A high-capacity iron-based lithium-ion battery cathode material α-lifeo 2 preparation method
A technology for lithium ion batteries and positive electrode materials, which is applied in the field of preparation of α-LiFeO2, a positive electrode material for high-capacity iron-based lithium ion batteries, can solve the problems of complicated synthesis methods, poor electrochemical performance, and impure products, and achieve electrochemical performance. Good, single phase, low price effect
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Embodiment 1
[0031] Dissolve 0.035mol (1.473g) of lithium hydroxide monohydrate and 0.004mol (1.616g) of ferric nitrate nonahydrate in an appropriate amount of absolute ethanol, and add the ferric nitrate solution dropwise to lithium hydroxide at room temperature and under magnetic stirring. Add 0.004mol (about 0.028g) lithium metal to the solution, and stir magnetically at room temperature for 5 hours to obtain a dark brown-brown precipitate; after centrifugation, wash repeatedly with absolute ethanol and deionized water for 5 times, and finally Wash with absolute ethanol to remove excess Li + and other impurity ions, and then put the final sample washed with absolute ethanol in a blast drying oven at 80°C for 4 hours, then manually grind the dried sample for 20 minutes, and then put the refined powder into an 80°C drying oven again Continue to dry for 20h in the middle to obtain lithium-rich layered α-LiFeO 2 Lithium-ion battery cathode material.
[0032] For the above α-LiFeO 2 Lithi...
Embodiment 2
[0034] Dissolve 0.109mol (7.211g) of anhydrous lithium acetate and 0.012mol (5.05g) of ferric nitrate nonahydrate in an appropriate amount of absolute ethanol, and add the ferric nitrate solution dropwise to anhydrous lithium acetate at room temperature and under magnetic stirring. In the solution, add 0.012mol (approximately 0.084g) lithium metal, stir magnetically at room temperature for 5h to obtain a dark brown-brown precipitate, after centrifugation, wash repeatedly 5-8 times with absolute ethanol and deionized water alternately, to remove excess Li + and other impurity ions, and then put the final sample washed with absolute ethanol in a blast drying oven at 80°C for 4 hours, then manually grind the dried sample for 20 minutes, and then put the refined powder into an 80°C drying oven again Continue to dry for 20h in the middle to obtain lithium-rich layered α-LiFeO 2 Lithium-ion battery cathode material. Use it as a positive electrode active material, mix it with acety...
Embodiment 3
[0036] Dissolve 0.048mol (2.016g) of lithium hydroxide monohydrate and 0.004mol (1.616g) of ferric nitrate nonahydrate in an appropriate amount of absolute ethanol, and add the ferric nitrate solution dropwise to hydrogen monohydrate at room temperature and under magnetic stirring. Add 0.004mol (about 0.028g) lithium metal to the lithium oxide solution, and continue magnetic stirring at room temperature for 5 hours to obtain a dark brown precipitate. After centrifugation, wash repeatedly with absolute ethanol and deionized water alternately. to remove excess Li + and other impurity ions, and then the final sample washed with absolute ethanol was dried in a blast drying oven at 80°C for 6 hours, and then the dried sample was manually ground for 20 minutes, and the obtained fine powder was dried again at 80°C Continue to dry in the box for 16h to obtain lithium-rich layered α-LiFeO 2 Lithium-ion battery cathode material. Use it as positive electrode active material, mix with a...
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