Positive electrode material for transition metal-doped sodium ion battery and preparation and application thereof
A technology for sodium-ion batteries and cathode materials, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of no improvement in electrical conductivity and low electrical conductivity, and achieve excellent cycle performance, small particle size, and electrical conductivity. boosted effect
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Embodiment 1
[0020] Example 1: (Transition metal Ti doping to prepare Na 3 V 1.9 Ti 0.1 (PO 4 ) 2 F 3 / C)
[0021] Weigh 2.520g sodium fluoride (both fluorine source and sodium source), 4.445g ammonium metavanadate, 0.159g titanium dioxide, 4.601g ammonium dihydrogen phosphate and 8.406g citric acid (both as carbon source and as reducing Add to 250mL agate ball milling pot, then add 80g agate balls and 60ml deionized water, put the ball milling pot in the ball mill, ball mill at 580rpm for 12h. Pour the resulting mixed solution (except the agate ball) into a beaker, wash the agate pellets with deionized water, pour the cleaning solution into the beaker, wash 3 times, stir with a magnet, evaporate the solvent at 80℃, and put it in 120 Keep it in an oven at ℃ for 8 hours to obtain precursor A. The precursor A is pre-sintered at 350°C for 5h and 750°C for 8h in a nitrogen atmosphere. After cooling, the transition metal-doped cathode material Na is obtained. 3 V 1.9 Ti 0.1 (PO 4 ) 2 F 3 / C.
Embodiment 2
[0022] Example 2: (Transition metal Fe doping to prepare Na 3 V 1.95 Fe 0.05 (PO 4 ) 2 F 3 / C)
[0023] Weigh 2.520g sodium fluoride (both fluorine source and sodium source), 4.562g ammonium metavanadate, 0.407g (FeNO 3 ) 3 ·9H 2 O, 4.601g ammonium dihydrogen phosphate and 8.406g citric acid (both as a carbon source and as a reducing agent), add them to a 250mL agate ball mill jar, then add 80g agate balls and 60ml deionized water, and place the ball mill jar In the ball mill, ball mill at a speed of 580 rpm for 12 hours. Pour the resulting mixed solution (except the agate ball) into a beaker, wash the agate pellets with deionized water, pour the cleaning solution into the beaker, wash 3 times, stir with a magnet, evaporate the solvent at 80℃, and put it in 120 Keep it in an oven at ℃ for 8 hours to obtain precursor A. The precursor A is pre-sintered at 350°C for 5h and 750°C for 8h in a nitrogen atmosphere. After cooling, the transition metal-doped cathode material Na is obtain...
Embodiment 3
[0024] Example 3: (Preparation of Na by doping transition metal Ni 3 V 1.93 Ni 0.07 (PO 4 ) 2 F 3 / C)
[0025] Weigh 2.520g sodium fluoride (both fluorine source and sodium source), 4.515g ammonium metavanadate, 0.404gNi(NO 3 ) 2 ·6H 2 O, 4.601g ammonium dihydrogen phosphate and 8.406g citric acid (both as a carbon source and as a reducing agent), add them to a 250mL agate ball mill jar, then add 80g agate balls and 60ml deionized water, and place the ball mill jar In the ball mill, ball mill at a speed of 580 rpm for 12 hours. Pour the resulting mixed solution (except the agate ball) into a beaker, wash the agate pellets with deionized water, pour the cleaning solution into the beaker, wash 3 times, stir with a magnet, evaporate the solvent at 80℃, and put it in 120 Keep it in an oven at ℃ for 8 hours to obtain precursor A. The precursor A is pre-sintered at 350°C for 5h and 750°C for 8h in a nitrogen atmosphere. After cooling, the transition metal-doped cathode material Na is ...
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