Large-scale synthesis of powders of solid-state electrolyte material particles for solid-state batteries, systems and methods thereof

Abstract

Various solid-state electrolyte materials having a desired chemical composition as well as method and apparatus of producing the solid-state electrolyte (SSE) materials are provided. The method includes drying a gas-liquid mixture to form a gas-solid mixture, obtaining powdered particles, and annealing the powdered particles to obtain crystalline products of the SSE material. The liquid mixture is prepared using stoichiometrically amounts of lithium-containing salt and one or more inorganic salts and then mixed with a gas. The salts are prepared in solutions and the molar ratio of the solutions of lithium-containing salt and the one or more inorganic metal salt are digitally controlled, thereby obtaining large scale synthesis of the SSE materials. The processing apparatus generally includes a mist generator, a power jetting chamber, one or more gas-solid separators, and one or more reactors. Various types of SSE materials can then be prepared and obtained.

1 . A solid-state electrolyte material, comprising,
 a ceramic material having a chemical composition of Li a  La b  Zr c  D1 d  D2 e  . . . DN n  O v , wherein 6.2≤a≤7.2, 2.8≤b≤3.5, 1.2≤c≤2.2, 2.0≤v≤12, and wherein at least one of D 1 , D 2 , . . . , D N  is a metal, N≥0, 0≤d≤0.8, 0≤e≤0.8, and 0≤n≤0.8, and being synthesized by a process, comprising:
 forming a liquid mixture of digitally-controlled stoichiometrically amounts of a lithium-containing salt, a lanthanum-containing salt, a zirconium-containing salt, and one or more inorganic metal salts containing one or more metals D 1 , D 2 , . . . , D N ; 
 mixing the liquid mixture with a first gas flow to form a gas-liquid mixture and jetting a mist of the gas-liquid mixture into a power jetting chamber at high speed; 
 drying the gas-liquid mixture for a first reaction time period of less than 20 min to undergo one or more oxidation reactions by delivering a second gas flow of a heated gas and forming a gas-solid mixture inside the power jetting chamber; 
 delivering the gas-solid mixture out of the power jetting chamber 
 obtaining powdered particles of the ceramic material; and 
 annealing the powdered particles for a second reaction time period of more than 2 hours to undergo a dynamic crystallization process in the presence of a third gas flow and form crystalline products, wherein the crystalline products of the ceramic material are in clusters under scanning electronic microscopy (SEM) analysis. 
   
     
     
         2 . The solid-state electrolyte material of  claim 1 , wherein the process further comprising:
 milling the crystalline products of the ceramic material to obtain nano-sized particles, wherein the tap density of the ceramic material is more than 1.0 g/ml.   
     
     
         3 . The solid-state electrolyte material of  claim 2 , wherein the tap density of the ceramic material is more than 1.4 g/ml after annealing the ceramic material at more than 900° C. at more than 8 hours. 
     
     
         4 . The solid-state electrolyte material of  claim 1 , wherein the second gas flow contains oxygen and the gas-liquid mixture is dried by delivering the second gas flow having a temperature of 200° C. or higher for less than 10 min. 
     
     
         5 . The solid-state electrolyte material of  claim 1 , wherein the powdered particles are annealed in the dynamic crystallization process in the presence of an oxygen gas flow. 
     
     
         6 . The solid-state electrolyte material of  claim 1 , wherein the process further comprising separating the gas-solid mixture to obtain the one or more solid particles of the ceramic material. 
     
     
         7 . The solid-state electrolyte material of  claim 1 , wherein the crystalline products as measured by X-ray diffraction (XRD) analysis are garnet type ceramic material with a cubic structure and its measured ionic conductivity (σ) is larger than 10 −4  S per centimeter at 25° C. 
     
     
         8 . The solid-state electrolyte material of  claim 1 , wherein the crystalline products as measured by X-ray diffraction (XRD) analysis are garnet type ceramic material with a tetragonal structure. 
     
     
         9 . The solid-state electrolyte material of  claim 1 , wherein D 1 , D 2 , . . . , D N  is selected from the group consisting of Al, Ta, Ti, Ge, Mg, Mn, Zr, Zn, Nb, Ce, Sn, Ga, Ba, Ac, Ca, Sc, V, Cr, Fe, Cu, B, As, Hf, Mo, W, Re, Ru, Rh, Pt, Ag, Os, Ir, Au, F, Cl, I, Br, and combinations thereof. 
     
     
         10 . The solid-state electrolyte material of  claim 1 , wherein the ceramic material is selected from the group consisting of Li 7 La 3 Zr 2 O 12 , Li 7 La 3 Zr 2 O 12  doped with one or more metals, Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.24 O 12 , Li 6.5 La 3 Zr 2 Al 0.22 O 12 , Li 6.76 La 2.87 Zr 2.0 Al 0.24 O 12.35 , Li 6.74 La 2.96 Zr 2.0 Al 0.25 O 12.45 , Li 6.27  La 3.22 Zr 2.0 Al 0.3 O 12.39 , Li 6.4 La 2.86 Zr 2.0 Al 0.24 O 11.98 , Li 6.43 La 2.93 Zr 2.0 Al 0.24 O 12.08 , Li 6.32 La 3.2 Zr 2.0 Al 0.46 O 12.9 , Li 6.57 La 2.99 Zr 2.0 Al 0.22 O 12.22 , Li 6.4 La 3 Zr 2 Al 0.2 O 12 , Li 6.54 La 2.82 Zr 2.0 Al 0.24 O 12.08 , Li 6.49 La 3.28 Zr 2.0 Al 0.31 O 12.7 , Li 6.28 La 3 Zr 2 Al 0.24 O 12 , Li 6.25 La 3.01 Zr 2.0 Al 0.22 O 11.92 , Li 6.49 La 3.02 Zr 2.0 Al 0.23 O 12.2 , Li 6.5 La 3 Zr 1.5 Ta 0.5 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Al 0.2 O 12 , Li 6.25 La 3 Zr 2 Al 0.25 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Ga 0.2 O 12 , Li 6.25 La 3 Zr 2 Ta 0.25 Ga 0.2 O 12 , Li 6.4 La 3 Zr 2 Ga 0.2 O 12 , Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 , Li 5 La 3 Nb 2 O 12 , Li 5 La 3 Ta 2 O 12 , Li 5 La 3 Ti 2 O 12 , Li 6 La 3 Sr 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ti 2 O 12 , Li 1.26 La 2.24 Ti 4 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , and combinations thereof. 
     
     
         11 . The solid-state electrolyte material of  claim 1 , wherein the process further comprising:
 sintering the crystalline products of the ceramic material at an annealing temperature of 900° C. or higher to further process the ceramic material; and   measuring the ionic conductivity of the ceramic material.   
     
     
         12 . The solid-state electrolyte material of  claim 1 , wherein the SPAN value (D 90 −D 10 )/D 50  of the crystalline products after annealing is 0.8<SPAN≤1.7. 
     
     
         13 . The solid-state electrolyte material of  claim 1 , wherein the SPAN value (D 90 −D 10 )/D 50  of the crystalline products after annealing is 0.8<SPAN≤1.0. 
     
     
         14 . The solid-state electrolyte material of  claim 1 , wherein the D 90  of the crystalline products after annealing are at between 20 μm and 40 μm, the D 10  are between 3 μm and 10 μm, the D 99  are between 35 μm and 60 μm, and the D 1  are between 0.1 μm and 3 μm. 
     
     
         15 . The solid-state electrolyte material of  claim 1 , wherein the D 50  of the crystalline products after annealing is between 10 μm and 18 μm. 
     
     
         16 . The solid-state electrolyte material of  claim 1 , wherein the lithium-containing salt is selected from a group consisting of lithium sulfate (Li 2 SO 4 ), lithium nitrate (LiNO 3 ), lithium carbonate (Li 2 CO 3 ), lithium acetate (LiCH 2 COO), lithium hydroxide (LiOH), lithium formate (LiCHO 2 ), lithium chloride (LiCl), and combinations thereof. 
     
     
         17 . The solid-state electrolyte material of  claim 16 , wherein the lithium-containing salt, the lanthanum-containing salt, the zirconium-containing salt, and the one or more inorganic metal salts are of the same type of acid salts. 
     
     
         18 . The solid-state electrolyte material of  claim 1 , wherein one of the one or more inorganic metal salts is selected from a group consisting of metal sulfate, metal phosphate, metal nitrate, metal carbonate, metal acetate, metal hydroxide, metal halogen compounds, formate, metal chloride, metal bromide, metal iodide, metal fluoride, and combinations thereof. 
     
     
         19 . A solid-state electrolyte material, comprising,
 a ceramic material having a chemical composition of Li a  La b  Zr c Al d  D1 e  . . . DN n  O v , wherein 6.2≤a≤7.2, 2.8≤b≤3.5, 1.2≤c≤2.2, 2.0≤v≤12, and wherein at least one of a 1 , . . . , D N  is a metal, N≥0, 0≤d≤0.8, 0≤e≤0.8, and 0≤n≤0.8, and being synthesized by a process, comprising:
 forming a liquid mixture of digitally-controlled stoichiometrically amounts of a lithium-containing salt, a lanthanum-containing salt, a zirconium-containing salt, and one or more inorganic salts containing one or more metals D 1 , D 2 , . . . , D N ; 
 jetting a mist of the liquid mixture by mixing the liquid mixture with a first gas flow into a power jetting chamber at high speed to form a gas-liquid mixture; 
 drying the gas-liquid mixture for a first reaction time period of less than 20 min to undergo one or more oxidation reactions by delivering a second gas flow of a heated gas and forming a gas-solid mixture inside the power jetting chamber; 
 delivering the gas-solid mixture out of the power jetting chamber 
 obtaining powdered particles of the ceramic material; and 
 annealing the powdered particles for a second reaction time period of more than 2 hours to undergo a dynamic crystallization process in the presence of a third gas flow and form crystalline products, wherein the crystalline products of the ceramic material are in clusters under scanning electronic microscopy (SEM) analysis. 
   
     
     
         20 . The solid-state electrolyte material of  claim 1 , wherein the ceramic material is selected from the group consisting of Li 7 La 3 Zr 2 O 12  doped with one or more metals, Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.24 O 12 , Li 6.5 La 3 Zr 2 Al 0.22 O 12 , Li 6.76 La 2.87 Zr 2.0 Al 0.24 O 12.35 , Li 6.74 La 2.96 Zr 2.0 Al 0.25 O 12.45 , Li 6.27  La 3.22 Zr 2.0 Al 0.3 O 12.39 , Li 6.4 La 2.86 Zr 2.0 Al 0.24 O 11.98 , Li 6.43 La 2.93 Zr 2.0 Al 0.24 O 12.08 , Li 6.32 La 3.2 Zr 2.0 Al 0.46 O 12.9 , Li 6.57 La 2.99 Zr 2.0 Al 0.22 O 12.22 , Li 6.4 La 3 Zr 2 Al 0.2 O 12 , Li 6.54 La 2.82 Zr 2.0 Al 0.24 O 12.08 , Li 6.49 La 3.28 Zr 2.0 Al 0.31 O 12.7 , Li 6.28 La 3 Zr 2 Al 0.24 O 12 , Li 6.25 La 3.01 Zr 2.0 Al 0.22 O 11.92 , Li 6.49 La 3.02 Zr 2.0 Al 0.23 O 12.2 , Li 6.5 La 3 Zr 1.5 Ta 0.5 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Al 0.2 O 12 , Li 6.25 La 3 Zr 2 Al 0.25 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Ga 0.2 O 12 , Li 6.25 La 3 Zr 2 Ta 0.25 Ga 0.2 O 12 , Li 6.4 La 3 Zr 2 Ga 0.2 O 12 , Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 , Li 5 La 3 Nb 2 O 12 , Li 5 La 3 Ta 2 O 12 , Li 5 La 3 Ti 2 O 12 , Li 6 La 3 Sr 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ti 2 O 12 , Li 1.26 La 2.24 Ti 4 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , and combinations thereof. 
     
     
         21 . A solid-state electrolyte material, comprising,
 a ceramic material selected from the group consisting of Li 7 La 3 Zr 2 O 12 , Li 7 La 3 Zr 2 O 12  doped with one or more metals, Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.25 O 12 , Li 6.5 La 3 Zr 2 Al 0.24 O 12 , Li 6.5 La 3 Zr 2 Al 0.22 O 12 , Li 6.76 La 2.87 Zr 2.0 Al 0.24 O 12.35 , Li 6.74 La 2.96 Zr 2.0 Al 0.25 O 12.45 , Li 6.27 La 3.22 Zr 2.0 Al 0.3 O 12.39 , Li 6.4 La 2.86 Zr 2.0 Al 0.24 O 11.98 , Li 6.43 La 2.93 Zr 2.0 Al 0.24 O 12.08 , Li 6.32 La 3.2 Zr 2.0 Al 0.46 O 12.9 , Li 6.57 La 2.99 Zr 2.0 Al 0.22 O 12.22 , Li 6.4 La 3 Zr 2 Al 0.2 O 12 , Li 6.54 La 2.82 Zr 2.0 Al 0.24 O 12.08 , Li 6.49 La 3.28 Zr 2.0 Al 0.31 O 12.7 , Li 6.28 La 3 Zr 2 Al 0.24 O 12 , Li 6.25 La 3.01 Zr 2.0 Al 0.22 O 11.92 , Li 6.49 La 3.02 Zr 2.0 Al 0.23 O 12.2 , Li 6.5 La 3 Zr 1.5 Ta 0.5 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Al 0.2 O 12 , Li 6.25 La 3 Zr 2 Al 0.25 O 12 , Li 6.15 La 3 Zr 1.75 Ta 0.25 Ga 0.2 O 12 , Li 6.25 La 3 Zr 2 Ta 0.25 Ga 0.2 O 12 , Li 6.4 La 3 Zr 2 Ga 0.2 O 12 , Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 , Li 5 La 3 Nb 2 O 12 , Li 5 La 3 Ta 2 O 12 , Li 5 La 3 Ti 2 O 12 , Li 6 La 3 Sr 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ta 2 O 12 , Li 6 La 3 Ba 1 Ti 2 O 12 , Li 1.26 La 2.24 Ti 4 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.36 La 2.24 Ti 4 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , Li 1.72 La 2.24 Ti 3.8 Ge 0.2 O 12 , and combinations thereof, and being synthesized by a process, comprising:
 forming a liquid mixture of digitally-controlled stoichiometrically amounts of a lithium-containing salt, a lanthanum-containing salt, a zirconium-containing salt, and one or more inorganic salts containing one or more metals D 1 , D 2 , . . . , D N ; 
 jetting a mist of the liquid mixture into a power jetting chamber to be mixed with a first gas flow to form a gas-liquid mixture; 
 drying the lithium-containing salt, the lanthanum-containing salt, the zirconium-containing salt together for a first reaction time period of less than 20 min to undergo one or more oxidation reactions by delivering a second gas flow of a heated gas and form powdered particles of the ceramic material; and 
 annealing the powdered particles for a second reaction time period of more than 2 hours to undergo a dynamic crystallization process in the presence of a third gas flow and form crystalline products of the ceramic material, wherein the final crystalline products of the ceramic material are in clusters under scanning electronic microscopy (SEM) analysis, and wherein the crystalline products of as measured by X-ray diffraction (XRD) analysis are garnet type ceramic material with a cubic structure and its measured ionic conductivity (σ) is larger than 10 −4  S per centimeter at 25° C.