ZIRCON TYPE AB04 MATERIALS AS MAGNESIUM CATHODES

Abstract

A composition MxABO.sub.4 can include: a composition ABO.sub.4, wherein M is selected from the group consisting of: Ca, Mg, and Na, wherein M is intercalated with ABO.sub.4, wherein x is greater than or equal to 0, wherein A includes at least one selected from the group consisting of: Dy, Er, Sm, Nd, Tm, Pr, Gd, Sc, Y, Eu, Ho, Tb, Bi, Lu, La, Yb, Ce, Zr, Hf, Th, U, Ce, In, Tl, Pa, Pu, Ba, Pb, and Sr, wherein B includes at least one selected from the group consisting of: B, P, V, Cr, As, Si, Ge, N, Nb, Mo, Ru, Sb, W, Re, Bi, Mn, Fe, Se, Tc, Sn, and Co, and wherein the composition ABO.sub.4 has a tetragonal structure.

Claims

1. A composition MxABO.sub.4, comprising: a composition ABO.sub.4, wherein M is selected from the group consisting of: Ca, Mg, and Na, wherein M is intercalated with ABO.sub.4, wherein x is greater than or equal to 0, wherein A includes at least one selected from the group consisting of: Dy, Er, Sm, Nd, Tm, Pr, Gd, Sc, Y, Eu, Ho, Tb, Bi, Lu, La, Yb, Ce, Zr, Hf, Th, U, Ce, In, Tl, Pa, Pu, Ba, Pb, and Sr, wherein B includes at least one selected from the group consisting of: B, P, V, Cr, As, Si, Ge, N, Nb, Mo, Ru, Sb, W, Re, Bi, Mn, Fe, Se, Tc, Sn, and Co, wherein the composition ABO.sub.4 has a crystal structure with a tetragonal I4_1/amd space group, and wherein the composition ABO.sub.4 has edge-sharing AO.sub.8 dodecahedral and BO.sub.4 tetrahedral.

2. The composition of claim 1, wherein A is Eu, Y, Yb, Sc, or a combination thereof.

3. The composition of claim 1, wherein B is Cr.

4. The composition of claim 1, wherein B is V.

5. The composition of claim 1, wherein the composition ABO.sub.4 is EuCrO.sub.4 and M is Mg, and the EuCro.sub.4 is made using a solid state method or a sol-gel method.

6. The composition of claim 1, wherein the composition ABO.sub.4 is EuVO.sub.4 and M is Mg, and the EuVO.sub.4 is made using a solid state method or a sol-gel method.

7. The composition of claim 1, wherein the composition ABO.sub.4 is YVO.sub.4 and M is Mg, and the YVO.sub.4 is made using a solid state method or a sol-gel method.

8. The composition of claim 1, wherein the composition ABO.sub.4 is ScVO.sub.4 and M is Mg, and the ScVO.sub.4 is made using a solid state method.

9. The composition of claim 1, wherein the composition ABO.sub.4 is YbVO.sub.4 and M is Mg, and the YbVO.sub.4 is made using a solid state method.

10-12. (canceled)

13. The composition of claim 1, wherein the composition ABO.sub.4 is YCrO.sub.4 and M is Mg.

14. The composition of claim 1, wherein the composition ABO.sub.4 is EuCrO.sub.4 and M is Ca or Na, and the EuCrO.sub.4 is made using a solid state method or a sol-gel method.

15. The composition of claim 1, wherein the composition ABO.sub.4 is EuVO.sub.4 and M is Ca or Na, and the EuVO.sub.4 is made using a solid state method or a sol-gel method.

16. The composition of claim 1, wherein the composition ABO.sub.4 is YVO.sub.4 and M is Ca or Na, and the YVO.sub.4 is made using a solid state method or a sol-gel method.

17. The composition of claim 1, wherein the composition ABO.sub.4 is ScVO.sub.4 and M is Ca or Na, and the ScVO.sub.4 is made using a solid state method.

18. The composition of claim 1, wherein the composition ABO.sub.4 is YbVO.sub.4 and M is Ca, and the YbVO.sub.4 is made using a solid state method.

19-33. (canceled)

34. A cathode including the composition of claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0008] The present disclosure will be better understood from reading the following description of non-limiting embodiments, with reference to the attached drawings, wherein below:

[0009] FIG. 1 illustrates an example of the crystal structure of EuCrO.sub.4 in accordance with certain implementations of the disclosed technology.

[0010] FIG. 2 illustrates an example of the structure of the Zircon family/host in accordance with certain implementations of the disclosed technology.

[0011] FIG. 3 illustrates an example of the structure of the Zircon family/intercalated in accordance with certain implementations of the disclosed technology.

[0012] FIG. 4 illustrates an example in which NEB showed low energy barrier in accordance with certain implementations of the disclosed technology.

[0013] FIG. 5 illustrates an example of probability density analysis for the Ca migration pathway in Ca.sub.xYVO.sub.4 from ab initio molecular dynamics calculations in accordance with certain implementations of the disclosed technology.

[0014] FIG. 6 illustrates an example of Ca.sub.xYVO.sub.4 diffusivity in accordance with certain implementations of the disclosed technology.

[0015] FIG. 7 illustrates an example of five different compositions that were tried with solid-state synthesis, four of which were synthesized with high purity in accordance with certain implementations of the disclosed technology.

[0016] FIG. 8 illustrates an example of electrochemical response of Zircon compounds observed in Mg ion batteries in accordance with certain implementations of the disclosed technology.

[0017] FIG. 9 illustrates an example of three compositions synthesized with sol-gel method in accordance with certain implementations of the disclosed technology.

[0018] FIG. 10 illustrates an example of electrochemical response of Zircon compounds observed in Mg ion batteries in accordance with certain implementations of the disclosed technology.

DETAILED DESCRIPTION

[0019] Implementations of the disclosed technology are generally directed to improved Mg, Ca, and Na cathodes.

[0020] FIG. 1 illustrates an example of crystal structure of EuCro.sub.4 demonstrating the structure type of the zircon-type ABO4 family in accordance with certain implementations of the disclosed technology.

[0021] Implementations of the disclosed technology present a significant improvement over current Mg cathodes with respect to improved Mg solid state mobility. Theoretical predictions using density functional theory have found the Mg migration barrier to be much lower in materials in the zircon-type ABO4 family: EuCro4, YCrO4 and YVO4 and comparable voltage, capacity and energy density to other Mg cathodes. Therefore, the disclosed invention offers an attractive alternative to currently available Mg cathodes. The YVO.sub.4 compound showed low diffusion barriers for Mg, Ca and Na, suggesting this compound family to be a promising cathode material in Mg/Ca/Na ion batteries.

[0022] Table 1 illustrates information pertaining to multiple compositions that were studied.

TABLE-US-00001 TABLE 1 Working Redox Energy barrier Experimentally Host ion center (meV) investigated EuCrO.sub.4 Mg Cr 107 Yes YCrO.sub.4 Mg Cr 121 Yes YVO.sub.4 MG/Ca/NA V 71/62/78 Yes EuVO4 Mg V Yes ScVO4 Mg V Yes

[0023] Table 2 illustrates comparisons to other Mg/Ca cathodes.

TABLE-US-00002 TABLE 2 Other ones Ours Spinel Layered Chevrel NASICON Mg.sub.xCrO.sub.4 Ca.sub.xYVO.sub.4 Mg.sub.xTi.sub.2S.sub.4 Mg.sub.xTiS.sub.2 Mg.sub.xMo.sub.6S.sub.8 Ca.sub.x[NaV.sub.2(PO.sub.4).sub.3 Avg. 2.1 V 0.8 V 0.89 1.2 0.99 3.2 Voltage (theory) Gravimetric 96 119 224 239 129 81 Capacity (mAh/g) Gravimetric 198 240 199 287 128 259 Energy Density (Wh/kg) Migration 107 62 615 1160 500 Barrier (meV)

[0024] FIG. 2 illustrates an example of the structure of the Zircon family/host where ABO.sub.4 with edge-sharing AO.sub.8 dodecahedral and BO.sub.4 tetrahedral and structure type: tetragonal (I4_1/amd).

[0025] FIG. 3 illustrates an example of the structure of the Zircon family/intercalated where M.sub.xABO4, M=Mg, Ca, Na and Ab initio calculations confirmed stable structures with Mg/Ca/Na inserted. As used herein, the term intercalated generally refers to the Ca, Mg, or Na are inserted into the ABO.sub.4 structure during chemical or electrochemical reactions.

[0026] FIG. 4 illustrates an example in which NEB calculations showed low energy barrier.

[0027] FIG. 5 illustrates an example of probability density analysis for the Ca migration pathway in Ca.sub.xYVO.sub.4 from ab initio molecular dynamics calculations.

[0028] FIG. 6 illustrates an example of Ca.sub.xYVO.sub.4 diffusivity.

[0029] FIG. 7 illustrates an example of five different compositions that were tried with solid-state synthesis, four of which were synthesized with high purity. In the example, precursors were mixed, then pellets were prepared, then they were annealed for 24 hours.

[0030] FIG. 8 illustrates an example of electrochemical response of Zircon compounds observed in Mg ion batteries.

[0031] FIG. 9 illustrates an example of three compositions synthesized with sol-gel method.

[0032] FIG. 10 illustrates an example of electrochemical response of Zircon compounds observed in Mg ion batteries.

A First Example: Preparation of EuCrO.SUB.4 .Cathode for Electrochemical Measurements

[0033] In an initial step, 140 mg of EuCrO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0034] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0035] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as EuCro.sub.4:C:PTFE=70:20:10.

[0036] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0037] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0038] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0039] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0040] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Mg.sub.3Bi.sub.2 anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

Second Example: Preparation of EuVO.SUB.4 .Cathode for Electrochemical Measurements

[0041] In an initial step, 140 mg of EuVO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0042] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0043] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as EuVO.sub.4:C:PTFE=70:20:10.

[0044] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0045] In a next step, the new mixture is rolled for several times (8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0046] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0047] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0048] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Mg.sub.3Bi.sub.2 anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

A Third Example: Preparation of YVO.SUB.4 .Cathode for Electrochemical Measurements

[0049] In an initial step, 140 mg of YVO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0050] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0051] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as YVO.sub.4:C:PTFE=70:20:10.

[0052] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0053] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0054] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0055] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0056] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Mg.sub.3Bi.sub.2 anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

A Fourth Example: Preparation of ScVO.SUB.4 .Cathode for Electrochemical Measurements

[0057] In an initial step, 140 mg of ScVO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0058] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0059] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene. (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as ScVO.sub.4:C:PTFE=70:20:10.

[0060] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0061] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0062] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0063] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0064] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Mg.sub.3Bi.sub.2 anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

A Fifth Example: Preparation of EuVO.SUB.4 .Cathode for Electrochemical Measurements

[0065] In an initial step, 140 mg of EuVO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0066] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0067] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as EuVO.sub.4:C:PTFE=70:20:10.

[0068] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0069] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0070] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0071] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0072] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Activated Carbon anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

A Sixth Example: Preparation of EuCrO.SUB.4 .Cathode for Electrochemical Measurements

[0073] In an initial step, 140 mg of EuCrO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0074] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0075] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as EuCrO.sub.4:C:PTFE=70:20:10.

[0076] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0077] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0078] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0079] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0080] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Activated Carbon anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

A Seventh Example: Preparation of YVO.SUB.4 .Cathode for Electrochemical Measurements

[0081] In an initial step, 140 mg of YVO.sub.4 powder is mixed with 40 mg of conductive Carbon are placed into ball mill jars inside the glovebox (under Argon atmosphere).

[0082] In a next step, the powders are mixed with planetary ball milling for 3 hours at 300 rpm.

[0083] In a next step, after ball milling, the mixture is transferred back to the glovebox and 20 mg of polytetrafluoroethylene (PTFE) is added to the mixture. By this way the overall composition of the cathode film is determined as YVO.sub.4:C:PTFE=70:20:10.

[0084] In a next step, PTFE added powders are mixed for at least 30 minutes in the glovebox with the help of mortar and pestle.

[0085] In a next step, the new mixture is rolled for several times (e.g., 8-10) in a stainless-steel plate to obtain a complete polymerization of the binder and homogeneous distribution of all the ingredients.

[0086] In a next step, after obtaining a homogeneous cathode film, rolling is continued to decrease the film thickness and circular samples with 1 cm.sup.2 surface area are punched out from the film.

[0087] In a next step, the weight of the circular sample is measured. Then, the sample is rolled again to decrease the thickness of the cathode film. The rolling and punching processes are repeated until the weight of the circular sample becomes 3 mg.

[0088] In a next step, after obtaining a sample with 3 mg weight and 1 cm.sup.2 surface area, the cathode film is placed into the 2-electrode coin cell and electrochemical performance against Activated Carbon anode in 0.5 M Mg (TFSI)2 in diglyme is tested.

[0089] In certain implementations where the composition ABO.sub.4 is EuCrO.sub.4, the M is Mg and the EuCrO.sub.4 is made using either a solid state method or a sol-gel method.

[0090] In certain implementations where the composition ABO.sub.4 is EuVO.sub.4, the M is Mg and the EuVO.sub.4 is made using either a solid state method or a sol-gel method.

[0091] In certain implementations where the composition ABO.sub.4 is YVO.sub.4, the M is Mg and the YVO.sub.4 is made using either a solid state method or a sol-gel method.

[0092] In certain implementations where the composition ABO.sub.4 is ScVO.sub.4, the M is Mg and the ScVO.sub.4 is made using a solid state method.

[0093] In certain implementations, the composition ABO.sub.4 is YCrO.sub.4 and the M is Mg.

[0094] In certain implementations where the composition ABO.sub.4 is EuCrO.sub.4, the M is Ca and the EuCrO.sub.4 is made using either a solid state method or a sol-gel method.

[0095] In certain implementations where the composition ABO.sub.4 is EuVO.sub.4, the M is Ca and the EuVO.sub.4 is made using either a solid state method or a sol-gel method.

[0096] In certain implementations where the composition ABO.sub.4 is YVO.sub.4, the M is Ca and the YVO.sub.4 is made using either a solid state method or a sol-gel method.

[0097] In certain implementations where the composition ABO.sub.4 is ScVO.sub.4, the M is Ca and the ScVO.sub.4 is made using a solid state method.

[0098] In certain implementations, the composition ABO.sub.4 is YCrO.sub.4 and the M is Ca.

[0099] In certain implementations where the composition ABO.sub.4 is EuCrO.sub.4, the M is Na and the EuCrO.sub.4 is made using either a solid state method or a sol-gel method.

[0100] In certain implementations where the composition ABO.sub.4 is EuVO.sub.4, the M is Na and the EuVO.sub.4 is made using either a solid state method or a sol-gel method.

[0101] In certain implementations where the composition ABO.sub.4 is YVO.sub.4, the M is Na and the YVO.sub.4 is made using either a solid state method or a sol-gel method.

[0102] In certain implementations where the composition ABO.sub.4 is ScVO.sub.4, the M is Na and the ScVO.sub.4 is made using a solid state method.

[0103] In certain implementations, the composition ABO.sub.4 is YCrO.sub.4 and the M is Na.

[0104] The previously described versions of the disclosed subject matter have many advantages that were either described or would be apparent to a person of ordinary skill. Even so, these advantages or features are not required in all versions of the disclosed apparatus, systems, or methods.

[0105] Additionally, this written description makes reference to particular features. It is to be understood that the disclosure in this specification includes all possible combinations of those particular features. Where a particular feature is disclosed in the context of a particular aspect or example, that feature can also be used, to the extent possible, in the context of other aspects and examples.

[0106] Also, when reference is made in this application to a method having two or more defined steps or operations, the defined steps or operations can be carried out in any order or simultaneously, unless the context excludes those possibilities.

[0107] Although specific examples of the invention have been illustrated and described for purposes of illustration, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, the invention should not be limited except as by the appended claims.