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Continuous electron ion fast conducting type double perovskite magnesium ion battery cathode material and preparation method thereof

A magnesium-ion battery and double perovskite technology, which is applied in battery electrodes, circuits, electrical components, etc., can solve the problems of complex matrix action mechanism, shorten the diffusion time of magnesium ions, and material lattice transformation, so as to accelerate the migration ability and The rate of redox reaction, the effect of reducing electron migration resistance and improving electronic conductivity

Inactive Publication Date: 2017-10-24
宁波吉电鑫新材料科技有限公司
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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 lower; 2, the product magnesium oxide after conversion reaction is electronic insulator and its magnesium ion diffusion activation energy is also higher, causes larger 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 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 and other problems; ion doping Doping is also an effective way to adjust the microstructure of the lattice and change the transport characteristics of lattice electrons and ions. However, the mechanism of ion doping or even multi-ion synergistic doping on the matrix is ​​very complicated, and the effect is often unpredictable.

Method used

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  • Continuous electron ion fast conducting type double perovskite magnesium ion battery cathode material and preparation method thereof

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Embodiment 1

[0021] Embodiment 1: Magnesium nitrate hexahydrate, lithium nitrate, tetrabutyl titanate, strontium nitrate, lanthanum nitrate hexahydrate, yttrium nitrate hexahydrate, copper nitrate trihydrate, zinc nitrate hexahydrate, niobium oxalate according to the stoichiometric formula Mg 0.8 Sr 0.2 La 0.5 Y 0.2 Li 0.3 Ti 0.8 Cu 0.1 Zn 0.1 NbO 6 Mix, add citric acid whose amount is 5.0 times of the total metal ion substance, add water and stir evenly to form a total metal ion concentration of 1.0mol L -1 The initial aqueous solution; mix and dissolve 6g acrylamide / 100mL water volume of acrylamide and 1g N,N'-methylenebisacrylamide / 100mL water volume N,N'-methylenebisacrylamide and water, and the acrylamide in the solution The amount of the substance is 0.5 times the amount of the total metal ion substance in the initial aqueous solution; use a polytetrafluoroethylene stirring paddle to stir at a speed of 1500rpm for 5 minutes, then raise it to 75°C at a speed of 5°C / min and main...

Embodiment 2

[0022] Embodiment 2: Magnesium nitrate hexahydrate, lithium nitrate, tetrabutyl titanate, strontium nitrate, lanthanum nitrate hexahydrate, yttrium nitrate hexahydrate, copper nitrate trihydrate, zinc nitrate hexahydrate, niobium oxalate according to the stoichiometric formula Mg 0.8 Sr 0.2 La 0.5 Y 0.2 Li 0.3 Ti 0.8 Cu 0.1 Zn 0.1 NbO 6 Mix, add citric acid whose amount is 7 times the amount of total metal ion substances, add water and stir evenly to form a total metal ion concentration of 1.5mol L -1 The initial aqueous solution; mix and dissolve 6g acrylamide / 100mL water volume of acrylamide and 1g N,N'-methylenebisacrylamide / 100mL water volume N,N'-methylenebisacrylamide and water, and the acrylamide in the solution The amount of the substance is 0.7 times the amount of the total metal ion substance in the initial aqueous solution; use a polytetrafluoroethylene stirring paddle to stir at a speed of 1700rpm for 10 minutes, then raise it to 80°C at a speed of 8°C / min a...

Embodiment 3

[0023] Embodiment 3: Magnesium nitrate hexahydrate, lithium nitrate, tetrabutyl titanate, strontium nitrate, lanthanum nitrate hexahydrate, yttrium nitrate hexahydrate, copper nitrate trihydrate, zinc nitrate hexahydrate, niobium oxalate according to the stoichiometric formula Mg 0.8 Sr 0.2 La 0.5 Y 0.2 Li 0.3 Ti 0.8 Cu 0.1 Zn 0.1 NbO 6 Mix, add citric acid whose amount is 10.0 times of the total metal ion substance, add water and stir evenly to form a total metal ion concentration of 2.5mol L -1 The initial aqueous solution; mix and dissolve 6g acrylamide / 100mL water volume of acrylamide and 1g N,N'-methylenebisacrylamide / 100mL water volume N,N'-methylenebisacrylamide and water, and the acrylamide in the solution The amount of the substance is 1.2 times the amount of the total metal ion substance in the initial aqueous solution; use a polytetrafluoroethylene stirring paddle to stir at a speed of 2000rpm for 15 minutes, then raise it to 85°C at a speed of 9°C / min and ma...

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Abstract

The invention provides a continuous electron ion fast conducting type double perovskite magnesium ion battery cathode material and a preparation method thereof. The cathode material is composed of Mg0.8Sr0.2La0.5Y0.2Li0.3Ti0.8Cu0.1Zn0.1NbO6, a continuous porous structure of gel is used as a template in a preparation process to form a continuous porous double perovskite structure product with mutually adhered particles; meanwhile, a continuous carbon film with high conductivity and adhered on the surface of an active material is formed by cracking under a protective gas; this morphology is conductive to reducing the grain boundary resistance and the electron transfer resistance, increasing the contact area with the electrolyte and having certain structure rigidity; the electronic conductivity is improved by the common occupation of the Mg and La on the A position and partial Sr substitution on the Mg position and the partial Y and Li substitution on the La position; and the stability of the perovskite structure is improved by the Cu and Zn doping on the B position, and the high-performance magnesium ion battery cathode material is formed at last.

Description

technical field [0001] The invention relates to the technical field of a method for manufacturing a negative electrode material of a magnesium ion battery. 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 caused by automobile exhaust are beco...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/485H01M4/131H01M4/1391
CPCH01M4/131H01M4/1391H01M4/485Y02E60/10
Inventor 水淼
Owner 宁波吉电鑫新材料科技有限公司
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