CN103456504A - Gel polymer electrolyte film, and manufacturing method and application for same - Google Patents

Gel polymer electrolyte film, and manufacturing method and application for same Download PDF

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CN103456504A
CN103456504A CN2012101756341A CN201210175634A CN103456504A CN 103456504 A CN103456504 A CN 103456504A CN 2012101756341 A CN2012101756341 A CN 2012101756341A CN 201210175634 A CN201210175634 A CN 201210175634A CN 103456504 A CN103456504 A CN 103456504A
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polymer electrolyte
gel polymer
electrolyte film
ionic liquid
hours
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周明杰
刘大喜
王要兵
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Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
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Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/13Energy storage using capacitors

Abstract

An embodiment of the invention discloses a gel polymer electrolyte film. The gel polymer electrolyte film is made of a mixed material. A polymer substrate material and ionic liquid are mixed to form the mixed material, a mass ratio of the polymer substrate material to the ionic liquid is 100:30-50, the polymer substrate material is polyacrylonitrile-methyl methacrylate, and the ionic liquid is N-methylpiperidine ionic liquid. The embodiment of the invention further discloses a manufacturing method and application for the gel polymer electrolyte film. The gel polymer electrolyte film, the manufacturing method and the application have the advantages that the safety performance is excellent, environments are protected, large-scale manufacturing is facilitated, and the like.

Description

A kind of gel polymer electrolyte film and its production and use
Technical field
The present invention relates to the electrochemical device association area, relate in particular to a kind of gel polymer electrolyte film and its production and use.
Background technology
Ultracapacitor is a kind of novel energy device between rechargeable battery and capacitor, have that volume is little, capacity is large, charging rate is fast, have extended cycle life, the advantage such as discharging efficiency is high, operating temperature range is wide, good reliability and contaminant-free maintenance-free, be a kind of novel, efficient, practical energy accumulating device, thereby be widely used in AC-battery power source of military field, device for mobile communication, computer and electric automobile etc.
The ultracapacitor working electrolyte is divided into aqueous electrolyte, organic liquid electrolyte and polymer dielectric.The decomposition voltage of aqueous electrolyte is low, thereby studies less.The advantage of now widely used liquid electrolyte is that conductivity is high, but inflammable owing to containing, volatile organic solvent, it discharges fuel gas in charge and discharge process, particularly under some unconventional condition of work, (as high-power, discharge and recharge, super-charge super-discharge etc.) produces the generation that gas is accelerated in large calorimetric meeting, cause inner pressure of battery to increase, Leakage Gas, blast even on fire, thereby have serious potential safety hazard.The studied persons of advantage such as polymer dielectric ultracapacitor and polymer electrolyte lithium-ion battery are safe because having, nothing is leaked, leakage current is little pay attention to.But under the solid polymer electrolyte room temperature, conductivity is lower by (10 -5~ 10 -4s/cm), use application to be restricted, thereby gel polymer electrolyte become research emphasis.
Summary of the invention
Given this, the embodiment of the present invention aims to provide a kind of gel polymer electrolyte film and preparation method thereof, has that security performance is high, environmental friendliness, is conducive to the characteristics such as extensive preparation, can be for the preparation of ultracapacitor.
The embodiment of the present invention provides a kind of gel polymer electrolyte film, the material of described gel polymer electrolyte film comprises the composite material that Polymers bottom material and ionic liquid are mixed to form, the mass ratio of described Polymers bottom material and described ionic liquid is 100:30 ~ 50, described Polymers bottom material is polyacrylonitrile-methyl methacrylate, and described ionic liquid is for having the compound as shown in structural formula (1):
Figure BDA00001709469200021
In formula, Y -for BF 4 -, PF 6 -, (CF 3sO 2) 2n -or CF 3sO 3 -.
Preferably, the matter average molecular weight of polyacrylonitrile-methyl methacrylate (P (AN-MMA)) is 10 ~ 500,000.
Correspondingly, the embodiment of the present invention also provides a kind of preparation method of gel polymer electrolyte film, comprises the following steps:
(1) ratio that is 1:1.05 ~ 1.2 with the halo propene carbonate according to mol ratio by the N-methyl piperidine is mixed, and is heated to 60 ℃ ~ 80 ℃ under inert gas shielding, and stirring reaction 48 ~ 72 hours obtains having the compd A that following structural formula means:
Figure BDA00001709469200022
In formula, X -for Cl -, Br -, I -;
(2) by described compd A and general formula, be M +y -salt according to the ratio of mol ratio 1: 1 ~ 1.1, mix, add deionized water, at room temperature stirring reaction is 4 ~ 24 hours, obtains having the ionic liquid meaned as structural formula (1):
Figure BDA00001709469200023
Wherein, M +for Na +, K +or NH 4 +; Y -for BF 4 -, PF 6 -, (CF 3sO 2) 2n -or CF 3sO 3 -;
(3) by described ionic liquid, with polyacrylonitrile-methyl methacrylate, according to mass ratio, be that 30 ~ 50:100 mixes; add organic solvent; under anhydrous and inert gas shielding; be heated to 40 ℃ ~ 60 ℃; the formation viscous solution that stirs, cast in described viscous solution on glass plate, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours; after cooling, peel off and obtain described gel polymer electrolyte film.
Step (1) is for to make the N-methyl piperidine react the process that makes compd A with the halo propene carbonate, and reaction equation is as follows:
Figure BDA00001709469200031
Wherein, RX is the halo propene carbonate.
Preferably, the halo propene carbonate is chlorocarbonic acid propylene, bromo propene carbonate or iodo propene carbonate.
Wherein, the structural formula of chlorocarbonic acid propylene, bromo propene carbonate and iodo propene carbonate is respectively:
Preferably, described inert gas is nitrogen (N 2) or argon gas (Ar 2).
Preferably, step (1) also comprises the following purification process to compd A: after completion of the reaction, that the reactant liquor of described reaction is standing cooling, use the ethyl acetate washed product, and, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours, obtain the compd A of purifying.
Step (2) is M for making compd A and general formula +y -reactant salt make ionic liquid, reaction equation is as follows:
Figure BDA00001709469200033
In formula, M +for Na +, K +or NH 4 +; Y -for BF 4 -, PF 6 -, (CF 3sO 2) 2n -or CF 3sO 3 -.
Preferably, step (2) also comprises the following purification process to described ionic liquid: after completion of the reaction, with carrene or chloroform extraction reactant liquor 1 ~ 5 time, collect extract, strip to using saturated AgNO with deionized water 3aqueous solution titration water by after the organic phase evaporation and concentration, and, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours, obtains the described ionic liquid of purifying till producing without precipitation.
Ionic liquid has the characteristics such as conductivity high (about 5ms/cm), fusing point low (30 ℃ of left and right), electrochemical window wide (5V left and right), has the advantages such as non-volatile, non-combustible, Heat stability is good with respect to inflammable, volatile, shortcoming, the ionic liquid such as thermal stability is bad of organic liquid.Therefore, in gel polymer electrolyte, mixed ionic liquid can reduce the use amount of organic liquid, has reduced electrolytical inflammability and volatility, has not only improved the fail safe of gel polymer electrolyte film, stability, and environmental friendliness.
Step (3) is for making N-methyl piperidine ionic liquid/polyacrylonitrile-methyl methacrylate (P (AN-MMA)) gel polymer electrolyte film.
Preferably, the matter average molecular weight of polyacrylonitrile-methyl methacrylate (P (AN-MMA)) is 10 ~ 500,000.
Preferably, organic solvent is the DMSO(dimethyl sulfoxide (DMSO)), the NMP(N-methyl pyrrolidone) or DMF(N, dinethylformamide).
Preferably, the mass ratio of organic solvent and polyacrylonitrile-methyl methacrylate is 20% ~ 30%.
In addition, the embodiment of the present invention also provides the purposes of the gel polymer electrolyte film prepared by said method in ultracapacitor.
Particularly, gel polymer electrolyte film is assembled into to ultracapacitor: by Graphene, (specific area is about 700m 2/ g), acetylene black and PVDF are Graphene according to mass ratio: the ratio of acetylene black: PVDF=85 ~ 90:3 ~ 7:3 ~ 10 is mixed, and Graphene: NMP=1:2 ~ 20 add NMP in mass ratio, fully stirs and makes it to become the slurry mixed; Then by the slurry blade coating on the aluminium foil cleaned through ethanol, under the vacuum of 0.01MPa, 100 ℃ are dried to constant weight, and are pressed into Graphene electrodes in 10 ~ 15MPa pressure lower roll, and are cut into the electrode disk; The gel polymer electrolyte film prepared is placed between two Graphene electrodes, and on stamping machine, the button capacitor is made in sealing.
Implement the embodiment of the present invention, there is following beneficial effect:
(1) gel polymer electrolyte film security performance provided by the invention is high, stability is high and environmental friendliness, is applicable to the electrochemical devices such as ultracapacitor;
(2) preparation method of gel polymer electrolyte film provided by the invention is easy and simple to handle, is conducive to realize large-scale production.
The accompanying drawing explanation
In order to be illustrated more clearly in the embodiment of the present invention or technical scheme of the prior art, below will the accompanying drawing of required use in embodiment or description of the Prior Art be briefly described, apparently, accompanying drawing in the following describes is only some embodiments of the present invention, for those of ordinary skills, under the prerequisite of not paying creative work, can also obtain according to these accompanying drawings other accompanying drawing.
Fig. 1 is preparation method's schematic flow sheet of gel polymer electrolyte film provided by the invention;
Fig. 2 is the constant current charge-discharge curve of the ultracapacitor of the embodiment of the present invention one.
Embodiment
Below in conjunction with the accompanying drawing in the embodiment of the present invention, the technical scheme in the embodiment of the present invention is clearly and completely described, obviously, described embodiment is only the present invention's part embodiment, rather than whole embodiment.Embodiment based in the present invention, those of ordinary skills, not making under the creative work prerequisite the every other embodiment obtained, belong to the scope of protection of the invention.
Embodiment 1
A kind of preparation method of gel polymer electrolyte film, comprise the steps:
(1) prepare chlorination N-propylene carbonate ester group-N-methyl piperidine
Add respectively (99g, 1mol) N-methyl piperidine and (149.6g, 1.1mol) chlorocarbonic acid propylene in the flask of 250mL, after mixing, at N 2under protection, be heated to 60 ℃, stirring reaction 72h, after completion of the reaction, the standing room temperature that is cooled to, use ethyl acetate washed product 3 times, and at 80 ℃ of lower vacuumize 48h, obtain lurid solid, be chlorination N-propylene carbonate ester group-N-methyl piperidine, yield is 70%;
(2) prepare N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate ion liquid
By the above-mentioned chlorination N-propylene carbonate ester group made-N-methyl piperidine (117.5g, 0.5mol) and NaBF 4(55g, 0.5mol) is dissolved in the 100mL deionized water, stirring reaction 4h at room temperature, after completion of the reaction, by 250mL dichloromethane extraction 3 times for reactant liquor, combining extraction liquid; Then at every turn with 60mL deionized water back extraction until with saturated AgNO 3till aqueous solution titration water produces without precipitation, after carrene is concentrated with Rotary Evaporators, at 80 ℃ of vacuumize 48h, obtain colourless liquid, be N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate ion liquid.
N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate ion liquid synthetic reaction formula is as follows:
Figure BDA00001709469200061
The nuclear magnetic resoance spectrum diagram data of N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate is as follows: 1H NMR (CDCl3,400MHz, ppm): 4.92 (m, 1H), 4.40 (d, 2H), (3.73 d, 2H), 3.26 (m, 4H), 2.95 (s, 3H), 1.74 (m, 4H), 1.29 (m, 2H).
(3) prepare N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate ion liquid/P (AN-MMA) gel polymer electrolyte film:
Add successively 100g P (AN-MMA) (matter average molecular weight 300,000), 50g N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate and 25g dimethyl sulfoxide (DMSO) in the there-necked flask of 500mL.Under the protection of dry inert nitrogen gas, be heated to 40 ℃, and stir and to allow P (AN-MMA) dissolve, make system become even viscous solution.The viscous solution that gained is mixed casts on clean glass plate, is transferred to rapidly in vacuum drying chamber, and under 80 ℃, dry 48h, slough solvent.After being cooled to room temperature, separating elastic membrane transparent on sheet glass and be N-propylene carbonate ester group-N-methyl piperidine tetrafluoroborate ion liquid/P (AN-MMA) gel polymer electrolyte film in glove box.
The N-propylene carbonate ester group that makes-N-methyl piperidine tetrafluoroborate ion liquid/P (AN-MMA) gel polymer electrolyte film is assembled into to ultracapacitor: (specific area is about 700m to take the 9g Graphene 2/ g), 0.5g acetylene black and 0.5g PVDF, and add 80g NMP, fully stir and make it to become the slurry mixed.Then by its blade coating on the aluminium foil cleaned through ethanol, under the vacuum of 0.01MPa, 100 ℃ are dried to constant weight, and are pressed into Graphene electrodes in 10MPa pressure lower roll, and are cut into the electrode disk.The above-mentioned gel polymer electrolyte prepared is placed between two Graphene electrodes, and on stamping machine, the button capacitor is made in sealing.
Utilize the charge-discharge test instrument to carry out the constant current charge-discharge test to the ultracapacitor assembled in the present embodiment, in the electrochemical window of 0 ~ 2.7V, with the electric current of 0.5A/g, record its charging and discharging curve as shown in Figure 2.
As can be seen from Figure 2, the prepared gel polymer electrolyte of the embodiment of the present invention is suitable for the electrolyte of ultracapacitor, and has stability preferably in the electrochemical window of 0 ~ 2.7V.
Embodiment 2
A kind of preparation method of gel polymer electrolyte film, comprise the steps:
(1) prepare bromination N-propylene carbonate ester group-N-methyl piperidine
Add respectively (99g, 1mol) N-methyl piperidine and (216g, 1.2mol) bromo propene carbonate in the flask of 250mL, after mixing, at N 2under protection, be heated to 70 ℃, stirring reaction 60h, after completion of the reaction, the standing room temperature that is cooled to, use ethyl acetate washed product 3 times, and at 90 ℃ of lower vacuumize 36h, obtain lurid solid, be bromination N-propylene carbonate ester group-N-methyl piperidine, yield is 75%;
(2) prepare N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate ionic liquid
By the above-mentioned bromination N-propylene carbonate ester group made-N-methyl piperidine (140.1g, 0.5mol) and KPF 6(101.2g, 0.55mol) is dissolved in the 100mL deionized water, stirring reaction 10h at room temperature, after completion of the reaction, by 250mL chloroform extraction 3 times for reactant liquor, combining extraction liquid; Then at every turn with 60mL deionized water back extraction until with saturated AgNO 3till aqueous solution titration water produces without precipitation, after carrene is concentrated with Rotary Evaporators, at 90 ℃ of vacuumize 36h, obtain colourless liquid, be N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate ionic liquid.
N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate ionic liquid synthetic reaction formula is as follows:
The nuclear magnetic resoance spectrum diagram data of N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate is as follows: 1HNMR (CDCl3,400MHz, ppm): 4.95 (m, 1H), 4.42 (d, 2H), (3.74 d, 2H), 3.27 (m, 4H), 2.97 (s, 3H), 1.76 (m, 4H), 1.31 (m, 2H).
(3) prepare N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate ionic liquid/P (AN-MMA) gel polymer electrolyte film:
Add successively 100g P (AN-MMA) (matter average molecular weight 100,000), 40g N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate and 20g NMP in the there-necked flask of 500mL.Under the protection of dry inert gas Ar2, be heated to 50 ℃, and stir and to allow P (AN-MMA) dissolve, make system become even viscous solution.The viscous solution that gained is mixed casts on clean glass plate, is transferred to rapidly in vacuum drying chamber, and under 90 ℃, dry 36h, slough solvent.After being cooled to room temperature, separating elastic membrane transparent on sheet glass and be N-propylene carbonate ester group-N-methyl piperidine hexafluorophosphate ionic liquid/P (AN-MMA) gel polymer electrolyte film in glove box.
The N-propylene carbonate ester group that makes-N-methyl piperidine hexafluorophosphate ionic liquid/P (AN-MMA) gel polymer electrolyte film is assembled into to ultracapacitor: take 8.5g Graphene (specific area is about 700m2/g), 0.4g acetylene black and 0.4g PVDF, and add 60g NMP, fully stir and make it to become the slurry mixed.Then by its blade coating on the aluminium foil cleaned through ethanol, under the vacuum of 0.01MPa, 100 ℃ are dried to constant weight, and are pressed into Graphene electrodes in 15MPa pressure lower roll, and are cut into the electrode disk.The above-mentioned N-propylene carbonate ester group prepared-N-methyl piperidine hexafluorophosphate ionic liquid/P (AN-MMA) gel polymer electrolyte film is placed between two Graphene electrodes, and on stamping machine, the button capacitor is made in sealing.
Utilize the charge-discharge test instrument to carry out the constant current charge-discharge test to the ultracapacitor assembled in the present embodiment, there is stability preferably in the electrochemical window of 0 ~ 2.7V.
Embodiment 3
A kind of preparation method of gel polymer electrolyte film, comprise the steps:
(1) prepare iodate N-propylene carbonate ester group-N-methyl piperidine
Add respectively (99g, 1mol) N-methyl piperidine and (239.4g, 1.05mol) iodo propene carbonate in the flask of 250mL, after mixing, at N 2under protection, be heated to 80 ℃, stirring reaction 48h, after completion of the reaction, the standing room temperature that is cooled to, use ethyl acetate washed product 5 times, and at 100 ℃ of lower vacuumize 24h, obtain lurid solid, be chlorination N-propylene carbonate ester group-N-methyl piperidine, yield is 80%;
(2) prepare two (fluoroform sulphonyl) the inferior amine salt ionic liquids of N-propylene carbonate ester group-N-methyl piperidine
By the above-mentioned iodate N-propylene carbonate ester group made-N-methyl piperidine (117.5g, 0.5mol) and two (fluoroform sulphonyl) imines potassium KTFSI (173.4g, 0.53mol) be dissolved in the 100mL deionized water, stirring reaction 24h at room temperature, after completion of the reaction, by reactant liquor 250mL dichloromethane extraction 3 times, combining extraction liquid; Then at every turn with 60mL deionized water back extraction until with saturated AgNO 3till aqueous solution titration water produces without precipitation, after carrene is concentrated with Rotary Evaporators, at 100 ℃ of vacuumize 24h, obtain colourless liquid, be two (fluoroform sulphonyl) the inferior amine salt ionic liquids of N-propylene carbonate ester group-N-methyl piperidine.
Two (fluoroform sulphonyl) the inferior amine salt ionic liquid synthetic reaction formulas of N-propylene carbonate ester group-N-methyl piperidine are as follows:
The nuclear magnetic resoance spectrum diagram data of two (fluoroform sulphonyl) inferior amine salts of N-propylene carbonate ester group-N-methyl piperidine is as follows: 4.96 (m, 1H), 4.44 (d, 2H), 3.75 (d, 2H), 3.28 (m, 4H), 2.99 (s, 3H), 1.77 (m, 4H), 1.33 (m, 2H).
(3) prepare two (fluoroform sulphonyl) inferior amine salt ionic liquid/P (AN-MMA) gel polymer electrolyte films of N-propylene carbonate ester group-N-methyl piperidine:
Add successively 100g P (AN-MMA) (matter average molecular weight 300,000), two (fluoroform sulphonyl) inferior amine salts of 30g N-propylene carbonate ester group-N-methyl piperidine and 30g DMF in the there-necked flask of 500mL.Under the protection of dry inert gas N2, be heated to 60 ℃, and stir and to allow P (AN-MMA) dissolve, make system become even viscous solution.The viscous solution that gained is mixed casts on clean glass plate, is transferred to rapidly in vacuum drying chamber, and under 100 ℃, dry 24h, slough solvent.After being cooled to room temperature, separating elastic membrane transparent on sheet glass and be two (fluoroform sulphonyl) inferior amine salt ionic liquid/P (AN-MMA) gel polymer electrolyte films of N-propylene carbonate ester group-N-methyl piperidine in glove box.
Two (fluoroform sulphonyl) inferior amine salt ionic liquid/P (AN-MMA) gel polymer electrolyte films of the N-propylene carbonate ester group that makes-N-methyl piperidine are assembled into to ultracapacitor: (specific area is about 700m to take the 9g Graphene 2/ g), 0.6g acetylene black and 0.8g PVDF, and add 150g NMP, fully stir and make it to become the slurry mixed.Then by its blade coating on the aluminium foil cleaned through ethanol, under the vacuum of 0.01MPa, 100 ℃ are dried to constant weight, and are pressed into Graphene electrodes in 15MPa pressure lower roll, and are cut into the electrode disk.The above-mentioned N-propylene carbonate ester group prepared-N-methyl piperidine hexafluorophosphate ionic liquid/P (AN-MMA) gel polymer electrolyte film is placed between two Graphene electrodes, and on stamping machine, the button capacitor is made in sealing.
Utilize the charge-discharge test instrument to carry out the constant current charge-discharge test to the ultracapacitor assembled in the present embodiment, there is stability preferably in the electrochemical window of 0 ~ 2.7V.
The above is the preferred embodiment of the present invention; it should be pointed out that for those skilled in the art, under the premise without departing from the principles of the invention; can also make some improvements and modifications, these improvements and modifications also are considered as protection scope of the present invention.

Claims (10)

1. a gel polymer electrolyte film, it is characterized in that, the material of described gel polymer electrolyte film is the composite material that Polymers bottom material and ionic liquid are mixed to form, the mass ratio of described Polymers bottom material and described ionic liquid is 100:30 ~ 50, described Polymers bottom material is polyacrylonitrile-methyl methacrylate, and described ionic liquid is for having the compound as shown in structural formula (1):
Figure FDA00001709469100011
Y in formula -for BF 4 -, PF 6 -, (CF 3sO 2) 2n -or CF 3sO 3 -.
2. gel polymer electrolyte film as claimed in claim 1, is characterized in that, the matter average molecular weight of described polyacrylonitrile-methyl methacrylate is 10 ~ 500,000.
3. the preparation method of a gel polymer electrolyte film, is characterized in that, comprises the following steps:
(1) ratio that is 1:1.05 ~ 1.2 with the halo propene carbonate according to mol ratio by the N-methyl piperidine is mixed, and is heated to 60 ℃ ~ 80 ℃ under inert gas shielding, and stirring reaction 48 ~ 72 hours obtains having the compd A that following structural formula means:
Figure FDA00001709469100012
In formula, X -for Cl -, Br -, I -;
(2) by described compd A and general formula, be M +y -salt according to mol ratio, be 1:1 ~ 1.1 ratio is mixed, add deionized water, at room temperature stirring reaction is 4 ~ 24 hours, obtains having the ionic liquid meaned as structural formula (1):
Figure FDA00001709469100013
Wherein, M +for Na +, K +or NH 4 +; Y -for BF 4 -, PF 6 -, (CF 3sO 2) 2n -or CF 3sO 3 -;
(3) ratio that is 30 ~ 50:100 with polyacrylonitrile-methyl methacrylate according to mass ratio by described ionic liquid is mixed; add organic solvent; under anhydrous and inert gas shielding; be heated to 40 ℃ ~ 60 ℃; the formation viscous solution that stirs, cast in described viscous solution on glass plate, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours; after cooling, peel off and obtain described gel polymer electrolyte film.
4. the preparation method of gel polymer electrolyte film as claimed in claim 3, is characterized in that, halo propene carbonate described in step (1) is chlorocarbonic acid propylene, bromo propene carbonate or iodo propene carbonate.
5. the preparation method of gel polymer electrolyte film as claimed in claim 3, is characterized in that, described inert gas is nitrogen or argon gas.
6. the preparation method of gel polymer electrolyte film as claimed in claim 3, it is characterized in that, step (1) also comprises the following purification process to described compd A: after completion of the reaction described, the reactant liquor of described reaction is standing cooling, use the ethyl acetate washed product, and, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours, obtain the described compd A of purifying.
7. the preparation method of gel polymer electrolyte film as claimed in claim 3, it is characterized in that, step (2) also comprises the following purification process to described ionic liquid: after completion of the reaction described, with carrene or chloroform extraction reactant liquor 1 ~ 5 time, collect extract, strip to using saturated AgNO with deionized water 3aqueous solution titration water by after the organic phase evaporation and concentration, and, 80 ℃ ~ 100 ℃ lower vacuumizes 24 hours ~ 48 hours, obtains the described ionic liquid of purifying till producing without precipitation.
8. the preparation method of gel polymer electrolyte film as claimed in claim 3, is characterized in that, the matter average molecular weight of described polyacrylonitrile-methyl methacrylate is 10 ~ 500,000.
9. the preparation method of gel polymer electrolyte film as claimed in claim 3, it is characterized in that, described in step (3), organic solvent is dimethyl sulfoxide (DMSO), 1-METHYLPYRROLIDONE or N, dinethylformamide, the mass ratio of described organic solvent and polyacrylonitrile-methyl methacrylate is 20% ~ 30%.
10. select as described in one as claim 3 ~ 9 purposes of gel polymer electrolyte film in ultracapacitor that method prepares.
CN2012101756341A 2012-05-31 2012-05-31 Gel polymer electrolyte film, and manufacturing method and application for same Pending CN103456504A (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060210876A1 (en) * 2005-03-17 2006-09-21 Takashi Kuboki Electrochemical device
CN1934212A (en) * 2004-04-19 2007-03-21 Lg化学株式会社 Gel polymer electrolyte containing ionic liquid and electrochromic device using the same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1934212A (en) * 2004-04-19 2007-03-21 Lg化学株式会社 Gel polymer electrolyte containing ionic liquid and electrochromic device using the same
US20060210876A1 (en) * 2005-03-17 2006-09-21 Takashi Kuboki Electrochemical device

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
G P PANDEY等: "Ionic liquid incorporated polymer electrolytes for supercapacitor application", 《INDIAN JOURNAL OF CHEMISTRY》 *
WEN LU等: "Incorporating Ionic Liquid Electrolytes into Polymer Gels for Solid-State Ultracapacitors", 《JOURNAL OF ELECTROCHEMICAL SOCIETY》 *

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Application publication date: 20131218