Pre-lithiation method of negative electrode for secondary battery
US-11183683-B2 · Nov 23, 2021 · US
US11575117B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11575117-B2 |
| Application number | US-201816465900-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 4, 2018 |
| Priority date | May 19, 2017 |
| Publication date | Feb 7, 2023 |
| Grant date | Feb 7, 2023 |
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A method for pre-lithiating a silicon oxide negative electrode for a secondary battery, specifically a method for pre-lithiation by immersing the silicon oxide negative electrode in an electrolytic solution for wetting, and by applying pressure while a lithium metal is in direct contact with the wetted silicon oxide negative electrode. The silicon oxide negative electrode for a secondary battery manufactured through pre-lithiation provided in the present disclosure has improved initial irreversibility, and a secondary battery manufactured using such a silicon oxide negative electrode for a secondary battery has excellent charge/discharge efficiency.
Opening claim text (preview).
The invention claimed is: 1. A method for pre-lithiating a silicon oxide negative electrode for a secondary battery, comprising; a first step of immersing the silicon oxide negative electrode for the secondary battery in an electrolyte solution for wetting, wherein the first step comprises immersing the silicon oxide negative electrode for the secondary battery in the electrolyte solution for 3 hours to 20 hours; and a second step of bringing the wetted silicon oxide negative electrode for the secondary battery into direct contact with a lithium metal, wherein the second step comprises bringing the wetted silicon oxide negative electrode for the secondary battery into direct contact with the lithium metal for 5 to 20 minutes, wherein the second step is performed in the electrolyte solution in the first step, and wherein the second step comprises bringing the wetted silicon oxide negative electrode for the secondary battery into direct contact with the lithium metal with a force of 1 to 10 kgf per unit area of 1.5 cm 2 . 2. The method of claim 1 , wherein the electrolyte solution in the first step is prepared by dissolving any one or two or more lithium salts selected from the group consisting of LiCl, LiBr, LiI, LiClO 4 , LiBF 4 , LiB 10 Cl 10 , LiPF 6 , LiCF 3 SO 3 , LiCF 3 CO 2 , LiAsF 6 , LiSbF 6 , LiAlCl 4 , CH 3 SO 3 Li, CF 3 SO 3 Li, (CF 3 SO 2 ) 2 NLi, chloroborane lithium, a lower aliphatic lithium carboxylate and lithium tetraphenylborate in a solvent. 3. The method of claim 2 , wherein the solvent is any one or a mixture of two or more selected from the group consisting of N-methyl-2-pyrrolidinone, propylene carbonate, ethylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, ethylmethyl carbonate, gamma-butyrolactone and 1,2-dimethoxy ethane. 4. The method of claim 1 , wherein the contact pressure is 0.2 to 5 kgf per 1.5 cm 2 . 5. The method of claim 1 , wherein the contact pressure is 0.5 to 2 kgf per 1.5 cm 2 .
Electrochemical doping, intercalation, occlusion or alloying · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx · CPC title
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
by coating on electrode collectors · CPC title
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