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Solid and liquid phase conversion mixed electrolyte as well as preparation method and application thereof

An electrolyte and hybrid technology, applied in the direction of fuel cell half-cells and primary battery half-cells, etc., can solve the problems of reduced battery life, reduced charge and discharge efficiency, and mutual conversion, so as to slow down the corrosion rate and improve Effects of energy density and cycle extension

Inactive Publication Date: 2012-07-04
LIAONING BROTHER ELECTRONICS TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Another major factor that determines the performance of lithium-air batteries is the electrolyte, of which solid electrolytes and gel electrolytes have good reliability and no electrolyte leakage, high specific energy, and wide cycle voltage, but the conductivity of most solid electrolytes at room temperature And the solubility is low; the organic electrolyte system is easy to cause the corrosion of the negative electrode lithium due to the use of water-containing organic solvents in the preparation, resulting in a decrease in the specific capacity of the lithium-air battery and a decrease in the charge-discharge efficiency; and the ionic liquid has a wide electrochemical window. Volatile, recyclable and other advantages, the application of new ionic liquids in the electrolyte research of lithium-air batteries has become a multidisciplinary research frontier
However, the ionic liquid currently used in lithium-air batteries only stays in the experimental stage, and it cannot be converted between solid phase and liquid phase with temperature changes. The pure liquid electrolyte makes the corrosion rate of the lithium metal negative electrode too fast, reducing the battery life

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0013] Step 1: In a three-neck flask equipped with a spherical condenser and a constant pressure dropping funnel, add 0.8 mol of N-methylimidazole and 80 mL of toluene, and 2 Warm up to 70°C under protection, slowly add 0.8 mol n-propane bromide dropwise under stirring, continue to react for 24 hours, let stand for 5 minutes to separate layers, discard the upper layer of toluene solution, wash the lower layer of yellow liquid with 50mL of toluene twice, 60°C After vacuum drying for 8 hours, bromo-1-methyl-3-propylimidazole was obtained as a yellow viscous liquid.

[0014] Step 2: Add 0.8 mol of KPF 6 Slowly drop the saturated aqueous solution into bromo-1-methyl-3-propylimidazole aqueous solution, stir at room temperature for 10 h, let it stand for 5 min to separate layers, take the oily liquid crude product in the lower layer, and wash repeatedly with deionized water until the water phase is free of Br — (detected with silver nitrate solution), vacuum dried to remove residua...

Embodiment 2

[0018] Step 1: In a three-neck flask equipped with a spherical condenser and a constant pressure dropping funnel, add 1.0 mol of N-methylimidazole and 100 mL of toluene, 2 Warm up to 80 °C under protection, slowly add 1.0 mol n-propane bromide dropwise under stirring, continue to react for 30 h, let stand for 10 min to separate layers, discard the upper layer of toluene solution, wash the lower layer of yellow liquid with 75 mL of toluene three times, 70 ℃ and vacuum-dried for 10 h to obtain a yellow viscous liquid of 1-methyl-3-propylimidazole bromide.

[0019] Step 2: Add 1.0 mol KPF 6 Saturated aqueous solution was slowly dropped into 1.0 mol bromo-1-methyl-3-propylimidazole aqueous solution, stirred at room temperature for 11 hours, allowed to stand for 10 minutes to separate layers, and the oily liquid crude product in the lower layer was removed, and deionized water was used repeatedly Wash until the aqueous phase is free of Br — (detected with silver nitrate solution)...

Embodiment 3

[0023] Step 1: In a three-necked flask equipped with a spherical condenser and a constant pressure dropping funnel, add 1.2 mol of N-methylimidazole and 120 mL of toluene, and 2 Under protection, the temperature was raised to 90 °C, and 1.2 mol of n-propane bromide was slowly added dropwise under stirring, and the reaction was continued for 36 h, and the layers were separated for 15 min, the upper layer of toluene solution was discarded, and the lower layer of yellow liquid was washed 3 times with 100 mL of toluene, 80 ℃ and vacuum-dried for 12 h to obtain bromo-1-methyl-3-propylimidazole yellow viscous liquid.

[0024] Step 2: Add 1.2 mol KPF 6 Slowly drop the saturated aqueous solution into bromo-1-methyl-3-propylimidazole aqueous solution, stir at room temperature for 12 h, let stand for 15 min to separate layers, take the oily liquid crude product in the lower layer, and wash repeatedly with deionized water until the water phase is free of Br — (detected with silver nitra...

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PUM

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Abstract

The invention discloses a solid and liquid phase conversion mixed electrolyte, a preparation method thereof and application thereof. The method comprises the following steps of: adding N-methylimidazole and methylbenzene, raising the temperature under the protection of N2, dropwise adding n-propyl bromide slowly, reacting the components continuously, standing the reaction product to be layered, discarding the methylbenzene solution on the upper layer, washing the yellow solution on the lower layer with methylbenzene, and drying the product in vacuum to obtain yellow thick liquid of 1-methyl-3-propylimidazolium; dropwise adding saturated aqueous solution of KPF6 into the yellow thick liquid slowly, stirring at the room temperature, standing the reaction product to be layered, repeatedly washing the crude product of oily liquid on the lower layer until no Br<1-> exists in the aqueous phase, and dehydrating the residual water to obtain pale-yellow 1-methyl-3-methylimidazolium hexafluorophosphate ionic liquid; and weighing LiPF6, and dissolving the LiPF6 in the liquid to prepare the mixed ionic liquid electrolyte. The electrolyte is in solid phase at low temperature and in liquid phase at high temperature, and can be converted between solid phase and liquid phase along with the change of temperature. The energy density of a lithium air battery prepared from the electrolyte can be improved, the corrosion speed of a lithium cathode can be slowed, and the cyclic times of the battery can be increased.

Description

technical field [0001] The invention relates to electrolyte preparation technology, in particular to a solid-liquid phase conversion mixed electrolyte and its preparation method and application. Background technique [0002] A lithium-air battery is a battery that uses lithium as the anode and oxygen in the air as the cathode reactant. Compared with lithium-ion batteries, it has a higher energy density because its cathode active material O 2 It can be obtained directly from the surrounding air without being stored in batteries. Theoretically, since oxygen is used as the cathode and the reactants are not limited, the capacity of the lithium-air battery depends only on the lithium electrode. At the same time, due to the high theoretical specific capacity of Li, the theoretical specific energy of the lithium-air battery can reach 11,140Wh / kg, This theoretical specific energy is higher than all current conventional power systems. Another major factor that determines the perfor...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M12/06
CPCY02E60/128
Inventor 蔡克迪彭亚晶孙曙光金振兴王道林王双龙牧伟芳
Owner LIAONING BROTHER ELECTRONICS TECH CO LTD
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