differ in the temperature at which weight loss starts. In the present invention, therefore, at least two different kinds of carbon should be contained in the composite particle (C). And containing different kinds of carbon in the negative active material allows the silicon expansion / contraction that occurs during charge / discharge to be reduced and, consequently, the contact conductivity in the particle of the negative active material can be retained.

Problems solved by technology

% to the weight of the composite particle (C), the amount of the electronic conductive additive (B) becomes insufficient to the amount of the silicon-containing particle (A), so that inadequate electronic conductivity causes the deterioration of the cycle performance.

Method used

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Examples

Experimental program
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embodiment a

Embodiment A1

[0084]Lithium cobalt oxide was used as a positive active material in the preparation of a non-aqueous electrolyte secondary battery of a prismatic type. FIG. 2 shows the cross sectional configuration of a non-aqueous electrolyte secondary battery of a prismatic type. In FIG. 2, the non-aqueous electrolyte secondary battery of a prismatic type is expressed as 41, winding-type electrodes as 42, an positive electrode as 43, a negative electrode as 44, a separator as 45, a battery case as 46, a battery cap as 47, a safety valve as 48, a positive terminal as 49, and a positive lead as 50.

[0085]The winding-type electrodes 42 is housed in the battery case 46, the battery case 46 is equipped with the safety valve 48, and the battery cap 47 and the battery case 46 are sealed up by means of laser welding. The positive terminal 49 is connected with the positive electrode 43 with the positive lead 50, and the negative electrode 44 is connected to the inner wall of the battery case ...

embodiments a2 to a5

, and Comparative Example A1

[0091]In these batteries, the following weight percentages were used as the amount of carbon coating in the composite particle (C): 0, 5, 40, 60, and 70 wt. %. Except for the above, the batteries have an identical configuration to that of Embodiment A1.

[0092]These non-aqueous electrolyte secondary batteries were charged at a constant current of 1 CmA and a constant voltage of 3.9 V at a temperature of 25° C. for 3 hours and made to reach a fully charged state. Subsequently, they were discharged at a current of 1 CmA until the voltages dropped to 2.45 V. These steps were taken as one cycle and the obtained discharge capacity was considered as the initial discharge capacity. After that, under the same conditions as the above, a total of 100 charge / discharge cycles were carried out, and the discharge capacity at the 1st cycle and a change in discharge capacity with an increase in the number of cycle times (capacity retention ratio according to cycle) were de...

embodiments a10 to a14

[0098]In these batteries, the following areas were used as the BET specific surface area of the composite particle (C): 1.0 m2 / g, 6.3 m2 / g, 10 m2 / g, 0.5 m2 / g, and 11.0 m2 / g. Except for the above, the batteries have an identical configuration to that of Embodiment A1.

[0099]In the same manner as the above, the discharge capacity at the 1st cycle and a change in discharge capacity with an increase in the number of cycle times (capacity retention ratio according to cycle) were determined. The results are shown in Table A3.

TABLE A3BET specificCapacity retentionDischargesurface arearatio accordingcapacity(m2 / g)to cycle (%)(mAh)EM A17.490640EM A101.085635EM A116.381638EM A1210.084620EM A130.562630EM A1411.079590

[0100]These results reveal that when the BET specific surface area of the composite particle (C) falls within the range of 1.0 to 10.0 m2 / g, satisfactory cycle performance is achieved. It is believed that when the BET specific surface area is less than 1.0 m2 / g, the current density ...

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Abstract

The present invention provides a non-aqueous electrolyte secondary battery including a positive electrode, a negative electrode having a negative active material, and a non-aqueous electrolyte; characterized in that the negative active material contains composite particle (C), which has silicon-containing particle (A) and electronic conductive additive (B), and carbon material (D), wherein the weight of the electronic conductive additive (B) falls within the range of 0.5 wt. % to 60 wt. % to the weight of the composite particle (C). The negative active material contains silicon which is capable of performing high discharge capacity, so that a non-aqueous electrolyte secondary battery having a large discharge capacity can be obtained. In addition, since the negative active material contains the electronic conductive additive (B) and the carbon material (D), the contact conductivity between the silicon-containing particle (A) or between the negative active material improves and, as a result, a non-aqueous electrolyte secondary battery having satisfactory cycle performance can be attained.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This is a divisional of application Ser. No. 10 / 513,664 filed Nov. 8, 2004, which is the National Stage of PCT / JP03 / 05654 filed May 6, 2003; the above noted prior applications are all hereby incorporated by reference.TECHNICAL FIELD[0002]The present invention relates to a non-aqueous electrolyte secondary battery.BACKGROUND ART[0003]In the past, carbon material has been used mainly as a negative active material for lithium-ion secondary batteries.[0004]These days, however, in the batteries which utilize carbon material as a negative active material, the discharge capacity is so enhanced as to be close to the theoretical capacity of carbon material. Such a present situation makes it difficult to further improve the discharge capacity of those batteries.[0005]In recent years, therefore, high-capacity negative active materials which can be alternatives to carbon material have been studied thoroughly. As one example of such high-capacity nega...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): H01M4/58H01M4/131H01M4/133H01M4/134H01M4/36H01M4/38H01M4/48H01M4/587H01M4/62
CPCH01M4/131H01M4/133H01M4/134H01M4/364H01M4/38H01M4/483H01M4/62H01M4/625H01M2004/021H01M2004/027Y02E60/122H01M4/366H01M4/587H01M4/386Y02E60/10H01M4/02H01M4/58H01M4/48H01M10/0525
Inventor TABUCHI, TORUAOKI, TOSHIYUKITESHIMA, MINORUNISHIE, KATSUSHI
Owner GS YUASA INT LTD
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