Patent Application
20230361346
The present disclosure relates to nonaqueous electrolytic solutions for energy storage devices including batteries and capacitors, especially for secondary batteries and devices known as supercapacitors.
There are two main types of batteries: primary and secondary. Primary batteries are also known as non-rechargeable batteries. Secondary batteries are also known as rechargeable batteries. A well-known type of rechargeable battery is the lithium-ion battery Lithium-ion batteries have a high energy density, no memory effect and low self-discharge..
Lithium-ion batteries are commonly used for portable electronics and electric vehicles. In the batteries lithium ions move from the negative electrode to the positive electrode during discharge and back when charging.
Typically, the electrolytic solutions include a nonaqueous solvent and an electrolyte salt, plus additives. The electrolyte is typically a mixture of organic carbonates such as ethylene carbonate, propylene carbonate, fluoroethylene carbonate, dialkyl carbonates such as ethyl methyl carbonate and ethers and polyethers such as dimethoxyethane containing a lithium-ion electrolyte salt. Many lithium salts can be used as the electrolyte salt; common examples include lithium hexafluorophosphate (LiPF6), lithium bis (fluorosulfonyl) imide (LiFSI) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI).
The electrolytic solution has to perform a number of separate roles within the battery.
The principal role of the electrolyte is to facilitate the flow of charge carriers between the cathode and anode. This occurs by transportation of metal ions within the battery to or from one or both of the anode and cathode, whereby on chemical reduction or oxidation, electrical charge is liberated/adopted.
Thus, the electrolyte needs to provide a medium which is capable of solvating and/or supporting the metal ions.
Due to the use of lithium electrolyte salts and the interchange of lithium ions with lithium metal, which is very reactive with water, as well as the sensitivity of other battery components to water, the electrolyte is usually non-aqueous.
Additionally, the electrolyte has to have suitable rheological properties to permit/enhance the flow of ions therein, at the typical operating temperature to which a battery is exposed and is expected to perform.
Moreover, the electrolyte has to be as chemically inert as possible. This is particularly relevant in the context of the expected lifetime of the battery regarding internal corrosion within the battery (e.g. of the electrodes and casing) and the issue of battery leakage. Also of importance within the consideration of chemical stability is flammability. Unfortunately, typical electrolyte solvents can be a safety hazard, since they often comprise a flammable material.
This can be problematic as in operation, when discharging or being discharged, batteries may accumulate heat. This is especially true for high density batteries such as lithium-ion batteries. It is therefore desirable that the electrolyte displays a low flammability, with other related properties such as a high flash point.
It is also desirable that the electrolyte does not present an environmental issue with regard to disposability after use or other environmental issue such as global warming potential.
“Regioselectivity in addition reactions of some binucleophilic reagents to (trifluoromethyl) acetylene” Stepanova et. al., Zhurnal Organicheskoi Khimii (1988), 24(4), 692-9 describes the preparation of a dioxolane having a CF3CH2 group, at relatively low levels of selectivity.
The listing or discussion of an independently prior published document in this specification should not necessarily be taken as an acknowledgement that the document is part of the state of the art or is common general knowledge.
It is an object of the present invention to provide a nonaqueous electrolytic solution, which provides improved properties over the nonaqueous electrolytic solution of the prior art.
According to a first aspect of the invention there is provided the use of a formulation comprising a metal ion and a compound of Formula 1 in a nonaqueous battery electrolyte formulation,
According to a second aspect of the invention there is provided the use of a nonaqueous battery electrolyte formulation comprising a formulation comprising a metal ion and a compound of Formula 1 in a battery.
According to a third aspect of the invention there is provided a battery electrolyte formulation comprising a formulation comprising a metal ion and a compound of Formula 1.
According to a fourth aspect of the invention there is provided a formulation comprising a metal ion and a compound of Formula 1, optionally in combination with a solvent.
According to a fifth aspect of the invention there is provided a battery comprising a battery electrolyte formulation comprising a metal ion and a compound of Formula 1.
According to a sixth aspect of the invention there is provided a method of reducing the flash point of a battery and/or a battery electrolyte formulation, comprising the addition of a formulation comprising a formulation comprising a metal ion and a compound of Formula 1.
According to a seventh aspect of the invention there is provided a method of powering an article comprising the use of a battery comprising a battery electrolyte formulation comprising a formulation comprising a metal ion and a compound of Formula 1.
According to an eighth aspect of the invention there is provided a method of retrofitting a battery electrolyte formulation comprising either (a) at least partial replacement of the battery electrolyte with a battery electrolyte formulation comprising a formulation comprising a metal ion and a compound of Formula 1, and/or (b) supplementation of the battery electrolyte with a battery electrolyte formulation comprising a compound of Formula 1.
According to a ninth aspect of the invention there is provided a method of preparing a battery electrolyte formulation comprising mixing a compound of Formula 1 with a metal ion containing salt and other solvents or co-solvents.
According to a tenth aspect of the invention there is provided a method of preparing a battery electrolyte formulation comprising mixing a composition comprising a compound of Formula 1 with a metal ion-containing compound,
According to an eleventh aspect of the invention there is provided a method of improving battery capacity/charge transfer within a battery/battery life/etc. by the use of a formulation comprising a metal ion and a compound of Formula 1.
According to a twelfth aspect of the invention there is provided a method of reducing the overpotential generated at one or both of the electrodes of a battery during cycling by the use of a formulation comprising a metal ion and a compound of Formula 1.
In reference to all aspects of the invention the preferred embodiment of Formula (1) is a partially fluorinated ether with the structure
wherein R1, R2, R3, R4 are independently selected from the group comprising H, F, Cl, Br, I, CF3, alkyl, fluoroalkyl, haloalkyl and R5 is independently selected from the group CF3, alkyl, fluoroalkyl, perfluoroalkyl, haloalkyl perfluorohaloalkyl.
Most preferably R5 methyl; preferably R1 and R2 are CF3 and R3 and R4 are H; alternatively R1 is CF3, R2 is H, one of R3 and R4 is F, and one of R3 and R4 is H; further alternatively R1 is CF3, R2 is H. and R3 and R4 are H.
In the aspects of the invention, the electrolyte formulation has been found to be surprisingly advantageous.
The advantages of using formulations comprising compounds of Formula 1 in electrolyte solvent compositions manifest themselves in a number of ways. Their presence can reduce the flammability of the electrolyte composition (such as when for example measured by flashpoint). Their oxidative stability makes them useful for batteries required to work in harsh conditions and at high temperatures, they are compatible with common electrode chemistries and can even enhance the performance of these electrodes through their interactions with them.
Additionally, electrolyte compositions comprising compounds of Formula 1 may have superior physical properties including low viscosity and a low melting point, yet a high boiling point with the associated advantage of little or no gas generation in use. The electrolyte formulation may wet and spread extremely well over surfaces, particularly fluorine-containing surfaces; this is postulated to result from a beneficial a relationship between its adhesive and cohesive forces, to yield a low contact angle.
Furthermore, electrolyte compositions that comprise compounds of Formula 1 may have superior electro-chemical properties, including improved capacity retention, reduced overpotential generation at one or both electrodes during cycling, improved cyclability and capacity retention, improved compatibility with other battery components e.g. separators and current collectors, and with all types of cathode and anode chemistries, including systems that operate across a range of voltages and especially high voltages, and which include additives such as silicon. In addition, the electrolyte formulations display good solvation of metal (e.g. lithium) salts and interaction with any other electrolyte solvents present.
Preferred features relating to the aspects of the invention follows below. Preferences and options for a given aspect, feature or parameter of the invention should, unless the context indicates otherwise, be regarded as having been disclosed in combination with any and all preferences and options for all aspects, features and parameters of the invention.
The electrolyte formulation will preferably comprise 0.1 wt % to 99.9 wt % of the compound of Formula 1, conveniently 50.0 wt % to 99.9 wt % of the compound of Formula 1.
The nonaqueous electrolytic solution further comprises a metal ion, Normally the metal ion comes from an ionic salt, such as a metal electrolyte salt. Typically the metal electrolyte salt is present in an amount of 0.1 to 90 wt % relative to the total mass of the nonaqueous electrolyte formulation depending on the application.
The metal salt generally comprises a salt of lithium, sodium, magnesium, calcium, lead, zinc, ammonium or nickel. (Here it is of course appreciated that “ammonium” is not a metal per se. However, ammonium is a cation and can form ionic salts that can act as electrolyte salts.
Preferably the metal salt comprises a salt of lithium, such as those selected from the group comprising lithium hexafluorophosphate (LiPF6), lithium hexafluoroarsenate monohydrate (LiAsF6), lithium perchlorate (LiClO4), lithium tetrafluoroborate (LiBF4), lithium triflate (LiSO3CF3), lithium bis(fluorosulfonyl)imide (LiFSI, Li(FSO2)2N) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI, Li(CF3SO2)2N).
Most preferably, the metal salt comprises LiPF6, LiFSI or LiTFSI. Thus, in a most preferred variant of the fourth aspect of the invention, there is provided a formulation comprising LiPF6, LiFSI, LiTFSI and a compound of Formula 1, optionally in combination with one or more co-solvents.
Alternatively the metal salt comprises a salt of ammonium. Most preferably ammonium refers to NH4+ quaternary ammonium cations or alternatively NH4−xRx+, where one or more hydrogen atoms are replaced by organic groups (indicated by R). Preferred examples of organic groups include C1-C20 alkyl, fluoroalkyl, perfluoroalkyl, haloalkyl perfluorohaloalkyl. Particularly preferred is tetraethyl ammonium.
Preferred ammonium salts include fluoroborates such as tetrafluoroborates, such as BF4−.
The nonaqueous electrolytic solution may comprise a solvent. Preferred examples of solvents include fluoroethylene carbonate (FEC) and/or propylene carbonate (PC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), ethylene carbonate (EC),dimethoxyethane (DME), dioxolane (DOL) or acetonitrile.
Where present, the additional solvent makes up from 0.1 wt % to 99.9 wt % of the liquid component of the electrolyte.
The nonaqueous electrolytic solution may include an additive.
Suitable additives may serve as surface film-forming agents, which form an ion permeable film on the surface of the positive electrode or the negative electrode. This can pre-empt a decomposition reaction of the nonaqueous electrolytic solution and the electrolyte salt occurring on the surface of the electrodes, thereby preventing the decomposition reaction of the nonaqueous electrolytic solution on the surface of the electrodes.
Examples of film-forming agent additives include vinylene carbonate (VC), ethylene sulfite (ES), lithium bis(oxalato)borate (LiBOB), cyclohexylbenzene (CHB) and ortho-terphenyl (OTP). The additives may be used singly, or two or more may be used in combination.
When present, the additive is present in an amount of 0.1 to 3 wt % relative to the total mass of the nonaqueous electrolyte formulation.
The battery may comprise a primary (non-rechargeable) or a secondary battery (rechargeable). Most preferably the battery comprises a secondary battery.
A battery comprising the nonaqueous electrolytic solutions will generally comprise several elements. Elements making up the preferred nonaqueous electrolyte secondary battery cell are described below. It is appreciated that other battery elements may be present (such as a temperature sensor); the list of battery components below is not intended to be exhaustive.
The battery generally comprises a positive and a negative electrode. Usually the electrodes are porous and permit metal ions (lithium ions) to move in and out of their structures with a process called insertion (intercalation) or extraction (deintercalation).
For rechargeable batteries (secondary batteries), the term cathode designates the electrode where reduction is taking place during the discharge cycle. For lithium-ion cells the positive electrode (“cathode”) is the lithium-based one.
The positive electrode is generally composed of a positive electrode current collector such as a metal foil, optionally with a positive electrode active material layer disposed on the positive electrode current collector.
The positive electrode current collector may be a foil of a metal that is stable at a range of potentials applied to the positive electrode, or a film having a skin layer of a metal that is stable at a range of potentials applied to the positive electrode, Aluminium (Al) is desirable as the metal that is stable at a range of potentials applied to the positive electrode.
The positive electrode active material layer generally includes a positive electrode active material, and other components such as a conductive agent and a binder. This is generally obtained by mixing the components in a solvent, applying the mixture onto the positive electrode current collector, followed by drying and rolling.
The positive electrode active material may be lithium (Li) or a lithium-containing transition metal oxide. The transition metal element may be at least one selected from the group consisting of scandium (Sc), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu) and yttrium (Y). Of these transition metal elements, manganese, cobalt and nickel are the most preferred.
Further, in certain embodiments transition metal fluorides may be preferred.
Some of the transition metal atoms in the transition metal oxide may be replaced by atoms of a non-transition metal element. The non-transition element may be selected from the group consisting of magnesium (Mg), aluminium (Al), lead (Pb), antimony (Sb) and boron (B). Of these non-transition metal elements, magnesium and aluminium are the most preferred.
Preferred examples of positive electrode active materials include lithium-containing transition metal oxides such as LiCoO2, LiNiO2, LiMn2O4, LiMnO2, LiNi1−yCoyO2 (0<y<1), LiNi1−y−z CoyMnzO2 (0<y+z<1) and LiNi1−y−zCoyAlzO2 (0<y+z<1). LiNi1−y−zCoyMnzO2 (0<y+z<0.5) and LiNi1−y−zCoyAlO2 (0<y+z<0.5) containing nickel in a proportion of not less than 50 mol % relative to all the transition metals are desirable from the perspective of cost and specific capacity. These positive electrode active materials contain a large amount of alkali components and thus accelerate the decomposition of nonaqueous electrolytic solutions to cause a decrease in durability. However, the nonaqueous electrolytic solution of the present disclosure is resistant to decomposition even when used in combination with these positive electrode active materials.
The positive electrode active material may be a lithium (Li) containing transition metal fluoride. The transition metal element may be at least one selected from the group consisting of scandium (Sc), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu) and yttrium (Y). Of these transition metal elements, manganese, cobalt and nickel are the most preferred.
Some of the transition metal atoms in the transition metal fluoride may be replaced by atoms of a non-transition metal element. The non-transition element may be selected from the group consisting of magnesium (Mg), aluminium (Al), lead (Pb), antimony (Sb) and boron (B). Of these non-transition metal elements, magnesium and aluminium are the most preferred.
A conductive agent may be used to increase the electron conductivity of the positive electrode active material layer. Preferred examples of the conductive agents include conductive carbon materials, metal powders and organic materials. Specific examples include carbon materials as acetylene black, ketjen black and graphite, metal powders as aluminium powder, and organic materials as phenylene derivatives.
A binder may be used to ensure good contact between the positive electrode active material and the conductive agent, and to increase the adhesion of the components such as the positive electrode active material with respect to the surface of the positive electrode current collector. Preferred examples of the binders include fluoropolymers and rubber polymers, such as polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF) ethylene-propylene-isoprene copolymer and ethylene-propylene-butadiene copolymer. The binder may be used in combination with a thickener such as carboxymethylcellulose (CMC) or polyethylene oxide (PEO).
The negative electrode is generally composed of a negative electrode current collector such as a metal foil, optionally with a negative electrode active material layer disposed on the negative electrode current collector.
The negative electrode current collector may be a foil of a metal, Copper (lithium-free) is suitable as the metal. Copper is easily processed at low cost and has good electron conductivity.
Generally, the negative electrode comprises carbon, such as graphite or graphene and/or lithium metal, In preferred embodiments, the negative electrode comprises graphite and/or lithium metal.
Silicon based materials can also be used for the negative electrode. A preferred form of silicon is in the form of nano-wires, which are preferably present on a support material. The support material may comprise a metal (such as steel) or a non-metal such as carbon.
The negative electrode may include an active material layer, Where present the active material layer includes a negative electrode active material and other components such as a binder. This is generally obtained by mixing the components in a solvent, applying the mixture onto the positive electrode current collector, followed by drying and rolling.
Negative electrode active materials are not particularly limited, provided the materials can store and release lithium ions. Examples of suitable negative electrode active materials include carbon materials, metals, alloys, metal oxides, metal nitrides, and lithium-intercalated carbon and silicon, Examples of carbon materials include natural/artificial graphite, and pitch-based carbon fibres. Preferred examples of metals include lithium (Li), silicon (Si), tin (Sn), germanium (Ge), indium (In), gallium (Ga), titanium (Ti), lithium alloys, silicon alloys and tin alloys. Examples of lithium-based material include lithium titanate (Li2TiO3).
The active material may can be in many forms such as a thin film, foil or supported on a three-dimensional matrix.
As with the positive electrode, the binder may be a fluoropolymer or a rubber polymer and is desirably a rubbery polymer, such as styrene-butadiene copolymer (SBR). The binder may be used in combination with a thickener.
In a preferred embodiment, the negative electrode is lithium metal, in a secondary battery; conveniently in such embodiments, but also in other embodiments with other negative electrodes and in other battery types, the electrolyte comprises LiTFSI and/or LiFSI, dimethoxyethane, and a compound of Formula 1.
A separator is preferably present between the positive electrode and the negative electrode. The separator has insulating properties. The separator may comprise a porous film having ion permeability. Examples of porous films include microporous thin films, woven fabrics and nonwoven fabrics. Suitable materials for the separators are polyolefins, such as polyethylene and polypropylene.
The battery components are preferably disposed within a protective case.
The case may comprise any suitable material which is resilient to provide support to the battery and an electrical contact to the device being powered,
In one embodiment the case comprises a metal material, preferably in sheet form, moulded into a battery shape. The metal material preferably comprises a number of portions adaptable be fitted together (e.g. by push-fitting) in the assembly of the battery. Preferably the case comprises an iron/steel-based material.
In another embodiment the case comprises a plastics material, moulded into a battery shape. The plastics material preferably comprises a number of portions adaptable be joined together (e.g. by push-fitting/adhesion) in the assembly of the battery. Preferably the case comprises a polymer such as polystyrene, polyethylene, polyvinyl chloride, polyvinylidene chloride, or polymonochlorofluoroethylene. The case may also comprise other additives for the plastics material, such as fillers or plasticisers. In this embodiment wherein the case for the battery predominantly comprises a plastics material, a portion of the casing may additionally comprise a conductive/metallic material to establish electrical contact with the device being powered by the battery.
The positive electrode and negative electrode may be wound or stacked together through a separator. Together with the nonaqueous electrolytic solution they are accommodated in the exterior case. The positive and negative electrodes are electrically connected to the exterior case in separate portions thereof.
A number/plurality of battery cells may be made up into a battery module. In a battery module the battery cells may be organised in series and/or in parallel. Typically, these are encased in a mechanical structure.
A battery pack may be assembled by connecting multiple modules together in a series or parallel. Typically, battery packs include further features such as sensors and controllers including battery management systems and thermal management systems. The battery pack generally includes an encasing housing structure to make up the final battery pack product.
The battery of the invention, in the form of an individual battery/cell, module and/or pack (and the electrolyte formulations therefor) are intended to be used in one or more of a variety of end products.
Preferred examples of end products include portable electronic devices, such as GPS navigation devices, cameras laptops, tablets and mobile phones. Other preferred examples of end products include vehicular devices (as provision of power for the propulsion system and/or for any electrical system or devices present therein), such as electrical bicycles and motorbikes, as well as automotive applications (including hybrid and purely electric vehicles).
Preferences and options for a given aspect, feature or parameter of the invention should, unless the context indicates otherwise, be regarded as having been disclosed in combination with any and all preferences and options for all other aspects, features and parameters of the invention.
The invention will now be illustrated with reference to the following non-limiting examples.
The following steps were followed.
2,3-epoxy-1,1,1,3-tetrafluoropropane was ring opened using the following procedure:
2,3-epoxy-1,1,1,3-tetrafluoropropane was ring opened using the following procedure:
2,3-epoxy-1,1,1- rifluoro-2-(trifluoromethyl)propane was ring opened using the following procedure:
The alcohol prepared in Example 1a and Examples 1b/1c, as described above was added to an aqueous solution comprising 20% NaOH and containing 2% tetra-n-butyl ammonium bromide (TBAB) at 0-5° C. A small excess of dimethyl sulfate was then added to this mixture with stirring. When the addition was complete, the reaction was stirred for 1 hour and allowed to warm to room temperature. The product was then recovered by distillation, dried over anhydrous MgSO4 and then redistilled over CaH2 to remove impurities and final traces of water.
Using this method, the two methyl ethers below were prepared:
Ether A: 19F NMR spectrum shows characteristic signals as follows
Ether B: 19F NMR spectrum shows characteristic signals as follows
Ethers A and B were used to prepare sample electrolyte formulations comprising:
Solutions were prepared comprising a 50:50 mix of the ether and co-solvent containing 1 M of a conducting salt. These solutions were found to comprise a single phase and be clear.
The Figures illustrates the results of various spectroscopic analytical techniques carried out on some of the reaction products from the Examples.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014633.8 | Sep 2020 | GB | national |
| 2102464.1 | Feb 2021 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2021/052334 | 9/9/2021 | WO |
