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Honeycomb stannic oxide material and preparation method thereof

A tin dioxide and honeycomb technology, applied in the field of honeycomb tin dioxide material and its preparation, can solve the problems of dispersive electron or ion transport obstacles, severe volume expansion, low agglomeration stability, etc., and achieve excellent electrochemical performance , the effect of enhancing conductivity

Inactive Publication Date: 2017-06-13
HUAZHONG UNIV OF SCI & TECH
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

For example, Lei Zhang et al. have prepared a porous tin dioxide hollow microcube structure by a selective etching method. The advantage is that the porous and hollow structure can provide more surface reaction sites, but the pure tin dioxide material is full of microcubes. The volume expansion during the discharge process is severe, and it is easy to agglomerate and has low stability, which brings great difficulties to the application of materials (Energy Environ.Sci., 2014, 7, 1013–1017); Jianping Li et al. prepared tin dioxide by template method / carbon core-shell sphere structure, the advantage is that the core-shell structure not only provides a certain buffer space, but also the carbon coating layer further avoids the agglomeration of tin dioxide, providing reliable cycle stability for the negative electrode material, however The dispersion of nanospheres leads to obstacles in the transport of electrons or ions during charge and discharge, which has a certain impact on the performance of electrode materials, especially the rate characteristics (CrystEngComm, 2014, 16, 517)

Method used

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  • Honeycomb stannic oxide material and preparation method thereof
  • Honeycomb stannic oxide material and preparation method thereof
  • Honeycomb stannic oxide material and preparation method thereof

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specific Embodiment approach 1

[0027] Specific embodiment one: present embodiment a kind of preparation method of honeycomb tin dioxide lithium (sodium) ion battery negative electrode material, realize according to the following steps:

[0028] Preparation of silica pellets: Measure 61.75mL of ethanol and 24.75mL of deionized water in the same beaker and mix evenly, then add 4.5mL of tetraethyl orthosilicate and 9mL of ammonia water with a mass fraction of 25% , stirred at room temperature for 8 hours, centrifuged and washed several times with deionized water and alcohol respectively and dried overnight at 60°C to obtain the product;

[0029] Preparation of tin dioxide-coated silica pellets: Weigh 0.04 g of silica pellets and ultrasonically disperse them in 60 mL of water-ethanol mixture to obtain a white suspension, wherein the volume fraction of ethanol is 37.5%; Then add 0.3g potassium stannate trihydrate and 1.8g urea and continue to stir for 5 minutes, transfer the suspension to a 100mL hydrothermal ke...

specific Embodiment approach 2

[0032] Embodiment 2: This embodiment is different from Embodiment 1 in that 0.2 g of glucose and 10 g of sodium chloride are dissolved in the dispersion in the step of preparing the honeycomb tin dioxide / carbon composite electrode material. Other parameters and specific implementation steps are the same as those in Embodiment 1. In Example 2, a larger proportion of carbon source was used, and the proportion of carbon in the prepared sample was increased to study the role played by the carbon layer in the designed structure.

[0033] In the steps of the above examples, under the condition that other steps and parameters remain unchanged, the amount of organic matter added in the preparation of the honeycomb tin dioxide / carbon composite electrode material is the key factor to control the experimental variables.

[0034] Two parameters are adopted in the embodiment, namely 0.1 g glucose and 0.2 g glucose. The difference between the two lies in the different proportions of organi...

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Abstract

The invention provides a preparation method of a honeycomb stannic oxide material, belongs to the technical field of preparation of lithium (sodium) ion battery electrode materials, and mainly aims to solve the problems of poor cycle stability and low specific capacity of conventional electrode materials. The method comprises the following steps: one, mixing a certain proportion of tetraethoxysilane, ethanol, water and ammonia water, stirring at room temperature to obtain silica beads; two, growing a layer of stannic oxide on the silica beads prepared in the step one by a hydrothermal method; and three, with sodium chloride as a template and glucose as a carbon source, carbonizing at high temperature to obtain a carbon film coating the nano beads, and etching silica by using sodium hydroxide, to obtain the honeycomb stannic oxide / carbon composite material. The stannic oxide / carbon composite material prepared by the template method shows excellent electrochemical performance such as high specific capacity and good cycle stability in lithium (sodium) ion batteries.

Description

technical field [0001] The invention belongs to the field of materials and electrochemical energy storage devices, and more specifically relates to a honeycomb tin dioxide material and a preparation method thereof. Background technique [0002] With the increasing demand for fossil fuels in modern life and industrial production, the earth is facing increasingly severe environmental problems, which also stimulates people to explore clean and renewable energy that can be applied on a large scale, and for most renewable energy, For example, solar energy and wind energy are intermittent, so the development of high-efficiency energy storage technology is particularly important for the large-scale application of renewable energy. [0003] As an excellent energy storage device, secondary lithium-ion batteries have developed rapidly in recent years and are widely used in various portable electronic devices and electric vehicles. At the same time, due to the limitation of lithium res...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01G19/02C01B32/05H01M4/48H01M10/0525H01M10/054
CPCC01G19/02C01P2002/72C01P2002/82C01P2002/88C01P2004/03C01P2004/04C01P2004/34C01P2004/62C01P2004/80C01P2006/40C01P2006/80H01M4/48H01M10/0525H01M10/054H01M2004/021Y02E60/10
Inventor 王春栋敖翔江建军
Owner HUAZHONG UNIV OF SCI & TECH
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