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A kind of negative electrode composite material sn/mxene@c and its preparation method

A composite material and negative electrode technology, which is applied in the field of negative electrode composite material Sn/MXene@C and its preparation, can solve the problems of not being able to effectively alleviate the volume effect, not having a stable frame structure, and not being able to form an SEI film, etc., to achieve good cycle stability High performance, wide applicability and low cost

Active Publication Date: 2021-03-05
CENT SOUTH UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] CN102231436A discloses a kind of preparation method of Sn-Sb / graphene nano-composite material, and has studied its electrochemical performance, experimental result shows that graphene-based Sn-Sb obviously improves as the charging and discharging capacity of lithium-ion battery negative electrode material; But this The research is to load Sn-Sb alloy on graphene. Because of its thin sheet structure, graphene does not have a stable frame structure, and its volume effect cannot be effectively alleviated during charging and discharging.
[0005] CN105720246A discloses a granular tin dioxide / two-dimensional nano-titanium carbide composite material, which uses a liquid phase method to prepare SnO 2 / Ti 3 C 2 composite material and showed that its electrochemical performance is superior to that of SnO alone in Li-ion batteries 2 materials; however, in this study, more dispersed in Ti 3 C 2 The interlayer and surface SnO of the material 2 The particles are still directly exposed on the surface of the composite material, which will lead to direct contact between the nanoparticles and the electrolyte, and the inability to form a stable SEI film, resulting in a large number of side reactions

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  • A kind of negative electrode composite material sn/mxene@c and its preparation method
  • A kind of negative electrode composite material sn/mxene@c and its preparation method
  • A kind of negative electrode composite material sn/mxene@c and its preparation method

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Embodiment 1

[0036] This embodiment includes the following steps:

[0037] (1) Add 1000 mg Ti 3 AlC 2 The powder was added to 30 g of hydrofluoric acid aqueous solution with a mass concentration of 40 wt%, and sealed with a plastic wrap, and stirred at a constant temperature of 95 °C for 7 h at a stirring speed of 600 rpm to etch away the Al layer, and the reacted The solution was centrifuged, then centrifuged and washed with deionized water for 6 times, until the pH of the lotion was neutral, the centrifugation speed was 10,000 rpm, and the centrifugation time was 10 min each time, and the cleaned precipitate was ultrasonicated with deionized water as solvent Disperse, the ultrasonic power is 400 W, the time is 2 h, the ultrasonic solution is centrifuged and washed twice with absolute ethanol, put in a 60 °C oven, and dried for 8 h to obtain MXene powder;

[0038](2) Weigh 100 mg of the MXene powder obtained in step (1), add it into 40 ml of absolute ethanol, and disperse it ultrasonica...

Embodiment 2

[0047] This embodiment includes the following steps:

[0048] (1) Add 1250 mg Ti 3 AlC 2 The powder was added to 40 g of hydrofluoric acid aqueous solution with a mass concentration of 35 wt%, and sealed with a plastic wrap, stirred at a constant temperature of 94 °C for 8 h, and kept at a stirring speed of 450 rpm, the Al layer was etched away, and the reaction solution was centrifuged. Centrifuge and wash with deionized water for 7 times until the pH of the lotion is neutral, the centrifugal speed is 9800 rpm, and the centrifugation time is 12 minutes each time. The precipitate after cleaning is ultrasonically dispersed with deionized water as a solvent. The ultrasonic power is 500 W, time 1.5 h, the ultrasonic solution was centrifuged and washed twice with absolute ethanol, placed in a 70 °C oven, and dried for 12 h to obtain Ti 2 C 3 powder;

[0049] (2) Weigh 160 mg of Ti obtained in step (1) 2 C 3 The powder was ultrasonically dispersed in 40ml deionized water for ...

Embodiment 3

[0057] This embodiment includes the following steps:

[0058] (1) Add 1100 mg Ti 3 AlC 2 The powder was added to 35 g of hydrofluoric acid aqueous solution with a mass concentration of 38 wt%, and sealed with a plastic wrap, at a constant temperature of 93°C, stirred for 7.5 h, and kept at a stirring speed of 650 rpm, etched away the Al layer, and centrifuged the reaction solution. Centrifuge and wash with deionized water for 7 times until the pH of the lotion is neutral, the centrifugal speed is 9500 rpm, and the centrifugation time is 11 minutes each time. The precipitate after cleaning is ultrasonically dispersed with deionized water as a solvent. The ultrasonic power is 300 W, time 3 h, the ultrasonic solution was centrifuged and washed twice with absolute ethanol, placed in an oven at 75 °C, and dried for 15 h to obtain Ti 2 C 3 powder;

[0059] (2) Weigh 80 mg of Ti obtained in step (1) 2 C 3 The powder was ultrasonically dispersed in 40 ml deionized water for 20 m...

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Abstract

The invention relates to a negative electrode composite material Sn / MXene@C and a preparation method thereof. The negative electrode composite material Sn / MXene @ C is of a multi-layer sandwich structure of which the surface layer is packaged by carbon, and the multi-layer sandwich structure is MXene of which Sn nanoparticles are embedded between layers. The preparation method comprises the following steps: sequentially adding PVP and soluble divalent tin salt into MXene dispersion liquid, uniformly mixing, and heating and evaporating to obtain sediments; and carrying out heat treatment on thesediments in a reducing atmosphere to obtain the Sn / MXene@C. The negative electrode composite material disclosed by the invention has a stable frame structure, and a battery assembled by the positiveelectrode prepared from the negative electrode composite material is high in specific capacity, good in cycling stability and good in rate capability. The preparation method is simple to operate andlow in preparation cost.

Description

technical field [0001] The invention relates to the field of negative electrode materials for lithium batteries, in particular to a negative electrode composite material Sn / MXene@C and a preparation method thereof. Background technique [0002] With the depletion of traditional fossil energy and the aggravation of environmental problems, the research on new energy development and storage technology is imminent. In the field of energy storage, lithium-ion batteries (LIBs) have become the most widely used energy storage devices due to their high capacity, small size, and light weight. However, with the continuous improvement of battery energy density requirements in the power battery market, technological breakthroughs in lithium battery systems have gradually encountered bottlenecks. The low theoretical specific capacity of traditional carbon anode materials is one of the main problems. Therefore, it is extremely important to develop anode materials with higher lithium stora...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/36H01M4/38H01M4/62H01M10/0525
CPCH01M4/366H01M4/387H01M4/625H01M4/628H01M10/0525H01M2004/021H01M2004/027Y02E60/10
Inventor 郑俊超左定川宋生超贺振江罗紫艳
Owner CENT SOUTH UNIV