RECHARGEABLE CALCIUM BATTERY

Abstract

A rechargeable calcium battery formed from a calcium metal anode, a cathode formed from a composite carbon/sulfur (C/S), a metal oxide, or a metal sulfide, and a multi-component electrolyte containing a mixture of different salts. The calcium anode is formed as a thin, pure calcium metal foil that is polished and combined with a copper collector for redox activity. The cathode may be formed from a carbon-sulfur (CS) composite or metal oxide/sulfide, such as CaM.sub.xO.sub.y or CaM.sub.xS.sub.y, or formed from binary and ternary metals, such as CaM1aM2bO.sub.y/S.sub.y and CaM.sub.1aM.sub.2bM.sub.3cO.sub.y/S.sub.y. The battery also includes a multi-component electrolyte including calcium salts, such as Ca(TSFI).sub.2, Ca(ClO.sub.4).sub.2, Ca(BF.sub.4).sub.2, and CaPF.sub.6, or the pairing of lithium, sodium and potassium salts with one of the anions, such as Ca(TFSI), NaPF.sub.6, and Li(TFSI).

Claims

1. A rechargeable battery, comprising: an anode formed from a foil including calcium; a cathode formed from a material selected from the group consisting of a carbon-sulfide composite, a metal oxide, a transition metal oxide or sulfide, a binary metal oxide or sulfide, and a ternary metal oxide sulfide; an electrolyte comprising an aprotic solvent and a cation salt selected from the group consisting of a calcium salt, a lithium salt, a sodium salt, or a potassium salt.

2. The rechargeable battery of claim 1, wherein the foil is polished.

3. The rechargeable battery of claim 2, wherein the anode further comprises a copper collector.

4. The rechargeable battery of claim 3, wherein the anode is microporous.

5. The rechargeable battery of claim 3, wherein the anode includes a mesh support.

6. The rechargeable battery of claim 1, wherein the material forming the cathode is CaM.sub.1aM.sub.2bO.sub.y/S.sub.y.

7. The rechargeable battery of claim 1, wherein the material forming the cathode is CaM.sub.1aM.sub.2bM.sub.3cO.sub.y/S.sub.y.

8. The rechargeable battery of claim 1, wherein the material forming the cathode is CaNiMnCoO.sub.2.

9. The rechargeable battery of claim 1, wherein the calcium salt is selected from the group consisting of Ca(TSFI).sub.2, Ca(ClO.sub.4).sub.2, Ca(BF.sub.4).sub.2, and CaPF.sub.6.

10. The rechargeable battery of claim 1, wherein the calcium salt is selected from the group consisting of Ca(trifluoromethanesulfonylimide).sub.2, NaPF.sub.6, and Li(trifluoromethanesulfonylimide).

11. The rechargeable battery of claim 1, wherein the aprotic solvent is a carbonate.

12. The rechargeable battery of claim 1, wherein the aprotic solvent is selected from the group consisting of ethyl carbonate, dimethyl carbonate, ethyl methyl carbonate, diethyl carbonate, acetonitrile, dimethyl fumarate, tetrahydrofuran.

13. The rechargeable battery of claim 11, wherein the aprotic solvent is a binary compound selected from the consisting of ethyl carbonate/dimethyl carbonate, ethyl carbonate/ethyl methyl carbonate, ethyl carbonate/diethyl carbonate, and ethyl carbonate/propylene carbonate.

14. The rechargeable battery of claim 11, wherein the aprotic solvent is ethyl carbonate/dimethyl carbonate/ethyl methyl carbonate.

15. The rechargeable battery of claim 1, wherein the aprotic solvent is an ionic liquid solvent selected from the group consisting of an alkyl imidazolium alkylsulfonate paired ionic liquid, 1-ethyl-3-methylimidazolium trifluoromethanesulfonate, 1-ethyl-3-methylimidazolium methanesulfonate, and 1-butyl-3-methylimidazolium trifluoromethanesulfonate.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

[0005] The present invention will be more fully understood and appreciated by reading the following Detailed Description in conjunction with the accompanying drawings, in which:

[0006] FIG. 1 is a schematic of a calcium battery according to the present invention;

[0007] FIG. 2 is a diagram of a first embodiment of a calcium battery according to the present invention; and

[0008] FIG. 3 is a diagram of a second embodiment of a calcium battery according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0009] Referring to the figures, wherein like numeral refer to like parts throughout, there is seen in FIG. 1 a rechargeable calcium battery 10 according to the present invention. Battery 10 comprises a calcium metal anode 12, a composite carbon/sulfur cathode 14, and a multi-component electrolyte 16 containing a cation salt in an aprotic solvent. More specifically, as seen in FIG. 2, the cation salt may be selected from the group consisting of Li, Na/K, and Ca salts. Alternatively, as seen in FIG. 3, cathode 14 may be formed from a binary metal oxide or sulfide that contains calcium and another metal, such as CaMxOy or CaMxSy.

[0010] Calcium metal anode 12 is the electron source and is formed as a thin, pure calcium metal foil. The foil is polished to a high level of smoothness using a SiC rotatory brush to ensure maximal contact with the electrolyte. Foil is combined with a copper (Cu) collector, which provides stable redox activity and electrical contact. Stainless steel may also be used.

[0011] The calcium metal anode may also be in the form of a microporous structure, or calcium metal deposits on a carbon support, or calcium metal deposits on a stainless steel mesh support. This form of anode increases surface area to increase overall areal current density.

[0012] Referring to FIG. 2, in the first embodiment, cathode 14 formed from a carbon-sulfur (CS) composite or metal oxide/sulfide (CaMxOy/CaMxSy) cathodes enables high-capacity storage of calcium ions as well as fast charge/discharge of the battery via the fast mobility of Ca. The carbon stabilizes the sulfur materials to mitigate degradation of the cathode during cycling. In the example of binary metal oxide or sulfide for cathode 14, the metal center can be any transition metal element, such as Ti, V, Cr, Mn, Fe, Co. Specific ratios for x/y are 1/3 and 2/4, with the former being a perovskite crystal structure and the latter being either of the spinel and post-spinel compounds.

[0013] Referring to FIG. 3, in another embodiment, cathode 14 comprises the use of binary and ternary transition metal compositions, such as CaM.sub.1aM.sub.2bO.sub.y/S.sub.y and CaM.sub.1aM.sub.2bM.sub.3cO.sub.y/S.sub.y. Another variation to the CaM.sub.xO.sub.y/CaM.sub.xS.sub.y are materials with layered structure, such as CaNiMnCoO.sub.2, as well as binary layered oxides selected from Ni, Mn, and Co. Different stochiometric ratios may be selected. Switching S for O, allows for tuning of the ion transport and charge/discharge kinetics. Specifically, perovskite (CaMO.sub.3) and spinel or post-spinel (CaM.sub.2O.sub.4) structures may be used. Both binary and ternary transitional metal oxides may be in the perovskite, spinel, post-spinel, or layer crystal structures.

[0014] In either embodiment, multi-component electrolyte 16 is selected to ensure stable cycling at high kinetics rates. Calcium salts that may be used are Ca(TSFI).sub.2, Ca(ClO.sub.4).sub.2, Ca(BF.sub.4).sub.2, and Ca(PF.sub.6).sub.2. Lithium, sodium and potassium salts may also be paired with one of these anions. As an example, the present invention may comprise Ca(TFSI), NaPF.sub.6, and Li(TFSI), where TFSI is trifluoromethanesulfonylimide. Multi-component electrolyte 16 is configured to enable several key functions. First, multi-component electrolyte 16 provides an increased mobility of Ca.sup.2+ ions via the Li salt to increase coordination with the electrolyte solvent and reduce coordination with Ca, thereby allowing the former greater mobility. Second, multi-component electrolyte 16 provides for the formation of a stable solid electrolyte interface via Na and/or K salts, which creates a protective layer over the calcium metal and has high transport coefficients for Ca.sup.2+ ions. Na and K are selected because they form a stable artificial solid electrolyte interface over the calcium anode to allow for stable redox activity and high calcium ion transport. Finally, multi-component electrolyte 16 facilitates battery charge transport via the native calcium salt. Multi-component electrolyte 16 may also comprise a variation where any of the salt components for their respective cation is also binary (CaX and CaY). In this option, the salt components further stabilize the electrodes and the respective cations enable charge transport. The solvent used for multi-component electrolyte 16 may comprise carbonate electrolytes, either as single components, binary, or ternary components. Examples include (single:) EC (ethyl carbonate), DMC (dimethyl carbonate), EMC (ethyl methyl carbonate), DEC (diethyl carbonate), ACN (acetonitrile), DMF (dimethyl fumarate), THE (tetrahydrofuran), (binary:) EC/DMC, EC/EMC, EC/DEC, and EC/PC (propylene carbonate), and (ternary:) EC/DMC/EMC. An additional variation of the solvent for the present invention comprises the use of ionic liquid solvents, such as alkyl imidazolium alkylsulfonate paired ionic liquids. Other examples include 1-ethyl-3-methylimidazolium trifluoromethanesulfonate, 1-ethyl-3-methylimidazolium methanesulfonate, and 1-butyl-3-methylimidazolium trifluoromethanesulfonate.

[0015] Battery 10 may further include a separator such as a standard separator formed from plastic or glass. Additionally, the separator may be a low ether content, crosslinked polymer gel, in which the electrolytes are swollen. The low ether content enables greater mobility in of the cations in the electrolyte, and can also help further stabilize the calcium metal anode interface. Examples include polytetrahydrofuran, but other low ether content polymers are acceptable. Polyethylene oxide is also acceptable.

[0016] Battery 10 enables a high discharge rate and stable long-life cycling. Based on the chemistry of the present invention, battery 10 has theoretical energy densities of 900 Wh/kg and theoretical capacities of 750 mAh/g, which have been at least partially confirmed with experimentation. Battery can provide open circuit voltages that range from 2.5 and 4 V.