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A kind of quasi-solid electrolyte and its preparation method and application

An electrolyte and quasi-solid-state technology, applied in solid electrolytes, non-aqueous electrolytes, circuits, etc., can solve the problems of interface stability and affect the cycle stability of lithium negative electrodes, and achieve excellent mechanical properties and chemical/electrochemical properties.

Active Publication Date: 2019-11-19
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is an interface stability problem between the ceramic electrolyte and lithium metal, and there is also an interface stability problem between the liquid electrolyte and lithium metal, which affects the cycle stability of the lithium negative electrode.

Method used

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  • A kind of quasi-solid electrolyte and its preparation method and application
  • A kind of quasi-solid electrolyte and its preparation method and application
  • A kind of quasi-solid electrolyte and its preparation method and application

Examples

Experimental program
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Embodiment 1

[0066] The ceramic electrolyte was prepared by the sol-gel method. 19.6 mL of 25% ammonia water was added dropwise to 10 mL of tetraisopropyl titanate, and the precipitate was obtained after magnetic stirring for 1 hour. The precipitate was filtered and dispersed in 40 mL of deionized water. Stir evenly, then add 80mL of oxalic acid with a concentration of 1mol / L, and stir well until the precipitate is completely dissolved to obtain solution A; add 1.832 g of LiNO 3 , 2.212g Al(NO 3 ) 3 ·9H 2 O, 7.751 grams (NH 4 ) 2 HPO 4 Add to the above-mentioned solution A in step, and stir thoroughly to obtain solution B; dissolve 6 grams of cetyltrimethylammonium bromide in 40 mL of absolute ethanol, and stir at 40°C for 2 hours to obtain solution C; C was added to solution B, fully stirred at 80 ℃ to obtain a colloidal precursor, and then the precursor was placed in a tube furnace, at a heating rate of 2 ℃ / min in an air atmosphere to 650 ℃, and in argon Calcined in an atmosphere for 12 ...

Embodiment 2

[0082] The ceramic electrolyte was prepared by the sol-gel method. 19.6 mL of 25% ammonia water was added dropwise to 10 mL of tetraisopropyl titanate, and the precipitate was obtained after magnetic stirring for 1 hour. The precipitate was filtered and dispersed in 40 mL of deionized water. Stir evenly, then add 80mL of oxalic acid with a concentration of 1mol / L, stir well until the precipitate is completely dissolved, and obtain solution A; add 1.761 g of LiNO 3 , 2.581 grams of Al(NO 3 ) 3 ·9H 2 O, 7.751 grams (NH 4 ) 2 HPO 4 Add to the above-mentioned solution in the step and obtain solution B after thorough stirring; dissolve 6 g of cetyltrimethylammonium bromide in 40 mL of absolute ethanol and stir at 40°C for 2 hours to obtain solution C; Add to solution B, stir well at 80°C to obtain a colloidal precursor, then place the precursor in a tube furnace and raise it to 600°C in an air atmosphere at a heating rate of 2°C / min, and place it in an argon atmosphere Calcined in me...

Embodiment 3

[0086] The ceramic electrolyte was prepared by the sol-gel method. 19.6 mL of 25% ammonia water was added dropwise to 10 mL of tetraisopropyl titanate, and the precipitate was obtained after magnetic stirring for 1 hour. The precipitate was filtered and dispersed in 40 mL of deionized water. Stir evenly, then add 80mL of oxalic acid with a concentration of 1mol / L, and stir well until the precipitate is completely dissolved to obtain solution A; add 1.902 g of LiNO 3 , 1.843 grams of Al(NO 3 ) 3 ·6H 2 O, 7.751 grams (NH 4 ) 2 HPO 4 Add to the above-mentioned solution in the step and obtain solution B after thorough stirring; dissolve 6 g of cetyltrimethylammonium bromide in 40 mL of absolute ethanol and stir at 40°C for 2 hours to obtain solution C; Add to solution B, stir well at 80°C to obtain a colloidal precursor, then place the precursor in a tube furnace, raise it to 550°C in an air atmosphere at a heating rate of 2°C / min, and place it in an argon atmosphere Calcined in med...

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Abstract

The invention discloses a quasi-solid electrolyte which is prepared from the following raw materials including a polymer, a ceramic electrolyte, lithium salt and ionic liquid; the polymer is preparedfrom polyvinylidene fluoride-hexafluoropropylene and polypropylene carbonate; the ceramic electrolyte is prepared from a principal-phase lithium titanium aluminum phosphate and impurity-phase TiP2O7 / TiO2; and the ionic liquid is fluorine-containing imidazolium ionic liquid. The invention also discloses the quasi-solid electrolyte which has high mechanical strength and toughness, high room-temperature lithium ion conductivity and high chemical / electrochemical stability with a metal lithium negative electrode and an oxide positive electrode, is used for a metal lithium cell, a lithium air cell and a lithium-sulfur battery and can realize good electrochemical performance.

Description

Technical field [0001] The invention relates to the field of a novel lithium battery solid electrolyte, in particular to a quasi-solid electrolyte and a preparation method and application thereof. Background technique [0002] With the rapid development of the new energy automobile industry, the requirements for the energy density of power batteries are getting higher and higher, and the energy density of traditional lithium-ion batteries is close to the bottleneck value, and the development of new lithium battery systems has become an urgent need at present. Substituting metal lithium for the graphite negative electrode of a lithium-ion battery can significantly increase the energy density of the battery and reduce the volume of the battery. However, the compatibility of metallic lithium with liquid electrolytes is poor, and metallic lithium is prone to form dendrites during repeated charging and discharging, and it is easy to pierce the diaphragm and cause safety problems. By ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M10/0562
CPCH01M10/0562H01M2300/0068Y02E60/10
Inventor 谢健朱崇佳孙秋实曹高劭赵新兵
Owner ZHEJIANG UNIV