Preparation method of manganese phosphate coated lithium-rich oxide positive electrode material
A manganese phosphate package and cathode material technology, applied in battery electrodes, electrochemical generators, electrical components, etc., can solve the problem of low Coulomb efficiency, poor high rate performance and cycle performance, and lithium-rich manganese-based cathode materials cannot achieve high capacity. and other problems, to achieve the effect of simple process, cheap raw materials and excellent electrochemical performance
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Embodiment 1
[0023] Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation: add an appropriate amount of NiSO 4 ·6H 2 O, CoSO 4 ·7H 2 O and MnSO 4 4H 2 O (molar ratio Ni:Co:Mn=0.21:0.08:0.54) was dissolved in deionized water containing 0.1mol / L ammonia water. Then 4mol / L NaOH aqueous solution is slowly added in the solution, and control solution pH=11, obtains (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 Precursor. Will (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 The precursor was filtered and dried with LiOH·H 2 O was mixed ball milled for 2 h, calcined in a muffle furnace at 400 °C for 5 h, and then at 800 °C for 15 h to obtain pure Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 powder, the molar ratio Li:Ni:Co:Mn=1.174:0.220:0.079:0.551 was determined by inductively coupled plasma mass spectrometry.
[0024] PPML 4 Coated Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation of Li-rich materials: adding an appropriate amount of Mn(CH 3 COO) 2 4H 2 O and citric acid were dissolved in 20 mL ethanol, Mn...
Embodiment 2
[0026] Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation: add an appropriate amount of NiSO 4 ·6H 2 O, CoSO 4 ·7H 2 O and MnSO 4 4H 2 O (molar ratio Ni:Co:Mn=0.21:0.08:0.54) was dissolved in deionized water containing 0.1mol / L ammonia water. Then 4mol / L NaOH aqueous solution is slowly added in the solution, and control solution pH=11, obtains (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 Precursor. Will (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 The precursor was filtered and dried with LiOH·H 2 O was mixed ball milled for 2 h, calcined in a muffle furnace at 400 °C for 5 h, and then calcined in a muffle furnace at 850 °C for 12 h to obtain pure Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 powder, the molar ratio Li:Ni:Co:Mn=1.182:0.208:0.084:0.536 was determined by inductively coupled plasma mass spectrometry.
[0027] PPML 4 Coated Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation of Li-rich materials: adding an appropriate amount of Mn(CH 3 COO) 2 4H 2 O and citric acid were d...
Embodiment 3
[0029] Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation: add an appropriate amount of NiSO 4 ·6H 2 O, CoSO 4 ·7H 2 O and MnSO 4 4H 2 O (molar ratio Ni:Co:Mn=0.21:0.08:0.54) was dissolved in deionized water containing 0.1mol / L ammonia water. Then 4mol / L NaOH aqueous solution is slowly added in the solution, and control solution pH=11, obtains (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 Precursor. Will (Ni 0.21 co 0.08 mn 0.54 )(OH) 2 The precursor was filtered and dried with LiOH·H 2 O was mixed ball milled for 2 h, calcined in a muffle furnace at 400 °C for 5 h, and then calcined in a muffle furnace at 900 °C for 10 h to obtain pure Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 powder, the molar ratio Li:Ni:Co:Mn=1.203:0.212:0.078:0.547 was determined by inductively coupled plasma mass spectrometry.
[0030] PPML 4 Coated Li 1.17 Ni 0.21 co 0.08 mn 0.54 o 2 Preparation of Li-rich materials: adding an appropriate amount of Mn(CH 3 COO) 2 4H 2 O and citric acid were d...
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