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A substrate-free niobium pentoxide nanosheet array negative electrode material and its preparation method and application

A niobium pentoxide and nanosheet array technology, which is applied in chemical instruments and methods, negative electrodes, inorganic chemistry, etc., can solve problems such as slow diffusion of lithium ions, improve electrochemical performance, save production costs, and increase stability. Effect

Active Publication Date: 2018-10-30
HUNAN UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] The technical problem to be solved in the present invention is to solve the problem of slow diffusion of lithium ions in niobium pentoxide crystals, by changing the diffusion distance of lithium ions, the electrochemical performance of niobium pentoxide as a negative electrode material is improved; A method for preparing a substrate-free niobium pentoxide nanosheet array anode material with high performance, excellent cycle performance, and stable structure. The preparation method has simple process, easy operation, and low cost

Method used

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  • A substrate-free niobium pentoxide nanosheet array negative electrode material and its preparation method and application
  • A substrate-free niobium pentoxide nanosheet array negative electrode material and its preparation method and application
  • A substrate-free niobium pentoxide nanosheet array negative electrode material and its preparation method and application

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Embodiment 1

[0031] At room temperature, dissolve niobium oxalate in 60 mL of mixed solvent a1 of deionized water and polyethylene glycol 6000 with a mass ratio of 10:3 to form a mixed solution A1. After stirring for the first time, add sodium hydroxide dropwise solution to obtain a mixed solution B1, to obtain a mixed solution B1 with a niobium ion concentration of 35 mmol / L and a sodium ion concentration of 0.19 mol / L; after the mixed solution B1 is sealed, the second stirring is performed, and after stirring for 3 hours, the mixed solution B1 is transferred Into an 80mL reactor, at 170°C, carry out hydrothermal reaction, the reaction time is 30h, after the reaction is completed, naturally cool to room temperature; move the obtained solution to a centrifuge for centrifugation, and centrifuge the obtained solid matter, successively After washing with deionized water and absolute ethanol for 3 times, drying at 110° C. for 12 hours, the substrate-free niobium pentoxide nanosheet array negati...

Embodiment 2

[0035]At room temperature, dissolve niobium chloride in 40 mL of mixed solvent a2 of deionized water and polyethylene glycol 16000 with a mass ratio of 3:7 to form a mixed solution A2. Potassium solution to obtain a mixed solution B2 with a concentration of niobium ions of 90 mmol / L and a concentration of potassium ions of 0.5 mol / L. After sealing the mixed solution B2, stir for the second time. After stirring for 0.5 h, transfer the mixed solution B2 to 80 mL In the reaction kettle, carry out hydrothermal reaction at 150°C, and the reaction time is 72h. After the reaction is completed, it is naturally cooled to room temperature, and the obtained solution is moved to a centrifuge device for centrifugation, and the centrifuged solid matter is used successively. After washing with deionized water and absolute ethanol three times respectively, drying at 150° C. for 8 hours, the substrate-free niobium pentoxide nanosheet array negative electrode material can be obtained.

Embodiment 3

[0037] At room temperature, dissolve niobium acetate in 60 mL of mixed solvent a3 of deionized water and polyvinyl alcohol 20000 with a mass ratio of 1:35 to form a mixed solution A3; after stirring for the first time, add potassium hydroxide solution dropwise Obtain mixed solution B3, obtain the niobium ion concentration and be 15mmol / L; In an 80mL reactor, conduct a hydrothermal reaction at 250°C for 6 hours. After the reaction is completed, cool it down to room temperature naturally, centrifuge, and wash the solid matter obtained by centrifugation with deionized water and absolute ethanol for 6 times. Drying at 80° C. for 16 hours can obtain the substrate-free niobium pentoxide nanosheet array negative electrode material.

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Abstract

The invention discloses a preparation method of a substrate-free niobium pentoxide nanosheet array negative electrode material. The method comprises the steps of dissolving soluble niobate into a mixed solvent of deionized water and polymeric alcohol and mixing evenly; adding a metal alkali solution or salt solution containing sodium ions and / or potassium ions to obtain a mixed solution; sealing the mixed solution, stirring, carrying out hydrothermal reaction on the stirred mixed solution, and after reaction is completed, naturally cooling to room temperature; and centrifugally treating the completely reacted solution to obtain the substrate-free niobium pentoxide nanosheet array negative electrode material. Through changing the diffusion distances of lithium ions, the problem of slow diffusion of existing lithium ions in niobium pentoxide crystals is solved, and the electrochemical properties of the niobium pentoxide as the negative electrode material are improved. The substrate-free niobium pentoxide nanosheet array negative electrode material has the characteristics of being stable in structure, good in cycle performance and excellent in rate capability, and the preparation method is simple in process, easy to operate and relatively low in cost.

Description

technical field [0001] The invention relates to a battery negative electrode material and its preparation, in particular to a baseless niobium pentoxide nanosheet array negative electrode material and its preparation method and application. Background technique [0002] Since the 1990s, lithium-ion batteries have been considered ideal for high-capacity, high-power batteries because of their high energy density, good cycle performance, and charge protection capabilities. However, due to the poor high-rate performance and limited theoretical capacity (about 372mAh / g) of commercialized traditional graphite anode materials, it is difficult to meet the performance requirements. In recent years, a series of Fe2O3, SnO2, Cu2O, NiO, Co3O4, MnO2, Si and other materials with high theoretical capacity have emerged. Although the specific capacity is high, the volume expansion problem is serious during the charge and discharge process, which can easily cause cracking and cracking of the ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G33/00H01M4/485H01M10/0525
CPCC01G33/00C01P2004/03C01P2004/04H01M4/485H01M10/0525H01M2004/027Y02E60/10
Inventor 陈晗石崇福向楷雄朱裔荣周伟陈宪宏
Owner HUNAN UNIV OF TECH