Method for preparing lithium iron phosphate electrode material by using twice carbon adding technology based on liquid phase mixing material
A technology of lithium iron phosphate and electrode materials, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of forming a good carbon coating on the surface of lithium iron phosphate particles, complicated processes, and increased energy consumption, and achieves a higher batch rate. secondary stability and product properties, lowering reaction temperature, and reducing production energy consumption
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Embodiment 1
[0041] Weigh 1.208gLiCl·H with the molar ratio of lithium: iron: phosphorus = 1:1:1 2 O, 5.406 g FeCl 3 ·6H 2 0, 2.3006gNH 4 h 2PO 4 , and 0.35g of sucrose, which were dissolved in 20ml of deionized water, and then placed in an oven at a temperature of 195°C and heated in a slightly boiling state. After it was completely dried, the obtained solid residue was mixed with absolute ethanol dissolved in 0.35g PEG400, and ball milled for 5h. The anhydrous ethanol in the obtained ball-milled product was dried, and a high-temperature carbothermal reduction reaction was carried out in a tube furnace under the protection of flowing argon. The reaction temperature was 750° C. and the reaction time was 8 hours. Such as figure 2 As shown, the position of the XRD diffraction peak is related to that of LiFePO 4 The standard card (JCPDS Card No. 83-2092) matches, indicating that the obtained product is LiFePO 4 .
Embodiment 2
[0043] The preparation steps in this example are exactly the same as those in Example 1 above. The difference is: Weigh 1.379g anhydrous lithium nitrate, 8.08gFe(NO 3 ) 3 9H 2 O, 2.3006gNH 4 h 2 PO 4 , and 1.25 g of sucrose as a reactant. Such as image 3 As shown, the position of the XRD diffraction peak is related to that of LiFePO 4 The standard card (JCPDS Card No. 83-2092) matches, indicating that the obtained product is LiFePO 4 . Figure 4 Shown is the SEM picture of the material, and the particle size of the material can be seen in the figure to be several hundred nanometers. Such as Figure 5 As shown, the initial discharge capacity of the material is 156mAh / g at a charge-discharge rate of 0.1C, and the plateau voltage difference is about 0.15V. exist Image 6 Among them, the discharge capacity of the material at 0.1C gradually increases with the activation of the battery and the full infiltration of the electrolyte in the first few cycles, reaching 163 mA...
Embodiment 3
[0045] The preparation steps in this example are exactly the same as those in Example 2 above. The difference is: (1) The molar ratio of the raw materials added is lithium: iron: phosphorus = 1.05:1:1. (2) 0.45g of PEG400 is added when chain organic matter is added. Such as Figure 7 As shown, the material in Example 3 has a discharge capacity of 158 mAh / g at 0.1C.
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