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A perovskite mgnbo3 magnesium-ion battery anode material synthesized by selective crystallization controlled by electric field

A magnesium ion battery, selective crystallization technology, applied in battery electrodes, secondary batteries, circuits, etc., can solve problems such as shortening the diffusion time of magnesium ions, material lattice transformation, and difficulty in particle electron conduction, so as to reduce electron migration resistance, Effect of reducing grain boundary resistance and increasing contact area

Active Publication Date: 2018-10-23
宁波吉电鑫新材料科技有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, it is still very difficult to take into account the rate performance and cycle capacity retention performance of the material.
The main reasons are as follows: 1. When the redox reaction occurs, the electrode material should have fast lithium ion intercalation and deintercalation and electronic conduction, that is, it should have good electronic conductivity and ion conductivity at the same time. Many negative electrode materials have high However, it is an electronic insulator, and some negative electrode materials are good electronic conductors, but the diffusion capacity of lithium ions is weak, which greatly increases the polarization of the battery; 2. Many electrode materials are intercalated with lithium ions and There is a large volume change during the deintercalation process, resulting in the breakage of electrode material particles and the loss of effective electrode materials during the cycle. The large volume change also brings about the transformation of the material lattice during the charging and discharging process to produce a second phase. seriously affect the performance of the battery
3. Lithium battery negative electrode material with conversion reaction mechanism, the electronic insulation of the reaction product lithium compound seriously affects the reversibility of the material
ABOs 3 When the alloy reaction is carried out, the oxide can react with two metals, which may produce alloy solid solutions in various phases. Due to the interaction of bimetals, it may also produce electrochemical characteristics that are completely different from those of single metals. Therefore, ABOs 3 Type oxide has the potential to become a high-performance magnesium-ion battery anode material, which may provide close to or more than 300mAh.g -1 The specific capacity, the volume change of the material that magnesium ions enter or exit is also small; however, the research and development of this material in magnesium ion batteries is basically blank
And its main problem is: 1, ionic conductivity and electron conductivity are low; 2, the product magnesium oxide after conversion reaction is electronic insulator and its magnesium ion diffusion activation energy is also higher, causes greater electrochemical polarization; 3. The synthesis temperature is high, which is easy to cause the growth and agglomeration of grains
[0014] In response to these problems, changing the morphology of the material can alleviate these problems to a certain extent. For example, reducing the particle size of the material to the nanometer scale can reduce the diffusion path of magnesium ions, shorten the diffusion time of magnesium ions, and improve the kinetics of the material. Performance; too small a particle size can easily cause difficulties in electronic conduction between particles; the same agglomeration between particles or too large particles can easily cause electrolyte penetration difficulties between particles, slow migration of magnesium ions, etc.

Method used

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  • A perovskite mgnbo3 magnesium-ion battery anode material synthesized by selective crystallization controlled by electric field

Examples

Experimental program
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Embodiment 1

[0021]Example 1: Magnesium nitrate hexahydrate and niobium hydroxide are put into a ball mill at a ratio of 1:1 in the amount of substance, the mass ratio of the ball mill and the material is 20:1, and ball milled at a speed of 400 rpm for 20 hours. The ball-milled material is heated up to 900°C at a rate of 10°C / min in a tube furnace, and then a DC voltage of 900V is applied to both ends of the tube furnace. Cool the furnace to 30°C; grind the cooled material in a mortar for 12 minutes, and immerse it in a saturated solution of lithium metaborate at a constant temperature of 30°C under constant stirring at a speed of 1200 rpm with a polytetrafluoroethylene stirring paddle. The mass ratio of the mass to the immersed cooled material was 10:1. After stirring for 9 minutes, the constant temperature was lowered to 22°C and stirring was continued for 15 minutes. After that, it was filtered and dried in a drying oven at 160°C for 10 hours. Then the dried material was heated to 550°C...

Embodiment 2

[0022] Example 2: Magnesium nitrate hexahydrate and niobium hydroxide are put into a ball mill at a ratio of 1:1 in the amount of substance, the mass ratio of the ball mill and the material is 20:1, and ball milled at a speed of 400 rpm for 15 hours. The ball-milled material is heated to 900°C at a rate of 8°C / min in a tube furnace, and then a DC voltage of 900V is applied to both ends of the tube furnace. Cool the furnace to 30°C; grind the cooled material in a mortar for 12 minutes, and immerse it in a saturated solution of lithium metaborate at a constant temperature of 30°C under constant stirring at a speed of 1000 rpm with a polytetrafluoroethylene stirring paddle. The mass ratio of the mass to the immersed cooled material was 10:1. After stirring for 7 minutes, the constant temperature was lowered to 20°C and stirred for 10 minutes, then filtered and dried in a drying oven at 140°C for 8 hours. Then the dried material was heated to 500°C at a rate of 8°C / min in a tube f...

Embodiment 3

[0023] Example 3: Magnesium nitrate hexahydrate and niobium hydroxide were put into a ball mill at a ratio of 1:1 in the amount of substance, the mass ratio of the ball mill and the material was 20:1, and ball milled at a speed of 200 rpm for 10 hours. The ball-milled material is heated to 800°C at a rate of 2°C / min in a tube furnace, and then a DC voltage of 600V is applied to both ends of the tube furnace. Cool the furnace to 30°C; grind the cooled material in a mortar for 6 minutes, and immerse it in a saturated solution of lithium metaborate at a constant temperature of 30°C under constant stirring at a speed of 900 rpm with a polytetrafluoroethylene stirring paddle. The mass ratio of the mass to the immersed cooled material was 10:1. After stirring for 5 minutes, the constant temperature was lowered to 18°C ​​and stirring was continued for 5 minutes. After that, it was filtered and dried in a drying oven at 120°C for 5 hours. Then the dried material was heated to 450°C at...

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Abstract

The invention provides a perovskite MgNbO3 magnesium ion battery negative electrode material synthesized through electric field regulation and control selective crystallization and a preparation method thereof. The material is characterized in that the crystallization characteristics of crystals with the lattice defects are changed by applying the electric field in the specific direction during high-temperature solid-phase reaction are utilized; particles with column-shaped appearances grow in the electric field directions; meanwhile, through the non-uniform crystallization on the surfaces of the particles with the column-shaped appearances, sintering agents are nonuniformly adhered on positions with the great surface curvature radius to form the continuous porous appearance. The appearance is favorable for reducing the grain boundary resistance and the electronic migration resistance; the oxidation-reduction reaction speed and the magnesium ion migration capability in the lattices and electrolyte are accelerated; certain structure rigidity is realized; the buffer is formed for the material volume change in the charging and discharging process, so that the high-performance magnesium ion battery negative material is formed.

Description

technical field [0001] The invention relates to the technical field of a method for manufacturing a high-performance perovskite composite magnesium-ion battery negative electrode material. Background technique [0002] Lithium-ion secondary batteries have the absolute advantages of high volume, weight-to-energy ratio, high voltage, low self-discharge rate, no memory effect, long cycle life, and high power density. Currently, the global mobile power market has an annual share of more than 30 billion US dollars and Gradually grow at a rate of more than 10%. Especially in recent years, with the gradual depletion of fossil energy, new energy sources such as solar energy, wind energy, and biomass energy have gradually become alternatives to traditional energy sources. Among them, wind energy and solar energy are intermittent, and a large amount of energy is used simultaneously to meet the needs of continuous power supply. Energy storage batteries; urban air quality problems caus...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G33/00H01M4/58H01M10/054
CPCC01G33/00C01P2006/40H01M4/5825H01M10/054Y02E60/10
Inventor 水淼
Owner 宁波吉电鑫新材料科技有限公司