CN1767101A - A kind of electrolyte that is used for electrochemical capacitor and preparation method thereof - Google Patents
A kind of electrolyte that is used for electrochemical capacitor and preparation method thereof Download PDFInfo
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- CN1767101A CN1767101A CNA2005100128010A CN200510012801A CN1767101A CN 1767101 A CN1767101 A CN 1767101A CN A2005100128010 A CNA2005100128010 A CN A2005100128010A CN 200510012801 A CN200510012801 A CN 200510012801A CN 1767101 A CN1767101 A CN 1767101A
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- electrolyte
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- electrochemical capacitor
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
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- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
It is standby as main electrolyte that a kind of electrolyte that is used for electrochemical capacitor is that chloride, nitrate, sulfate, molybdate or the chromate of Fe, Co, Ni, Cu, Mn, Cr or Mo metal is made into the aqueous solution of 0.1M~saturated solution respectively, HNO
3, H
2SO
4Or the aqueous solution that HCl is made into 0.5~8M respectively mixed one or more main electrolyte and one or more auxiliary electrolyte in 1: 10 by volume~10: 1 as auxiliary electrolyte, electrolyte of the present invention.
Description
Technical field
The invention belongs to and relate to a kind of electrolyte and preparation method thereof, the electrochemical capacitor preparation method of electrolyte that specifically can produce high specific capacitance.
Background technology
Ultracapacitor with regard to its performance be between a kind of energy between traditional capacitor and battery, its accumulate mechanism has electric double layer capacitance mechanism and pseudo capacitance mechanism.No matter but its electrolyte of which kind of accumulate mechanism all is the electrochemistry inertia, except a large amount of negative ions and charge-conduction is provided, any chemical reaction can not take place.Inorganic electrolyte liquid such as KOH, Na
2SO
4, though KCl, NaCl, LiCl etc. have conductivity preferably.But for porous carbon electrode material, its single electric double layer capacitance mechanism makes that single electrode can be too not high than electric capacity.Though organic electrolyte has the operation potential window of broad, its viscosity is big, electric conductivity is poor than inorganic electrolyte liquid.This can influence the high-power charge-discharge performance of electrochemical capacitor widely.In addition, under the identical situation of electrode material, the single electrode of organic electrolyte also compares electric capacity far below the single electrode of inorganic electrolyte liquid than electric capacity.In a word, single electric double layer capacitance mechanism is owing to be subjected to the restriction of electrode material specific area, and its specific capacitance is difficult to have significantly raising on existing basis.
Summary of the invention
The objective of the invention is to prepare a kind of be applicable to electrochemical capacitor, can produce electrolyte of high specific capacitance and preparation method thereof.
The present invention with elements such as Fe, Co, Ni, Cu, Mn, Cr, Mo as active material.Chloride, nitrate, sulfate and permanganate, molybdate and chromate etc. with metals such as Fe, Co, Ni, Cu, Mn, Cr, Mo are main electrolyte, with good strong electrolyte solution of electric conductivity such as auxiliary electrolyte sulfuric acid, nitric acid, hydrochloric acid, convert into mixed electrolytic solution with two or more components.In charge and discharge process, the active metallic ion generation electrochemical redox reaction that main electrolyte is contained generates various reactive electro to as Fe
3+/ Fe
2+, Co
3+, Co
2+/ Co and Cu
2+, Cu
+/ Cu etc., thus very big pseudo capacitance amount produced; And auxiliary electrolyte so the adding of auxiliary electrolyte both provided a large amount of ions for the generation of electric double layer capacitance, has been improved the electric conductivity of electrolyte because good electric conductivity is arranged simultaneously again.
Electrolyte of the present invention consists of:
Chloride, nitrate, sulfate, molybdate or the chromate of Fe, Co, Ni, Cu, Mn, Cr or Mo metal is made into the aqueous solution of 0.1M~saturated solution respectively as main electrolyte, HNO
3, H
2SO
4Or the aqueous solution that HCl is made into 0.5~8M respectively is as auxiliary electrolyte, and the volume ratio of main electrolyte and auxiliary electrolyte is to form electrolyte in 1: 10~10: 1.
Preparation method of the present invention is as follows:
It is standby as main electrolyte that chloride, nitrate, sulfate, molybdate or the chromate of Fe, Co, Ni, Cu, Mn, Cr or Mo metal is made into the aqueous solution of 0.1M~saturated solution respectively, HNO
3, H
2SO
4Or the aqueous solution that HCl is made into 0.5~8M respectively mixed main electrolyte and auxiliary electrolyte in 1: 10 by volume~10: 1 as auxiliary electrolyte, must convert electrolyte of the present invention.
Electrolyte of the present invention is applicable to that electrode is the electrochemical capacitor of all carbonaceous porous material such as active carbon, nano carbon tube, activated carbon fiber, activated carbon microballon, charcoal-aero gel etc.
The present invention has following advantage:
1. the prepared electrochemical capacitor of the present invention is different from general electrolyte part with electrolyte and is to contain in the electrolyte active material that can produce pseudo capacitance, thereby can greatly improve the capacitor charging/discharging capacity;
2. prepared electrolyte abundant raw material of the present invention, cheap is applicable to all carbonaceous porous materials, and good practicality is arranged.
Embodiment
The comparative example
With the BET specific area is 2780m
2The porous charcoal of/g is an electrode material, and (mass ratio) graphite powder adds 15% (mass ratio) PTFE emulsion (concentration is 60%) and is binding agent down together, fully stirring, compression molding under the pressure of 10MPa in doping 30%.With 2M H
2SO
4Be electrolyte.Under current density I=0.2A/g (porous charcoal, the down with) condition during constant current charge-discharge, ultracapacitor single electrode quality is 258F/g (porous charcoal) (be as the criterion with discharge capacity, down with) than electric capacity; The result that cyclic voltammetry (dV/dt=5mV/S) records is 262F/g.Its cyclic voltammetry curve is typical electric double layer capacitance feature.
Embodiment 1
Electrode material and preparation condition thereof are the same.With 1.5M FeSO
4Solution and 2M H
2SO
4Solution is made electrolyte with 1: 10 mixed mixed solution of converting of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 545F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 562F/g.Charge/discharge capacity has cyclical stability preferably along with the cycle-index increase tends towards stability gradually.
Embodiment 2
Electrode material and preparation condition thereof are the same.With 1M CuSO
4Solution and 2M H
2SO
4Solution is made electrolyte with 10: 1 mixed mixed solutions of converting of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 710F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 712F/g.Charge/discharge capacity has cyclical stability preferably along with the cycle-index increase tends towards stability gradually.
Embodiment 3
Electrode material and preparation condition thereof are the same.With 2M CuCl
2Solution and 2M H
2SO
4Solution is made electrolyte with 3: 7 mixed mixed solutions of converting of volume ratio.The ultracapacitor single electrode quality that cyclic voltammetry (dV/dt=5mV/S) records reaches 912F/g than electric capacity; The result is 710F/g when dV/dt=10mV/S.Contrast as can be known with the cyclic voltammetry curve of embodiment 2 that the electrochemical reaction mechanism of active material changes, the invertibity of electrode process improves.
Embodiment 4
With the BET specific area is 1530m
2The weak point of/g is cut the inkstone Portland of active carbon fibre Wesy and is pulverized, with the BET specific area be 2780m
2The porous charcoal of/g is evenly mixed with 2: 1 ratios, and the graphite powder of doping 20% adds 12%PTFE emulsion (concentration is 60%) and is binding agent, fully stirs compression molding under the pressure of 10MPa.With 1.5M NiCl
2Solution and 1.5M Ni (NO
3)
2Solution and 6MH
2SO
4Solution is with 2: 3: 5 mixed electrolyte of converting into of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 508F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 519F/g.
Embodiment 5
Electrode material and preparation condition thereof are with embodiment 4.With 1M MnSO
4Solution, 1M MnCl
2With 4M HNO
3Solution is with 2: 2: 3 mixed electrolyte of converting into of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 485F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 501F/g.
Embodiment 6
With the BET specific area is 870m
2The activated carbon microballon of/g (micron order) is an electrode material, and the graphite powder of doping 10% adds 6%PTFE emulsion (concentration is 60%) and is binding agent, fully stirs compression molding under the pressure of 6MPa.With 1M K
2Cr
2O
7Solution, 0.5M CrSO
4Solution and 6M HNO
3Solution is with 1: 1: 1 mixed electrolyte of converting into of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 276F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 290F/g.
Embodiment 7
Electrode material and preparation condition thereof are with embodiment 6.With 0.5MNa
2MoO
4Solution and 0.5M HCl solution and 6M H
2SO
4Solution is with 1: 1: 1 mixed electrolyte of converting into of volume ratio.During constant current charge-discharge, ultracapacitor single electrode quality reaches 310F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 335F/g.
Embodiment 8
With the BET specific area is 820m
2The charcoal-aero gel of/g is an electrode material, and the graphite powder of doping 20% adds 10%PTFE emulsion (concentration is 60%) and is binding agent, fully stirs compression molding under the pressure of 6MPa.With 0.5M CoCl
3Solution, 1M CoSO
4Solution and 4M H
2SO
4Solution is converted into electrolyte so that volume ratio 1: 1: 1 is mixed, and during constant current charge-discharge, ultracapacitor single electrode quality reaches 330F/g than electric capacity under current density I=0.2A/g condition; The result that cyclic voltammetry (dV/dt=5mV/S) records is 352F/g.
Claims (2)
1, a kind of electrolyte that is used for electrochemical capacitor is characterized in that chloride, nitrate, sulfate, molybdate or the chromate of Fe, Co, Ni, Cu, Mn, Cr or Mo metal is made into the aqueous solution of 0.1M~saturated solution respectively as main electrolyte, HNO
3, H
2SO
4Or the aqueous solution that HCl is made into 0.5~8M respectively is as auxiliary electrolyte, and the volume ratio of one or more main electrolyte and one or more auxiliary electrolyte is to form electrolyte in 1: 10~10: 1.
2, a kind of preparation method who is used for the electrolyte of electrochemical capacitor as claimed in claim 1 is characterized in that comprising the steps:
It is standby as main electrolyte that chloride, nitrate, sulfate, molybdate or the chromate of Fe, Co, Ni, Cu, Mn, Cr or Mo metal is made into the aqueous solution of 0.1M~saturated solution respectively, HNO
3, H
2SO
4Or the aqueous solution that HCl is made into 0.5~8M respectively mixed one or more main electrolyte and one or more auxiliary electrolyte in 1: 10 by volume~10: 1 as auxiliary electrolyte, electrolyte of the present invention.
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CNB2005100128010A CN100501888C (en) | 2005-09-08 | 2005-09-08 | Electrolyte for electrochemical capacitor and its preparing method |
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CNB2005100128010A CN100501888C (en) | 2005-09-08 | 2005-09-08 | Electrolyte for electrochemical capacitor and its preparing method |
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CN1767101A true CN1767101A (en) | 2006-05-03 |
CN100501888C CN100501888C (en) | 2009-06-17 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102280266A (en) * | 2011-05-30 | 2011-12-14 | 大连交通大学 | Super capacitor with superposed liquid-flow pseudocapacitance |
CN103474253A (en) * | 2013-09-30 | 2013-12-25 | 武汉理工大学 | Porous carbon microsphere electrode materials based on surface function functional group, preparing method of materials, super capacitor of materials, and preparing method of super capacitor |
CN107680811A (en) * | 2017-11-18 | 2018-02-09 | 陈馨雅 | A kind of electrolyte for aluminum electrolytic capacitor |
CN108538634A (en) * | 2018-05-25 | 2018-09-14 | 北京化工大学 | A kind of water system compounding electrolyte and its preparation method and application |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69432788T2 (en) * | 1993-12-03 | 2004-04-08 | Matsushita Electric Industrial Co., Ltd., Kadoma | ELECTROLYTE SOLUTION AND ELECTROCHEMICAL ELEMENT MADE THEREOF |
JP2002008948A (en) * | 2000-06-19 | 2002-01-11 | Matsushita Electric Ind Co Ltd | Electric double-layer capacitor |
-
2005
- 2005-09-08 CN CNB2005100128010A patent/CN100501888C/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102280266A (en) * | 2011-05-30 | 2011-12-14 | 大连交通大学 | Super capacitor with superposed liquid-flow pseudocapacitance |
CN103474253A (en) * | 2013-09-30 | 2013-12-25 | 武汉理工大学 | Porous carbon microsphere electrode materials based on surface function functional group, preparing method of materials, super capacitor of materials, and preparing method of super capacitor |
CN103474253B (en) * | 2013-09-30 | 2016-01-06 | 武汉理工大学 | Based on function of surface functional group porous carbon microsphere electrode material and preparation method thereof, its ultracapacitor and preparation method |
CN107680811A (en) * | 2017-11-18 | 2018-02-09 | 陈馨雅 | A kind of electrolyte for aluminum electrolytic capacitor |
CN108538634A (en) * | 2018-05-25 | 2018-09-14 | 北京化工大学 | A kind of water system compounding electrolyte and its preparation method and application |
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Publication number | Publication date |
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CN100501888C (en) | 2009-06-17 |
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