A carbon coating method of hydrothermal lithium iron phosphate
A technology of lithium iron phosphate and lithium iron phosphate is applied in the field of preparation technology of positive electrode materials for lithium ion batteries, which can solve the problems of low tap density of products, low electrode compaction density, uneven carbon layer, poor electrical conductivity, etc., and achieve excellent electrical conductivity. Chemical properties, uniform composition, good batch stability
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Embodiment 1
[0029] According to the patent ZL201010031395.3, the white powder of lithium iron phosphate was prepared. The specific steps are as follows: 555.7g ferrous sulfate heptahydrate (2mol) was dissolved and diluted to 2.0L; 237.4g 85% phosphoric acid (2.06mol) was diluted to 0.5L; 251.8g lithium hydroxide monohydrate (6mol) was dissolved in water and diluted to 1.5L. Add the phosphoric acid solution and the lithium hydroxide solution into a 5L autoclave with a sealed feeding tube and a cooling coil, purge the inside of the autoclave with an inert gas (nitrogen) to make all the air escape, seal the autoclave, and heat from room temperature with stirring at a speed of 200rpm to 40°C, open the feed valve and exhaust valve, and add the ferrous sulfate solution prepared above under stirring at a feed rate of 300mL / min. Seal the autoclave, and after stirring for 20 minutes, open the feed valve and exhaust valve, and then add the prepared lithium hydroxide solution as a pH regulator, whi...
Embodiment 2
[0032] Embodiment 2 (compared with embodiment 1, oxidation degree is different)
[0033] The lithium iron phosphate powder in Example 1 was placed in an electric blast drying oven, kept at 180°C for 1h, taken out, and the Fe 3+ The content is 2.0%. Other steps are the same as in Example 1. The electrochemical performance, carbon content and ferric iron content of the product are shown in Table 1.
Embodiment 3
[0038] Embodiment 3 (olefin ratio 1:7)
[0039] Place the oxidized lithium iron phosphate powder in Example 1 in a tube furnace, first pass high-purity argon into it, and in the high-purity argon atmosphere, control the heating rate to 4°C / min, and heat from room temperature to 570°C , and keep it warm for 2 hours, continue to increase the temperature in the furnace to 630°C at a heating rate of 4°C / min, and then replace it with a reaction gas with a volume ratio of 2-butene and argon of 1:7, and control the gas flow rate to 50mL / min , after 4h, the gas was switched to high-purity argon again, and naturally cooled to below 100°C to obtain LiFePO 4 / C Composite. The electrochemical performance, carbon content and ferric iron content of the product are shown in Table 1.
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