A preparing method and application of a positive electrode material of a lithium ion battery
A technology for lithium-ion batteries and cathode materials, applied in the field of functional material preparation, can solve the problems of difficult to provide high energy density, poor cycle stability, low specific capacity, etc., to increase lithium storage sites and maintain integrity. , the effect of prolonging the cycle life
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Embodiment 1
[0023] 1) First, synthesize vanadyl oxalate according to the existing literature: take (1.2g, 6.60mmol) of V 2 O 5 Add to 80 mL of water, and then add (2.4 g, 19.00 mmol) of oxalic acid dihydrate. Transfer the above aqueous solution to a 250 mL evaporating dish and stir at 60°C until it is completely dry, and then put it in a vacuum oven at 60°C to dry overnight.
[0024] 2) Synthesis of V@M-1 precursor: take Fe(NO 3 ) 3 ·9H 2 O (1.62g, 4.00mmol) was added to 4mL of water to dissolve, and then vanadyl oxalate (1.0g, 4.00mmol) prepared above was added to the above solution and stirred until completely dissolved. Another trimesic acid (420mg, 2.00mmol) was added to the above solution and stirred overnight. Finally, the above solution was transferred to a hydrothermal reactor, heated at 130°C for 24 hours, and then naturally cooled to room temperature. The product was washed twice with water, DMF and methanol in turn. Place it in a blast drying oven at 70°C and dry overnight, and ...
Embodiment 2
[0027] 1) First, synthesize vanadyl oxalate according to the literature: take (0.6g, 3.30mmol) of V 2 O 5 Add to 40 mL of water, and then add (1.2 g, 9.5 mmol) of oxalic acid dihydrate. The above aqueous solution was transferred to a 250 mL evaporating dish and stirred at 80°C until it was completely dry, and then placed in a vacuum oven at 60°C to dry overnight.
[0028] 2) Synthesis of V@M-1 precursor: take Fe(NO 3 ) 3 ·9H 2 O (2.02g, 5.00mmol) was added to 5mL of water to dissolve, and then vanadyl oxalate (1.0g, 4.0mmol) prepared above was added to the above solution and stirred until completely dissolved. Another trimesic acid (840 mg, 4.00 mmol) was added to the above solution and stirred overnight. Finally, the above solution was transferred to a hydrothermal reactor, heated at 140°C for 24 hours, and then naturally cooled to room temperature. The product was washed twice with water, DMF and methanol in turn. Place it in a blast drying oven at 70°C and dry overnight, and...
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