Preparation method of lithium battery negative electrode material iron-based binary composite metal oxide
A negative electrode material, binary composite technology, applied in battery electrodes, electrical components, secondary batteries, etc., can solve the problems of complex operation steps, difficult to popularize on a large scale, difficult to control reaction conditions, etc. Easy-to-control conditions and uniform results
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[0013] The invention provides a method for preparing an iron-based binary composite metal oxide as a lithium battery negative electrode material, comprising the following steps:
[0014] Step 1. Prepare polymer microemulsion beads with a particle size of 50-500 nm by emulsion polymerization, and centrifuge the polymer microemulsion beads to obtain a template material with long-range order and reverse opal structure; M source compound, iron The source compound is mixed according to the ratio of the amount of substances M: Fe=0.95~1.05:1.95~2.05 and prepared into an alcohol solution or aqueous solution with a total concentration of metal ions of 1~3mol / L, and the M is a transition metal other than iron. any one;
[0015] Step 2. Soak the template material obtained in step 1 in the alcohol solution or aqueous solution obtained in step 1 for 10 to 60 minutes, then suction filter, and then dry the solid obtained after suction filtration at 50 to 100°C for 2 to 14 hours;
[0016] S...
Embodiment 1
[0030] Polymethyl methacrylate microemulsion beads with a particle size of 50nm were prepared by emulsion polymerization, and the polymethyl methacrylate microemulsion beads were centrifuged to form template materials with long-range order and anti-opal structure; The source compound and the iron source compound are mixed according to the ratio of the amount of substances Zn:Fe=0.95:1.95 and prepared into an ethylene glycol and methanol solution with a total metal ion concentration of 1mol / L, and the volume ratio of the solvent ethylene glycol and methanol is 1:2 , the M source compound is one or more of the acetylacetonate compound, acetic acid compound or nitric acid compound of M, and the iron source compound is one or more of the acetylacetonate compound, acetic acid compound or nitric acid compound of Fe ;
[0031]Step 2. Soak the template material obtained in step 1 in the alcohol solution or aqueous solution obtained in step 1 for 10 minutes, then suction filter, and th...
Embodiment 2
[0034] Polymethyl methacrylate microemulsion beads with a particle size of 500nm were prepared by emulsion polymerization, and the polymethyl methacrylate microemulsion beads were centrifuged to obtain template materials with long-range order and anti-opal structure; the copper source Compounds and iron source compounds are mixed according to the ratio of the amount of substances Cu: Fe=1.05:2.05 and prepared into an aqueous solution with a total concentration of metal ions of 3mol / L. The M source compound is an acetylacetonate compound, an acetic acid compound or a nitric acid compound. One or more of them, the iron source compound is one or more of Fe acetylacetonate compounds, acetic acid compounds or nitric acid compounds;
[0035] Step 2. Soak the template material obtained in step 1 in the alcohol solution or aqueous solution obtained in step 1 for 10-60 minutes, then suction filter, and then dry the solid obtained after suction filtration at 100° C. for 14 hours;
[003...
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