Active material for nonaqueous secondary battery and nonaqueous secondary battery using same
A non-aqueous secondary battery and active material technology, applied in the direction of secondary batteries, non-aqueous electrolyte batteries, non-aqueous electrolyte batteries, etc., can solve problems such as poor high-temperature cycle characteristics, difficult coexistence of safe battery performance, and reduced capacity
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[0058] Hereinafter, although the present invention is still explained in detail by examples, the present invention is not limited to these at all. In addition, unless specifically stated otherwise, electrodes for charge / discharge tests and flat cells were produced according to the following methods.
[0059] In the mixture of composite particles and acetylene black conductive substance that can be doped / de-doped with alkali metal ions as active material, add active material: conductive substance: binding agent=86: 10: 4 (weight ratio) as A 1-methyl-2-pyrrolidone (hereinafter may be referred to as NMP) solution of PVDF as a binder, and kneading to obtain a paste. The paste was coated on a #100 stainless steel mesh as a current collector, and dried at 150° C. for 8 hours under vacuum to obtain an electrode.
[0060] By putting the obtained electrode; with a solution as an electrolyte, wherein ethylene carbonate (hereinafter may be referred to as EC), dimethyl carbonate (hereina...
Embodiment 1
[0078] (1) Synthesis of composite particles
[0079] In the glove box of argon atmosphere, a predetermined amount of aluminum isopropoxide (hereinafter may be referred to as AIPO) is dissolved in 2-propanol (hereinafter may be referred to as IPA) fully dehydrated with molecular sieves, and the composite particles R1 are dispersed, Then, it was taken out from the glove box, and the IPA was evaporated by a rotary evaporator, and the surface of the composite particle R1 was coated with AIPO. Here, the ratio of Al in the coated AIPO to Ni in the composite particles R1 was determined to be Al:Ni=0.02:0.85 (expressed in molar ratio). Then, it was hydrolyzed by standing still in a hygrostat maintaining a temperature of 30° C. and a relative humidity of 10% for 19 hours, and then dried at 50° C. for 4 hours in a vacuum. The dried product of gain is put into the tubular furnace that alumina core tube is arranged, in oxygen flow, roasts 1 hour at 720 ℃, obtains the powdered composite p...
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