High voltage cathode materials for non-aqueous ammonia based

Abstract

Novel, high voltage cathode active materials for non-aqueous ammonia based primary and reserve batteries are described therein, as well as non-aqueous electrolytes supporting high voltage, and various anodes, separators and cell constructions are disclosed. Said materials provide higher power output at low temperatures over prior art ammonia based batteries.

Claims

1. A non-aqueous reserve battery having ammonia based electrolyte, an alkaline earth metal based anode, a porous electrically non-conductive separator, and a cathode, which cathode's active materials are selected from the group including persulfate salt, molybdenum oxide, and a permanganate salt.

2. A non-aqueous battery as described in claim 1, in which said cathode active material with a binder and conductive carbon powder is coated on a conductive substrate material.

3. A non-aqueous battery as described in claim 1, in which said cathode active material with a fibrous binder and carbon conductive powder included therein is in a pad form, and said pad is in contact with a conductive substrate material.

4. A non-aqueous battery as described in claim 1, in which said cathode active material with a binder and conductive carbon is doped into a porous conductive substrate material.

5. A non-aqueous battery as described in claim 1, in which said cathode active material with a binder and conductive carbon is pressed onto a conductive substrate material.

6. A non-aqueous battery as described in claim 1, which battery has horizontally stacked flat circular cells.

7. A non-aqueous battery as described in claim 1, which battery is in a cylindrical form having said cathode wound.

8. A non-aqueous battery as described in claim 1, in which battery said separator(s)' material is a porous glass non-woven paper.

9. A non-aqueous battery as described in claim 1, in which battery said separator(s)' material is a porous polymer film.

10. A non-aqueous battery as described in claim 1, in which said electrolyte is non-aqueous and contains ammonia NH.sub.3 with at least one salt selected from the group including: LiPF.sub.6, LiBF.sub.4, LiTFSI, LiSCN, NH.sub.4SCN, KSCN, and LiNO.sub.3, dissolved therein.

11. A non-aqueous reserve battery described in claim 1, in which said persulfate salt has a general structure represented by the formula: X.sub.2S.sub.2O.sub.8, wherein X is a cation with an ionic charge 1+ selected from the group including: Na.sup.+, K.sup.+, and NH.sub.4.sup.+ with associated anion of S.sub.2O.sub.8.sup.2.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The nature and characteristic features of the invention will be more readily understood from the following description taken in connection with the accompanying drawing forming part thereof, in which:

(2) FIG. 1 is a sectional side elevational view of cylindrical ammonia based primary or reserve battery, having flat circular electrodes and the electrolyte in the ampoule placed on top of the cells.

(3) FIG. 2 is a sectional side elevational view of cylindrical ammonia based primary or reserve battery, having cylindrically wound electrodes and the electrolyte in the ampoule placed in the center of the battery.

(4) FIG. 3 is a discharge time (first 60 seconds) versus voltage diagram for cells made with standard m-dinitrobenzene type cathodes discharged at 10 mA/cm.sup.2 and 40 mA/cm.sup.2 over discharge temperature range of 45 to +25 C.

(5) FIG. 4 is a discharge time (first 60 seconds) versus voltage diagram for cells made with ammonium persulfate type cathodes discharged at 10 mA/cm.sup.2 and 40 mA/cm.sup.2 over discharge temperature range of 45 to +25 C.

(6) FIG. 5 is a discharge time (first 60 seconds) versus voltage diagram for cells made with molybdenum oxide type cathodes discharged at 10 mA/cm.sup.2 and 40 mA/cm.sup.2 over discharge temperature range of 45 to +25 C.

(7) FIG. 6 is a discharge time (first 60 seconds) versus voltage diagram for cells made with the selected cathodes discharged at 10 mA/cm.sup.2 and 40 mA/cm.sup.2 at 45 C.

(8) It should, of course, be understood that the description and drawings herein are merely illustrative, and that various modifications and changes can be made in the compositions and the structures disclosed without departing from the spirit of the invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

(9) When referring to the preferred embodiments, certain terminology will be utilized for the sake of clarity. Use of such terminology is intended to encompass not only the described embodiments, but also technical equivalents, which operate and function substantially same way to bring about the same results.

(10) Referring now to the FIG. 1, which is one embodiment of the invention, showing ammonium based low temperature primary or reserve battery 1 of the invention, which battery comprises: an alkali metal, such as magnesium foil anode 2; in contact with tabbed metal current collector 3; a cathode 4, such as persulfate based salt like (NH.sub.4).sub.2S.sub.2O.sub.8, or K.sub.2S.sub.2O.sub.8, or Na.sub.2S.sub.2O.sub.8, coated on tabbed stainless steel collector 5 and in contact with the cathode 4; a separator 6, such as 90% porous non-woven glass paper, between said anode 2 and cathode 4; and an electrolyte 7, such as ammonia NH.sub.3 with a salt like KSCN dissolved therein, and the electrolyte is stored in a separate pressure ampoule 8, preferably of a glass material, placed next to the battery components 2 to 6. The cathode 4 with collector 5 is insulated by ring 9.

(11) The battery 1 is sealed dry in moisture-proof metal enclosure 3, with metal plug 10, insulating layer 11, and positive metal pin 12, sealed by a glass seal 13, and is activated by mechanically punching the wall of the ampoule 8. The activation is done only when the battery 1 is needed to power a device.

(12) The battery may be multi-celled with the cells connected in parallel. (not shown). All structures are heat and pressure and corrosion resistant.

(13) Referring now to the FIG. 2, which is another embodiment of the invention, showing ammonium based low temperature primary or reserve battery 1A of the invention, comprising: an alkali metal, such as lithium foil anode 2A, in contact with metal case 3A, as current collector; a cathode 4A such as molybdenum oxide MoO.sub.3, or a permanganate in contact with and coated on stainless steel grid collector 5A, and both are cylindrically wound over pressure ampoule 8A; a separator 6A, such as 90% porous non-woven glass paper between said cathode 4A and anode 2A; and electrolyte 7A, such as ammonia NH.sub.3 with a salt like LiPF.sub.6 dissolved therein and stored in the pressure ampoule 8A, preferably of glass material.

(14) Battery components 2A to 6A are sealed dry in moisture-proof enclosure 9A, comprising the metal case 3A, insulating layer 11A, metal plug 10A with positive metal pin 12A, connected to metal disc 5B, and sealed with a glass seal 13A.

(15) The collector 5A is in contact with the metal disk 5B having the pin 12A attached.

(16) The battery 1A is activated by mechanically punching the wall of the ampoule 8A, only if the battery 1A is needed to power a device. All structures are heat and pressure and corrosion resistant.

(17) The cathodes 4 and 4A described and shown in FIGS. 1 and 2 may be coated on the current collectors 5 and 5A by known various methods via a slurry comprising the active material, plastic binder and conductive carbon powder in a solvent, which solvent evaporates after coating.

(18) Additionally, the described materials of the same named components may be interchangeable between the FIGS. 1 and 2. For example, the cathode 4 material persulfate salt may be used in cathode 4A and replace the molybdenum oxide, and vice versa.

(19) The cathode's persulfate salt of the invention has a general structure represented by the formula: X.sub.2S.sub.2O.sub.8, wherein X is representative of a cation with an ionic charge 1+(such as Na+, K+, NH.sub.4+) with associated anion of S.sub.2O.sub.8.sup.2, which is another embodiment of the invention.

(20) The battery electrolyte of the invention is non-aqueous electrolyte, and comprises at least one non-aqueous solvent selected from the group including: NH.sub.3, methyl format, diethyl ether and dimethoxy ether, with at least one salt selected from the group including: LiPF.sub.6, LiBF.sub.4, LiTFSI, LiSCN, NH.sub.4SCN, KSCN and LiNO.sub.3, dissolved therein, which is another embodiment of the invention.

(21) The above cathode's active material structure may be also made in pad form, using a fibrous binder in combination with a conductive substrate, which is another embodiment of the invention. (Not shown).

(22) Another cathode structure may have also the above active materials doped into porous conductive substrate, which is another embodiment of the invention. (Not shown).

(23) Another cathode structure may have also the above active materials with a binder pressed into a conductive substrate, which is another embodiment of the invention. (Not shown).

(24) Another cathode structure made of the above materials may be also made as a casted free-standing film or plate, in contact with a current collector, which is another embodiment of the invention. (Not shown).

(25) The separators in the described batteries of the invention may be also made from a porous polymer or a solid state ion conductive film.

(26) The anodes in the described batteries of the invention may be also composed from alloyed alkali metal, or alkaline earth metal, or alloyed alkaline earth metal.

(27) The FIGS. 3, 4, 5, and 6 are showing discharge times versus voltage of the cells having different cathodes at various temperatures for a comparison.

(28) The cathodes are based on: ammonium persulfate, molybdenum oxide and m-DNB.

(29) It will thus be seen, that high power density, low temperature ammonium based batteries have been provided, with which the objects of the invention are achieved.