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A kind of synthetic method and application of vanadium oxide

A synthesis method and technology of vanadium oxide, applied in vanadium oxide, active material electrodes, electrochemical generators, etc., can solve problems such as poor controllability, harsh experimental parameters, and difficult microstructure, and achieve smooth surface and large specific surface area , the effect of high battery capacity and cycle stability

Active Publication Date: 2022-08-05
JIANGNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Based on the multivalent state of vanadium, it is possible to control the vanadium oxide VO 2 The synthesis and its microstructure are very difficult. The current chemical synthesis methods often use strong reducing agents, which makes the reaction process less controllable and leads to the formation of VO 2 The experimental parameters are harsh, and it is necessary to develop new synthetic methods to realize the synthesis of vanadium oxide VO 2 Controllable synthesis of , and realize the application of high-capacity aqueous zinc-ion batteries

Method used

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  • A kind of synthetic method and application of vanadium oxide
  • A kind of synthetic method and application of vanadium oxide
  • A kind of synthetic method and application of vanadium oxide

Examples

Experimental program
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Embodiment 1

[0033] Weigh 0.46g of ammonium metavanadate into a beaker, weigh 50mL of deionized water into the beaker, stir for 30 minutes until the ammonium metavanadate is completely dissolved, add 37% concentrated hydrochloric acid, adjust the pH value to 1.1, at room temperature Continue stirring for 10 minutes; add 0.4 mL of aniline solution (analytical grade), the concentration of aniline in the solution is 86.6 mmol / L, and continue to stir at room temperature for 10 minutes; transfer the above solution into a 90 mL reaction kettle, react at 200 ° C for 24 h, and centrifuge after ethanol and Deionized water was washed and centrifuged three times each, and the product was dried at 50°C under air. The x-ray diffraction pattern of the product is shown in figure 1 , the scanning electron microscope image is shown in figure 2 , see the electrochemical performance test results image 3 .

[0034] from figure 1 It can be seen that the material has high purity and good crystallinity. B...

Embodiment 2

[0038] Weigh 0.46g of ammonium metavanadate into a beaker, measure 50mL of deionized water into the beaker, stir for 30 minutes until the ammonium metavanadate is completely dissolved, add 37% concentrated hydrochloric acid, adjust the pH value to 0.9, at room temperature Continue stirring for 10 minutes; add 0.4 mL of aniline solution (analytical grade), the concentration of aniline in the solution is 86.3 mmol / L, and continue to stir at room temperature for 10 minutes; transfer the above solution into a 90 mL reaction kettle, react at 200 ° C for 24 hours, and centrifuge after ethanol and Deionized water was washed and centrifuged 3 times each, and the product was dried at 50 °C under air. The X-ray diffraction pattern of the product is shown in Figure 4 , for VO 2 (B) Phase structure.

Embodiment 3

[0040] Weigh 0.46g of ammonium metavanadate into a beaker, weigh 50mL of deionized water into the beaker, stir for 30 minutes until the ammonium metavanadate is completely dissolved, add 37% concentrated hydrochloric acid, adjust the pH value to 0.7, at room temperature Continue stirring for 10 minutes; add 0.4 mL of aniline solution (analytical grade), the concentration of aniline in the solution is 85.7 mmol / L, and continue to stir at room temperature for 10 minutes; transfer the above solution into a 90 mL reaction kettle, and react at 200 ° C for 24 h. After centrifugation, ethanol and Deionized water was washed and centrifuged 3 times each, and the product was dried at 50 °C under air. The X-ray diffraction pattern of the product is shown in Figure 5 , for VO2 (B) Phase structure.

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Abstract

The invention provides a synthesis method and application of vanadium oxide, and belongs to the technical field of battery materials. The synthesis method includes: adjusting the pH value of the vanadate aqueous solution to 0.7-1.1 with an aqueous hydrochloric acid solution; adding the obtained solution to aniline and mixing, subjecting the obtained solution to hydrothermal reaction, and separating solid-liquid to obtain the solid phase to obtain the vanadium oxide. The invention provides a kind of vanadium oxide VO with simple synthesis process and low cost 2 synthetic method. The method is a one-step synthesis, the synthesis route is clear, the secondary treatment of the sample is not required, and the obtained sample has excellent capacity and cycle stability in the aqueous zinc-ion battery.

Description

technical field [0001] The invention belongs to the technical field of battery materials, and in particular relates to a synthesis method and application of vanadium oxide. Background technique [0002] Commercial lithium-ion batteries have many problems, including low content of lithium resources, high price, and flammable and explosive safety problems when using organic electrolytes. It is an urgent need to develop new secondary batteries to replace lithium batteries. Aqueous zinc-ion batteries have the advantages of abundant zinc reserves, low price, high environmental tolerance, high battery capacity and cycle stability, and high safety and environmental friendliness of water-based electrolytes. It is possible to replace lithium-ion batteries. options. [0003] Vanadium oxide material is a commonly used cathode material for aqueous zinc-ion batteries. The valence states of vanadium include +5, +4, +3, +2, etc., and multivalent vanadium oxides can make aqueous zinc-ion b...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G31/02H01M4/48H01M10/36
CPCC01G31/02H01M4/48H01M10/36H01M2004/028C01P2004/20C01P2004/30C01P2004/52C01P2002/72C01P2004/03C01P2006/40C01P2004/62C01P2004/61Y02E60/10
Inventor 聂延光袁心邹彤张友鹏王赞尧
Owner JIANGNAN UNIV
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