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Magnesium-doped positive electrode material for magnesium ion battery and preparation method thereof

A technology for magnesium ion batteries and positive electrode materials, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of poor compatibility between materials and electrolytes, slow dynamic insertion of magnesium, and difficulty in moving embedded materials, etc., to achieve scale Chemical industry production, stable crystal structure, improved electrical conductivity and electrochemical activity

Active Publication Date: 2017-10-24
NINGBO POLYTECHNIC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] There are two main obstacles to the technological development of magnesium-ion batteries: first, in the process of charging and discharging, a surface passivation film will be formed on the surface of the electrode material. Unlike lithium, the surface film of lithium can conduct lithium ions, while The passivation film formed on the surface of the magnesium electrode is difficult to conduct divalent magnesium ions, so that the deposition and dissolution of magnesium can proceed smoothly; Intercalation, the movement in the intercalation material is difficult, and there are few matrix materials for the rapid intercalation of magnesium ions, so the selection of positive electrode materials has become an important issue. Finding suitable positive electrode materials is the key to the research of magnesium ion batteries
[0004] People have carried out research on the positive electrode materials of magnesium ion batteries, and most of the positive electrode materials of magnesium ion batteries are inorganic transition metal compounds, concentrated as oxides (such as V 2 o 5 ), sulfide (such as the sulfide Mo of the Chevrel phase 6 S 8 ), phosphate polyanions (such as Mg 0.5+y (Fe y Ti 1-y ) 2 (PO 4 ) 3 ), etc., the main problems of these materials are: poor compatibility between materials and electrolyte, slow kinetics of magnesium intercalation, low intercalation capacity, large charge-discharge voltage difference, and poor cycle performance

Method used

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  • Magnesium-doped positive electrode material for magnesium ion battery and preparation method thereof
  • Magnesium-doped positive electrode material for magnesium ion battery and preparation method thereof
  • Magnesium-doped positive electrode material for magnesium ion battery and preparation method thereof

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Effect test

Embodiment 1

[0032] A method for preparing a magnesium-site doped magnesium ion battery cathode material includes the following steps:

[0033] Accurately weigh 0.98mol of Mg(OH) 2 , 0.02mol of Ca(OH) 2 , 1.0mol of Ni(OH) 2 , Add an appropriate amount of deionized water, ball mill and mix uniformly, take it out and dry at 120°C, pre-burn at 400°C for 2 hours, and crush into powder. Weigh 1.0 mol of tetraethylorthosilicate, add the solid powder, tetraethylorthosilicate and 5.75g of citric acid into a stainless steel tank lined with polytetrafluoroethylene, mix thoroughly in anhydrous ethanol solvent, and in a sealed state Incubate at 210°C for 4 days to obtain a gel. After drying the gel, it was mixed with 32 grams of glucose and ball milled, and sintered in an inert atmosphere at 1050°C for 6 hours to obtain a carbon-coated magnesium ion battery cathode material Mg 0.98 Ca 0.02 NiSiO 4 .

[0034] Performance Testing:

[0035] The synthesized magnesium ion battery cathode material Mg 0.98 Ca 0.0...

Embodiment 2

[0039] Accurately weigh 0.97mol of magnesium acetate, 0.03mol of strontium oxalate, 1.0mol of nickel oxalate, add an appropriate amount of deionized water, ball mill and mix uniformly, take it out, dry at 120°C, pre-fire at 350°C for 4 hours, and crush into powder . Weigh 1.0 mol of tetraethylorthosilicate, add the solid powder, tetraethylorthosilicate and 9.2g of citric acid to a stainless steel tank lined with polytetrafluoroethylene, mix well in anhydrous ethanol solvent, and in a sealed state Incubate at 260°C for 2 days to obtain a gel. After drying the gel, it was mixed with 45 grams of glucose and ball milled, and sintered in an inert atmosphere at 1100°C for 4 hours to obtain a carbon-coated magnesium ion battery cathode material Mg 0.97 Sr 0.03 NiSiO 4 .

[0040] Performance Testing:

[0041] The synthesized magnesium ion battery cathode material Mg 0.97 Sr 0.03 NiSiO 4 Mix uniformly with acetylene black and polytetrafluoroethylene at a mass ratio of about 75:15:10. Use ...

Embodiment 3

[0043] Accurately weigh 0.99 mol of magnesium oxalate, 0.01 mol of barium hydroxide, and 1.0 mol of nickel acetate, add an appropriate amount of deionized water, ball mill and mix uniformly, take it out, dry at 120°C, pre-burn at 380°C for 3 hours, and crush into powder. Weigh 1.0 mol of tetraethylorthosilicate, add the solid powder, tetraethylorthosilicate and 10.5g of citric acid into a stainless steel tank lined with polytetrafluoroethylene, mix thoroughly in anhydrous ethanol solvent, and in a sealed state Incubate at 300°C for 1 day to obtain a gel. After drying the gel, it was mixed with 25 grams of polyethylene glycol and ball milled, and sintered in an inert atmosphere at 950°C for 6 hours to obtain a carbon-coated magnesium ion battery cathode material Mg 0.99 Ba 0.01 NiSiO 4 .

[0044] The synthesized magnesium ion battery cathode material Mg 0.99 Ba 0.01 NiSiO 4 Mix uniformly with acetylene black and polytetrafluoroethylene at a mass ratio of about 75:15:10. Use a fil...

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Abstract

The invention relates to a magnesium-doped positive electrode material for a magnesium ion battery and a preparation method thereof, and belongs to positive electrode materials for rechargeable batteries in energy materials. The molecular formula of the positive electrode material is Mg(1-x)AxNiSiO4, wherein A is one of doping elements Ca, Sr and Ba, and x is equal to 0.001 to 0.08. The preparation method comprises the following steps: accurately weighing a magnesium source compound, a doping element compound and a nickel source compound according to the atom mole ratio of Mg, A to Ai being (1-x): x: 1, adding an appropriate amount of deionized water, ball-milling and mixing uniformly, drying after taking out the mixture, and firing to obtain solid powder. Tetraethyl orthosilicate is weighed in proportion according to the atom mole ratio of Ni to Si being 1: 1, the solid powder, the tetraethyl orthosilicate and an appropriate amount of citric acid are sufficiently mixed in an absolute ethyl alcohol solvent, and the mixture is put in a stainless steel tank to obtain a gel substance. Then, mixed ball-milling is carried out with a carbon source compound, and sintering is carried out in an inert atmosphere for a few hours, so that the carbon coated positive electrode material Mg(1-x)AxNiSiO4 for the magnesium ion battery is obtained.

Description

Technical field [0001] The invention belongs to the field of preparation of cathode materials for magnesium ion batteries, and particularly relates to a magnesium site-doped nickel magnesium silicate anode material Mg for magnesium ion batteries (1-x) A x NiSiO 4 And its preparation method. Background technique [0002] Lithium-ion batteries are currently the most widely used secondary batteries. However, the global lithium resources are not rich. Lithium-ion batteries have greater safety hazards in the application process, especially when used as power batteries, forcing people to develop lithium-ion batteries At the same time, strive to find other secondary battery systems. In recent years, certain progress has been made in the research of magnesium-ion batteries. The diagonal positions of magnesium and lithium in the periodic table, according to the law of diagonals, have many similarities in their chemical properties. Magnesium reserves are very abundant on the earth. my cou...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/58H01M4/525H01M4/46H01M10/0525
CPCH01M4/466H01M4/525H01M4/5825H01M10/0525Y02E60/10
Inventor 袁正勇彭振博
Owner NINGBO POLYTECHNIC
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