Graphene-coated titanium niobium oxide composite electrode material, lithium primary battery and preparation method thereof
A graphene-coated, titanium-niobium oxide technology, applied in the direction of active material electrodes, non-aqueous electrolyte batteries, dry batteries, etc., can solve the problems of low conductivity and reduced output power capacity, and achieve high energy density, low cost, Good material consistency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0041] The graphene-coated titanium-niobium oxide composite electrode material described in this embodiment includes TiNb 2 o 7 Inner core and graphene cladding layer, the mass fraction of graphene cladding layer is 1%. The specific preparation method is as follows:
[0042] Weigh 23.42g of anatase-type titanium dioxide and 76.58g of niobium pentoxide according to the molar ratio Ti:Nb=1:2, after ball milling for 10 hours, sinter in air at 1100°C for 12 hours, and then oxidize the produced titanium niobium After 10 hours of ball milling with graphene powder (content 1%), sintering 4h under the nitrogen atmosphere of 750 ℃, then after the sintered material is ground and pulverized, adopt resistance tester to test the resistance of powder, test powder resistance is 80Ω; the powder is prepared into an electrode, and the electrode preparation method is as follows: take 90% titanium niobium oxide, 5% Super_P conductive agent, 5% Solvay Solef 5130 binder and NMP as solvent, these ...
Embodiment 2
[0044] The graphene-coated titanium-niobium oxide composite electrode material described in this embodiment includes TiNb 1.9 o 6.75 Inner core and graphene cladding layer, the mass fraction of graphene cladding layer is 0.8%. The specific preparation method is as follows:
[0045] Weigh 23.42g of anatase titanium dioxide and 76.58g of niobium pentoxide according to the molar ratio Ti:Nb=1:2, after ball milling for 10 hours, sinter in air at 1000°C for 12 hours, and then oxidize the produced titanium niobium After 10 hours of ball milling with graphene powder (content 0.8%), sintering 4h under the nitrogen atmosphere of 750 ℃, then after the material after sintering is ground and pulverized, adopt resistance tester to test the resistance of powder, test powder resistance is 103Ω; the powder is prepared into an electrode, and the electrode preparation method is as follows: take 90% of titanium niobium oxide, 5% of Super_P conductive agent, 5% of Solvay’s Solef 5130 binder and...
Embodiment 3
[0047] The graphene-coated titanium-niobium oxide composite electrode material described in this embodiment includes TiNb 2 o 7 Inner core and graphene cladding layer, the mass fraction of graphene cladding layer is 1.2%. The specific preparation method is as follows:
[0048] Weigh 23.42g of anatase titanium dioxide and 76.58g of niobium pentoxide according to the molar ratio Ti:Nb=1:2, after ball milling for 10 hours, sinter in air at 1200°C for 12 hours, and then oxidize the produced titanium niobium After 10 hours of ball milling with graphene powder (content 1.2%), sintering 4h under the nitrogen atmosphere of 750 ℃, then after the material after sintering is ground and pulverized, adopt resistance tester to test the resistance of powder, test powder resistance is 70Ω; the powder is prepared into an electrode, and the electrode preparation method is as follows: take 90% titanium niobium oxide, 5% Super_P conductive agent, 5% Solvay Solef 5130 binder and NMP as solvent, ...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com