Electrolyte for use in an all inorganic rechargeable cell and lithium inorganic cell containing the improved electrolyte

An improved electrolyte is provided in a lithium/sulfur dioxide rechargea cell, the electrolyte comprising a solution of a stable, highly conductive liquid electrolyte complex LiAlCl.sub.4 --3SO.sub.2 and up to about 50 percent by weight of sulfuryl chloride as a cosolvent.

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Description

This invention relates in general to an improved electrolyte for use in all inorganic rechargeable cell and to an all inorganic rechargeable cell including the improved electrolyte and in particular to an improved electrolyte for use in a lithium/SO.sub.2 rechargeable cell and to a lithium/SO.sub.2 rechargeable cell including the improved electrolyte.

BACKGROUND OF THE INVENTION

An all inorganic Li/SO.sub.2 rechargeable cell generally includes a lithium anode, a porous carbon cathode and a stable highly conductive liquid electrolyte complex LiAlCl.sub.4 --xSO.sub.2. This complex is rapidly formed when the commonly used LiAlCl.sub.4 electrolyte salt reacts with SO.sub.2 gas or SO.sub.2 liquid. Although the initially formed liquid complex has the formula LiAlCl.sub.4 --3SO.sub.2, additional lowered LiAlCl.sub.4 salt concentration can be achieved at will by diluting the above electrolyte with additional SO.sub.2. Thus, electrolyte with formulas LiAlCl--xSO.sub.2 where x is at least 3 can be prepared. The starting electrolyte LiAlCl.sub.4 --3SO.sub.2 has a very high specific conductivity of 0.1 S/cm. The fact that this is the highest known conductivity for any ambient temperature non aqueous electrolyte makes this general class of electrolytes extremely valuable.

One difficulty with the use of this electrolyte is however, that during cell discharge, the insoluble reduction product is deposited in the porous carbon cathode. Simultaneously, some of the LiAlCl.sub.4 electrolyte salt is also precipitated in the porous carbon cathode. The coprecipitation of electrolyte salt is partially responsible for the severely reduced capacity currently plaguing this system.

SUMMARY OF THE INVENTION

The general object of this invention is to provide an improved lithium inorganic rechargeable cell system. A more particular object is to minimize or even eliminate LiAlCl.sub.4 coprecipitation and thus improve cell capacity.

It has been found that the aforementioned objects can be attained by adding a suitable cosolvent to the electrolyte to allow excess LiAlCl.sub.4 that would normally precipitate to dissolve. The requirements of an effective cosolvent are:

(A) The cosolvent should be capable of rapidly dissolving the LiAlCl.sub.4 salt and, in order to minimize IR losses, must in the process form a reasonably conducting electrolyte solution.

(B) The cosolvent should be extremely miscible with liquid SO.sub.2.

(C) The cosolvent must not become easily oxidized during cell charging which typically takes place at 4.0 volts relative to lithium.

(D) The cosolvent should not become chemically degraded in the presence of AlCl.sub.3 or chlorine, both of which are formed during cell charging.

A particularly effective cosolvent has been found to be sulfuryl chloride, SO.sub.2 Cl.sub.2. One would not expect that the addition of SO.sub.2 Cl.sub.2 as a cosolvent would be able to improve cell capacity in Li/SO.sub.2 rechargeable cells since the specific conductivity of pure SO.sub.2 Cl.sub.2 is very poor. That is, pure SO.sub.2 Cl.sub.2 is one million times less conductive than is the LiAlCl.sub.4 --3SO.sub.2 electrolyte.

Experimental results were obtained in small laboratory cells. The cells include a lithium anode, a porous carbon cathode made from high surface area carbon black and a LiAlCl.sub.4 electrolyte salt.

The following electrolytes were tested: (1) LiAlCl--3SO.sub.2 ; (2) LiAlCl.sub.4 --3SO.sub.2 +10% SO.sub.2 Cl.sub.2 ; (3) LiAlCl.sub.4 --3SO.sub.2 +20% SO.sub.2 Cl.sub.2 ; and (4) LiAlCl.sub.4 --SO.sub.2 Cl.sub.2

The results of these experiments are shown in the following Table:

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                      FIRST                                                    

                      CYCLE      TENTH CYCLE                                   

                      CAPACITY   CAPACITY                                      

     ELECTROLYTE      mAH        mAH                                           

     ______________________________________                                    

     LiAlCl.sub.4 --3SO.sub.2                                                  

                       9         14                                            

     LiAlCl.sub.4 --3SO.sub.2 + 10% SO.sub.2 Cl.sub.2                          

                      32         20                                            

     LiAlCl.sub.4 --3SO.sub.2 + 20% SO.sub.2 Cl.sub.2                          

                      52         18                                            

     LiAlCl.sub.4 --SO.sub.2 Cl.sub.2                                          

                      20          0                                            

     ______________________________________                                    

The results clearly show that Li/LiAlCl.sub.4 --3SO.sub.2 cells constructed with 10% and 20% added SO.sub.2 Cl.sub.2 had longer capacities than either Li/LiAlCl.sub.4 --3SO.sub.2 cells or even Li/LiAlCl.sub.4 --SO.sub.2 Cl.sub.2 cells. It is clear that on the TENTH CYCLE, the advantage of the addition of low percentages of SO.sub.2 Cl.sub.2 is evident. Cells containing more than 50% added SO.sub.2 Cl.sub.2 could not be cycled ten times.

We wish it to be understood that we do not desire to be limited to the exact details as described for obvious modifications will occur to a person skilled in the art.

Claims

1. An improved electrolyte for use in an all inorganic rechargeable cell, said electrolyte comprising a solution of a stable, highly conductive liquid electrolyte complex LiAlCl--XSO.sub.2 where x is at least 3, and up to about 50 percent by weight of a cosolvent that is: (a) capable of rapidly dissolving a LiAlCl.sub.4 salt and in the process forming a reasonably conducting electrolyte solution; (b) extremely miscible with liquid SO.sub.2; (c) not easily oxidized during cell charging; and (d) not chemically degraded in the presence of reaction products formed during cell charging.

2. An improved electrolyte according to claim 1 wherein the cosolvent is sulfuryl chloride.

3. An improved electrolyte for use in a lithium/sulfur dioxide rechargeable cell, said electrolyte comprising a solution of a stable, highly conductive liquid electrolyte complex LiAlCl--xSO.sub.2, where x is at least 3, and up to about 50 percent by weight of a cosolvent that is:

(a) capable of rapidly dissolving LiAlCl.sub.4 salt and in the process forming a reasonably conducting electrolyte solution;
(b) extremly miscible with liquid SO.sub.2; (c) not easily oxidized during cell charging which takes place at about 4.0 volts relative to lithium; and (d) not chemically degraded in the presence of AlCl.sub.3 or Cl.sub.2, both of which are formed during cell charging.

4. An improved electrolyte according to claim 3 wherein the liquid complex has the formula LiAlCl.sub.4 --3SO.sub.2.

5. An improved electrolyte according to claim 4 wherein the cosolvent is from about 10 percent to about 20 percent by weight of the electrolyte of sulfuryl chloride.

6. An improved electrolyte according to claim 3 wherein the cosolvent is sulfuryl chloride.

7. A lithium inorganic rechargeable electrochemical cell comprising lithium as the anode, a porous carbon as the cathode, and a solution of a stable, highly conductive liquid electrolyte complex LiAlCl.sub.4 --xSO.sub.2 awhere x is at least 3, and up to about 50 percent by weight of a cosolvent that is: (A) capable of readily dissolving LiAlCl.sub.4 salt and in the process forming a reasonably conducting electrolyte solution; (B) extremely miscible with liquid SO.sub.2; (C) not easily oxidized during cell charging which takes place at about 4.0 volts relative to lithium; and (D) not chemically degraded in the presence of AlCl.sub.3 or Cl.sub.2, both of which are formed during cell charging; as the electrolyte.

8. A lithium inorganic rechargeable electrochemical cell according to claim 7 wherein the liquid complex has the formula LiAlCl--3SO.sub.2.

9. A lithium inorganic rechargeable electrochemical cell according to claim 8 wherein the cosolvent is from about 10 percent to about 20 percent by weight of the electrolyte of sulfuryl chloride.

10. A lithium inorganic rechargeable electrochemical cell according to claim 7 wherein the cosolvent is sulfuryl chloride.

Referenced Cited
U.S. Patent Documents
RE30661 June 30, 1981 Eisenberg
4375502 March 1, 1983 Gabano
4547441 October 15, 1985 Vallin et al.
Foreign Patent Documents
2140146 March 1973 DEX
Patent History
Patent number: H496
Type: Grant
Filed: Aug 10, 1987
Date of Patent: Jul 5, 1988
Assignee: The United States of America as represented by the Secretary of the Army (Washington, DC)
Inventors: Robert J. Mammone (South Plainfield, NJ), Michael Binder (Brooklyn, NY)
Primary Examiner: John F. Terapane
Assistant Examiner: Eric Jorgensen
Attorneys: Sheldon Kanars, Jeremiah G. Murray, Roy E. Gordon
Application Number: 7/84,278
Classifications
Current U.S. Class: Fluid Active Material Or Two-fluid Electrolyte Combination Having Areas Of Nonmixture (429/101); 429/196; 429/197; 252/622
International Classification: H01M 458; H01M 624;