Electrolyte and lithium ion secondary battery
A technology of electrolyte and lithium salt, which is applied in the field of electrolyte and can solve problems such as battery performance degradation
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[0120]
[0121] The method for preparing the electrolytic solution of the present embodiment may be a method as long as the above-mentioned non-aqueous solvent, the lithium salt, the above-mentioned fluorine-containing ether compound, and the above-mentioned optional components added as necessary can be uniformly dissolved or dispersed. , can be prepared in the same manner as known electrolytic solutions.
[0122] 《Lithium-ion secondary battery》
[0123] The lithium ion secondary battery of the present invention includes the electrolytic solution of the present invention described above. As for the configuration other than the electrolytic solution, a conventionally known configuration of a lithium ion secondary battery can be used.
[0124] Hereinafter, an embodiment having a usable configuration will be described.
[0125] As a configuration of the lithium ion secondary battery of the present embodiment, for example, an electrode element and an electrolytic solution in w...
Embodiment 1
[0156]
[0157] Will contain spinel LiNi 0.5 mn 1.5 o 4 A slurry of 92% by mass, 4% by mass of Ketjen Black, and 4% by mass of polyvinylidene fluoride was coated on a positive electrode current collector 1A made of aluminum foil (thickness 20 μm) and dried to prepare a positive electrode 1 with a thickness of 175 μm. In the same manner, a double-sided electrode obtained by coating the positive electrode 1 on both surfaces of the positive electrode current collector 1A and drying it was prepared.
[0158]
[0159] A slurry containing 85% by mass of SiO with an average particle diameter of 15 μm and 15% by mass of polyamic acid was coated on a negative electrode collector 2A made of copper foil (thickness 10 μm) and dried to prepare a negative electrode 2 with a thickness of 46 μm. The as-prepared anode was annealed at 350 °C for 3 h under a nitrogen atmosphere to cure the binder.
[0160]
[0161] The components shown in Table 1 were mixed so as to have the final conce...
Embodiment 2
[0167] When preparing the electrolytic solution, vinylboronic acid (N-methyliminodiacetic acid) methyl ester was further added as a boron compound so that the final concentration was 0.09% by mass, and it was carried out in the same manner as in Example 1.
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