USRE31414E - Electrolyte salts for non aqueous electrochemical cells - Google Patents
Electrolyte salts for non aqueous electrochemical cells Download PDFInfo
- Publication number
- USRE31414E USRE31414E US06/199,160 US19916080A USRE31414E US RE31414 E USRE31414 E US RE31414E US 19916080 A US19916080 A US 19916080A US RE31414 E USRE31414 E US RE31414E
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- US
- United States
- Prior art keywords
- cell
- lithium
- electrolyte salt
- electrolyte
- fluid
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G15/00—Compounds of gallium, indium or thallium
- C01G15/006—Compounds containing, besides gallium, indium, or thallium, two or more other elements, with the exception of oxygen or hydrogen
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
Definitions
- This invention relates to electrolyte salts for electrochemical cells particularly non-aqueous high energy density cells and more particularly inorganic cells having fluid depolarizers such as thionyl chloride.
- thionyl chloride SOCl 2
- SOCl 2 thionyl chloride
- an electrolyte salt must fulfill several criteria. It should of course, have a high ionic or electrical conductivity for material transport upon cell discharge.
- the electrolyte salt should also be highly soluble in the fluid depolarizer/electrolyte whereby such conductivity may be practically attained.
- electrolyte salt should be stable with respect to both the fluid depolarizer/electrolyte solvent and the anode metal.
- Electrolyte salts or solutes used in thionyl chloride depolarized cells are, for example, described at length in U.S. Pat. No. 3,926,699.
- the most preferred and the most widely used electrolyte salt or solute having the above described requisite properties is lithium tetrachloroaluminate (LiAlCl 4 ).
- LiAlCl 4 lithium tetrachloroaluminate
- the present invention generally comprises the use of novel electrolyte salts in high energy density, non-aqueous electrochemical cells.
- the electrolyte salts have the general formula M(ZX 4 ) n .
- M represents the alkali or alkaline earth metals such as lithium, sodium, potassium, rubidium, beryllium, magnesium, and calcium, and generally though not necessarily corresponds to the metal used as the anode of the electrochemical cell.
- Z represents .[.a member selected from the group consisting of.]. gallium, .[.indium or thallium,.].
- the preferred electrolyte salts are those in which "X" is chlorine such as lithium tetrachlorogallate, .[.lithium tetrachloroindate and lithium tetrachlorothallate.]. with the most preferred salt being lithium tetrachlorogallate.
- the anodes useful in high energy density cells containing the novel electrolyte of the present invention include one or more of the aforementioned lithium and other alkali or alkaline earth metals such as sodium, potassium, rubidium, beryllium, magnesium, calcium and other metals above hydrogen in the EMF series.
- novel electrolyte salts of the present invention have particular utility in cells containing fluid depolarizer/electrolyte solvents such as thionyl chloride which cells are capable of being discharged at high rate.
- fluid depolarizer/electrolyte solvents include fluid oxyhalides, non-metallic oxides and non-metallic halides and mixtures thereof such as phosphorous oxychloride (POCl 3 ), selenium oxychloride (SeOCl 2 ), sulfur dioxide (SO 2 ), sulfur trioxide (SO 3 ), vanadium oxytri-chloride (VOCl 3 ), chromyl chloride (CrO 2 Cl 2 ), sulfuric oxychloride (SO 2 Cl 2 ), Nitryl chloride (NO 2 Cl), nitrosyl chloride (NOCl), nitrogen dioxide (NO 2 ), sulfur monochloride (S 2 Cl 2 ) and sulfur monobromide (S 2 Br 2 ).
- electrolyte salts have been described for particular utility in fluid cathode depolarizer/electrolyte solvent cells they may be utilized in other cells requiring electrolyte salts such as those containing solid cathodes such as metal chromates and dichromates, vanadates, molybdates, halides, oxides, permanganates, iodates and carbon monofluoride and organic electrolyte solvents such as tetrahydrofuran, propylene carbonate, dimethyl sulfite, dimethyl sulfoxide, N-nitrosodimethylamine, gamma-butyrolactone, dimethyl carbonate, methyl formate, butyl formate, dimethoxyethane, acetonitrile and N,N-dimethyl formamide.
- solid cathodes such as metal chromates and dichromates, vanadates, molybdates, halides, oxides, permanganates, iodates and
- the salts of the present invention are utilized in the same manner as prior art cells whereby they are simply dissolved in the electrolyte salt solvent to the desired concentration.
- the following examples set forth, by way of illustration, the preparation of a salt of the present invention, the testing of its stability with respect to cell components and its performance in electrochemical cells generally and as compared to cells containing an electrolyte salt of the prior art. It is understood that the following examples are for illustrative purposes only with the invention not to be limited thereby.
- LiGaCl 4 is prepared by mixing and melting equimolar amounts of anhydrous GaCl 3 and LiCl together. A one molar .[.LiGaCl 4 -SoCl 2 .]. LiGaCl 4 -.Iadd.SOCl 2 .Iaddend. solution is prepared (with the LiGaCl 4 being readily soluble in SOCl 2 ) and the ionic conductivity is measured and is found to be 1.13 ⁇ 10 -2 ohm -1 cm -1 at room temperature. This compares favorably with the conductivity of a similar solution of 1 molar LiAlCl 4 --SOCl 2 which is 1.6 ⁇ 10 -2 ohm -1 cm -1 . The conductivity of LiGaCl 4 is thus suitable for a Li/SOCl 2 cell with high discharge rate capability.
- D size cells (OD 1.30", L 2.38") are constructed by winding a lithium anode, having the dimensions of 21.25" ⁇ 2" ⁇ 0.015" with a carbon cathode on expanded nickel metal, having the dimensions 20 ⁇ 1.75" ⁇ 0.025", and two layers of glass fiber paper separators.
- the cells are each filled with 45 grams of the 1 molar LiGaCl 4 --SOCl 2 solution of Examples I and II.
- the cells are discharged at various currents with the results given in Table I.
- a cell is constructed in accordance with the procedure of Example III but with a 1 molar solution of LiAlCl 4 --SOCl 2 instead of LiGaCl 4 --SOCl 2 .
- the cell is discharged at 3.0 A and delivers 9.0 amp hours with about a 3 volt constant potential.
- the 9.0 amp hours attained with a cell containing a LiAlCl 4 electrolyte salt is nearly 20% less than that attained under identical conditions with an identical cell containing the electrolyte salt of the present invention.
Abstract
Novel electrolyte salts having high current carrying capability for non-aqueous electrochemical cells particularly those containing fluid depolarizer/electrolyte solvents. The salts have the general formula M(ZX4)n with "M" being an alkali or alkaline earth metal, "Z" being gallium, .[.indium or thallium,.]. "X" being a halogen and "n" being either 1 or 2.
Description
This invention relates to electrolyte salts for electrochemical cells particularly non-aqueous high energy density cells and more particularly inorganic cells having fluid depolarizers such as thionyl chloride.
Recently much effort has been expended in the development of high energy density cell systems which provide both higher voltages and total capacity (volumetric and gravimetric) than those of the Leclanche or alkaline cells having zinc anodes. The high energy density cell systems are centered around the use of active metals (metals above hydrogen in the EMF series which are unstable in aqueous environments) as anodes in non-aqueous solution cells. Lithium in particular has shown great promise as an anode material because of its high potential and low weight.
Various cell systems have been developed utilizing lithium as the anode electrode material. The ones showing the most promise in terms of voltage stability and high discharge capability, are those having fluid cathode depolarizers which serve the dual function of electrolyte salt solvent and cathode depolarizer. When a cell of this type is not being discharged, the fluid depolarizer/electrolyte solvent reacts with the anode metal to a limited extent with a protective coating being formed on the surface of the anode. Full reaction between the anode and fluid depolarizer with which it is in contact is thereby substantially prevented. However, upon discharge the protective coating is dissipated such that the cell can function.
One of the most common of such fluid depolarizer/electrolyte solvents is thionyl chloride (SOCl2) which, in combination with lithium, provides a cell couple having an exceedingly high voltage (˜4 volts), discharge capability, energy density, and stability of discharge. However, a limiting factor in the utility especially with respect to high rate discharge) of cells containing a Li/SOCl2 couple in the electrolyte salt used therein. Generally an electrolyte salt must fulfill several criteria. It should of course, have a high ionic or electrical conductivity for material transport upon cell discharge. The electrolyte salt should also be highly soluble in the fluid depolarizer/electrolyte whereby such conductivity may be practically attained. Additionally, the electrolyte salt should be stable with respect to both the fluid depolarizer/electrolyte solvent and the anode metal. Electrolyte salts or solutes used in thionyl chloride depolarized cells are, for example, described at length in U.S. Pat. No. 3,926,699. Of the enumerated salts in the aforesaid patent the most preferred and the most widely used electrolyte salt or solute having the above described requisite properties, is lithium tetrachloroaluminate (LiAlCl4). However, under conditions of high rate discharge, the energy density of cells containing lithium tetrachloroaluminate has been found to be substantially reduced.
It is an object of the present invention to provide novel electrolyte salts for non-aqueous electrochemical cells.
It is a further object of the present invention to provide novel electrolyte salts for use in high energy density cells having fluid depolarizer/electrolyte solvents such as thionyl chloride wherein the high rate discharge capability of such cells is improved without substantial loss of capacity.
These and other objects, features and advantages will be more evident from the following discussion.
The present invention generally comprises the use of novel electrolyte salts in high energy density, non-aqueous electrochemical cells. The electrolyte salts have the general formula M(ZX4)n. "M" represents the alkali or alkaline earth metals such as lithium, sodium, potassium, rubidium, beryllium, magnesium, and calcium, and generally though not necessarily corresponds to the metal used as the anode of the electrochemical cell. "Z" represents .[.a member selected from the group consisting of.]. gallium, .[.indium or thallium,.]. "X" represents a halogen or mixture of halogens which halogens are chlorine, bromine, iodine and fluorine and "n" represents either 1 or 2 with the value thereof being determined by whether "M" is an alkali metal in which instance n=1 or whether "M" is an alkaline earth metal in which instance n=2.
The preferred electrolyte salts are those in which "X" is chlorine such as lithium tetrachlorogallate, .[.lithium tetrachloroindate and lithium tetrachlorothallate.]. with the most preferred salt being lithium tetrachlorogallate.
The anodes useful in high energy density cells containing the novel electrolyte of the present invention include one or more of the aforementioned lithium and other alkali or alkaline earth metals such as sodium, potassium, rubidium, beryllium, magnesium, calcium and other metals above hydrogen in the EMF series.
The novel electrolyte salts of the present invention have particular utility in cells containing fluid depolarizer/electrolyte solvents such as thionyl chloride which cells are capable of being discharged at high rate. Examples of other fluid depolarizer/electrolyte solvents include fluid oxyhalides, non-metallic oxides and non-metallic halides and mixtures thereof such as phosphorous oxychloride (POCl3), selenium oxychloride (SeOCl2), sulfur dioxide (SO2), sulfur trioxide (SO3), vanadium oxytri-chloride (VOCl3), chromyl chloride (CrO2 Cl2), sulfuric oxychloride (SO2 Cl2), Nitryl chloride (NO2 Cl), nitrosyl chloride (NOCl), nitrogen dioxide (NO2), sulfur monochloride (S2 Cl2) and sulfur monobromide (S2 Br2). Each of the above can be used together with thionyl chloride (SOCl2) as fluid depolarizer/electrolyte solvent or separately.
Though the above electrolyte salts have been described for particular utility in fluid cathode depolarizer/electrolyte solvent cells they may be utilized in other cells requiring electrolyte salts such as those containing solid cathodes such as metal chromates and dichromates, vanadates, molybdates, halides, oxides, permanganates, iodates and carbon monofluoride and organic electrolyte solvents such as tetrahydrofuran, propylene carbonate, dimethyl sulfite, dimethyl sulfoxide, N-nitrosodimethylamine, gamma-butyrolactone, dimethyl carbonate, methyl formate, butyl formate, dimethoxyethane, acetonitrile and N,N-dimethyl formamide.
The salts of the present invention are utilized in the same manner as prior art cells whereby they are simply dissolved in the electrolyte salt solvent to the desired concentration. The following examples, set forth, by way of illustration, the preparation of a salt of the present invention, the testing of its stability with respect to cell components and its performance in electrochemical cells generally and as compared to cells containing an electrolyte salt of the prior art. It is understood that the following examples are for illustrative purposes only with the invention not to be limited thereby.
LiGaCl4 is prepared by mixing and melting equimolar amounts of anhydrous GaCl3 and LiCl together. A one molar .[.LiGaCl4 -SoCl2.]. LiGaCl4 -.Iadd.SOCl2 .Iaddend. solution is prepared (with the LiGaCl4 being readily soluble in SOCl2) and the ionic conductivity is measured and is found to be 1.13×10-2 ohm-1 cm-1 at room temperature. This compares favorably with the conductivity of a similar solution of 1 molar LiAlCl4 --SOCl2 which is 1.6×10-2 ohm-1 cm-1. The conductivity of LiGaCl4 is thus suitable for a Li/SOCl2 cell with high discharge rate capability.
Shiny pieces of lithium foil are added to the LiGaCl4 --SOCl2 solution of Example I and refluxed for 8 days at about 85° C. At the end of the refluxing period the lithium pieces are found to be bright and shiny indicating that the LiGaCl4 --SOCl2 is chemically compatible with lithium and is therefore useful as an electrolyte in a lithium anode cell. The absence of discoloration and/or corrosion indicates that a protective coating of sufficient but minimal thickness is formed on the surface of the lithium with discoloration indicating a too thick coating and corrosion indicating the absence of a coating.
Several "D" size cells (OD 1.30", L 2.38") are constructed by winding a lithium anode, having the dimensions of 21.25"×2"×0.015" with a carbon cathode on expanded nickel metal, having the dimensions 20×1.75"×0.025", and two layers of glass fiber paper separators. The cells are each filled with 45 grams of the 1 molar LiGaCl4 --SOCl2 solution of Examples I and II. The cells are discharged at various currents with the results given in Table I.
TABLE I
______________________________________
Cell Discharge Current
Voltage amp hours to 2 volts
______________________________________
1 0.13 amps 3.6 14
2 0.10 3.5 13.4
3 1.0 3.3 12.4
4 3.0 3.0 11
______________________________________
Several cells made in accordance with Example III are stored for varying lengths of time at 25° C. and discharged at a current rate of 1 amp with the discharge characteristics as a function of storage time given in Table II.
TABLE II
______________________________________
Storage duration
Capacity to 2.0 volts at
Cell at 25° C. (months)
1A (amp hours)
______________________________________
5 0 12.5
6 1 12.3
7 2 11.9
8 5 11.0
______________________________________
A cell is constructed in accordance with the procedure of Example III but with a 1 molar solution of LiAlCl4 --SOCl2 instead of LiGaCl4 --SOCl2. The cell is discharged at 3.0 A and delivers 9.0 amp hours with about a 3 volt constant potential.
The 9.0 amp hours attained with a cell containing a LiAlCl4 electrolyte salt is nearly 20% less than that attained under identical conditions with an identical cell containing the electrolyte salt of the present invention.
The above examples are for illustrative purposes only. It is understood that changes and variations with respect to cell components utilized with the electrolyte salts of the present invention may be made without departing from the scope of the present invention as defined in the following claims.
Claims (8)
1. A non-aqueous electrochemical cell comprising an anode, comprised of one or more metals above hydrogen in the EMF series, a cathode depolarizer and a dissolved electrolyte salt characterized in that the electrolyte salt has the formula M(ZX4)n wherein "M" is selected from the group consisting of alkali and alkaline earth metals, "Z" is .[.selected from the group consisting of.]. gallium, .[.indium and thallium,.]. "X" is selected from the group consisting of chlorine, bromine, iodine, fluorine and mixtures thereof, and "n" is 1 when "M" is an alkali metal and "n" is 2 when "M" is an alkaline earth metal.
2. The cell of claim 1 wherein said cathode depolarizer is a fluid and functions as a solvent for said electrolyte salt.
3. The cell of claim 2 wherein said cathode depolarizer is selected from the group consisting of fluid oxyhalides, non-metallic oxides, non-metallic halides and mixtures thereof.
4. The cell of claim 3 wherein said cathode depolarizer is thionyl chloride (SOCl2).
5. The cell of claim 1 wherein said metal is lithium.
6. The cell of claim 4 wherein said metal is lithium. .[.7. The cell of claim 1 wherein said electrolyte salt is selected from the group consisting of lithium tetrachlorogallate, lithium tetrachloroindate and
lithium tetrachlorothallate..]. 8. The cell of claim 1 wherein said
electrolyte salt is lithium tetrachlorogallate. 9. The cell of claim 6 wherein said electrolyte salt is lithium tetrachlorogallate. .Iadd. 10. A non-aqueous electrochemical cell comprising a lithium anode, a fluid cathode depolarizer and an electrolyte salt dissolved in said fluid cathode depolarizer characterized in that said electrolyte salt consists of LiGaCl4. .Iaddend.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/199,160 USRE31414E (en) | 1978-11-02 | 1980-10-21 | Electrolyte salts for non aqueous electrochemical cells |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/956,833 US4177329A (en) | 1978-11-02 | 1978-11-02 | Electrolyte salts for non aqueous electrochemical cells |
| US06/199,160 USRE31414E (en) | 1978-11-02 | 1980-10-21 | Electrolyte salts for non aqueous electrochemical cells |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/956,833 Reissue US4177329A (en) | 1978-11-02 | 1978-11-02 | Electrolyte salts for non aqueous electrochemical cells |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE31414E true USRE31414E (en) | 1983-10-11 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/199,160 Expired - Lifetime USRE31414E (en) | 1978-11-02 | 1980-10-21 | Electrolyte salts for non aqueous electrochemical cells |
Country Status (1)
| Country | Link |
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| US (1) | USRE31414E (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5766797A (en) * | 1996-11-27 | 1998-06-16 | Medtronic, Inc. | Electrolyte for LI/SVO batteries |
| US6017656A (en) | 1996-11-27 | 2000-01-25 | Medtronic, Inc. | Electrolyte for electrochemical cells having cathodes containing silver vanadium oxide |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3926669A (en) * | 1972-11-13 | 1975-12-16 | Gte Laboratories Inc | Electrochemical cells having an electrolytic solution comprising a covalent inorganic oxyhalide solvent |
| US4060674A (en) * | 1976-12-14 | 1977-11-29 | Exxon Research And Engineering Company | Alkali metal anode-containing cells having electrolytes of organometallic-alkali metal salts and organic solvents |
| US4071664A (en) * | 1977-04-01 | 1978-01-31 | P. R. Mallory & Co. Inc. | Electrolyte salt additive |
| US4074019A (en) * | 1977-03-01 | 1978-02-14 | Exxon Research & Engineering Co. | Cell having fluorinated carbon cathode and solvated alkali metal salt electrolyte |
| US4075397A (en) * | 1977-03-01 | 1978-02-21 | Exxon Research & Engineering Co. | Cell having chalcogenide cathode and solvated alkali metal salt electrolyte |
| US4117213A (en) * | 1977-08-24 | 1978-09-26 | Exxon Research & Engineering Co. | Alkali metal salts of complex anions containing heteroatom substituents and electrolyte compositions containing these |
-
1980
- 1980-10-21 US US06/199,160 patent/USRE31414E/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3926669A (en) * | 1972-11-13 | 1975-12-16 | Gte Laboratories Inc | Electrochemical cells having an electrolytic solution comprising a covalent inorganic oxyhalide solvent |
| US4060674A (en) * | 1976-12-14 | 1977-11-29 | Exxon Research And Engineering Company | Alkali metal anode-containing cells having electrolytes of organometallic-alkali metal salts and organic solvents |
| US4074019A (en) * | 1977-03-01 | 1978-02-14 | Exxon Research & Engineering Co. | Cell having fluorinated carbon cathode and solvated alkali metal salt electrolyte |
| US4075397A (en) * | 1977-03-01 | 1978-02-21 | Exxon Research & Engineering Co. | Cell having chalcogenide cathode and solvated alkali metal salt electrolyte |
| US4071664A (en) * | 1977-04-01 | 1978-01-31 | P. R. Mallory & Co. Inc. | Electrolyte salt additive |
| US4117213A (en) * | 1977-08-24 | 1978-09-26 | Exxon Research & Engineering Co. | Alkali metal salts of complex anions containing heteroatom substituents and electrolyte compositions containing these |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5766797A (en) * | 1996-11-27 | 1998-06-16 | Medtronic, Inc. | Electrolyte for LI/SVO batteries |
| US6017656A (en) | 1996-11-27 | 2000-01-25 | Medtronic, Inc. | Electrolyte for electrochemical cells having cathodes containing silver vanadium oxide |
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