Zinc-base complex oxide/graphene composite material, and preparation method and application thereof
A technology of composite materials and oxides, which is applied in the direction of electrical components, battery electrodes, circuits, etc., can solve the problems of large volume change and capacity attenuation, and achieve the effects of simple process, improved electrochemical performance, and uniform distribution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] FeCl with a molar ratio of 2:1 3 ·6H 2 O and ZnCl 2 Dissolve in deionized water to make 80 mL of Fe 3+ and Zn 2+ Total concentration is 0.015mol / L solution, add 29 milligrams of GO again and make mixed solution; The mixed solution is placed in the capacity and is in the autoclave (filling degree 80%, volume percentage) of 100 milliliters, then with 6mol / L Adjust the pH value of NaOH aqueous solution to 10, and feed oxygen to saturation, then seal the reactor, react at 220°C for 32 hours, and cool to room temperature naturally; collect the solid reaction product, pass the product through deionized water and absolute ethanol Alternately repeated washing, drying, to obtain 0.107g ZnFe 2 o 4 / graphene composite material, wherein the weight percentage of graphene is 11%.
[0037] The X-ray diffraction spectrum of the composite material of gained, transmission electron micrograph and scanning electron micrograph are respectively as follows figure 1 , figure 2 with i...
Embodiment 2
[0040] MnC with a molar ratio of 2:1 2 o 4 2H 2 O and ZnSO 4 ·7H 2 O was dissolved in ethylene glycol to make 80 mL of Mn 2+ and Zn 2+ Total concentration is the solution of 0.03mol / L, add 38 milligrams of GO again and make mixed solution; The mixed solution is placed in the capacity and is in the autoclave of 100 milliliters (filling degree 80%, percent by volume), adjust pH with 25wt% ammonia water The value is adjusted to 11, and oxygen is passed to saturation (at O 2 Under saturated conditions, Mn 2+ is oxidized to Mn 3+ ), then the reactor was sealed, reacted at 220°C for 36 hours, and cooled naturally to room temperature; the solid reaction product was collected, and the product was washed alternately and repeatedly with deionized water and absolute ethanol, and dried to obtain 0.205g ZnMn 2 o 4 / graphene composite material, wherein the weight percentage of graphene is 7.4%.
[0041] It can be seen from the X-ray diffraction spectrum and transmission electron m...
Embodiment 3
[0044] NiSO with a molar ratio of 2:1 4 ·6H 2 O and ZnC 2 o 4 2H 2 O was dissolved in anhydrous methanol to make 80 mL of Ni 2+ and Zn 2+ A solution with a total concentration of 0.09mol / L was added to prepare a mixed solution with 59 mg of GO; the mixed solution was placed in a high-pressure reactor (filling degree 80%, volume percentage) with a capacity of 100 ml, and the KOH of 6mol / L The pH value of the aqueous solution was adjusted to 9, and oxygen was introduced to saturation (at O 2 Under saturated conditions, Ni 2+ Can be oxidized to Ni 3+ ), then the reactor was sealed, reacted at 240°C for 48 hours, and cooled naturally to room temperature; the solid reaction product was collected, and the product was washed alternately and repeatedly with deionized water and absolute ethanol, and dried to obtain 0.615g ZnNi 2 o 4 / graphene composite material, wherein the weight percentage of graphene is 3.8%.
[0045] It can be seen from the X-ray diffraction spectrum and ...
PUM
Property | Measurement | Unit |
---|---|---|
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