CN114614086A - Electrolyte containing fluorine substituted phosphorus nitrogen cyclic compound and battery composed of electrolyte - Google Patents
Electrolyte containing fluorine substituted phosphorus nitrogen cyclic compound and battery composed of electrolyte Download PDFInfo
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- CN114614086A CN114614086A CN202210301016.0A CN202210301016A CN114614086A CN 114614086 A CN114614086 A CN 114614086A CN 202210301016 A CN202210301016 A CN 202210301016A CN 114614086 A CN114614086 A CN 114614086A
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/58—Liquid electrolytes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/58—Liquid electrolytes
- H01G11/64—Liquid electrolytes characterised by additives
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0567—Liquid materials characterised by the additives
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- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
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- Manufacturing & Machinery (AREA)
- General Chemical & Material Sciences (AREA)
- Secondary Cells (AREA)
Abstract
The invention discloses an electrolyte containing a fluorine substituted phosphorus nitrogen cyclic compound and a battery composed of the electrolyte. The electrolyte comprises electrolyte, organic solvent and a fluoro-phosphorus nitrogen cyclic compound shown as a formula I. When the electrolyte is used in a battery, the electrolyte is added with the compound shown in the formula I, so that the multi-aspect performance of the battery is improved, the 3C discharge rate of the battery at normal temperature is more than 78.1% at 3C charging rate, the 1C discharge rate at-20 ℃ is more than 78.8%, the capacity retention rate of 3C charging/1C discharging cycle after 800 cycles at normal temperature is more than 81.4%, the capacity retention rate of 3C charging/1C discharging cycle at high temperature of 45 ℃ is more than 80.2%, and the comprehensive performance is excellent.
Description
Technical Field
The invention belongs to the technical field of electrochemical energy storage, and particularly relates to an electrolyte containing a fluoro-phosphorus-nitrogen cyclic compound and a battery composed of the electrolyte.
Background
Currently, organic electrolyte materials used in the lithium battery industry are mainly alkyl carbonate compounds and LiPF6Lithium salt system, the performance of which is greatly reduced at high temperature (above 60 ℃), while the power battery for electric automobile requires a higher working temperature range (about-30 to 80 ℃); moreover, the alkyl carbonate organic electrolyte material has high flammability, so that the safety has great hidden trouble; especially in the field of hybrid and all-electric automotive applications, long-term cycling problems and safety are important factors that limit the practical application of these materials.
The electrolyte is an important component of the lithium ion battery, and plays a role in transmitting lithium ions between the positive electrode and the negative electrode. The safety, charge-discharge cycle, working temperature range and charge-discharge capacity of the battery are all important in relation to the electrochemical performance of the electrolyte. The traditional functional components in the electrolyte play a key role in prolonging the service life of the battery, but no long-term effective measure is provided for delaying or inhibiting the generation of lithium dendrites, so that the safety performance of the battery and the service life of charge-discharge cycles are greatly influenced.
The requirement of high energy density and the requirement of high temperature and high voltage stability of the battery are higher and higher, so that the development of an electrolyte for improving the stable charge and discharge cycle of the battery is very important.
Disclosure of Invention
The invention aims to provide an electrolyte containing a fluorine substituted phosphorus nitrogen cyclic compound and a battery composed of the electrolyte.
The electrolyte containing the fluoro substituted phosphorus nitrogen cyclic compound comprises an electrolyte, an organic solvent and the fluoro substituted phosphorus nitrogen cyclic compound shown as a formula I;
the electrolyte comprises XClO4、XPF6、XBF4、XTFSI、XFSI、XBOB、XODFB、XCF3SO3Or XAsF6Any one or a combination of at least two of; wherein X is Li, Na or K.
The organic solvent includes any one of carbonate, carboxylate, fluorocarboxylate, propionate, fluoroether or aromatic hydrocarbon or a combination of at least two thereof.
The carbonate includes a halogenated carbonate and/or a non-halogenated carbonate; the non-halogenated carbonate comprises any one or the combination of at least two of ethylene carbonate, propylene carbonate, diethyl carbonate, dimethyl carbonate or ethyl methyl carbonate; the halogenated carbonate comprises any one or the combination of at least two of fluoroethylene carbonate, difluoroethylene carbonate, difluoropropylene carbonate, ethyl trifluoroacetate, trifluoroethyl methyl carbonate, trifluoromethyl ethylene carbonate, 4-trifluoromethyl ethylene carbonate, chloroethylene carbonate, bis (2,2, 2-trifluoroethyl) carbonate, methyl trifluoropropionate, 3,3, 3-trifluoro ethyl acetate, 2-trifluoromethyl methyl benzoate, 4,4, 4-trifluoro ethyl butyrate or 1,1,1,3,3, 3-hexafluoroisopropyl acrylate.
The carboxylic acid ester comprises halogenated carboxylic acid ester and/or non-halogenated carboxylic acid ester; the non-halogenated carboxylic acid ester comprises any one or a combination of at least two of propyl butyrate, propyl acetate, isopropyl acetate, butyl propionate, isopropyl propionate, ethyl butyrate, methyl propionate, ethyl propionate or propyl propionate; the halogenated carboxylic acid ester comprises any one or a combination of at least two of propyl fluorobutyrate, propyl fluoroacetate, isopropyl fluoroacetate, butyl fluoropropionate, isopropyl fluoropropionate, ethyl fluorobutyrate, methyl fluoropropionate, ethyl fluoropropionate and propyl fluoropropionate.
The fluorine ether is a fluorine ether having 7 or less carbon atoms.
The aromatic hydrocarbon comprises halogenated aromatic hydrocarbon and/or non-halogenated aromatic hydrocarbon; the halogenated aromatic hydrocarbon comprises any one or the combination of at least two of monofluorobenzene, difluorobenzene, 1,3, 5-trifluorobenzene, trifluorotoluene, 2-fluorotoluene or 2, 4-dichlorotrifluorotoluene.
The weight percentage of the electrolyte in the electrolyte is 8-49%; the weight percentage of the organic solvent in the electrolyte is 1-85%; the weight percentage of the fluoro phosphorus nitrogen cyclic compound shown in the formula I in the electrolyte is 0.01-20%.
A battery comprises the electrolyte.
The battery comprises a lithium ion battery, a sodium ion battery, a potassium ion battery or a super capacitor; the negative electrode material of the lithium ion battery comprises any one or the combination of at least two of graphite, soft carbon, hard carbon, a composite material of monocrystalline silicon and graphite, a composite material of silicon oxide and graphite, and lithium titanate or niobium pentoxide.
The invention has the beneficial effects that: the electrolyte disclosed by the invention is added with the compound shown in the formula I, so that when the electrolyte is used in a battery, the multi-aspect performance of the obtained battery is improved, the 3C discharge rate at normal temperature in the battery is more than 78.1% at 3C charge rate, the 1C discharge rate at-20 ℃ is more than 78.8%, the capacity retention rate of 3C charge/1C discharge cycle after 800 cycles at normal temperature is more than 81.4%, the capacity retention rate of 3C charge/1C discharge cycle after 45 ℃ high temperature is more than 80.2%, and the comprehensive performance is excellent.
Detailed Description
In order that the invention may be more fully understood, reference will now be made to the following description. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete.
The general test platform used in the examples is as follows:
the experimental anode adopts a binder PVDF-S5130, a composite conductive agent Super-P/KS-6 (the mass ratio of Super-P: KS-6 is 2: 1), a 622 nickel cobalt manganese ternary anode material or a lithium cobaltate anode material, a solvent NMP (N-methyl-2-pyrrolidone, N-methyl pyrrolidone), a cathode adopts C-P15, a conductive agent Super-P solvent CMC, H2O and a binder SBR as raw materials, the wet pulping process is respectively adopted to prepare slurry, the viscosity of the anode is adjusted to 10000-13000 mPa.s, the viscosity of the cathode is adjusted to 1500-3000 mPa.s, the N/P ratio is designed to be 1.12, the capacity is 1671mAh, the lithium ion battery is subjected to coating, slicing, rolling, splitting, drying at 140 ℃ for 8H, sealing tape pasting, winding the battery core, drying at 80 ℃ for 48H, and then the lithium ion battery is placed for 24H according to the following different electrolyte formulas, And preparing the lithium ion soft package battery by formation, primary final sealing, aging and secondary final sealing, and then testing the cycle performance and the safety performance of the battery.
The fluorinated phosphazene cyclic compounds used in examples 1-7 were custom-made to Shijiazhuang Santa Clay chemical (purity 99.5%).
The electrolyte compositions of examples 1 to 11 and comparative examples 1 and 2 are shown in table 1.
The compositions of the electrolytes provided in examples 1 to 11 and comparative examples 1 and 2 were all in weight ratio and each contained 1% VC and 1% PS, as shown in table 1.
TABLE 1 (in the tables, all are weight ratios)
The electrolytes described in examples 1-10 and comparative example 1 were added to a 1.67Ah lithium ion battery containing a graphite negative electrode material (fir P15), NCM622 nickel cobalt manganese ternary material;
the following tests were performed:
(1) charge rate performance: the 1C current is 1.67A, and the 3C current is 5.01A; the charge and discharge potential range is 2.75V-4.35V. The charging rate of the 3C at the normal temperature is a ratio of a capacity C2 of the 3C constant current charging to a 1C constant current charging capacity C1.
(2) Cycle performance: the range of charging and discharging potential is 2.75V-4.35V, the charging current is 3C (5.01A) to 4.35V, the constant voltage charging of 4.35V is carried out until the cut-off current is less than or equal to 0.02C (0.0334A), after standing for 5 minutes, 1C (1.67A) is discharged to 2.75V, and the standing is carried out for 5 minutes; thus, the charge and discharge are cycled.
(3) Low-temperature discharge performance: the 1C (1.67A) discharge capacity at 25 ℃ was C1, and after full charge at 4.35V and freezing at-20 ℃ for 4 hours, the discharge was 1C (1.67A) to 2.75V, and the discharge capacity was C2. The discharge rate at-20 ℃ was C2/C1.
The electrolyte described in example 11 and comparative example 2 was added to a battery whose negative electrode material was a silicon-carbon negative electrode material (fibrate S420) and whose positive electrode material was 4.5V lithium cobalt oxide to prepare a 1.85Ah lithium ion battery;
the following tests were performed:
(1) charge rate performance: the 1C current is 1.85A, and the 3C current is 5.55A; the charge and discharge potential range is 2.75V-4.50V. The charging rate of the 3C at the normal temperature is a ratio of a capacity C2 of the 3C constant current charging to a 1C constant current charging capacity C1.
(2) Cycle performance: the range of charging and discharging potential is 2.75V-4.50V, the charging current is 3C (5.55A) to 4.50V, the charging is carried out at 4.50V with constant voltage until the cut-off current is less than or equal to 0.02C (0.037A), after standing for 5 minutes, 1C (1.85A) is discharged to 2.75V, and the standing is carried out for 5 minutes; thus, the charge and discharge are cycled.
(3) Low-temperature discharge performance: the 1C (1.85A) discharge capacity at 25 ℃ at room temperature was designated as C1, and after full charge at 4.5V and freezing at-20 ℃ for 4 hours, the discharge was 1C (1.85A) to 2.75V, and the discharge capacity was designated as C2. The discharge rate at-20 ℃ was C2/C1.
The test results are summarized in tables 2 to 4.
TABLE 2
TABLE 3
TABLE 4
As can be seen from the analysis of data in tables 2-4, when the electrolyte disclosed by the invention is used in a battery, the multi-aspect performance of the battery is improved by adding the compound shown in the formula I, the 3C discharge rate at normal temperature in the battery disclosed by the invention is more than 78.1%, the 1C discharge rate at 20 ℃ is more than 78.8%, the capacity retention rate of 3C charge/1C discharge cycle at 800 times of normal temperature cycle is more than 81.4%, the capacity retention rate of 800 times of 3C charge/1C discharge cycle at 45 ℃ is more than 80.2%, and the comprehensive performance is excellent.
As can be seen from the analysis of comparative example 1 and example 3, the performance of comparative example 1 is inferior to that of example 3, and the electrolyte added with the fluoro-phosphorus-nitrogen cyclic compound shown in the formula I is proved to be capable of improving the comprehensive performance and the safety performance of the battery. Analysis of comparative example 2 and example 11 revealed similar results. The electrolyte added with the fluoro-phosphorus-nitrogen cyclic compound shown in the formula I is proved to be beneficial to the charge-discharge cycle performance and the low-temperature discharge performance of a silicon-containing material or graphite serving as a negative electrode and a ternary material or cobalt acid lithium battery.
The above-mentioned embodiments only express several embodiments of the present invention, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the inventive concept, which falls within the scope of the present invention. Therefore, the protection scope of the present patent shall be subject to the appended claims.
Claims (10)
2. the fluorinated phosphorus nitrogen-containing cyclic compound electrolyte solution of claim 1, wherein the electrolyte comprises XClO4、XPF6、XBF4、XTFSI、XFSI、XBOB、XODFB、XCF3SO3Or XAsF6Any one or a combination of at least two of; wherein X is Li, Na or K.
3. The electrolyte as claimed in claim 1, wherein the organic solvent includes any one or a combination of at least two of carbonate, carboxylate, fluorocarboxylate, propionate, fluoroether or aromatic hydrocarbon.
4. The electrolyte solution containing a fluorinated phosphorus-nitrogen cyclic compound according to claim 1, wherein the carbonate comprises a halogenated carbonate and/or a non-halogenated carbonate; the non-halogenated carbonate comprises any one or the combination of at least two of ethylene carbonate, propylene carbonate, diethyl carbonate, dimethyl carbonate or ethyl methyl carbonate; the halogenated carbonate comprises any one or the combination of at least two of fluoroethylene carbonate, difluoroethylene carbonate, difluoropropylene carbonate, ethyl trifluoroacetate, trifluoroethyl methyl carbonate, trifluoromethyl ethylene carbonate, 4-trifluoromethyl ethylene carbonate, chloroethylene carbonate, bis (2,2, 2-trifluoroethyl) carbonate, methyl trifluoropropionate, 3,3, 3-trifluoro ethyl acetate, 2-trifluoromethyl methyl benzoate, 4,4, 4-trifluoro ethyl butyrate or 1,1,1,3,3, 3-hexafluoroisopropyl acrylate.
5. The electrolyte of claim 1, wherein the carboxylic acid ester comprises a halogenated carboxylic acid ester and/or a non-halogenated carboxylic acid ester; the non-halogenated carboxylic acid ester comprises any one or a combination of at least two of propyl butyrate, propyl acetate, isopropyl acetate, butyl propionate, isopropyl propionate, ethyl butyrate, methyl propionate, ethyl propionate or propyl propionate; the halogenated carboxylic acid ester comprises any one or a combination of at least two of propyl fluorobutyrate, propyl fluoroacetate, isopropyl fluoroacetate, butyl fluoropropionate, isopropyl fluoropropionate, ethyl fluorobutyrate, methyl fluoropropionate, ethyl fluoropropionate and propyl fluoropropionate.
6. The electrolyte solution containing a fluorinated phosphorus-nitrogen-containing cyclic compound according to claim 1, wherein the fluoroether is fluoroether having 7 or less carbon atoms.
7. The electrolyte as claimed in claim 1, wherein the aromatic hydrocarbon includes halogenated aromatic hydrocarbon and/or non-halogenated aromatic hydrocarbon; the halogenated aromatic hydrocarbon comprises any one or the combination of at least two of monofluorobenzene, difluorobenzene, 1,3, 5-trifluorobenzene, trifluorotoluene, 2-fluorotoluene or 2, 4-dichlorotrifluorotoluene.
8. The electrolyte solution containing the fluorinated phosphorus-nitrogen cyclic compound according to claim 1, wherein the weight percentage of the electrolyte solution in the electrolyte solution is 8 to 49%; the weight percentage of the organic solvent in the electrolyte is 1-85%; the weight percentage of the fluoro phosphorus nitrogen cyclic compound shown in the formula I in the electrolyte is 0.01-20%.
9. A battery comprising the electrolyte of any one of claims 1-8.
10. The battery of claim 9, wherein the battery comprises a lithium ion battery, a sodium ion battery, a potassium ion battery, or a supercapacitor; the negative electrode material of the lithium ion battery comprises any one or the combination of at least two of graphite, soft carbon, hard carbon, a composite material of monocrystalline silicon and graphite, a composite material of silicon oxide and graphite, and lithium titanate or niobium pentoxide.
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Citations (7)
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JP2001023687A (en) * | 1999-07-09 | 2001-01-26 | Sony Corp | Nonaqueous electrolyte battery |
CN101057355A (en) * | 2004-10-05 | 2007-10-17 | 株式会社普利司通 | Nonaqueous electrolyte solution, and nonaqueous electrolyte battery having same |
CN101663790A (en) * | 2007-04-20 | 2010-03-03 | 三菱化学株式会社 | Nonaqueous electrolyte solution and nonaqueous electrolyte secondary battery using same |
JP2014002972A (en) * | 2012-06-20 | 2014-01-09 | Fujifilm Corp | Electrolytic solution for nonaqueous secondary battery, and nonaqueous electrolytic solution secondary battery |
US20150221987A1 (en) * | 2012-10-11 | 2015-08-06 | Fujifilm Corporation | Electrolytic solution for non-aqueous secondary battery, and non-aqueous electrolytic solution secondary battery |
CN107857780A (en) * | 2016-09-22 | 2018-03-30 | 微宏动力系统(湖州)有限公司 | A kind of synthetic method of fluoro phosphonitrile compound, fluoro phosphonitrile compound and battery electrolytic solution |
CN112970141A (en) * | 2018-10-30 | 2021-06-15 | 新强能电池公司 | Silicon-based energy storage device with electrolyte additive containing phosphazene |
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- 2022-03-24 CN CN202210301016.0A patent/CN114614086A/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2001023687A (en) * | 1999-07-09 | 2001-01-26 | Sony Corp | Nonaqueous electrolyte battery |
CN101057355A (en) * | 2004-10-05 | 2007-10-17 | 株式会社普利司通 | Nonaqueous electrolyte solution, and nonaqueous electrolyte battery having same |
CN101663790A (en) * | 2007-04-20 | 2010-03-03 | 三菱化学株式会社 | Nonaqueous electrolyte solution and nonaqueous electrolyte secondary battery using same |
JP2014002972A (en) * | 2012-06-20 | 2014-01-09 | Fujifilm Corp | Electrolytic solution for nonaqueous secondary battery, and nonaqueous electrolytic solution secondary battery |
US20150221987A1 (en) * | 2012-10-11 | 2015-08-06 | Fujifilm Corporation | Electrolytic solution for non-aqueous secondary battery, and non-aqueous electrolytic solution secondary battery |
CN107857780A (en) * | 2016-09-22 | 2018-03-30 | 微宏动力系统(湖州)有限公司 | A kind of synthetic method of fluoro phosphonitrile compound, fluoro phosphonitrile compound and battery electrolytic solution |
CN112970141A (en) * | 2018-10-30 | 2021-06-15 | 新强能电池公司 | Silicon-based energy storage device with electrolyte additive containing phosphazene |
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