Lithium-sulfur battery flexible electrode material and preparation method and application thereof
A lithium-sulfur battery and flexible electrode technology, applied in the field of lithium-sulfur battery flexible electrode materials and their preparation, can solve the problems of not easy to scale up production, limited sulfur binding capacity, loss of active material, etc., achieve excellent cycle stability, improve binding The effect of increasing power and conductivity
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2018-07-10
Smart Images

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Abstract
Description
technical field
[0001] The invention relates to the technical field of lithium-sulfur batteries, in particular to a flexible electrode material for lithium-sulfur batteries and its preparation method and application. Background technique
[0002] With the continuous development of flexible devices and wearable electronic products, independently supported hybrid cathode materials have become one of the development trends of flexible lithium-sulfur batteries, and are also a hot spot in current research.
[0003] At present, single-walled carbon nanotubes are also widely used as current collectors for flexible batteries. However, lithium polysulfides are generated during charging and discharging of lithium-sulfur batteries, and the generated lithium polysulfides can often be dissolved in organic electrolytes. The active material is lost. Therefore, the current research focuses on finding a material that can be used as a carrier to wrap the sulfur element well so that it can bin...
Examples
Embodiment 1
[0062] A flexible electrode material for lithium-sulfur batteries, including single-walled carbon nanotube-wound VO x nano hollow spheres, the VO x The nano hollow sphere is coated with sulfur element.
[0063] Its preparation method is as follows:
[0064] (1) Dissolve 0.05g of vanadyl acetylacetonate into 20mL of N-N dimethylformamide solution, stir at room temperature for 2h, transfer the solution to a polytetrafluoroethylene reactor, then transfer the reactor to a drying oven to raise the temperature To 200 ℃, keep 21h, then naturally cool to room temperature. Take out the suspension in the reaction kettle, centrifuge at 8000r / min for 5min, collect the precipitate, wash with absolute ethanol for 3 times, then dry at 50°C for 10h, and collect VO with a particle size of about 200nm x Hollow balls, such as figure 1 , figure 2 shown.
[0065] (2) will VO x Mix hollow spheres with sulfur powder at a mass ratio of 1:2, put them into a sealed glass container with a cover ...
Embodiment 2
[0068] The only difference from Example 1 is that the mass of vanadyl acetylacetonate is 0.1 g.
[0069] As a result, step (1) collects VO with a particle size of about 400nm x Hollow balls, such as Figure 4 , Figure 5 shown;
[0070] Step (2) to get VO x Solid spheres complexed with sulfur, such as Image 6 As shown, through elemental analysis, it is found that the core of the obtained solid sphere is sulfur element, and the shell is VO x . The resulting flexible film product is denoted VHS-400@S / SWCNT.
Embodiment 3
[0072] The only difference from Example 1 is that the mass of vanadyl acetylacetonate is 0.3g.
[0073] As a result, step (1) collects VO with a particle size of about 900nm x Hollow balls, such as Figure 7 , Figure 8 shown;
[0074] Step (2) to get VO x Solid spheres complexed with sulfur, such as Figure 9 As shown, through elemental analysis, it is found that the core of the obtained solid sphere is sulfur element, and the shell is VO x . The resulting flexible film product is denoted VHS-900@S / SWCNT.