A SOLID-STATE ELECTROLYTE FOR SOLID-STATE RECHARGEABLE SODIUM-IONS BATTERIES

Abstract

The present invention provides a solid-state electrolyte for solid-state rechargeable sodium-ions batteries comprising: Na in a molar content x of at least 3.50 and of at most 4.00, Sn in a molar content y of at least 0.50 and of at most 1.00, As in a molar content z superior to 0.00, preferably of at least 0.10, and of at most 0.50, S in a molar content of 4.00.

Claims

1-13. (canceled)

14. A solid-state electrolyte for solid-state rechargeable sodium-ions batteries comprising: Na in a molar content x of at least 3.50 and of at most 4.00, Sn in a molar content y of at least 0.50 and of at most 1.00, As in a molar content z of more than 0.20 and less than 0.30, and S in a molar content of 4.00.

15. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, having a general formula Na.sub.xSn.sub.yAs.sub.zS.sub.4, wherein 3.55?x?3.95.

16. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 15, wherein 3.70?x?3.80.

17. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, wherein 0.55?y?0.95.

18. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 17, wherein 0.70?y?0.80.

19. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, wherein 0.21?z?0.29.

20. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according claim 19, wherein 0.24?z?0.26.

21. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, wherein 3.70?x?3.80, 0.70?y?0.80 and 0.21?z?0.29.

22. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, having a sodium ionic conductivity of superior to 0.30 mS/cm at a temperature of 30? C. and at least 1.00 mS/cm at a temperature of 60? C.

23. Solid-state electrolyte for solid-state rechargeable sodium-ions batteries according to claim 14, comprising a space group of I41/acd having 13.0 ??lattice constant a?15.0 ?, 25.0 ??lattice constant c?30.0 ?, as determined by XRD.

24. A process for manufacturing a solid-state electrolyte according to any of the preceding claims, said process comprising: a first step of mixing Na.sub.2S, SnS.sub.2, As.sub.2S.sub.3, and S powder in an inert atmosphere so as to obtain a mixture; a second step of pressing said mixture under a pressure between 50 and 400 MPa, so as to obtain a pellet; and a third step of firing said pellet at a temperature between 300? C. and 700? C. during a period of time comprised between 1 and 20 hours.

25. A positive electrode for solid-state rechargeable sodium-ions batteries, comprising a solid-state electrolyte according to claim 14.

26. A solid-state rechargeable sodium-ions battery comprising a solid-state electrolyte according to claim 14.

Description

DESCRIPTION OF THE FIGURES

[0013] By means of further guidance, figures are included to better appreciate the teaching of the present invention. Said figures are intended to assist the description of the invention and are nowhere intended as a limitation of the presently disclosed invention. The figures and symbols contained therein have the meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

[0014] FIG. 1 shows the X-ray diffraction (XRD) patterns of Examples 1 to 4 and Comparative Example 1.

[0015] FIG. 2 shows Arrhenius plots of conductivities of EX3 and Na.sub.3.75Sn.sub.0.75Sb.sub.0.25S.sub.4.00 according to Heo et al. x axis indicates 1000/T (K.sup.?1) whereby T is a temperature (K) and y axis indicates an ionic conductivity.

DETAILED DESCRIPTION OF THE INVENTION

[0016] In a first aspect, the present invention provides a solid-state electrolyte for solid-state rechargeable sodium-ions batteries comprising: [0017] Na in a molar content x of at least 3.50 and of at most 4.00, [0018] Sn in a molar content y of at least 0.50 and of at most 1.00, [0019] As in a molar content z superior to 0.00, preferably of at least 0.10, and of at most 0.50, [0020] S in a molar content of 4.00.

[0021] In a preferred embodiment the solid-state electrolyte comprises a compound comprising [0022] Na in a molar content x of at least 3.50 and of at most 4.00, [0023] Sn in a molar content y of at least 0.50 and of at most 1.00, [0024] As in a molar content z superior to 0.00, preferably of at least 0.10, and of at most 0.50, [0025] S in a molar content of 4.00.

[0026] In a preferred embodiment, the solid-state electrolyte according to the first aspect has a general formula Na.sub.xSn.sub.yAs.sub.zS.sub.4, wherein 3.50?x?4.00, 0.50?y<1.00, and 0.00<z?0.50, preferably 0.10?z?0.50.

[0027] Preferably, the molar content x is inferior or equal to 3.90 and preferably x is superior or equal to 3.70.

[0028] In a highly preferred embodiment, the solid-state electrolyte is according to the first aspect, wherein 3.55?x?3.95, preferably 3.60?x?3.90, more preferably 3.65?x?3.85. In a more highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein 3.70?x?3.80, preferably 3.71?x?3.79, more preferably 3.72?x?3.78, even more preferably 3.73?x?3.77, most preferably 3.74?x?3.76. In an even more highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein 3.70?x?3.80, more preferably 3.72?x?3.78, most preferably 3.74?x?3.76. In a highest preferred embodiment the solid-state electrolyte is according to the first aspect, wherein x=3.75.

[0029] Preferably, the molar content y is inferior or equal to 0.90 and preferably y is superior or equal to 0.70.

[0030] In a highly preferred embodiment, the solid-state electrolyte is according to the first aspect, wherein 0.55?y?0.95, preferably 0.60?y?0.90, more preferably 0.65?y?0.85. In an more highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein 0.70?y?0.80, preferably 0.71?y?0.79, more preferably 0.72?y?0.78, even more preferably 0.73?y?0.77, most preferably 0.74?y?0.76. In an even more highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein 0.70?y?0.80, more preferably 0.72?y?0.78, most preferably 0.74?y?0.76. In a highest preferred embodiment the solid-state electrolyte is according to the first aspect, wherein y=0.75.

[0031] Preferably, the molar content z is inferior or equal to 0.30.

[0032] In a highly preferred embodiment, the solid-state electrolyte is according to the first aspect, wherein As is in a molar content z of more than 0.20 and less than 0.30.

[0033] In a more highly preferred embodiment, the solid-state electrolyte is according to the first aspect, wherein 0.21?z?0.30, preferably 0.21?z?0.29, more preferably 0.22?z?0.29, even more preferably 0.22?z?0.28, even more preferably 0.23?z?0.28, even more preferably 0.24?z?0.28, even more preferably 0.24?z?0.27, most preferably 0.24?z?0.26. In an even more highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein 0.21?z?0.29, preferably 0.23?z?0.27, most preferably 0.24?z?0.26. In a highest preferred embodiment the solid-state electrolyte is according to the first aspect, wherein z=0.25.

[0034] In a highly preferred embodiment the solid-state electrolyte is according to the first aspect, wherein [0035] 3.70?x?3.80, preferably 3.72?x?3.78, more preferably 3.74?x?3.76; [0036] 0.70?y?0.80, preferably 0.72?y?0.78, more preferably 0.74?y?0.76; and [0037] 0.21?z?0.29, preferably 0.23?z?0.27, more preferably 0.24?z?0.26.

[0038] In a highest preferred embodiment the solid-state electrolyte is according to the first aspect, wherein x=3.75, y=0.75 and z=0.25.

[0039] In a preferred embodiment, the solid-state electrolyte according to the first aspect has a sodium ionic conductivity of superior to 0.30 mS/cm at a temperature of 30? C. and at least 1.00 mS/cm at a temperature of 60? C.

[0040] In a preferred embodiment, the solid-state electrolyte according to the first aspect comprises a space group of I41/acd having 13.0 ??lattice constant a?15.0 ?, 25.0 ??lattice constant c?30.0 ?, as determined by XRD.

[0041] In a second aspect, the present invention provides a process for manufacturing the solid-state electrolyte according to the first aspect. The process comprises: [0042] a first step of mixing Na.sub.2S, SnS.sub.2, As.sub.2S.sub.3, and S powder in an inert atmosphere so as to obtain a mixture, a second step of pressing said mixture under a pressure between 50-400 MPa, and a third step of firing said pellet at a temperature between 300? C. and 700? C. during a period of time comprised between 1 and 20 hours.

[0043] In a preferred embodiment the pressing of said mixture occurs under a pressure between 70-300 MPa, preferably a pressure between 80-200 MPa, more preferably between 100-150 MPa. Alternatively, and in an equally preferred embodiment, the pressing of said mixture occurs in mold having a diameter of 0.5-2 cm, preferably 0.75-1.25 cm, and under a weight between 0.1 and 5 tons, preferably 0.5 and 1.5 tons.

[0044] In a third aspect, the present invention provides a positive electrode for solid-state rechargeable sodium-ions batteries, comprising a solid-state electrolyte according to any of the preceding claims.

[0045] In a fourth aspect, the present invention provides a solid-state rechargeable sodium-ions battery comprising a solid-state electrolyte according to the first aspect of the invention.

EXAMPLES

1. Description of Analysis Method

[0046] 1.1. Powder X-Ray Diffraction

[0047] The powder X-ray diffraction (XRD) data are collected at 25? C. with an X-ray diffractometer (Rigaku Miniflex 600) using a Cu X-ray tube (?=1.5418 ?), a secondary graphite (002) monochromator, and an angular range of 10??2??80?. The crystal structure is refined using the powder profile refinement program, Generalized Structure and Analysis Software (GSAS, B. G. Toby, J. Appl. Cryst. 2001, 34(2), 210-213).

[0048] 1.2. Electrochemical Impedance Spectroscopy (EIS)

[0049] The sodium ion conductivity is measured by the AC impedance method using an ion-blocking symmetric cell of Ti/Solid-state electrolyte/Ti in a polyether ether ketone (PEEK) mold (diameter=10 mm), wherein the Ti rod is used as a current collector. The cold pressed pellets were prepared at 3 ton pressure. Frequency is applied from 1 MHz to 100 mHz using EC-Lab software on a Biologic SP-200 single-channel potentiostat. Measurement is conducted at various temperature (30, 45, 60, 75, and 90? C.). The sodium ionic conductivity (?) is calculated by below equation;

[00001]$?\left(S/\mathrm{cm}\right)=\frac{L}{R?A},$

where L is the thickness of the pellet (cm), A is the area of the pellet (cm.sup.2), and R is the resistance obtained by the electrochemical impedance spectroscopy (S.sup.?1).

2. Examples and Comparative Examples

Example 1

[0050] A Na.sub.3.90Sn.sub.0.90As.sub.0.10S.sub.4 powder is prepared by mixing, pelletizing, and subsequent heat treatment according to the following process: [0051] Step 1) Mixing: Na.sub.2S, SnS.sub.2, As.sub.2S.sub.3, and S powder are mixed according to the molar ratio of Na:Sn:As:S=3.90:0.90:0.10:4.00 using a mortar with a pestle. Since the starting and resultant materials are hygroscopic and air-sensitive, all reactants and products are handled in a dry Argon-filled glove box. [0052] Step 2) Pelletizing: the mixed powder is pelletized in a mold having a diameter of 1 cm by applying 1.0 ton weight. Then, the pelletized sample is placed in a carbon-coated fused-silica ampoule and vacuum-sealed. [0053] Step 3) Heat treatment: the reactants were heated to 400? C. at a rate of 2? C./min in a box furnace, held at this temperature for 12 hours, and cooled to room temperature naturally. After the reaction was completed, the ampoule is opened inside the Argon-filled glove box. The prepared powder is labelled as EX1.

Example 2, Example 3, and Example 4

[0054] Samples of Example 2, 3, and 4 are prepared according to the same procedure as EX1 except that different amount of Na.sub.2S, SnS.sub.2, As.sub.2S.sub.3, and S powder are used during step 1 according to the molar ratio illustrated in Table 1. The prepared powders are labelled as EX2, EX3, and EX4, respectively.

Comparative Example 1

[0055] A Na.sub.4SnS.sub.4 powder is prepared according to the same procedure as EX1 except that no As.sub.2S.sub.3 is used in step 1. The prepared powder is labelled as CEX1.

TABLE-US-00001 TABLE 1 Summary of the information of the samples according to Examples 1 to 4 and Comparative Example 1 Na.sub.xSn.sub.yAs.sub.zS.sub.4 Sample ID x y z ? (mS/cm) EX1 3.90 0.90 0.10 0.21 EX2 3.80 0.80 0.20 0.24 EX3 3.75 0.75 0.25 0.52 EX4 3.70 0.70 0.30 0.17 CEX1 4.00 1.00 0.00 <10.sup.?5 Heo et al* Na.sub.3.75Sn.sub.0.75Sb.sub.0.25S.sub.4 0.30 *Adv. Energy Mater. 8, 1702716 (2018)

TABLE-US-00002 TABLE 2 Summary of the ionic conductivity of Na.sub.3.75Sn.sub.0.75As.sub.0.25S.sub.4 as a function of the temperature ? (mS/cm) ? (mS/cm) of T (? C.) of EX3 Na.sub.3.75Sn.sub.0.75Sb.sub.0.25S.sub.4 30 0.52 0.30 45 0.62 60 1.03 0.90 75 1.68 90 1.97

[0056] Table 1 summarizes the molar ratio of the Na, Sn, and As elements and the sodium ionic conductivity (?, mS/cm) at 30? C. of the solid-state electrolytes manufactured from Example 1, 2, 3, 4 and Comparative Example 1. According to Table 1, it is observed that the solid-state electrolyte having a general formula Na.sub.xSn.sub.yAs.sub.zS.sub.4, wherein 3.50?x?4.00, 0.50?y<1.00, and 0.00<z?0.50, preferably 0.10?z?0.50, has a significantly higher ionic conductivity than the solid-state electrolyte having a formula Na.sub.4SnS.sub.4. Furthermore, Table 2 and FIG. 2 summarizes the ionic conductivity of Na.sub.3.75Sn.sub.0.75As.sub.0.25S.sub.4 and Na.sub.3.75Sn.sub.0.75Sb.sub.0.25S.sub.4 according to Heo et al. at various temperatures by the aforementioned EIS method. According to Table 2, the ionic conductivity at over 60? C. shows over 1.00 mS/cm and this is enough to be conducted in a solid-state rechargeable sodium-ions battery. This observation indicates that the use of Na.sub.3.75Sn.sub.0.75As.sub.0.25S.sub.4 as a solid-state electrolyte according to the present invention provides a higher ionic conductivity than the use of Na.sub.4SnS.sub.4 which is used as an ion insulator due to a low ionic conductivity. As shown in FIG. 2, the ionic conductivity of solid-state electrolytes increases as an operating temperature increases. EX3 has generally a higher ionic conductivity than Na.sub.3.75Sn.sub.0.75Sb.sub.0.25S.sub.4 at any temperature. Therefore, when EX3 is used in a solid-state rechargeable sodium-ions battery, a required ionic conductivity is achievable at a relatively lower operation temperature, which is a benefit for designing a battery management system.

[0057] About the structures of the compounds from Examples 1 to 4, FIG. 1 shows that the series of Na.sub.xSn.sub.yAs.sub.zS.sub.4 are manufactured properly. As the XRD data of Na.sub.3.70Sn.sub.0.70As.sub.0.30S.sub.4 from FIG. 1 suggest, a solid-state electrolyte Na.sub.3.70Sn.sub.0.70As.sub.0.30S.sub.4 has some impurities so that a solid-state electrolyte Na.sub.xSn.sub.yAs.sub.zS.sub.4 having z lower than 0.30 is more preferred. The Na.sub.3.75Sn.sub.0.75As.sub.0.25S.sub.4 has a structure of a space group of I41/acd that a lattice constant a is 13.7074 ?, c is 27.3628 ?, and ?, ?, and ? is 90?.