Material for lithium-sulfur battery positive electrode and preparation method thereof

A lithium-sulfur battery and positive electrode technology, applied in the field of lithium-sulfur battery positive electrode materials and its preparation, can solve the problems of reducing the electrochemical performance of composite materials, the inability to synthesize composite materials with high efficiency, and reducing the tap density, so as to improve Coulombic efficiency and cycle stability, good cycle stability and Coulombic efficiency, the effect of reducing volume expansion

Pending Publication Date: 2020-07-31
INT ACAD OF OPTOELECTRONICS AT ZHAOQING SOUTH CHINA NORMAL UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

There are some defects in the composite method, for example: the high-energy ball milling method can only pulverize the elemental sulfur to the submicron scale, and cannot be in good contact with carbon; the sulfur may agglomerate in the high-temperature heat treatment method; the gas-phase loading method has higher requirements for the instrument , poor experimental consistency and other shortcomings
[0005] At present, the carbon-coated mesoporous vanadium nitride nanowire film in the prior art r

Method used

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  • Material for lithium-sulfur battery positive electrode and preparation method thereof

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Experimental program
Comparison scheme
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Example Embodiment

[0030] Example 1

[0031] The material used for the positive electrode of the lithium-sulfur battery is a self-supporting mesoporous vanadium nitride nanowire / carbon nanotube composite material with a three-dimensional independent network structure.

[0032] The preparation method of the material comprises the following steps:

[0033] (1) Preparation of vanadium oxide nanowires: first, 0.1 g of ammonium metavanadate with a purity of 99% was added to 40 mL of deionized water, and stirred to form a uniform dispersion solution; then nitric acid was added dropwise to adjust the pH value of the dispersion solution to 2, and the Stir for 1 hour at room temperature and transfer to a high pressure reaction kettle with a capacity of 60 mL and heat at 180 ° C for 24 hours for reaction. After the reaction is completed, the reaction kettle is naturally cooled to room temperature, and the precipitate obtained from the reaction is repeatedly washed with deionized water and ethanol. 3 time...

Example Embodiment

[0036] Example 2

[0037] The preparation method of the material comprises the following steps:

[0038](1) Preparation of vanadium oxide nanowires: first, 0.3 g of ammonium metavanadate was added to 80 mL of deionized water, and stirred to form a uniform dispersion solution; then nitric acid was added dropwise to adjust the pH value of the dispersion solution to 3, and stirred at room temperature for 2 h and Transfer to the reaction kettle and heat it at 190 °C for 24 hours to react. After the reaction is completed, the reaction kettle is naturally cooled to room temperature, and the precipitate obtained from the reaction is washed 5 times with deionized water and ethanol, and dried at 60 °C under vacuum conditions. 12h to obtain vanadium oxide nanowires;

[0039] (2) Preparation of mesoporous vanadium nitride nanowires: placing the vanadium oxide nanowires obtained in step (1) in a flow rate of 30sccmNH 3 The reaction was carried out by heating to 550°C at a heating rate o...

Example Embodiment

[0041] Example 3

[0042] The preparation method of the material comprises the following steps:

[0043] (1) Preparation of vanadium oxide nanowires: firstly, 0.2 g of ammonium metavanadate was added to 60 mL of deionized water, and stirred to form a uniform dispersion solution; then nitric acid was added dropwise to adjust the pH value of the dispersion solution to 2, and stirred at room temperature for 2 h and Transfer to the reaction kettle and heat it for 24 hours at 170 °C for reaction. After the reaction is completed, the reaction kettle is naturally cooled to room temperature, and the precipitate obtained from the reaction is washed 4 times with deionized water and ethanol, respectively, and dried at 70 °C under vacuum conditions. 12h to obtain vanadium oxide nanowires;

[0044] (2) Preparation of mesoporous vanadium nitride nanowires: placing the vanadium oxide nanowires obtained in step (1) in a flow rate of 30sccmNH 3 The reaction was carried out by heating to 550°...

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Abstract

The invention belongs to the technical field of lithium-sulfur batteries, and particularly relates to a material for a lithium-sulfur battery positive electrode and a preparation method of the material. The material is a self-supporting mesoporous vanadium nitride nanowire/carbon nanotube composite material with a three-dimensional network structure. According to the material, the vanadium nitridenanowire with the mesoporous structure is connected with the carbon nanotube to form the self-supporting three-dimensional network structure; the material has high conductivity, ultrahigh specific surface area and excellent mechanical properties; and the method is simple, effective and easy to operate.

Description

technical field [0001] The invention belongs to the technical field of lithium-sulfur batteries, and in particular relates to a material for the positive electrode of lithium-sulfur batteries and a preparation method thereof. Background technique [0002] In the high-tech era, the demand for high-energy storage devices is increasing. Lithium-sulfur batteries are known for their extremely high theoretical energy density (2500Wh·kg -1 ) become one of the most promising rechargeable batteries. Lithium-sulfur battery is a battery system with metallic lithium as the negative electrode and elemental sulfur as the positive electrode. The sulfur positive electrode usually chooses an appropriate mixing ratio of active materials, conductive agents and binders; at the same time, due to the natural abundance of sulfur, low cost and environmental The advantages such as friendliness have made lithium-sulfur batteries arouse great interest in the academic circle in recent years. [0003]...

Claims

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Application Information

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IPC IPC(8): H01M4/62H01M10/052C01B21/06C01B32/168B82Y30/00
CPCH01M4/625H01M4/628H01M10/052C01B21/0617C01B32/168B82Y30/00C01P2004/80C01P2006/40H01M2004/021H01M2004/028Y02E60/10
Inventor 王新刘加兵
Owner INT ACAD OF OPTOELECTRONICS AT ZHAOQING SOUTH CHINA NORMAL UNIV
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