Lithium secondary battery
A technology for lithium secondary batteries and battery casings, applied in secondary batteries, lithium storage batteries, batteries, etc., can solve problems such as increased risk, and achieve the effects of excellent safety, expansion inhibition, and good storage characteristics
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Embodiment 1
[0287]
[0288] The above-mentioned lithium-containing composite oxide A and LiCoO as other lithium-containing composite oxide 2 The mass ratio shown in Table 1 was measured and mixed for 30 minutes using a Henschel mixer to obtain a mixture. 100 parts by mass of the obtained mixture (positive electrode active material), 20 parts by mass of a solution of PVDF and P(TFE-VDF) dissolved in NMP as a binder, and an average fiber of a conductive additive were mixed using a twin-screw kneader. 1.04 parts by mass of carbon fibers with a length of 100 nm and an average fiber diameter of 10 nm were kneaded with 1.04 parts by mass of graphite, and NMP was added to adjust the viscosity to prepare a paste containing a positive electrode mixture. In addition, the usage amount of the NMP solution of PVDF and P(TFE-VDF) is such that the amount of dissolved PVDF and P(TFE-VDF) is higher than that of the lithium-containing composite oxide A and LiCoO 2 The amounts of 2.34% by mass and 0.26% ...
Embodiment 2~5、8
[0306] In addition to the above-mentioned lithium-containing composite oxide A and LiCoO in the positive electrode active material 2 The positive electrode prepared in the same manner as in Example 1, and the non-aqueous electrolytic solution prepared in the same manner as in Example 1 except that the mixing ratio was changed as shown in Table 1, except that the amount of TEPA added was as shown in Table 2. Other than that, it carried out similarly to Example 1, and produced the lithium secondary battery.
Embodiment 6
[0308] Except for using the positive electrode prepared in the same manner as in Example 1, except that the above-mentioned lithium-containing composite oxide B was used instead of the above-mentioned lithium-containing composite oxide A, and the addition amount of TEPA was changed as shown in Table 2, it was the same as in Example 1. A lithium secondary battery was produced in the same manner as in Example 1 except that the prepared non-aqueous electrolytic solution was handled in the same manner.
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