ELECTROCHEMICAL CELL HAVING SOLID IONICALLY CONDUCTING POLYMER MATERIAL
20210226220 · 2021-07-22
Inventors
- Michael A. Zimmerman (No. Andover, MA, US)
- Alexei B. Gavrilov (Woburn, MA, US)
- Ting Liu (Wilmington, MA, US)
Cpc classification
H01M4/62
ELECTRICITY
C08G75/0209
CHEMISTRY; METALLURGY
H01M4/131
ELECTRICITY
Y02E60/10
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
H01M4/58
ELECTRICITY
H01M10/054
ELECTRICITY
International classification
H01M4/62
ELECTRICITY
C08G75/0209
CHEMISTRY; METALLURGY
H01M10/054
ELECTRICITY
H01M4/131
ELECTRICITY
H01M4/36
ELECTRICITY
H01M4/58
ELECTRICITY
Abstract
The invention features an electrochemical cell having an anode and a cathode; wherein at least one of the anode and cathode includes a solid ionically conducting polymer material that can ionically conduct hydroxyl ions.
Claims
1. An electrochemical cell for producing electrical energy via an electrochemical reaction comprising an anode and a cathode; and wherein at least one of the anode and the cathode comprise a solid ionically conducting polymer material; wherein the solid ionically conducting polymer material can ionically conduct hydroxyl ions, whereby the solid ionically conducting polymer material can conduct hydroxyl ions during said electrochemical reaction.
2. The cell of claim 1, wherein the cathode can produce hydroxyl ions during the electrochemical reaction.
3. The cell of claim 1, wherein the solid ionically conducting polymer material has a crystallinity index of at least or greater that about 30%.
4. The cell of claim 1, wherein the solid ionically conducting polymer material comprises at least one hydroxyl ion and has an OH— diffusivity greater that 10.sup.11 at a temperature in the range of 20° C. to 26° C.
5. The cell of claim 1, wherein the cathode comprises an active material that generates a hydroxyl ion during electrochemical reaction.
6. The cell of claim 1, wherein the anode comprises the solid ionically conducting polymer material and further comprises an anode electrochemically active material, wherein the solid ionically conducting polymer material and anode electrochemically active material are mixed, whereby the solid ionically conducting polymer material can ionically conduct hydroxyl ions to the anode electrochemically active material.
7. The cell of claim 1, wherein the cathode comprises the solid ionically conducting polymer material and further comprises a cathode electrochemically active material, wherein the solid ionically conducting polymer material and cathode electrochemically active material are mixed, whereby the solid ionically conducting polymer material can ionically conduct hydroxyl ions to the cathode electrochemically active material.
8. The cell of claim 6, wherein at least a portion of the solid ionically conducting polymer material is in contact with the anode electrochemically active material.
9. The cell of claim 7, wherein at least a portion of the solid ionically conducting polymer material is in contact with the cathode electrochemically active material.
10. The cell of claim 1, wherein the cathode comprises manganese dioxide, and wherein the cell has a specific capacity greater than 308 mAh/g manganese dioxide.
11. The cell of claim 1, wherein the solid ionically conducting polymer material is positioned interposed between the anode and cathode whereby the solid ionically conducting polymer material conducts hydroxyl ions between the anode and cathode.
12. The cell of claim 1, wherein the cathode comprises the solid ionically conducting polymer material, and wherein the amount of the solid ionically conducting polymer material ranges between 1 and 40 weight percent of the cathode.
13. The cell of claim 1, wherein the cell is rechargeable, and wherein the cathode comprises the manganese dioxide, and wherein the amount of manganese dioxide ranges between 20 and 90 weight percent of the cathode.
14. The cell of claim 1, wherein the cell is primary, and wherein the cathode comprises the manganese dioxide, and wherein the amount of manganese dioxide ranges between 50 and 95 weight percent of the cathode.
15. The cell of claim 1, wherein the cell further comprises a liquid electrolyte, wherein the liquid electrolyte comprises hydroxyl ions.
16. The cell of claim 1, wherein both the anode and cathode comprise the solid ionically conducting polymer material, wherein the cell is solid state and does not contain any liquid electrolyte, whereby ionic conductivity of the cell is enabled via the solid ionically conducting polymer material.
17. The cell of claim 1, wherein the anode comprises zinc, and the cathode comprises manganese dioxide, wherein the cell is primary.
18. The cell of claim 1, wherein the anode comprises zinc, and the cathode comprises manganese dioxide, wherein the cell is secondary.
19. The cell of claim 1, wherein the anode comprises aluminum, and the cathode comprises manganese dioxide, wherein the cell is primary.
20. The cell of claim 1, wherein the anode comprises zinc, and the cathode is fluidly connected to oxygen, whereby the oxygen acts as a cathode electrochemically active material.
Description
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE INVENTION
[0092] This application is a continuation-in-part of U.S. application Ser. No. 14/559,430, filed Dec. 3, 2014. U.S. Provisional application Ser. No. 62/342,432, filed May 27, 2016 is hereby incorporated by reference for all purposes.
[0093] The invention comprises a solid, ionically conductive polymer material including a base polymer, a dopant, and at least one compound including an ion source. The polymer material has a capacity for ionic conduction over a wide temperature range including room temperature. It is believed that ion “hopping” occurs from a high density of atomic sites. Thus, the polymer material can function as a means for supplying ions and has significant material strength.
[0094] For the purposes of this application, the term “polymer” refers to a polymer having a crystalline or semi-crystalline structure. In some applications, the solid, ionically conductive polymer material can be molded into shapes which can be folded back on itself allowing for new physical formats depending on the application. The base polymer is selected depending upon the desired properties of the composition in relation to the desired application.
[0095] For purposes of the application, the term “dopant” refers to electron acceptors or oxidants or electron donors. The dopant is selected depending upon the desired properties of the composition in relation to the desired application.
[0096] Similarly, the compound including an ion source is selected depending upon the desired properties of the composition in relation to the desired application.
[0097] I. Li.sup.+ Chemistries
[0098] In one aspect, the invention relates to a solid polymer electrolyte including the solid, ionically conductive polymer material in a lithium ion battery.
[0099] In this aspect, the base polymer is characterized as having a crystallinity value of between 30% and 100%, and preferably between 50% and 100%. The base polymer has a glass transition temperature of above 80° C., and preferably above 120° C., and more preferably above 150° C., and most preferably above 200° C. The base polymer has a melting temperature of above 250° C., and preferably above 280° C., and more preferably above 320° C. The molecular weight of the monomeric unit of the base polymer of the invention is in the 100-200 gm/mol range and can be greater than 200 gm/mol.
[0100] In this aspect, the dopant is an electron acceptor, such as, for non-limiting examples, 2,3-dicyano-5,6-dichlorodicyanoquinone (C.sub.8Cl.sub.2N.sub.2O.sub.2) also known as DDQ, Tetracyanoethylene(C.sub.6N.sub.4) known as TCNE, and sulfur trioxide (SO.sub.3). A preferred dopant is DDQ.
[0101] Typical compounds including an ion source for use in this aspect of the invention include, but are not limited to, Li.sub.2O, LiOH, ZnO, TiO.sub.2, Al.sub.3O.sub.2, and the like. The compounds containing appropriate ions which are in stable form can be modified after creation of the solid, polymer electrolytic film.
[0102] Other additives, such as carbon particles nanotubes and the like, can be added to the solid, polymer electrolyte including the solid, ionically conducting material to further enhance electrical conductivity or current density.
[0103] The novel solid polymer electrolyte enables a lighter weight and much safer architecture by eliminating the need for heavy and bulky metal hermetic packaging and protection circuitry. A novel solid polymer battery including the solid polymer electrolyte can be of smaller size, lighter weight and higher energy density than liquid electrolyte batteries of the same capacity. The novel solid polymer battery also benefits from less complex manufacturing processes, lower cost and reduced safety hazard, as the electrolyte material is non-flammable. The novel solid polymer battery is capable of cell voltages greater than 4.2 volts and is stable against higher and lower voltages. The novel solid polymer electrolyte can be formed into various shapes by extrusion (and co-extrusion), molding and other techniques such that different form factors can be provided for the battery. Particular shapes can be made to fit into differently shaped enclosures in devices or equipment being powered. In addition, the novel solid polymer battery does not require a separator, as with liquid electrolyte batteries, between the electrolyte and electrodes. The weight of the novel solid polymer battery is substantially less than a battery of conventional construction having similar capacity. In some embodiments, the weight of the novel solid polymer battery can be less than half the weight of a conventional battery.
[0104] In another aspect of the invention, a solid polymer electrolyte including the solid, ionically conducting polymer material is in the form of an ionic polymer film. An electrode material is directly applied to each surface of the ionic polymer film and a foil charge collector or terminal is applied over each electrode surface. A light weight protective polymer covering can be applied over the terminals to complete the film based structure. The film based structure forms a thin film battery which is flexible and can be rolled or folded into intended shapes to suit installation requirements.
[0105] In yet another aspect of the invention, a solid polymer electrolyte including the solid, ionically conducting polymer material is in the form of an ionic polymer hollow monofilament. Electrode materials and charge collectors are directly applied (co-extruded) to each surface of the solid, ionically conductive polymer material and a terminal is applied at each electrode surface. A light weight protective polymer covering can be applied over the terminals to complete the structure. The structure forms a battery which is thin, flexible, and can be coiled into intended shapes to suit installation requirements, including very small applications.
[0106] In still another aspect of the invention, a solid polymer electrolyte including the solid, ionically conducting polymer material has a desired molded shape. Anode and cathode electrode materials can be disposed on respective opposite surfaces of the solid polymer electrolyte to form a cell unit. Electrical terminals can be provided on the anode and cathode electrodes of each cell unit for interconnection with other cell units to provide a multi cell battery or for connection to a utilization device.
[0107] In aspects of the invention relating to batteries, the electrode materials (cathode and anode) can be combined with a form of the novel solid, ionically conductive polymer material to further facilitate ionic movement between the two electrodes. This is analogous to a conventional liquid electrolyte soaked into each electrode material in a convention lithium-ion battery.
[0108] Films of solid, ionically conducting polymer materials of the present invention have been extruded in thickness ranging upwards from 0.0003 inches. The ionic surface conductivity of the films has been measured using a standard test of AC-Electrochemical Impedance Spectroscopy (EIS) known to those of ordinary skill in the art. Samples of the solid, ionically conducting polymer material film were sandwiched between stainless steel blocking electrodes and placed in a test fixture. AC-impedance was recorded in the range from 800 KHz to 100 Hz using a Biologic VSP test system to determine the electrolyte conductivity. The results of the surface conductivity measurements are illustrated in
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[0110] The solid, ionically conductive polymer material of the invention offers three key advantages in its polymer performance characteristics: (1) It has an expansive temperature range. In lab-scale testing, the crystalline polymer has shown high ionic conductivity both at room temperature and over a wide temperature range. (2) It is non-flammable. The polymer self-extinguishes, passing the UL-V0 Flammability Test. The ability to operate at room temperature and the non-flammable characteristics demonstrate a transformative safety improvement that eliminates expensive thermal management systems. (3) It offers low-cost bulk manufacturing. Rather than spraying the polymer onto electrodes, the polymer material can be extruded into a thin film via a roll-to-roll process, an industry standard for plastics manufacturing. After the film is extruded, it can be coated with the electrode and charge collector materials to build a battery “from the inside out.” This enables thin, flexible form factors without the need for hermetic packaging, resulting in easy integration into vehicle and storage applications at low cost.
[0111] It is believed that the solid, ionically conducting polymer material of the present invention creates a new ionic conduction mechanism that provides a higher density of sites for ionic transport and allows the conducting material to maintain higher voltages without risk of thermal runaway or damage to ion transport sites from, for example, lithiation. This characteristic enables the solid, ionically conducting polymer material to be durable for anode materials and higher voltage cathode thin-film applications, resulting in higher energy densities for batteries which may be used in vehicle and stationary storage applications. The ability to maintain high voltages within a solid, ionically conductive polymer material which is mechanically robust, chemical and moisture resistant, and nonflammable not only at room temperature, but over a wide range of temperatures, allows integration with high performance electrodes without costly thermal and safety mechanisms employed by the industry today.
[0112] Batteries employing the solid polymer electrolyte including the solid, ionically conductive polymer material of the invention are characterized by an energy density improvement over current commercially available electrolytes, as well as a performance range of −40° C. to 150° C. with minimal conductivity degradation. The solid polymer electrolyte can be extruded by a process that produces polymers of a thickness of 6 microns, which enables thin-film formats under commercial manufacturing conditions at batch scale. Further, such extrusion processes enables high throughput, low-cost manufacturing lines for the production of the solid polymer electrolyte, and the processes can be integrated into a variety of product lines, including lithium and zinc battery manufacture. Battery costs can be reduced by up to 50%.
[0113] In addition, the solid, ionically conductive polymer material is not limited to use in batteries, but can be used in any device or composition that includes an electrolyte material. For example, the novel solid, ionically conductive polymer material can be used in electrochromic devices, electrochemical sensors, supercapacitors and fuel cells.
[0114] Flammability of the solid polymer electrolyte including the solid, ionically conductive polymer material of the invention was tested using a UL94 flame test. For a polymer to be rated UL94-VO, it must “self-extinguish” within 10 seconds and ‘not drip”. The solid polymer electrolyte was tested for this property and it was determined that it self-extinguished with 2 seconds, did not drip, and therefore easily passed the VO rating.
[0115] In addition to the properties of ionic conductivity, flame resistance, high temperature behavior, and good mechanical properties, it is preferable that the solid polymer electrolyte including the solid, ionically conductive polymer material of the invention is electrochemically stable at low and high potentials. The traditional test for the electrochemical stability is cyclic voltammetry, when working electrode potential is ramped linearly versus time. In this test, the polymer is sandwiched between a lithium metal anode and blocking stainless steel electrode. A voltage is applied and it is swept positively to a high value (greater than 4 volts vs. Li) for stability towards oxidation and negatively to a low value (0V vs. Li or less) for stability towards reduction. The current output is measured to determine if any significant reaction occurs at the electrode interface. High current output at high positive potential would signify oxidation reaction taking place, suggesting instability with cathode materials operating at these or more positive potentials (such as many metal oxides). High current output at low potentials would signify that a reduction reaction takes place, suggesting instability with anodes operating at these or more negative potentials (such as metal Li or lithiated carbon).
[0116] The solid polymer electrolyte including the solid, ionically conductive polymer material of the invention is able to achieve the following properties: A) high ionic conductivity at room temperature and over a wide temperature range (at least −10° C. to +60° C.); B) non-flammability; C) extrudability into thin films allowing for reel-reel processing and a new way of manufacturing; D) compatibility with Lithium metal and other active materials. Accordingly, this invention allows for the fabrication of a true solid state battery. The invention allows for a new generation of batteries having the following properties:
[0117] No safety issues;
[0118] New form factors;
[0119] Large increases in energy density; and
[0120] large improvements in cost of energy storage.
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[0122] In other aspects, the invention provides methods for making Li batteries including the solid, ionically conducting polymer material of the invention.
[0123] In yet another aspect, the invention provides a method of manufacturing of an ionic polymer film including the solid, ionically conductive polymer material of the invention which involves heating the film to a temperature around 295° C., and then casting the film onto a chill roll which solidifies the plastic. This extrusion method is shown in
[0124] II. OH.sup.− Chemistries
[0125] The invention also relates to a solid, ionically conducting polymer material which is engineered to transmit OH.sup.−ions, thereby making it applicable for alkaline batteries. For the purposes of present invention, the term “alkaline battery or alkaline batteries” refers to a battery or batteries utilizing alkaline (OH.sup.− containing) electrolyte. Such battery chemistries include, but not limited to, Zn/MnO.sub.2, Zn/Ni, Fe/Ni, Zn/air, Al/air, Ni/metal hydride, silver oxide and others. Zn/MnO.sub.2 chemistry is probably the most widely used and is the main choice for consumer batteries. Although many of the embodiments described herein are related to Zn/MnO.sub.2 chemistry, a person of ordinary skill in the art would understand that the same principles are applicable broadly to other alkaline systems.
[0126] Alkaline batteries rely on the transport of OH.sup.− ions to conduct electricity. In most cases, the OH.sup.− ion is also a participant in the electrochemical process. For instance, during the discharge of a Zn/MnO.sub.2 battery, the zinc anode releases 2 electrons and consumes OH.sup.− ions:
[0127] (1) Zn+4OH.sup.−.fwdarw.Zn(OH).sub.4.sup.2−+2e.sup.−
[0128] (2) Zn+2OH.sup.−.fwdarw.Zn(OH).sub.2+2e.sup.−.fwdarw.ZnO+H.sub.2O
[0129] (3) Zn(OH).sub.2.fwdarw.ZnO+H.sub.2O
[0130] During early stages of discharge of the battery, reaction (1) produces soluble zincate ions, which can be found in the separator and cathode [Linden's Handbook of Batteries, Fourth Edition]. At a certain point, the electrolyte will become saturated with zincates and the reaction product will change to insoluble Zn(OH).sub.2 (2). Eventually, the anode will become depleted of water and the zinc hydroxide dehydrates by equation (3). In rechargeable batteries, the reactions are reversed during charging of the battery. Formation of soluble zincate ions during the initial step of the Zn discharge may hinder recharging.
[0131] The cathode reaction involves a reduction of Mn.sup.4+ to Mn.sup.3+ by a proton insertion mechanism, resulting in the release of OH.sup.− ions (4). The theoretical specific MnO.sub.2 capacity for such 1-electron reduction is 308 mAh/g. Slow rate discharge to lower voltages may lead to further discharge of MnOOH as depicted by equation (5), which results in 410 mAh/g total specific capacity (1.33 e). In most prior art applications, the MnO.sub.2 discharge is limited to the 1-electron process. Utilization of the active is further adversely affected by the formation of soluble low-valent Mn species.
[0132] (4) MnO.sub.2+e.sup.−+H.sub.2O.fwdarw.MnOOH+OH.sup.−
[0133] (5) 3MnOOH+e.sup.−.fwdarw.Mn.sub.3O.sub.4+H.sub.2O+OH.sup.−
[0134] (6) MnO.sub.2+2 e.sup.−+2H.sub.2O.fwdarw.Mn(OH).sub.2+2OH.sup.−
[0135] Although MnO.sub.2 can theoretically experience a 2-electron reduction according to equation (6) with a theoretical specific capacity of 616 mAh/g, in practice with prior art batteries, it is not demonstrated. The crystalline structure rearrangement with the formation of inactive phases, such as Hausmanite Mn.sub.3O.sub.4, and out-diffusion of soluble products are among the factors limiting cathode capacity.
[0136] U.S. Pat. No. 7,972,726 describes the use of pentavalent bismuth metal oxides to enhance the overall discharge performance of alkaline cells. Cathode containing 10% AgBiO.sub.3 and 90% electrolytic MnO.sub.2 was shown to deliver 351 mAh/g to 0.8V cut-off at 10 mA/g discharge rate, compared to 287 mAh/g for 100% MnO.sub.2 and 200 mAh/g for 100% AgBiO.sub.3. The 351 mAh/g specific capacity corresponds to a 1.13 electron discharge of MnO.sub.2 and represents the highest specific capacity delivered at practically useful discharge rates and voltage ranges.
[0137] In principle, reaction (4) can be reversible, opening the possibility for a rechargeable Zn/MnO.sub.2 battery. In practice, the crystalline structure collapse and formation of soluble products allow only for shallow cycling.
[0138] Bismuth- or lead-modified MnO.sub.2 materials, disclosed in U.S. Pat. Nos. 5,156,934 and 5,660,953, were claimed to be capable of delivering about 80% of the theoretical 2-electron discharge capacity for many cycles. It was theorized in literature [Y. F. Yao, N. Gupta, H. S. Wroblowa, J. Electroanal. Chem., 223 (1987), 107; H. S. Wroblowa, N. Gupta, J. Electroanal. Chem., 238 (1987) 93; D. Y. Qu, L. Bai, C. F. Castledine, B. E. Conway, J. Electroanal. Chem., 365 (1994), 247] that bismuth or lead cations can stabilize crystalline structure of MnO.sub.2 during discharge and/or allow for reaction (6) to proceed via heterogeneous mechanism involving soluble Mn.sup.2+ species. Containing said Mn.sup.2+ species seems to be the key for attaining high MnO.sub.2 utilization and reversibility. In high carbon content (30-70%) cathodes per U.S. Pat. Nos. 5,156,934 and 5,660,953, the resulting highly porous structure was able to absorb soluble species. However, there is no data to suggest that a complete cell utilizing these cathodes was built or that this worked using a Zn anode.
[0139] Thus, a polymer electrolyte which prevents dissolution and transport of low-valent manganese species and zincate ions, would be highly beneficial to improve MnO.sub.2 utilization and achieve rechargeability of Zn/MnO.sub.2 cells.
[0140] In addition to proton insertion, MnO.sub.2 can undergo reduction by Li intercalation. It has been suggested [M. Minakshi, P. Singh, J. Solid State Electrochem, 16 (2012), 1487] that the Li insertion can stabilize MnO.sub.2 structure upon reduction and enable rechargeability.
[0141] The solid, ionically conductive polymer material of the invention, engineered to conduct Li+ and OH.sup.− ions, opens the possibility to tune MnO.sub.2 discharge mechanism in favor of either proton or lithium insertion, which can serve as an additional tool to improve cycle life.
[0142] Accordingly, in one aspect, the invention provides a polymer material including a base polymer, a dopant and at least one compound including an ion source, wherein the polymer material is a solid, ionically conducting polymer material having mobility for OH.sup.− ions. For the purposes of the application, the term “mobility for OH.sup.− ions” refers to a diffusivity of greater than 10.sup.−11 cm.sup.2/sec or a conductivity of 10.sup.−4 S/cm, at a room temperature of between 20° C. and 26° C. The solid, ionically conducting polymer material is suitable for use in alkaline cells.
[0143] In different aspects, the invention provides an electrolyte including the solid, ionically conductive polymer material having mobility for OH.sup.− ions, wherein the electrolyte is a solid polymer electrolyte for use in alkaline batteries; an electrode or electrodes including said solid polymer electrolyte; and/or a cell or cells including said electrode or electrodes.
[0144] In another aspect, the invention provides electrodes, cathodes and anodes including a solid polymer electrolyte for use in alkaline cells, wherein the solid polymer electrolyte includes a solid, ionically conducting polymer material having mobility for OH.sup.− ions. In yet another aspect, the invention provides an electrolyte interposed between cathode and anode, where at least one of the electrolyte, cathode and anode includes the solid, ionically conductive polymer material having mobility for OH.sup.− ions. In another aspect, the invention provides an alkaline battery including a cathode layer, an electrolyte layer and an anode layer, wherein at least one of the layers includes a solid, ionically conducting polymer material having mobility for OH.sup.− ions. The latter aspect is exemplarily illustrated in
[0145] The base polymer of the solid, ionically conducting polymer material having mobility for OH.sup.− ions is a crystalline or semi-crystalline polymer, which typically has a crystallinity value between 30% and 100%, and preferably between 50% and 100%. The base polymer of this aspect of the invention has a glass transition temperature above 80° C., and preferably above 120° C., and more preferably above 150° C., and most preferably above 200° C. The base polymer has a melting temperature of above 250° C., and preferably above 280° C., and more preferably above 280° C., and most preferably above 300° C.
[0146] The dopant of the solid, ionically conducting polymer material having mobility for OH.sup.− ions is an electron acceptor or oxidant. Typical dopants for use in this aspect of the invention are DDQ, TCNE, SO.sub.3, etc.
[0147] The compound including an ion source of the solid, ionically conducting polymer material having mobility for OH.sup.− ions includes a salt, a hydroxide, an oxide or other material containing hydroxyl ions or convertible to such materials, including, but not limited to, LiOH, NaOH, KOH, Li.sub.2O, LiNO.sub.3, etc.
[0148] The solid, ionically conductive material having mobility for OH.sup.− ions is characterized by a minimum conductivity of 1×10.sup.4 S/cm at room temperature and/or a diffusivity of OH.sup.− ions at room temperature of greater than 10.sup.−11 cm.sup.2/sec.
[0149] The cathode of the present invention relating to OH.sup.− chemistries includes MnO.sub.2, NiOOH, AgO, air (O.sub.2) or similar active materials. MnO.sub.2 is a preferred material and can be in the form of β-MnO.sub.2 (pyrolusite), ramsdellite, γ-MnO.sub.2, ε-MnO.sub.2, λ-MnO.sub.2 and other MnO.sub.2 phases or mixtures thereof, including, but not limited to, EMD and CMD.
[0150] The cathode of the present invention relating to OH.sup.− chemistries is prepared by mixing cathode active material with the components of the solid, ionically conducting polymer material of the invention including the base polymer, the dopant and a compound including a source of ions prior to formation of the solid, ionically conducting polymer material to form a mixture. Alternatively, the cathode active material is mixed with the solid, ionically conducting polymer material already formed.
[0151] The mixture is molded and/or extruded at temperatures between 180° C. and 350° C., and preferably between 190° C. and 350° C., and more preferably between 280° C. and 350° C., and most preferably between 290° C. and 325° C. The cathode active material can include various forms such as, for non-limiting examples, a powder form, a particle form, a fiber form, and/or a sheet form. The cathode of the present invention includes active material in an amount of between 10 w. % and 90 wt. %, and preferably in an amount of between 25 wt. % and 90 wt. %, and more preferably in an amount of between 50 wt. % and 90 wt. %, relative to the total cathode weight. The cathode can further include an electrically conductive additive, such as a carbon black component, a natural graphite component, a synthetic graphite component, a graphene component, a conductive polymer component, a metal particles component, and/or other like electrically conductive additives. The cathode can include the electrically conductive additives in an amount of between 0 wt. % and 25 wt. %, and preferably in an amount of between 10 wt. % and 15 wt. % relative to the total cathode weight. The cathode of the present invention relating to OH.sup.− chemistries can further include one or more functional additives for improving performance. The cathode active material can be encapsulated by the solid, ionically conducting polymer material of the invention.
[0152] The anode of the present invention relating to OH.sup.− chemistries can include an active material of Zn, in the form of zinc powder, zinc flakes and other shapes, zinc sheets, and other shapes. All such forms of zinc can be alloyed to minimize zinc corrosion.
[0153] The anode of the present invention relating to OH.sup.− chemistries is prepared by mixing anode active material with the components of the solid, ionically conducting polymer material of the invention including the base polymer, the dopant and a compound including a source of ions prior to formation of the solid, ionically conducting polymer material to form a mixture. Alternatively, the anode active material is mixed with the solid, ionically conducting polymer material already formed. The mixture is molded and/or extruded at temperatures between 180° C. and 350° C. The anode of the present invention includes active material in an amount of between 10 w. % and 90 wt. %, and preferably in an amount of between 25 wt. % and 90 wt. %, and more preferably in an amount of between 50 wt. % and 90 wt. %, relative to the total anode weight. The anode can further include an electrically conductive additive, such as a carbon black component, a natural graphite component, a synthetic graphite component, a graphene component, a conductive polymer component, a metal particles component, and/or other like electrically conductive additives. The anode can include the electrically conductive additives in an amount of between 0 wt. % and 25 wt. %, and preferably in an amount of between 10 wt. % and 15 wt. % relative to the total anode weight. The anode of the present invention relating to OH.sup.− chemistries can further include one or more functional additives for improving performance. The anode active material can be encapsulated by the solid, ionically conducting polymer material of the invention.
[0154] In another aspect, the invention provides a Zn/MnO.sub.2 battery including an electrolyte interposed between a MnO.sub.2 cathode and a Zn anode. The electrolyte in this aspect can include the solid, ionically conducting material of the invention having mobility for OH.sup.− ions or can include a traditional separator filled with liquid electrolyte. The cathode can include the solid, ionically conducting material having mobility for OH.sup.− ions of the invention or can include a commercial MnO.sub.2 cathode. The anode in this aspect can include the solid, ionically conducting material of the invention having mobility for OH.sup.− ions or can include a Zn foil, a Zn mesh or a Zn anode manufactured by other methods. In the Zn/MnO.sub.2 battery of the invention, the solid, electronically conducting polymer material of the invention having mobility for OH.sup.− ions is included in at least one of the cathode, the anode and the electrolyte.
[0155] III. Polymer-MnO.sub.2 Composite Cathode
[0156] The invention further relates to a polymer-MnO.sub.2 composite cathode with a high specific capacity and a primary alkaline cell including the cathode. More specifically, the invention further relates to a polymer-MnO.sub.2 composite cathode with a specific capacity close to theoretical 2-electron discharge and a primary alkaline cell comprising the cathode. The alkaline cell can be discharged at current densities comparable to that of commercial alkaline cells, while useful capacity is delivered to typical 0.8V voltage cut-off.
[0157] In different aspects, the invention features a cathode that is made of a MnO.sub.2 active material including a plurality of active MnO.sub.2 particles intermixed with a solid, ionically conductive polymer material including a base polymer, a dopant, and a compound including an ion source and a method of making said cathode. In other aspects, the invention features an electrochemical cell including a cathode, an anode and a separator disposed between the cathode and the anode, and a method for making said cathode. The cathode is made of a MnO.sub.2 active material including a plurality of active MnO.sub.2 particles intermixed with a solid, ionically conductive polymer material including a base polymer, a dopant, and a compound including an ion source. The cathode and the electrochemical cell of the present invention are characterized by flat discharge curves.
[0158] In the aspects of the invention related to the polymer-MnO.sub.2 composite cathode, the base polymer can be a semicrystalline polymer. The base polymer can be selected from a group which consists of a conjugated polymer or a polymer which can easily be oxidized. Non-limiting examples of the base polymers used in this aspect of the invention include PPS, PPO, PEEK, PPA, etc .
[0159] In the aspects of the invention related to the polymer-MnO.sub.2 composite cathode, the dopant is an electron acceptor or oxidant. Non-limiting examples of dopants are DDQ, tetracyanoethylene also known as TCNE, SO.sub.3, ozone, transition metal oxides, including MnO.sub.2, or any suitable electron acceptor, etc.
[0160] In the aspects of the invention related to the polymer-MnO.sub.2 composite cathode, the compound including the ion source is a salt, a hydroxide, an oxide or other material containing hydroxyl ions or convertible to such materials, including, but not limited to, LiOH, NaOH, KOH, Li.sub.2O, LiNO.sub.3, etc.
[0161] In the aspects of the invention related to the polymer-MnO.sub.2 composite cathode, the MnO.sub.2 active material can be in the form of β-MnO.sub.2 (pyrolusite), ramsdellite, γ-MnO.sub.2, ε-MnO.sub.2, λ-MnO.sub.2 and other MnO.sub.2 phases or mixtures thereof, including, but not limited to, EMD and CMD.
[0162] The cathode related to the polymer-MnO.sub.2 composite cathode can be made prepared by mixing a plurality of active MnO.sub.2 particles and a solid, ionically conducting polymer material including a base polymer, a dopant and a compound including an ion source, and heating the mixture to a specific temperature for a specific time. Said heating can optionally be performed while applying pressure.
[0163] In one embodiment, the polymer-MnO.sub.2 composite cathode of the present invention can be prepared by compression molding at a temperature of between The mixture is molded and/or extruded at temperatures between 180 and 350° C., and preferably between 190° C. and 350° C., and more preferably between 280° C. and 350° C., and most preferably between 290° C. and 325° C. In other embodiments, the heating is optionally conducted at a pressure of between 150-2000 PSI, and preferably between 150-1000 PSI and more preferably between 150-500 PSI, and most preferably between 150-250 PSI. The MnO.sub.2 active material can be in an amount of between 5 wt. % and 95 wt. % and preferably between 50 wt. % and 90 wt. % relative to the total weight of the composite cathode. The composite cathode can include a filler in the amount of between 5 wt. % and 50 wt. %, and preferably between 10 wt. % and 50 wt. %, and more preferably between 20 wt. % and 40 wt. %, and most preferably between 25 wt. % and 35 wt. % relative to the total weight of the composite cathode. The dopant can be added in the amount corresponding to a base polymer/dopant molar ratio between 2 and 10. and preferably between 2 and 8, and more preferably between 2 and 6, and most preferably between 3 and 5. The composite cathode can include an electrically conductive additive, such as a carbon black component, a natural and/or a synthetic graphite component, a graphene component, an electrically conductive polymer component, a metal particles component, and another component, wherein the electrically conductive component is in the amount of between 5 wt. % and 25 wt. %, and preferably between 15 wt. % and 25 wt. %, and more preferably between 18 wt. % and 22 wt. % relative to the total weight of the composite cathode. The MnO.sub.2 active material in the composite cathode can be encapsulated by solid, ionically conducting polymer material of the invention.
[0164] In a preferred embodiment, the invention features an alkaline battery including said polymer-MnO.sub.2 composite cathode and a Zn anode. The Zn anode can be in the form of slurry including Zn or Zn alloy powder, KOH, gelling agent and optionally other additives. The Zn anode can further include an electrically conductive additive, similar to the composite cathode.
[0165] The anode related to the polymer-MnO.sub.2 composite of the invention can include Zn, Al, Fe, metal hydride alloys or similar materials. Zn and Al are preferred materials and can be in the form of pure metals or specially designed alloys. The separator can be a traditional non-woven separator used in alkaline batteries. Electrolyte is KOH, NaOH, LiOH etc. solution in water. Alkali concentration can be between 4 and 9 M. The Electrolyte can further contain an electronically conductive additive and/or a functional additive.
[0166] IV. Polymer-Sulfur Cathode
[0167] In addition, the invention relates to a composite polymer-sulfur cathode. The composite polymer-sulfur cathode includes a sulfur component and a solid, ionically conducting polymer material including a base polymer, a dopant and a compound including a source of ions. The composite polymer-sulfur cathode is characterized as having a high specific capacity and a high capacity retention when employed in a secondary lithium or Li-ion sulfur cell. The composite cathode is characterized as having a specific capacity of greater than 200 milliamp-hr/gm, and preferably greater than 500 milliamp-hr/gm, and more preferably greater than 750 milliamp-hr/gm, and most preferably greater than 1000 milliamp-hr/gm. The composite cathode is characterized as having a retention of least 50% and preferably at least 80% for over 500 recharge/discharge cycles. The composite polymer-sulfur cathode of the present invention has direct application to low-cost, large-scale manufacturing enabled by the unique polymer used in this composite electrode. The composite polymer-sulfur cathode of the invention can provide high performance while simultaneously meeting the requirements for producing low-cost batteries.
[0168] Notably, sulfur cathodes reduce during discharge to create sequentially lower order polysulfides through the sequence illustrated in the following equation:
S.sub.8.fwdarw.Li.sub.2S.sub.8.fwdarw.Li.sub.2S.sub.4.fwdarw.Li.sub.2S.sub.2.fwdarw.Li.sub.2S
[0169] The intermediate polysulfides between Li.sub.2S.sub.8 and Li.sub.2S.sub.4 are soluble in liquid electrolytes. Thus, dissolved polysulfide particles are able to migrate (or “shuttle”) across porous separators and react directly with the anode and cathode during cycling. The polysulfide shuttle produces parasitic reactions with the lithium anode and re-oxidation at the cathode, all causing capacity loss. Furthermore, aspects of this shuttle reaction are irreversible, leading to self-discharge and low cycle life that has, until now, plagued lithium sulfur batteries.
[0170] The present invention demonstrates a composite polymer-sulfur cathode including a sulfur component and a solid, ionically conducting polymer material. This cathode can be extruded into a flexible, thin film via a roll-to-roll process. Such thin films enable thin, flexible form factors which can be incorporated into novel flexible battery designs. As shown in the examples which follow, this composite polymer-sulfur cathode can include an electrically conductive addition such as, for example, an inexpensive carbon black component, such as Timcal C45, which is already in use for many commercial battery products. In addition to the exemplary carbon black component, the composite polymer-sulfur cathode can include other electrically conductive additives such as, for non-limiting examples, a carbon component including but not limited to carbon fibers, a graphene component, a graphite component, metallic particles or other metal additives, and an electrically conductive polymer.
[0171] The engineering properties of the composite polymer-sulfur cathode allow the extrusion of the cathode into a wide range of possible thicknesses, which in turn provides important advantages in terms of flexibility in design in large-scale cathode manufacturing. The composite polymer-sulfur cathode can be extruded as thin as 5 microns and up to thicknesses greater than several 100 microns.
[0172] A comparison of the process steps necessary for producing standard lithium ion cathodes with those necessary to produce the inventive composite polymer-sulfur cathode is instructive relative to the inherent lower cost of the composite polymer-sulfur cathode manufacturing.
[0173] In addition to extrusion, the composite polymer-sulfur cathode can be formed by injection molding, compression molding, or any other process involving heat, or other techniques known by those skilled in the art for engineering plastics.
[0174] The composite polymer-sulfur cathode includes a sulfur component and a solid, ionically conducting polymer material including a base polymer, a dopant and a compound including a source of ions, as discussed above.
[0175] The base polymer includes liquid crystal polymers and polyphenylene sulfide (PPS), or any semicrystalline polymer with a crystallinity index greater than 30%, or other typical oxygen acceptors.
[0176] The dopant includes electron acceptors which activate the ionic conduction mechanism. These electron acceptors can be pre-mixed along with the other ingredients, or supplied in the vapor phase as a post doping process. Typical electron acceptor dopants suitable for use include, but are not limited to: 2,3-dichloro-5,6-dicyano -1,4-benzoquinone (DDQ) (C.sub.8Cl.sub.2N.sub.2O.sub.2), Tetracyanoethylene (TCNE) (C.sub.6N4), and sulfur trioxide (SO.sub.3).
[0177] The compounds including an ion source include, but are not limited to Li.sub.2O and LiOH. Use of composite polymer-sulfur cathodes in Li/Sulfur test cells has shown that the composite polymer-stable cathodes are stable to lithium, sulfur, and organic electrolytes typically used in lithium/sulfur batteries.
[0178] The base polymer is a nonflammable polymer which has been shown to self-extinguish and pass the UL-VO Flammability test. The non-flammability of the base polymer is a safety benefit to batteries employing the composite polymer-sulfur cathode. The incorporation of the non-flammable composite polymer-sulfur cathode into a cell with non-flammable electrolyte will further improve the safety of the battery, an important attribute for high energy density batteries.
[0179] The sulfur component can include non-reduced and/or reduced forms of sulfur including elemental sulfur. In particular, the composite polymer-sulfur cathode includes a sulfur component including the fully lithiated form of sulfur (Li.sub.2S), wherein the Li.sub.2S, is a solid . The composite polymer-sulfur cathode can also include a carbon component. The advantage to using the fully lithiated form of sulfur is that it provides a lithium source for a sulfur battery with a Li Ion anode, which, unlike metal Li, must by lithiated during initial charge. Combination of a sulfur cathode with a Li-ion anode provides benefit in preventing the formation of lithium dendrites which can be formed after cycling lithium anodes. Dendrites are caused by a non-uniform plating of lithium onto the lithium metal anode during charging. These dendrites can grow through separator materials and cause internal short circuits between cathode and anode, often leading to high temperatures and compromised safety of the battery. Materials that reversibly incorporate lithium, either through intercalation or alloying, lessen the chance for dendrite formation and have been proposed for use in high safety lithium/sulfur cells. The composite polymer-sulfur cathode can be used with an anode material such as, for example, a carbon-based (petroleum coke, amorphous carbon, graphite, carbon nano tubes, graphene, etc.) material, Sn, SnO, SnO.sub.2 and Sn-based composite oxides, including composites with transition metals, such as Co, Cu, Fe, Mn, Ni, etc. Furthermore, silicon has shown promise as a lithium ion anode material, in the elemental form, or as an oxide or composite material, as described for tin. Other lithium alloying materials (for example, Ge, Pb, B, etc.) could also be used for this purpose. Oxides of iron, such as Fe2O.sub.3 or Fe3O.sub.4 and various vanadium oxide materials have also been shown to reversibly incorporate lithium as a Li-ion anode material. Anode materials may be considered in different forms, including amorphous and crystalline, and nano-sized particles as well as nano-tubes.
[0180] The composite polymer-sulfur cathode can be combined with a standard liquid electrolyte, a standard nonwoven separator, and/or an electrolyte including a solid, ionically conducting polymer material with no liquid electrolyte. An example of a standard organic electrolyte solution includes a lithium salt, such as lithium bis(trifluoromethane sulfonyl)imide (LiTFSI), dissolved in a mixture of 1,3-dioxolane (DOL) and 1,2-dimethoxyethane (DME). Additives, such as LiNO.sub.3, can be added to the electrolyte to improve cell performance. Other lithium salts can be utilized in organic liquid electrolyte, including: LiPF.sub.6, LiBF.sub.4, LiAsF.sub.6, lithium triflate, among others. Additionally, other organic solvents can be used, such as propylene carbonate (PC), ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), fluoroethylene carbonate (FEC), as a few examples, either alone or as mixtures together or with DOL and DME. Examples of standard nonwoven separators include polypropylene (PP), polyethylene (PE), and combinations of PP/PE films. Other separator materials include polyimide, PTFE, ceramic coated films and glass-mat separators. All of the above materials can be used with the composite polymer-sulfur cathode. Further, the composite polymer-sulfur cathode could also be utilized in a gel-polymer system, where for example, a PVDF-based polymer is swelled with an organic electrolyte.
[0181] It is believed that the ability of the composite polymer-sulfur cathode to provide lithium ionic conductivity improves the performance of the cell by limiting the polysulfide shuttle mechanism, while simultaneously providing a sulfur cathode with high voltage. Furthermore, this unique engineering composite polymer-sulfur cathode allows for the large scale, low cost manufacturing necessary for commercial viability of the cathode.
[0182] Thus, the unique composite polymer-sulfur cathode has numerous potential benefits to batteries, including: [0183] Improved safety, under normal and abuse conditions [0184] Enabling new battery form factors [0185] Large increase in energy density over existing Li-ion cells [0186] Prevention of the polysulfide shuttle mechanism, leading to greater charge/discharge reversibility [0187] Large decrease in manufacturing cost (raw materials, process and capital equipment) leading to improvement in the cost of energy storage
[0188] V. Alkaline Cells
[0189] In an aspect, a rechargeable Zn/MnO.sub.2 battery for low rate applications that can match or surpass lithium-ion performance while delivering improved safety, robustness, and lower cost is described.
[0190] It has been observed that certain cathode formulations comprising the solid ionically conductive polymer material can demonstrate much higher active material utilization at low rates, while displaying steeper decline upon the discharge rate increase. This is illustrated by
[0191] Zinc and polymer content in the anode were optimized, specifically: zinc type and particle size, composition and process to make solid polymer electrolyte for the desired anode performance, and ZnO and other functional additives were introduced to reduce zinc passivation. The combined effect of higher zinc surface area and improved stability result in improved performance and prolonged cycle life. Embedding Zn particles into the polymer matrix prevents shape change, agglomeration and dendrite growth.
[0192] The cathode, optimized to increase capacity above 300 mAh/g shows specific MnO.sub.2 capacity improvement that has a drastic impact on the cell energy density of pouch cells as illustrated by
[0193] In an aspect, a rechargeable Zn/MnO.sub.2 batteries incorporating the solid ionically conducting polymer material for high rate and high temperature applications is described.
[0194] Good active material utilization and high-rate performance of coin cells is preserved upon increasing manganese dioxide content 80% by weight or above. Since high active material loadings are essential to achieving high energy density, the significance of this finding is hard to overstate. The improvements in discharge capacity resulting from optimization of the manganese dioxide content are shown in
[0195] Cathode densities of 2.5-3.0 g/cc are sufficient to attain high energy density. High-rate performance under these conditions can be limited by a zinc foil anode, rather than the cathode. A zinc anode with increased surface area to replace zinc foil shows improved performance.
[0196] To increase the anode rate capability and improve cycle life, the anode is improved by optimizing zinc and anode polymer content, optimizing zinc type and particle size, and introducing ZnO and other functional additives (such as manganese salts) to reduce zinc passivation and corrosion. The combined effect of higher zinc surface area and improved stability results in improved performance at high discharge rates and prolonged cycle life. Further it was found that embedding zinc particles into the polymer matrix prevents shape change, agglomeration and dendrite growth.
[0197] Cells matching or surpassing current state-of-the-art Li-ion systems in energy/power density, demonstrating >85% capacity retention at 15 C discharge; safe to operate at 80-100oC; and having a minimum life of 500 cycles were produced. These packs of Zn/MnO2 cells will not require complicated battery management and charge control circuitry, and additional energy density benefits and cost reduction is expected on the pack level.
Example 1
[0198] Solid polymer electrolyte was made by mixing PPS base polymer and ion source compound LiOH monohydrate in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS. The mixture was heat treated at 325/250° C. for 30 minutes under moderate pressure (500-1000 PSI). After cooling, the resulting material was grinded and placed into NMR fixture.
[0199] Self-diffusion coefficients were determined by using pulsed field gradient solid state NMR technique. The results shown in
Example 2
[0200] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67 wt. % to 33 wt. %, respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 50% β-MnO2 from Alfa Aesar, 5% of Bi2O3 and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0201] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250° C. for 30 minutes under moderate pressure (500-1000 PSI), yielding cathode disc 1 inch in diameter and about 0.15 mm thick. The resulting disc was punched to 19 mm diameter and used as a cathode to assemble test cells, containing commercial non-woven separator (NKK) and Zn foils anode. 6M LiOH was added as electrolyte.
[0202] Cells were discharged under constant current conditions of 0.5 mA/cm.sup.2 using Biologic VSP test system. The specific capacity of MnO.sub.2 was 303 mAh/g or close to theoretical 1e.sup.−discharge.
Example 3
[0203] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 50% β-MnO.sub.2 form Alfa Aesar, 5% of Bi.sub.2O.sub.3 and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0204] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and 1.6-1.8 mm thick.
[0205] The resulting cathodes were used to assemble test cells, containing commercial non-woven separator (NKK) and Zn anode slurry extracted from commercial alkaline cells. 6M KOH solution in water was used as electrolyte.
[0206] Cells were discharged under constant current conditions using Biologic VSP test system. The specific capacity of MnO.sub.2 was close to 600 mAh/g at C/9 discharge rate (35 mA/g), or close to theoretical 2 e.sup.− discharge.
[0207]
Example 4
[0208] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 50% β-MnO.sub.2 form Alfa Aesar, 5% of Bi.sub.2O.sub.3 and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0209] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250° C. for 30 minutes under moderate pressure (500-1000 PSI), yielding cathode disc 1″ in diameter and about 0.15 mm thick.
[0210] The resulting disc was punched to 19 mm diameter and used as a cathode to assemble test cells, containing commercial non-woven separator (NKK) and Zn foil anode. 6M LiOH was added as electrolyte.
[0211] The cells were discharged and charged using a Biologic VSP test system. Discharge was conducted at 0.5 mA/cm.sup.2 current to 0.8 V cut-off. Charge was performed at 0.25 mA/cm.sup.2 to 1.65 V, then held at 1.65V for 3 hours or until current declined to 0.02 mA/cm.sup.2. Every few cycles passivated Zn anode and separator were replaced with fresh. Specific capacity of MnO.sub.2 as a function of cycle number in cells per Example 4 is plotted at
Example 5
[0212] A 2035 coin cell was assembled using the solid polymer electrolyte of Example 1, the cathode of Example 2 and a Zn foil as anode. The cell was discharged and charged using a Biologic VSP test system. Discharge was conducted at 0.25 mA/cm.sup.2 current to 0.8 V cut-off. Charge was performed at 0.25 mA/cm.sup.2 to 1.65 V, then held at 1.65V for 3 hours or until current declined to 0.02 mA/cm.sup.2. The cell demonstrated reversible behavior during such cycling.
Example 6
[0213] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 55% β-MnO.sub.2 form Alfa Aesar and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0214] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1 inch in diameter and about 0.15 mm thick.
[0215] The test cell was assembled using the resulting cathode, electrolyte per Example 1 and anode made of Zn powder. The cell was discharged using Biologic VSP test system at 0.5 mA/cm.sup.2 current density to 0.8 V cut-off. Specific capacity of MnO.sub.2 was 401 mAh/g or more than theoretical 1-electron discharge.
Example 7
[0216] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Anode was prepared by additionally mixing 60% of Zn powder and 10% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0217] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and about 0.15 mm thick.
[0218] The 2035 coin cell was assembled using the resulting anode, cathode per example 2 and commercial NKK separator, containing saturated LiOH as electrolyte.
[0219] The control coin cell was made using Zn foil as anode, cathode per Example 2 and commercial NKK separator containing saturated LiOH as electrolyte.
[0220] The cells were discharged using a Biologic VSP test system at 0.5 mA/cm.sup.2 current density. The discharge profile with anode of the present invention shows higher capacity at slightly higher voltage, which can be related to increased surface area of Zn anode and retention of soluble zincates inside the anode structure.
Example 8
[0221] PPS base polymer and an ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Anode was prepared by additionally mixing 60% of Al powder and 10% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS. The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and about 0.15 mm thick.
[0222] The resulting anode was tested in test cell containing Zn counter electrode and commercial separator containing ZnSO4 electrolyte. Anode made of Al foil was tested as a control.
[0223] The anode was polarized potentiodynamically at 1 mV/s sweep rate using Biologic VSP test system.
Comparative Example 9
[0224] Discharge profile of Duracell Coppertop AA cell at 250 mA discharge was taken from the datasheet. Amount of MnO.sub.2 in the cell was calculated by comparison of published specifications and MSDS, yielding between 8.4 and 9.6 g. Simple conversion results in current density between 26 and 30 mA/g. Product of service hours (per datasheet) and discharge current yields total capacity, which can be converted to specific capacity by dividing it by weight of MnO.sub.2. Voltage profile of the Coppertop AA cell as a function of specific MnO.sub.2 capacity, calculated in such manner, is shown at
Comparative Example 10
[0225] AA cells were purchased in retail store and subjected to 250 mA discharge, corresponding to mid-rate test, using a Maccor 4300 system. Table 10.1 shows performance of commercial AA cells under 250 mA continuous discharge. Total capacity delivered to 0.9 V cut-off is shown in Table 10.1. Assuming amount of MnO.sub.2 in the cells is the same as Comparative example 9, the total capacity of the cell can be converted to specific capacity of MnO.sub.2. As one can see, under these discharge conditions commercial AA cells deliver between 200 and 280 mAh/g. Even taking into account positive effect of intermittent discharge and extending voltage cut-off to 0.8V, it is a fare statement that commercial alkaline cells operate within 1-electron reduction of MnO.sub.2, described by equation (1), and are limited to 308 mAh/g.
TABLE-US-00001 TABLE 10.1 Total Specific Capacity Capacity (mAh/g) Cell Ah Min Max Rayovac 2.15 224 256 Rayovac 2.11 220 251 Energizer Max 1.84 191 219 Energizer Max 1.82 190 217 Duracell Coppertop 2.15 224 256 Duracell Coppertop 2.13 222 254 Duracell Quantum 2.35 244 279 Duracell Quantum 2.33 243 277
Comparative Example 11 per U.S. Pat. No. 7,972,726
[0226]
Example 12
[0227] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 50% β-MnO.sub.2 from Alfa Aesar, 5% of Bi.sub.2O.sub.3 and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0228] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and 1.6-1.8 mm thick.
[0229] The resulting cathodes were used to assemble test cells, containing commercial non-woven separator (NKK) and Zn anode slurry extracted from commercial alkaline cells. 6M KOH solution in water was used as electrolyte.
[0230] Cell was discharged under constant current conditions using Biologic VSP test system.
Example 13
[0231] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 50% EMD from Tronox (mixture of γ- and ε-MnO.sub.2), 5% of Bi2O3 and 15% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0232] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc inch in diameter and 1.6-1.8 mm thick.
[0233] The resulting cathodes were used to assemble test cells, containing commercial non-woven separator (NKK) and Zn anode slurry extracted from commercial alkaline cells. 6M KOH solution in water was used as electrolyte.
[0234] Cells were discharged under constant current conditions using Biologic VSP test system.
Example 14
[0235] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 80% EMD from Tronox (mixture of γ- and ε-MnO.sub.2), 5% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0236] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and 1.6-1.8 mm thick.
[0237] The resulting cathodes were used to assemble test cells, containing commercial non-woven separator (NKK) and Zn anode slurry extracted from commercial alkaline cells. 7M KOH solution in water was used as electrolyte.
[0238] The cell was discharged under constant current conditions at a rate of 9 mA/g using Biologic VSP test system. The specific capacity of MnO.sub.2 was 590 mAh/g.
Example 15
[0239] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (by wt.), respectively, and mixed using jet milling. Cathode was prepared by additionally mixing 80% EMD from Erachem (mixture of γ- and ε-MnO.sub.2), 5% of C45 carbon black. DDQ dopant was added to the resulting mixture in the amount of 1 mole of DDQ per 4.2 moles of PPS.
[0240] The mixture was compression molded onto stainless steel mesh (Dexmet) at 325/250 C for 30 minutes under moderate pressure (500-1000 psi), yielding cathode disc 1″ in diameter and 1.6-1.8 mm thick.
[0241] The resulting cathodes were used to assemble test cells, containing commercial non-woven separator (NKK) and Zn anode slurry extracted from commercial alkaline cells. 7M KOH solution in water was used as electrolyte.
[0242] The cell was discharged under constant current conditions at a rate of 9.5 mA/g using Biologic VSP test system. The specific capacity of MnO.sub.2 was 541 mAh/g.
Example 16
[0243] PPS base polymer and ion source compound LiOH monohydrate were added together in the proportion of 67% to 33% (wt/wt), respectively, and were mixed using jet milling. The mixture was compression molded at 325° C/250° C. for 30 minutes under low pressure. The polymer-sulfur composite cathode was prepared by additionally mixing from 25% to 50% of sulfur powder, 5% to 15% of C45 carbon black, and 0% to 10% LiNO.sub.3 with the solid, ionically conducting polymer material. The materials were compression molded onto stainless steel mesh (Dexmet) at 120° C. for 30 minutes, yielding a cathode disc 15 mm in diameter and 0.3 to 0.4 mm thick.
[0244] The resulting cathodes were used to assemble test cells in 2035 coin cell hardware. Polypropylene separator (Celgard) 25 microns thick and 19 mm in diameter was used along with lithium foil anode material, 15 mm in diameter. A liquid electrolyte of 1M LiTFSI salt dissolved in a 50/50 (vol/vol) mixture of DOL/DME was used, with 0.5M LiNO.sub.3 additive. The cells were assembled in an argon gas filled glovebox, with low oxygen and water levels.
[0245] Cells were discharged under constant current conditions (1 mA) using a Maccor 4600 battery test system. Discharge was terminated at a voltage of 1.75 V.
[0246]
Example 17
[0247] Composite polymer-sulfur cathodes were manufactured as described in Example 16. These cathodes were assembled into coin cells using lithium metal anodes, polypropylene separator, and 1M LiTFSI in DOL/DME electrolyte with 0.5M LiNO.sub.3 additive.
[0248] Cells were discharged under constant current conditions (1 mA) using a Maccor 4600 battery test system. Discharge was terminated at a voltage of 1.75 V. Charge was accomplished in two steps, the first at a lower charge rate of 0.2 mA current to a maximum voltage of 2.3 V, and the second charge step at a higher rate of 1 mA current to a maximum voltage of 2.45 V. The overall charge capacity was limited for these test cells. These cells were allowed to cycle several times at room temperature.
[0249]
Comparative Example 18
[0250] A noteworthy example of a highly ordered interwoven composite electrode is presented in the literature [Ji, X.; Lee, K. T.; Nazar, L. F. Nature Materials 2009, 8, 500-506]. This composite cathode utilized CMK-3 mesoporous carbon with sulfur entrenched in the pores through heat treatment at 155° C.
[0251] The composite cathode in this example was slurry-cast from cyclopentanone onto a carbon coated aluminum current collector. The cathode utilized 84 wt % CMK-3/S composite, 8 wt % Super-S carbon and 8 wt % PVDF binder. The electrolyte was composed of 1.2 M LiPF6 in ethyl methyl sulphone, and Li metal was used as the anode. In comparison, the results for the composite polymer-sulfur cathode of the invention, as described in Example 16, are plotted on the same graph. It is apparent that the composite polymer-sulfur cathode of the invention gives as good, or better, results than literature examples of composite sulfur cathodes.
Comparative Example 19
[0252] The use of sulfur-conductive polymer composites as cathodes for lithium batteries has been demonstrated. In one case, polyacrylonitrile (PAN) is sulfurized to form a conductive and chemically active cathode material. The sulfurization of the polymer takes place at a relatively high temperature of ˜300° C. An example of the discharge curve for this material is shown in
Example 20
[0253] Solid polymer electrolyte samples were made by mixing SRT802 (Liquid Crystal Polymer) polymer with lithium hydroxide monohydrate, as a compound comprising ion source, in a proportion 2:1, respectively (by weight). DDQ was used a dopant. Weight ratio of polymer to dopant was 2:1. Mixtures were heat treated at 325/250° C. for 30 minutes under moderate pressure (500-1000 PSI). The ionic surface conductivity of the samples were measured using standard AC-EIS. Samples were sandwiched between stainless steel blocking electrodes and placed in test fixture. AC-impedance was recorded in the range from 800 KHz to 100 Hz using Biologic VSP test system to determine the electrolyte conductivity. Six samples were prepared and tested. Average conductivity was 3.7×10.sup.4 S/cm with about 19% standard deviation. The results are shown in the following Table 20.1.
TABLE-US-00002 TABLE 20.1 Conductivity Sample (S/cm) 1 3.42E−04 2 4.78E−04 3 4.09E−04 4 2.69E−04 5 3.46E−04 6 4.04E−04 Average 3.75E−04 Standard Deviation 7.18E−05 Standard Deviation % 19.2%
Example 21
[0254] Solid polymer electrolyte samples were made by mixing SRT900(Liquid Crystal Polymer) polymer with lithium hydroxide monohydrate, as a compound comprising ion source, in a proportion 2:1, respectively (by weight). DDQ was used a dopant. Weight ratio of polymer to dopant was 2:1. Mixtures were heat treated at 325/250 C for 30 minutes under moderate pressure (500-1000 psi). Samples were sandwiched between stainless steel electrodes and placed in test fixture. AC-impedance was recorded in the range from 800 KHz to 100 Hz using Biologic VSP test system to determine the electrolyte conductivity. Six samples were prepared and tested. Average conductivity was 1.5 ×10.sup.−3 S/cm with about 25% standard deviation. The results are shown in the following Table 21.1
TABLE-US-00003 TABLE 21.1 Conductivity Sample (S/cm) 1 1.14E−03 2 1.39E−03 3 1.59E−03 4 1.31E−03 5 1.20E−03 6 2.13E−03 Average 1.46E−03 Standard Deviation 3.63E−04 Standard Deviation % 24.9%
Example 22
[0255] Polymer electrolyte samples were made by mixing polymer and compound comprising ion source in various proportions. DDQ was used a dopant. Molar ratio of polymer to dopant was 4.2. Mixtures were heat treated at 325/250 C for 30 minutes under moderate pressure (500-1000 psi). Samples were sandwiched between stainless steel electrodes and placed in test fixture. AC-impedance was recorded in the range from 800 KHz to 100 Hz using Biologic VSP test system to determine the electrolyte conductivity.
[0256] Results are shown in the table below. High observed conductivity suggests that the polymer electrolyte can conduct multiple ions, including to Li.sup.+, K.sup.+, Na.sup.+, Ca.sup.2+, Mg.sup.2+, Al.sup.3+, OH.sup.− and Cl.sup.−.
TABLE-US-00004 Ion Ion Source Conductivity Source Wt. % (S/cm) Li.sub.2O 33% 1.9E−04 Na.sub.2O 33% 4.2E−05 MgO 33% 6.3E−07 CaCl.sub.2 33% 6.2E−03 MgCl.sub.2 20% 8.0E−03 AlCl.sub.3 15% 2.4E−03 NaOH 50% 1.3E−04 KOH 50% 2.2E−04
[0257] Ability to conduct ions other than Li.sup.+ opens new applications for the polymer electrolyte. Sodium- and potassium-based energy storage systems are viewed as alternative to Li-ion, driven primarily by low cost and relative abundance of the raw materials.
[0258] Calcium, magnesium and aluminum conductivity is important developing multivalent intercalation systems, potentially capable of increasing energy density beyond capabilities of Li-ion batteries. There is also a possibility to utilize such materials to create power sources with metal anodes, more stable and less costly than lithium.
[0259] Hydroxyl conductivity is crucial for numerous alkaline chemistries, including Zn/MnO.sub.2, Ni/Zn, Ni—Cd, Ni-MH, Zn-air, Al-air. Polymer electrolytes conducting hydroxyl ions can be also used in alkaline fuel cells and super capacitors.
Example 23
[0260] Solid ionically conductive polymer material:
[0261] Polyphenylene sulphide “PPS” (base polymer) and tetrachloro-1,4-benzoquinone “chloranil” are mixed and heated to form a solid intermediate polymer material, that when mixed with a compound including a source of ions forms the solid ionically conductive polymer material. The compound comprises 10-50% by weight of the base polymer. The heating step raises the temperature of the reactants to 250-350 oC, and takes from about 10 minutes to 8 hours to overnight. In an aspect, the solid ionically conductive polymer material or its intermediate or its reactants can be mixed with additives (e.g. electrically conductive carbons) to form a composite that is both ionically conductive and provides the functional attribute of the additive (e.g. electrical conductivity).
[0262] Zn Anode:
[0263] Zinc powder (pure powder or zinc powder alloyed with bismuth, indium, calcium, aluminum and other alloying agents known in the art) is mixed with solid intermediate polymer material, lithium hydroxide, conductive carbon additive (e.g C45 or KS6L graphite by Tincal, EC600—a high surface area carbon from AkzoNobel, etc), additives zinc oxide and/or other corrosion-resistive additives. PVDF or Kynar PVDF is used as binder, with NMP as a solvent. A mixer (e.g. Thinky) can be used and if used to mix the mixture is mixed until a homogeneous slurry is obtained (e.g. 10-30 min at 2000 rpm). The slurry is then casted by a doctor blade technique onto a current collector (stainless steel, titanium or nickel foil), which has a thin layer of graphite primer pre-coated. Electrodes were then dried at 80-120° C. for 2-12 hours, calendared and sliced into desired dimensions for coin cells or pouch cells.
[0264] MnO.sub.2 Cathode:
[0265] EMD MnO.sub.2 powder mixed with conductive additive (e.g. C45, KS6L graphite, EC600 high surface area carbon, etc), solid intermediate polymer material, and the ionic compound lithium hydroxide. PVDF (Polyvinylidene fluoride) or Kynar PVDF is used as binder, with NMP (N-Methyl-2-pyrrolidone) as solvent. A Thinky brand mixer is used to mix the mixture for 10-30 min at 2000 rpm until a homogeneous slurry is obtained. The slurry is then casted by a doctor blade technique onto a current collector (stainless steel, titanium or nickel foil), which has a thin layer of graphite primer pre-coated. Electrodes were then dried at 80-120° C. for 2-12 hours, calendared and sliced into desired dimensions for coin cells or pouch cells. Overall, the solid ionically conductive polymer material comprises about 2-30 weight % of the total cathode weight, and the active (EMD in this case) is about 20-80 wt %, carbon is about 3-30 wt %, and liquid electrolyte
[0266] Electrolyte:
[0267] Various electrolytes can be used. In an aspect the electrolyte formulation is an aqueous solution containing 36 wt. % potassium hydroxide with zinc oxide as an additive. In an aspect, a 1-3 molar concentration of zinc sulfate salt, with the addition of additives 0.5-4 wt. % of manganese sulfate (or other Mn(ii) salts) is used. These aqueous electrolytes can be added to 0.5-2 wt. % of a gelling agent, e.g. poly(ethylene glycol) di-acid (or other gelling agents known in the art). In an aspect, the solid ionically conductive polymer material is used as the electrolyte, a separator is not required, and a small amount of KOH solution or other liquid electrolyte solution can be optionally added to the anode or cathode.
[0268] Cell Construction:
[0269] CR2032 coin cells, bobbin cylindrical cell, and single-layer and multi-layer pouch cells have all been made using the same cathode and anode combination. Cell assembly steps are the same as commonly used in the industry, including electrode slurry, closing, crimping, Use a coin cell as an example, a cathode and an anode are sandwiched between a layer of non-woven separator that soaked with the above described zinc sulfate liquid electrolyte as described above.
[0270] Although this construction is described as a secondary cell, it has been found useful as a primary battery also.
[0271] Referring to Table 23.1, there is shown multiple constructions using the solid ionically conducting polymer material. Listed are a primary construction, three (1-3) secondary alkaline constructions including a solid-state formulation, and a zinc air construction.
[0272] Secondary formulation (1) corresponds to
[0273] Secondary formulation (2) corresponds to
[0274] While the present invention has been described in conjunction with preferred embodiments, one of ordinary skill, after reading the foregoing specification, will be able to effect various changes, substitutions of equivalents, and other alterations to that set forth herein. It is therefore intended that the protection granted by Letters Patent hereon be limited only by the definitions contained in the appended claims and equivalents thereof.