1595 results about "Trifluoromethyl" patented technology

The invention relates to an electrolyte additive, an electrolyte and a battery. The electrolyte additive comprises a first additive and lithium trifluoromethanesulfinate, the structural formula of the first additive is as shown in a formula (I): # imgabs0 # formula (I), and in the electrolyte additive, the mass ratio of the first additive to the lithium trifluoromethanesulfinate is 0.02-10. When the electrolyte additive is added into the electrolyte of the battery, the rate capability and the high-temperature performance of the battery can be effectively improved.

The invention belongs to the technical field of refrigerants, and provides a mixed refrigerant for replacing R290 and a preparation method and application thereof, the mixed refrigerant comprises a first component, a second component and a third component; the first component is trans-1, 2-difluoroethylene, the second component is 2, 3, 3, 3-tetrafluoropropene, and the third component is trifluoromethyl methyl ether; compared with R290 refrigerants in the prior art, the mixed refrigerant has the advantages that flammable and explosive components do not exist, and high-risk combustible gas clusters cannot be formed due to density layering after leakage, so that the mixed refrigerant has high safety performance, and the safety level can be not lower than A2L; the mixed refrigerant has the environment-friendly characteristic of low GWP, the GWP is smaller than or equal to 150, and the environment-friendly requirement is met; the thermophysical property and the refrigeration and / or heating cycle performance of the mixed refrigerant are similar to or better than those of R290; the mixed refrigerant can be used for directly replacing an R290 refrigerant.

The invention relates to environment-friendly hydrophobic ink and a preparation method thereof, and belongs to the technical field of water-based ink. A copolymerization modifier capable of being combined in a water-based polyacrylate emulsion in an initiation polymerization mode in the stage of preparing the modified water-based polyacrylate emulsion is prepared, and an o-hydroxy aromatic ketone structure in the copolymerization modifier can endow water-based ink with lasting ultraviolet absorption performance; the trifluoromethyl structure can reduce the surface energy of the water-based ink, and the benzimidazole ring structure can form stable coordinate bonds with metal ions, so that the bonding performance of the water-based ink and a metal substrate is enhanced; when the copolymerization modifier is used for modifying the water-based polyacrylate emulsion, the long-term performance, the hydrophobic and oil-resistant performance and the adhesion performance on the surface of a metal base material of the finished water-based ink can be effectively improved.

The application discloses a specific palmitoyl transferase inhibitor and application thereof, and an active ingredient of the palmitoyl transferase inhibitor is 4-(3-(2-(trifluoromethyl)-9H-thioxanthene-9-ylidene)propyl)-1-piperazine ethanol or a salt thereof. Current palmitoylation inhibitors, 2-bromohexadecanoic acid (2-BP), cerulenin and tunicamycin can all inhibit protein palmitoylation in cells, but all are not selective. And the existing palmitoylation inhibitors are similar to endogenous fatty acids, and inevitably affect lipid metabolism in the body, which limits the clinical application. The application discloses, for the first time, the application of 4-(3-(2-(trifluoromethyl)-9H-thioxanthene-9-ylidene)propyl)-1-piperazine ethanol as a specific palmitoyl transferase inhibitor, and the palmitoyl transferase inhibitor is better in specificity and reversible in inhibition.

The invention discloses an antibacterial material rich in a bismuth metal organic framework and a preparation method thereof, the method comprises the following steps: adding an indole monomer and an alcohol monomer into a solvent, and then adding nitrosalicylaldehyde into the solvent to obtain a spiropyran compound; the preparation method comprises the following steps: adding humic acid into a binary solvent consisting of dioxane and butanol to obtain a mixed solution; the ratio of the mass of the humic acid to the volume of the binary solvent is (2-3): (20-40) g / ml; sequentially adding a bismuth source, 2-bromo-5-(trifluoromethyl) pyridine and 4-(trifluoromethyl) phenylboronic acid into the mixed solution to obtain a bismuth metal organic framework; and adding the spiropyran compound into the bismuth metal organic framework to obtain the antibacterial material rich in the bismuth metal organic framework. The antibacterial capability of the antibacterial material is improved.

The invention discloses a preparation method of lithium trifluoromethanesulfinate, and belongs to the field of lithium ion battery materials. The preparation method of the lithium trifluoromethanesulfinate comprises the following steps: 1, mixing trifluoromethanesulfonyl chloride, lithium sulfite, lithium bicarbonate and a first solvent, and heating to react; 2, dissolving the concentrated crude product in a second solvent, and filtering and separating a lithium sulfate solid; and 3, concentrating the filtrate, adding a third solvent, uniformly stirring, filtering and separating the lithium chloride solid, and concentrating to obtain the lithium trifluoromethanesulfinate. According to the method for preparing the lithium trifluoromethanesulfinate, the yield can reach 94%, the operation is simple, byproducts are easy to separate, and the method is suitable for industrial production. In addition, the obtained by-product lithium sulfate can be used for preparing lithium sulfide, the by-product lithium chloride can be used for preparing solid electrolyte, and resource utilization is achieved.

The invention relates to a green preparation method of fluopyram intermediate 3-chloro-5-(trifluoromethyl)-2-ethylaminopyridine, which comprises the following steps: step 1, Ullmann reaction: coupling 3-chloro-2-methyl-5-trifluoromethylpyridine (C1) and N-bromomethyl phthalimide (C2) in the presence of a copper catalyst and potassium tert-butoxide to generate an intermediate (C3); and step 2, hydrolysis reaction: hydrolyzing the intermediate (C3) in the presence of hydrazine sulfate and an alkaline condition to generate the fluopyram intermediate 3-chloro-5-(trifluoromethyl)-2-ethylamino pyridine. The method has the advantages of short synthesis steps, easily available raw materials, no use of high-toxicity cyanogen compounds, low catalyst cost, difficult poisoning, recycling, simple post-treatment process, and less waste liquid generation, greatly reduces the production cost, improves the production safety, reduces the waste liquid discharge amount, and accords with the idea of green synthesis.

The invention discloses an imidazolium ionic liquid modified magnesium ion battery electrolyte and a preparation method and application thereof. The imidazolium ionic liquid modified magnesium ion battery electrolyte is obtained by fully dissolving [EOE-A-Im] [TFSI] ionic liquid in an APC electrolyte. Wherein [EOE-A-Im] [TFSI] is a 1-allyl-3-(2-ethoxyethyl)-1H-imidazole-3-onium bis (trifluoromethylsulfonyl) imine salt, and APC is a total phenyl complex. The imidazolium ionic liquid modified magnesium ion battery electrolyte disclosed by the invention is relatively wide in electrochemical window, excellent in compatibility with electrodes, high in magnesium deposition-dissolution efficiency, low in overpotential and good in cycling stability; and the preparation method of the imidazolium ionic liquid modified magnesium ion battery electrolyte is simple and environment-friendly, and accords with green industrial production.

The present disclosure relates to pharmaceutically acceptable salts, cocrystals, and crystalline forms thereof, of a compound which is N—((S)-1-(3-(4-chloro-3-(methylsulfonamido)-1-(2,2,2-trifluoroethyl)-1H-indazol-7-yl)-6-(3-methyl-3-(methylsulfonyl)but-1-yn-1-yl)pyridin-2-yl)-2-(3,5-difluorophenyl)ethyl)-2- ((3bS,4aR)-5,5-difluoro-3-(trifluoromethyl)-3b,4,4a,5-tetrahydro-TH-cyclopropa[3,4]cyclopenta[1,2-c]pyrazol-1-yl)acetamide, which is useful in the treatment of a Retroviridae viral infection including an infection caused by the HIV virus.

The invention discloses a lithium metal battery eutectic gel electrolyte and a preparation method and application thereof, and belongs to the field of solid electrolyte. The eutectic gel electrolyte is prepared by carrying out a photocuring reaction on a photocuring precursor solution containing a photoinitiator, and the photocuring precursor solution contains a bi-component liquid compound and a deep eutectic solvent; the two-component liquid compound comprises 4-acryloyl morpholine and a photocurable polyethylene glycol derivative; the deep eutectic solvent is formed from a liquid mixture comprising succinonitrile, lithium bis (trifluoromethylsulfonyl) imide and fluoroethylene carbonate. The eutectic gel electrolyte is composed of a deep eutectic solvent with functional groups such as cyano and sulfonyloxy, and a polymer electrolyte with functional groups such as ether oxygen and a unique skeleton structure. The advantages of high ionic conductivity, wide electrochemical window, high interface stability and the like can be endowed based on the interaction between functional groups and the space confinement effect of a polymer electrolyte skeleton structure.

The invention discloses a low-temperature-resistant working electrolyte for a liquid capacitor and a preparation method of the low-temperature-resistant working electrolyte, and relates to the technical field of electrolytes for capacitors. The low-temperature-resistant working electrolyte is prepared from the following raw materials: ethylene glycol, an auxiliary solvent, a solute, ammonium hypophosphite, a synergist, a stabilizer, 1-ethyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imine, boron nitride nanosheets and 2, 2, 2-trifluoroethyl acrylate. According to the invention, while the auxiliary solvent with a specific proportion is added, the synergist capable of improving the conductivity, the cycle life, the low-temperature ion mobility and the low-temperature power density and the 2, 2, 2-trifluoroethyl acrylate capable of further improving the electrochemical performance stability at the low temperature are also introduced, so that the low-temperature electrochemical performance of the lithium ion battery is improved. And a specific preparation method capable of preventing agglomeration and improving the smoothness of an ion conduction path is combined. Therefore, the electrolyte is more excellent in chemical performance at low temperature and wider in application prospect.

The embodiment of the invention discloses a preparation method of trifluoromethyl sulfinate. The preparation method comprises the following steps: reacting a trifluoromethyl sulfinyl reagent with an amino compound containing hydroxyl to obtain a trifluoromethyl sulfinate intermediate; and reacting the trifluoromethyl sulfinate intermediate with alkali metal salt in an organic solvent to obtain the trifluoromethyl sulfinate. According to the embodiment of the invention, firstly, the trifluoromethyl sulfinyl reagent reacts with the amino compound containing the hydroxyl group to obtain the trifluoromethyl sulfinate intermediate, and then the trifluoromethyl sulfinate and the alkali metal salt react in the organic solvent, so that the high-purity trifluoromethyl sulfinate can be prepared with high yield under mild conditions. The yield and the purity of the target product are effectively improved, and meanwhile, the production condition requirement and the environmental pollution degree are reduced, so that large-scale production and application are facilitated.

The invention relates to a compound containing a thiophene group, a device and equipment. In the structural formula of the compound, R1, R2, R3, R4, R5, R6, R7, R8, R9 and R10 are independently selected from hydrogen, halogen, cyano, trifluoromethyl, triphenylamine and derivatives thereof, methoxyl, aryl and derivatives thereof, cyanobiphenyl and naphthyl; the compound can be used for preparing a photovoltaic device and photovoltaic equipment and is used for improving the efficiency and stability of the photovoltaic device.

The invention discloses a bio-based fiber reinforced composite material and a preparation method thereof, and belongs to the technical field of bio-based fiber composite materials. The bio-based fiber reinforced composite material is prepared from the following raw materials in parts by weight: 60 to 80 parts of nylon 6, 10 to 20 parts of bio-based aramid fiber, 5 to 10 parts of modified carbon fiber, 2 to 6 parts of hyperbranched polyester modified zinc oxide and 1 to 3 parts of antioxidant, the bio-based aramid fiber is prepared by reacting 2, 5-furandicarbonyl chloride with two diamine monomers, and the two diamine monomers respectively contain trifluoromethyl and sulfuryl; the modified carbon fiber is obtained by grafting polyamidoamine on the surface of carbon fiber; the hyperbranched polyester terminal group of the hyperbranched polyester modified zinc oxide contains an epoxy group. The modified carbon fiber, the bio-based aramid fiber and the hyperbranched polyester modified zinc oxide are added into the nylon matrix, so that the composite material is endowed with good ultraviolet resistance, comprehensive mechanical properties and durability.

The invention relates to a flame-retardant high-temperature-resistant fiber woven fabric and a preparation process thereof, and belongs to the technical field of textiles. The preparation method comprises the following steps: grafting and crosslinking a self-made grafting monomer and polyvinyl chloride, and then weaving to obtain the modified polyvinyl chloride fiber fabric; a phosphate group in the monomer can promote surface carbonization to form a protective carbon layer, silicate generated by decomposition of a siloxy group at a high temperature is combined with the carbon layer to improve the strength and melt viscosity of the carbon layer, and the phosphate group and the siloxy group synergistically enhance the flame retardance and the molten drop resistance of the fabric; a cyclic phosphate group and a pyridine ring are connected to form a rigid structure with relatively high thermal stability, chain segment movement is limited, a plurality of siloxy groups in a monomer are crosslinked to form a crosslinked network, molecular chain segments are difficult to move, and the combination of the rigid group and the crosslinked network improves the high temperature resistance of the fabric and effectively improves the mechanical properties of the fabric; in addition, the positively charged quaternary ammonium salt structure in the monomer improves the antistatic performance of the fabric, and cooperates with trifluoromethyl to destroy the structural integrity of bacterial cells, so that the fabric achieves efficient bacteriostasis.

The invention relates to the technical field of sodium-ion batteries, in particular to a sodium-ion battery non-aqueous electrolyte, a sodium-ion battery, a battery module, a battery pack and a power utilization device.The sodium-ion battery non-aqueous electrolyte comprises sodium salt, an organic solvent and a functional additive, the sodium salt comprises sodium bis (fluorosulfonyl) imide and sodium hexafluorophosphate, and the organic solvent comprises sodium bis (fluorosulfonyl) imide and sodium hexafluorophosphate. The molar ratio of the sodium bis (fluorosulfonyl) imide to the sodium hexafluorophosphate is (8: 2)-(7: 3); the organic solvent is prepared from chain carbonate and cyclic carbonate, and the functional additive is prepared from 2-trifluoromethyl-1, 3-propene sultone and 1-fluoro-2-methyl-ethylene carbonate. According to the invention, the ionic conductivity and thermal stability of the sodium-ion battery electrolyte can be improved through reasonable proportioning and use of the double-ion sodium salt, and meanwhile, corrosion of sodium bis (fluorosulfonyl) imide to an aluminum structural part can also be avoided. The sodium salt and the functional additive cooperate with each other to form an effective interface film on the surface of the electrode, so that the high-temperature storage performance and the high-temperature cycle performance of the sodium ion battery can be remarkably improved.

The invention belongs to the technical field of medicinal chemistry, and particularly relates to a 3-sulfamoyl benzamide compound as well as a preparation method and application thereof. The 3-sulfamoyl benzamide compound has a structure as shown in a formula I. In the formula I, X is chlorine or trifluoromethyl; r1 and R2 are independently C1-4 alkyl or R1, R2 and N atoms connected with R1 and R2 jointly form a heterocyclic group, and the heterocyclic group is a substituted or unsubstituted five-membered or six-membered heterocyclic group; and when the heterocyclic group is a substituted heterocyclic group, the substituent group in the substituted heterocyclic group is one or more of C1-4 alkyl, phenyl and acetyl. The 3-sulfamoyl benzamide compound disclosed by the invention has a remarkable proliferation inhibition effect on HCT116 colon cancer cells, HeLa human cervical cancer cells, MDA-MB-231 human breast cancer cells and A375 human malignant melanoma cells.

The invention relates to the technical field of synthesis of pyroxasulfone intermediates, in particular to a synthesis method and application of a pyroxasulfone intermediate. Comprising the following preparation steps: (1) adding a reaction solvent into sodium formaldehyde sulfoxylate, adding 1-methyl-3-trifluoromethyl-5-hydroxy-1H-pyrazole, heating, and completely reacting to obtain sodium hydroxypyrazole methyl sulfinate; and (2) cooling the reaction liquid, adding acetonitrile and alkali liquor, introducing monochlorodifluoromethane gas, after the reaction is completed, concentrating, removing acetonitrile and water, adding methanol, stirring, filtering, and concentrating the filtrate to obtain the pyroxasulfone intermediate difluoromethoxy pyrazole methyl sodium sulfinate. The specific reaction process is as follows. According to the method, the sodium formaldehyde sulfoxylate which is low in cost and easy to obtain is used, synthesis of a 5, 5-dimethyl-4, 5-dihydroisoxazole thioether compound is avoided when pyroxasulfone is prepared from the intermediate obtained in the invention, three wastes and production cost are reduced, industrial production is easy to realize, and the method has relatively high practical value.

The invention discloses a high-temperature and high-pressure electrolyte additive, an electrolyte containing the high-temperature and high-pressure electrolyte additive and a lithium ion battery. The electrolyte additive is selected from at least one of cyclic borate compounds. According to the invention, after the cyclic borate compound (such as bis (pinacol) diboron or 3-(trifluoromethyl) phenylboronic acid pinacol ester compound) is applied to the high-nickel lithium ion battery as the electrolyte additive, the battery can still maintain the capacity greater than or equal to 88% at the working voltage of 2.8-4.5 V (55 DEG C, and 300 cycles), meanwhile, the rate capability of the battery is improved, and the service life of the battery is prolonged. Compared with a battery without the cyclic borate compound additive, the cyclic borate compound additive is greatly improved under the same battery test condition. The cyclic borate additive is added into the electrolyte, so that the cycle performance of the lithium ion battery at high temperature and high voltage can be improved, and the rate capability of the battery can be improved.

The invention relates to the technical field of adhesives, and discloses an imidazolium ionic liquid and a preparation method and application thereof, the preparation method comprises the following steps: reacting omega-bromoalcohol with 1-(methoxymethyl) imidazole in acetonitrile, and washing with methyl tert-butyl ether to obtain a target ionic liquid precursor; and dissolving the product in acetonitrile, adding 4-trifluoromethyl phenyl isocyanate, and washing with methyl tert-butyl ether after the reaction is finished, thereby obtaining the target imidazolium ionic liquid. The imidazolium ionic liquid disclosed by the invention is applied to a PVB (Polyvinyl Butyral) adhesive, and the PVB adhesive shows excellent adhesion strength in a macroscopic adhesion performance test on the basis of multiple interactions, and particularly has excellent adhesion strength on aluminum. The obtained adhesive can be universally adapted to various substrates such as metal substrates and macromolecule substrates, and finally high-strength and high-durability intelligent adhesion performance is achieved.

The invention belongs to the technical field of organic synthesis, and particularly relates to a pyroxasulfone preparation method which specifically comprises the following steps: dissolving 3-(5-difluoromethoxy-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethylthio)-5, 5-dimethyl-2-isoxazoline serving as a raw material with a solvent, then adding a boron compound, finally dropwise adding hydrogen peroxide, and reacting at room temperature to obtain the pyroxasulfone. Reacting for several hours to obtain pyroxasulfone; the adopted boron compound is cheap and easy to obtain, so that the use of a transition metal catalyst is avoided, and the raw material cost is reduced; organic acid reagents with heavy odor are not used, waste water and solid waste are less, and the method has great advantages in the aspect of environmental protection; the method is simple to operate, free of complex treatment steps and suitable for industrial production, and when the boron compound is selected from sodium metaborate, sodium perborate or a mixture of borax and sodium metaborate, the yield and purity of the process are higher, and sulfoxide impurities are fewer.

The invention discloses a fluorinated COF enhanced PVDF-HFP composite gel polymer electrolyte. The fluorinated COF enhanced PVDF-HFP composite gel polymer electrolyte is prepared from the following raw materials: polyvinylidene fluoride-co-hexafluoropropylene, a fluorinated covalent organic framework containing an ether oxygen bond and a carbon-carbon unsaturated double bond, bis (trifluoromethylsulfonyl) imide anion ionic liquid and fluorine-containing imide lithium salt, the fluorinated covalent organic framework containing the ether-oxygen bond and the carbon-carbon unsaturated double bond is prepared by carrying out condensation reaction on a perfluorophenylene-containing module and the ether-oxygen bond-containing aromatic module. According to the electrolyte, PVDF-HFP is used as a polymer matrix, bis (trifluoromethylsulfonyl) imidogen ionic liquid is used as a functional phase and a plasticizer, imide lithium salt is used as a lithium ion source, fluorinated COF containing ether oxygen bonds and olefinic bonds is introduced, and the electrolyte has high ionic conductivity, high lithium ion transference number, excellent mechanical property and interface stability; the method is especially suitable for a high-safety lithium metal battery system.

Processes and methods of preparing Compound (I) are disclosed. Crystalline forms of Compound (I), pharmaceutically acceptable salts, solvates, hydrates, and cocrystals thereof, pharmaceutical compositions comprising the same, methods of treating cystic fibrosis using the same, and methods for making the same are also disclosed.

The invention belongs to the technical field of chemical synthesis, and relates to a method for continuously synthesizing 4-bromo-2-p-chlorophenyl-5-trifluoromethyl pyrrole-3-nitrile by a microchannel reactor, which comprises the following steps: pumping a substrate solution to a first plate type micro-reaction module; respectively pumping the bromination reagent solution to a first plate type micro-reaction module, a second plate type micro-reaction module and a third plate type micro-reaction module to obtain a reaction base solution; the reaction base solution is introduced into a fourth plate type micro-reaction module, n-heptane is pumped to the fourth plate type micro-reaction module and a fifth plate type micro-reaction module, deionized water is pumped to the fourth plate type micro-reaction module and the fifth plate type micro-reaction module, and extract liquor is obtained; and carrying out separation, evaporation recovery and recrystallization to obtain a finished product. Through the multi-stage series design of the micro-channel reactor, catalytic bromination replaces traditional bromine oxidation and reaction-extraction in-situ integration, and the three major problems of low efficiency, serious pollution and poor safety of an intermittent process are solved.

The invention discloses an acid-alkali-resistant high-weather-resistant insulating powder coating as well as a preparation method and application thereof in the aspect of sound screens of high-speed guardrails, and relates to the technical field of fluorocarbon resin powder coatings. The insulating powder coating with acid and alkali resistance and high weather resistance is prepared from the following raw materials in parts by weight: 15 to 25 parts of fluorocarbon resin, 40 to 50 parts of polyester resin, 5 to 12 parts of curing agent, 0.5 to 2 parts of accelerant, 3 to 8 parts of corrosion-resistant agent, 2 to 5 parts of weather-resistant agent, 1 to 2 parts of flatting agent, 0.3 to 1 part of benzoin and 10 to 15 parts of inorganic nano filler. The preparation method comprises the following steps: reacting 4-trifluoromethylphenol with 6-bromo-1-hexene to obtain an intermediate 1, generating an intermediate 2 from the intermediate 1 under the action of m-chloroperoxybenzoic acid, and reacting the intermediate 2 with amino-terminated polyether to generate the corrosion-resistant agent. The acid-base-resistant high-weather-resistant insulating powder coating prepared by the invention has good acid-base resistance, heat aging resistance and light aging resistance.

The invention relates to a sodium ion battery and a phosphate flame-retardant electrolyte thereof. The electrolyte solution includes: a solvent including trimethyl phosphate (TMP) and hydrofluoroether; a sodium salt; and an additive containing sodium tetrakis (3, 5-bis (trifluoromethyl) phenyl) borate. The electrolyte is low in cost, high in safety, good in interface compatibility and excellent in electrochemical performance.

The invention belongs to the technical field of oil exploitation, and relates to a drag reducer for fracturing and a preparation method thereof. The preparation method comprises the following steps: adding 1, 5-hexadiene-3, 4-diol and a catalyst into a high-pressure reactor, raising the temperature, introducing ethylene oxide, raising the temperature, carrying out a heat preservation reaction, stopping heating, and cooling to 50 DEG C or below; adjusting the pH value to 2-3 by using phosphoric acid, adding sulfamic acid, heating, preserving heat and reacting, and cooling to below 40 DEG C; the preparation method comprises the following steps: adding deionized water, 2-(trifluoromethyl) acrylic acid and methacryloylethyl sulphobetaine, stirring and dissolving, adjusting the pH value to 7-8, adding an initiator, heating and carrying out a heat preservation reaction to obtain a viscous liquid; and settling, centrifuging, cleaning and drying to obtain the product drag reducer. The drag reducer has the characteristics of high viscosity and high drag reduction rate.

The invention relates to the technical field of lithium battery solid electrolyte, and discloses a composite solid electrolyte based on a fluorinated metal organic framework and a preparation method and application thereof. The composite solid electrolyte comprises a polymer, a lithium salt and a fluorinated metal organic framework material, wherein the mass ratio of the polymer to the lithium salt is 1: (0.3-0.5), and the dosage of the fluorinated metal organic framework material is 5-20wt% of the total amount of the polymer and the lithium salt. The composite solid electrolyte provided by the invention contains ZIF-8-xFL, and a phenolic hydroxyl group of the ZIF-8-xFL efficiently eliminates O < 2->. Generated on a positive electrode interface under high voltage through an electron delocalization effect, so that a chain oxidation reaction of a positive electrode / electrolyte interface under high voltage is inhibited; a coordinated unsaturated site formed by triazolyl and Zn < 2 + > has an anchoring effect on TFSI <-> anions, so that the migration number of Li < + > is increased; and the trifluoromethyl group with strong electronegativity is preferentially decomposed in the electrochemical reduction process, and is induced to form a solid electrolyte interface layer rich in inorganic F / N, so that the interface ion transmission kinetics and mechanical stability are remarkably improved.

The invention relates to a high-voltage polyoxyethylene (PEO)-based solid electrolyte and a preparation method thereof, and belongs to the technical field of solid-state battery materials. The electrolyte is composed of a polymer substrate, an inorganic filler, a cosolvent and a lithium salt, the polymer substrate is a PEO-polyacrylonitrile (PAN) composite substrate; the inorganic filler is lithium titanium aluminum phosphate LATP, and the cosolvent is fluoroethylene carbonate FEC; the lithium salt is lithium bis (trifluoromethanesulfonic acid) imide LiTFSI and lithium difluoro (oxalato) borate LiDFOB; the dispersing agent is acetonitrile ACN. The method has the advantages that PEO and FEC are complexed to form a new structure, and room-temperature efficient operation of a single-salt (LiTFSI) system is realized; and meanwhile, LiDFOB is cooperatively introduced to construct a stable passivation layer on a positive electrode interface, FEC synchronously induces to generate LiF-rich stable SEI on a lithium negative electrode, and the interface compatibility and electrochemical stability of the electrolyte to a high-voltage electrode are remarkably improved.

The invention discloses lithium ion diaphragm coating slurry and a preparation method and application thereof.The lithium ion battery diaphragm comprises a base membrane and a coating on the base membrane, the coating comprises a dispersing agent, potassium carboxymethyl cellulose and side-chain modified polyvinylidene fluoride, and the method for preparing the side-chain modified polyvinylidene fluoride comprises the steps that vinylidene fluoride, hexafluoropropylene, (S)-4-pentene-1, 2, 4-triazole-1, 2, 4-triazole-1, 2, 4-triazole-1, 2, 4-triazole-1, 2, 4-triazole-1, 2, 4-triazole-1, 3-triazole-1, 3-triazole-1, 2-triazole-1, the preparation method comprises the following steps: uniformly mixing 1, 2-diol, (S)-3-(trifluoromethyl) adipyl dichloride, an initiator, an auxiliary agent and a solvent, and reacting for 9-12 hours in an inert gas atmosphere at 75-80 DEG C under a stirring condition to obtain a reaction solution; and carrying out spray drying on the reaction liquid to obtain the side chain modified polyvinylidene fluoride. The coating slurry provided by the invention can realize firm bonding between the diaphragm and a pole piece at room temperature, improves the stability and safety of a battery structure, and remarkably reduces the internal resistance of the battery diaphragm at the same time.