Facile synthesis of solid sodium ion-conductive electrolytes

Patent metadata

Field	Value
Publication number	US-11685694-B2
Application number	US-201916686137-A
Country	US
Kind code	B2
Filing date	Nov 16, 2019
Priority date	Oct 10, 2019
Publication date	Jun 27, 2023
Grant date	Jun 27, 2023

Abstract

Disclosed is a rapid, reproducible solution-based method to synthesize solid sodium ion-conductive materials. The method includes: (a) forming an aqueous mixture of (i) at least one sodium salt, and (ii) at least one metal oxide; (b) adding at least one phosphorous precursor as a neutralizing agent into the mixture; (c) concentrating the mixture to form a paste; (d) calcining or removing liquid from the paste to form a solid; and (e) sintering the solid at a high temperature to form a dense, non-porous, sodium ion-conductive material. Solid sodium ion-conductive materials have electrochemical applications, including use as solid electrolytes for batteries.

First claim

We claim:

1. A method comprising:
(a) forming an alkaline mixture by mixing together in a liquid,
(i) at least one sodium salt comprising a sodium cation and a basic anion, and
(ii) at least one metal oxide;

(b) neutralizing the alkaline mixture with a solution comprising at least one phosphorous precursor;
(c) concentrating the neutralized mixture by heating at 180° C. for 1-2 hours to form a paste;
(d) calcinating the paste at 700° C. for 3 hours to remove liquid from the paste and to form a solid; and
(e) sintering the solid at a temperature in the range of 900° C. to 1250° C. for 2-4 hours, wherein the sintered solid is an ion-conductive ceramic comprising sodium, at least one metal, oxygen, and phosphorous.

2. The method of claim 1 , wherein the at least one phosphorous precursor is selected from the group consisting of phosphoric acid (H 3 PO 4 ), disodium phosphate (Na 2 HPO 4 ), monosodium phosphate (NaH 2 PO 4 ), ammonium dihydrogen phosphate (NH 4 H 2 PO 4 ), calcium phosphate (Ca 3 (PO 4 ) 2 ), triethyl phosphate ((C 2 H 5 ) 3 PO 4 ), trimethyl phosphate ((CH 3 ) 3 PO 4 ), tributyl phosphate ((C 4 H 9 ) 3 PO 4 ), aluminum phosphate (AlPO 4 ), sodium phosphate (Na 3 PO 4 ), zinc phosphate (Zn 3 (PO 4 ) 2 ), silver phosphate (Ag 3 PO 4 ), lithium phosphate (Li 3 PO 4 ), and combinations thereof.

3. The method of claim 1 , wherein the at least one sodium salt is selected from the group consisting of sodium carbonate (Na 2 CO 3 ), sodium bicarbonate (Na 2 HCO 3 ), sodium nitrate (NaNO 3 ), sodium acetate (NaOOCCH 3 ), sodium oxalate (Na 2 C 2 O 4 ), sodium hydroxide (NaOH), sodium chloride (NaCl), sodium bromide (NaBr), sodium fluoride (NaF), and combinations thereof.

4. The method of claim 1 , wherein the at least one metal oxide is selected from the group consisting of aluminum oxide (Al 2 O 3 ), silicon oxide (SiO 2 ), lanthanum oxide (La 2 O 3 ), zirconium dioxide (ZrO 2 ), zinc oxide (ZnO), cadmium oxide (CdO), yttrium oxide (Y 2 O 3 ), scandium oxide (Sc 2 O 3 ), titanium oxide (TiO 2 ), cobalt oxide (CoO), nickel oxide (NiO), niobium oxide (NbO, NbO 2 , or Nb 2 O 5 ), iron oxide (Fe 3 O 4 ), and combinations thereof.

5. The method of claim 1 , wherein the at least one metal oxide is zirconium dioxide and silicon dioxide, and the at least one metal in the ion-conductive ceramic is zirconium and silicon.

6. The method of claim 1 , wherein the ion-conductive ceramic has the formula of Na 1+x Zr 2 Si x P 3−x O 12 , wherein 0<x<3.

7. The method of claim 1 , wherein the ion-conductive ceramic has the formula of Na 1+x Zr 2 Si x P 3−1 O 12 , wherein 1.5<x<2.5; the alkaline mixture of (a) has an excess of 1-3 mol % of sodium salt; and the ion-conductive ceramic has an ionic conductivity in the range of 10 −4 to 10 −2 S/cm.

8. The method of claim 1 , further comprising sonicating the neutralized alkaline mixture at (b) prior to concentrating.

9. The method of claim 1 , wherein the solid at (d) is milled for 1 hour to form a powder prior to the sintering.

10. The method of claim 9 , wherein the powder is pressed into pellets prior to the sintering.

11. The method of claim 1 , wherein the aqueous mixture at (a) further comprises (iii) at least one doping metal precursor.

12. The method of claim 11 , wherein the at least one doping metal precursor is selected from the group consisting of germanium oxide (GeO 2 ), cobalt nitrate (Co(NO 3 ) 2 , lanthanum oxide (La 2 O 3 ), zirconium oxide (ZrO 2 ), cerium oxide (CeO 2 ), and combinations thereof.

13. A method comprising:
(a) forming an aqueous mixture by mixing together in a liquid,
(i) at least one sodium salt comprising a sodium cation and a basic anion,
(ii) at least one metal oxide, and
(iii) at least one phosphorous precursor as a neutralizing agent;

(b) concentrating the aqueous mixture by heating at 180° C. for 1-2 hours to form a paste;
(c) calcinating the paste at 700° C. for 3 hours to remove any liquid from the paste and to form a solid; and
(d) sintering the solid at a temperature in the range of 900° C. to 1250° C. for 2-4 hours, wherein the sintered solid is an ion-conductive ceramic comprising sodium, at least one metal, oxygen, and phosphorous.

14. The method of claim 13 , wherein the phosphorous precursor is selected from the group consisting of phosphoric acid (H 3 PO 4 ), disodium phosphate (Na 2 HPO 4 ), monosodium phosphate (NaH 2 PO 4 ), ammonium dihydrogen phosphate (NH 4 H 2 PO 4 ), calcium phosphate (Ca 3 (PO 4 ) 2 ), triethyl phosphate ((C 2 H 5 ) 3 PO 4 ), trimethyl phosphate ((CH 3 ) 3 PO 4 ), tributyl phosphate ((C 4 H 9 ) 3 PO 4 ), aluminum phosphate (AlPO 4 ), sodium phosphate (Na 3 PO 4 ), zinc phosphate (Zn 3 (PO 4 ) 2 ), silver phosphate (Ag 3 PO 4 ), lithium phosphate (Li 3 PO 4 ), and combinations thereof.

15. The method of claim 13 , wherein the at least one sodium salt is selected from the group consisting of sodium carbonate (Na 2 CO 3 ), sodium bicarbonate (Na 2 HCO 3 ), sodium nitrate (NaNO 3 ), sodium acetate (NaOOCCH 3 ), sodium oxalate (Na 2 C 2 O 4 ), sodium hydroxide (NaOH), sodium chloride (NaCl), sodium bromide (NaBr), sodium fluoride (NaF), and combinations thereof.

16. The method of claim 13 , wherein the at least one metal oxide is selected from the group consisting of aluminum oxide (Al 2 O 3 ), silicon oxide (SiO 2 ), lanthanum oxide (La 2 O 3 ), zirconium dioxide (ZrO 2 ), zinc oxide (ZnO), cadmium oxide (CdO), yttrium oxide (Y 2 O 3 ), scandium oxide (Sc 2 O 3 ), titanium oxide (TiO 2 ), cobalt oxide (CoO), nickel oxide (NiO), niobium oxide (NbO, NbO 2 , or Nb 2 O 5 ), iron oxide (Fe 3 O 4 ), and combinations thereof.

17. The method of claim 13 , wherein the least one metal oxide is zirconium dioxide and silicon dioxide, and the at least one metal in the ion-conductive ceramic is zirconium and silicon.

18. The method of claim 13 , wherein the ion-conductive ceramic has the formula of Na 1+x Zr 2 Si x P 3−x O 12 , wherein 0<x<3.

19. The method of claim 13 , wherein the ion-conductive ceramic has the formula of Na 1+x Zr 2 Si x P 3−1 O 12 , wherein 1.5<x</2.5′, the mixture of (a) comprises an excess of 1-3 mol % of sodium salt, and the ion-conductive ceramic has an ionic conductivity in the range of 10 −4 to 10 −2 S/cm.

20. The method of claim 13 , further comprising sonicating the aqueous mixture at (a) prior to concentrating.

21. The method of claim 13 , further comprising wherein the solid at (c) is milled for 1 hour to form a powder prior to the sintering.

22. The method of claim 21 , wherein the powder is pressed into pellets prior to the sintering.

23. The method of claim 13 , wherein the aqueous mixture at (a) further includes (iv) at least one doping metal precursor.

24. The method of claim 23 , wherein the at least one doping metal precursor is selected from the group consisting of germanium oxide (GeO 2 ), cobalt nitrate (Co(NO 3 ) 2 , lanthanum oxide (La 2 O 3 ), zirconium oxide (ZrO 2 ), cerium oxide (CeO 2 ), and combinations thereof.

25. A method comprising:
(a) forming an alkaline mixture by mixing together in a liquid,
(i) at least one sodium salt comprising a sodium cation and a basic anion, and
(ii) at least one metal oxide;

(b) neutralizing the alkaline mixture with a solution of phosphoric acid (H 3 PO 4 );
(c) concentrating the neutralized mixture by heating at 180° C. for 1-2 hours to form a paste;
(d) calcinating the paste at 700° C. for 3 hours to remove liquid from the

Assignees

• IBM
• Repsol Sa

Inventors

• Ansari Younes
• Na Young-Hye
• Nguyen Khanh
• Moreno-Ortiz Francisco José Alía

Classifications

• C04B35/62615

  High energy or reactive ball milling · CPC title

• C04B35/447 Primary

  based on phosphates {, e.g. hydroxyapatite} · CPC title

• C04B2235/3418

  Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint · CPC title

• H01M2300/0077

  based on zirconium oxide · CPC title

• H01M6/186

  Only oxysalts-containing solid electrolytes · CPC title