Carbon-coated active-material complex and lithium-ion battery
A technology of active material and electrode active material, applied in the direction of active material electrodes, lithium batteries, non-aqueous electrolyte batteries, etc., can solve the problem of low electronic conductivity and achieve the effect of internal resistance suppression
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Embodiment 1
[0140] (Production of carbon-coated active material complex (electrode material))
[0141] In 2L (liter) of water, mix 4 mol of lithium acetate (LiCH 3 COO), 2mol of iron (II) sulfate (FeSO 4 ), 2mol of phosphoric acid (H 3 PO 4 ) to prepare a homogeneous slurry mixture.
[0142] Next, this mixture was stored in a pressure-resistant airtight container with a capacity of 8 L, and hydrothermal synthesis was performed at 200° C. for 1 hour.
[0143] Thereafter, the obtained precipitate was washed with water to obtain precursor particles of an electrode active material in the form of a filter cake.
[0144] On the other hand, 150 g (in terms of solid content) of the precursor of the electrode active material, an aqueous polyvinyl alcohol solution obtained by dissolving 7.0 g of polyvinyl alcohol (PVA) as an organic compound in 100 g of water, and 100 g of polyvinyl alcohol as a pore forming agent Phosphoric acid (H 3 PO 4 )0.001mol, lithium acetate (LiCH 3 COO) 0.001 mol w...
Embodiment 2
[0173] Phosphoric acid (H 3 PO 4 )0.005mol, lithium acetate (LiCH 3 COO) 0.005 mol was used as a pore forming agent, and the carbon-coated active material complex and lithium ion battery of Example 2 were produced similarly to Example 1, and it evaluated.
[0174] Table 1 shows the evaluation results.
Embodiment 3
[0176] Phosphoric acid (H 3 PO 4 )0.0005mol, lithium acetate (LiCH 3 COO) 0.0005 mol was used as a pore forming agent, and the carbon-coated active material complex and lithium ion battery of Example 3 were produced similarly to Example 1, and it evaluated.
[0177] Table 1 shows the evaluation results.
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