Solid composite electrode with coated materials

Abstract

A solid-state composite electrode includes active electrode particles, ionically conductive particles, and electrically conductive particles. Each of the ionically conductive particles is at least partially coated with an isolation material that inhibits inter-diffusion of the ionically conductive particles with the active electrode particles. A battery cell includes a first current collector, a solid electrolyte layer, a first solid-state composite electrode having ionically conductive particles coated with an isolation material and positioned between the first current collector and the solid electrolyte layer, a second current collector, and a second electrode positioned between the solid electrolyte layer and the second current collector. A method of forming a solid-state composite electrode includes mixing together active electrode particles and electrically conductive particles with ionically conductive particles that are each at least partially coated with an isolation material. The mixture is formed into a film via tape-casting, and sintered at a temperature greater than 600° C.

Claims

1. A method of forming a solid-state composite electrode, comprising: mixing together particles of an active electrode material, particles of an ionically conductive material, and particles of an electrically conductive material, wherein each of the particles of the ionically conductive material is at least partially coated with an isolation material configured to inhibit inter-diffusion of the active electrode material with the ionically conductive material to form a mixture; mixing a polymer binder together with the mixture of the particles of the active electrode material, the particles of the ionically conductive material, and the particles of the electrically conductive material; forming the mixture mixed with the polymer binder into a film via a tape-casting process; heating the film to 500° C. or greater in an oxygen containing atmosphere until the polymer binder is at least substantially burned off; and sintering the film, after the polymer binder is at least substantially burned off, at a temperature greater than 600° C. to form a solid-state composite electrode.

2. The method of claim 1, wherein the coating of the isolation material on each of the particles of the ionically conductive material is formed via: a gel coating process; or a pulsed laser deposition process.

3. The method of claim 1, wherein the sintering is a co-sintering process that includes sintering the film with at least one of: (i) particles for forming a solid electrolyte layer, or particles for forming a solid electrolyte layer and a film for forming a further solid-state composite electrode; and (ii) at least one current collector.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 depicts a plan schematic of a conventional composite solid-state electrode.

(2) FIG. 2 depicts a detail schematic of an interface between particles of the electrode of FIG. 1.

(3) FIG. 3 depicts a plan schematic of an exemplary embodiment of a composite solid-state electrode with particles having an isolation coating.

(4) FIG. 4 depicts a detail schematic of an interface between particles of the electrode of FIG. 3.

(5) FIGS. 5, 6a, and 6b depict different exemplary embodiments of a composite solid-state electrode with particles having an isolation coating.

(6) FIGS. 7 and 8 depict flow diagrams of different exemplary embodiments of methods of applying an isolation coating to particles for a composite solid-state electrode.

(7) FIGS. 9 and 10 depict flow diagrams of different exemplary embodiments of methods of forming a composite solid-state electrode with particles having an isolation coating.

(8) FIG. 11 depicts an exemplary embodiment of a cell that includes a composite solid-state electrode with particles having an isolation coating.

DETAILED DESCRIPTION

(9) For the purposes of promoting an understanding of the principles of the embodiments described herein, reference is now made to the drawings and descriptions in the following written specification. No limitation to the scope of the subject matter is intended by the references. This disclosure also includes any alterations and modifications to the illustrated embodiments and includes further applications of the principles of the described embodiments as would normally occur to one skilled in the art to which this document pertains.

(10) FIG. 3 depicts a plan schematic of an exemplary embodiment of a solid state composite electrode 100 according to this disclosure. The electrode includes particles of active material 102, particles of ionically conductive material 104, and particles of electronically conductive material 106. The particles 102-106 are held together in close contact as a result of a sintering process.

(11) In some embodiments, the electrode 100 is a cathode, and the active material particles 102 include any acceptable cathode material such as, for example, a nickel-cobalt-magnesium-oxide material, a nickel-cobalt-aluminum-oxide material, a lithium-cobalt-oxide material, a lithium-iron-phosphate material, a lithium-titanium-oxide material, sulfide-based materials, spinel materials, and combinations thereof. In some embodiments, the electrode 100 is an anode, and the active material particles 102 include any acceptable anode material such as, for example, lithium titanate.

(12) Any acceptable solid electrolyte material is usable as the ionically conductive material for the ionically conductive particles 104 such as, for example, Li.sub.7La.sub.3Zr.sub.2O.sub.12 (also known as “LLZO”), a lithium aluminum titanium phosphate material, a lithium lanthanum titanate material, or combinations thereof. Any acceptable electrically conductive material is usable for the particles of electronically conductive material 106 such as, for example, a graphite material, an oxide material such as TiO.sub.2, SnO.sub.2, In.sub.2O.sub.3, ZnO, and ITO, or combinations thereof.

(13) Each of the particles of active material 102 includes an isolation coating 108. The coating 108 is formed from a material or materials that, when located between the active material of the particles 102 and the ionically conductive material for the particles 104, inhibits intermixing of the active material and the ionically conductive material. Additionally, the material of the coating 108 does not intermix with either of the active material of the particles 102 or the ionically conductive material of the particles 104. In particular, the coating 108 inhibits inter-diffusion during high temperatures, such as during a sintering process. In some embodiments, inhibiting of intermixing and/or inter-diffusion of the active material and the ionically conductive material reduces interfacial impedance between the active material and the ionically conductive material relative to conventional electrodes. In some embodiments, inhibiting intermixing and/or inter-diffusion improves power capability during discharge relative to conventional electrodes.

(14) In some embodiments, the coating 108 is formed from at least one of LiBO.sub.3, Li.sub.4SiO.sub.4, Li.sub.3PO.sub.4, or the like. In some embodiments, the coating material is a mixture of approximately 60% Li.sub.4SiO.sub.4 and approximately 40% Li.sub.3PO.sub.4 by weight. Other materials are used for the coating 108 in other embodiments. In some embodiments, the coating 108 on each of the particles 102 has a thickness that is less than or equal to 1,000 nanometers. In some embodiments, the thickness of the coating 108 is less than or equal to 100 nanometers. Other thicknesses are used in other embodiments.

(15) In some embodiments, each of the particles 102 is at least partially coated with the isolation coating 108. In some embodiments, each of the particles 102 is at least substantially coated with the isolation coating 108. In some embodiments, each of the particles 102 is completely coated with the isolation coating 108.

(16) FIG. 4 depicts a detail schematic of an interface 110 between an active material particle 102′ and an ionically conductive particle 104′ after having been sintered together. The isolation coating 108′ on the active material particle 102′ causes a reduction in inter-diffusion present between the active material of the particle 102′ and the ionically conductive material of the particle 104′ relative to the inter-diffusion depicted in FIG. 2. In the embodiment depicted in FIG. 4, the isolation coating 108′ completely inhibits inter-diffusion between the active material of the particle 102′ and the ionically conductive material of the particle 104′.

(17) While the embodiment in FIGS. 3 and 4 includes an isolation coating 108 on the particles of active material 102, in other embodiments, an isolation coating is included on other particles in addition to or instead of the active particles. FIG. 5 depicts another exemplary embodiment of a solid state composite electrode 500. The electrode includes particles of active material 502, particles of ionically conductive material 504, and particles of electronically conductive material 506. The particles 502-506 are held together in close contact as a result of a sintering process. In this embodiment, each of the particles of ionically conductive material 504 includes an isolation coating 508.

(18) FIG. 6a depicts a further exemplary embodiment of a solid state composite electrode 600. The electrode includes particles of active material 602, particles of ionically conductive material 604, and particles of electronically conductive material 606. The particles 602-606 are held together in close contact as a result of a sintering process. In this embodiment, each of the particles of active electrode material 602 includes an isolation coating 608, and each of the particles of ionically conductive material 604 includes an isolation coating 608′.

(19) In some embodiments, the isolation coating 608 is the same as the isolation coating 608′. In some embodiments, the isolation coating 608 and the isolation coating 608′ include different materials. In some embodiments, each of the particles 602 and 604 is at least partially coated with the isolation coating 608. In some embodiments, each of the particles 602 and 604 is at least substantially coated with the isolation coating 608. In some embodiments, each of the particles 602 and 604 is completely coated with the isolation coating 608.

(20) FIG. 6b depicts a further exemplary embodiment of a solid state composite electrode 601. The electrode includes particles of active material 602, particles of ionically conductive material 604, and particles of electronically conductive material 606′. The particles 602, 604, and 606′ are held together in close contact as a result of a sintering process. In this embodiment, each of the particles of active electrode material 602 includes an isolation coating 608, each of the particles of ionically conductive material 604 includes an isolation coating 608′, and each of the particles of electronically conductive material 606′ includes an isolation coating 608″.

(21) In some embodiments, the isolation coatings 608, 608′, and 608″ are the same. In some embodiments, the isolation coatings 608, 608′, and 608″ include different materials. In some embodiments, each of the particles 602, 604, and 606′ is at least partially coated with the isolation coating 608. In some embodiments, each of the particles 602, 604, and 606′ is at least substantially coated with the isolation coating 608. In some embodiments, each of the particles 602, 604, and 606′ is completely coated with the isolation coating 608.

(22) FIG. 7 depicts a flow diagram of an exemplary method 700 for producing particles with an isolation material at least partially coated each particle via a gel coating process. The method starts at block 702. At block 704, precursor solutes for forming an isolation coating are added with a cross-linking agent to a solvent to form a solution. In some embodiments where the isolation coating includes a mixture of 60% by weight Li.sub.4SiO.sub.4 and 40% by weight Li.sub.3PO.sub.4, the precursor solutes include approximately stoichiometric amounts of a lithium precursor and a phosphate precursor. In some embodiments, the lithium precursor is CH.sub.3COOLi or Li acetyl actonate. In some embodiments, the phosphate precursor is H.sub.3PO.sub.4 or NH.sub.42H.sub.2PO.sub.4. In some embodiments, the cross-linking agent is Si(OC.sub.2H.sub.5).sub.4. In some embodiments, the solvent is ethanol, water, or combinations thereof. Other materials for the precursor solutes, the cross-linking agent, and the solvent are used in other embodiments.

(23) At block 706, the solution is formed into a gel, i.e., a sol solution. Any acceptable method of forming a gel is usable. In some embodiments, forming the gel includes resting the solution for a period of time such as, for example, 24-48 hours, to enable sedimentation of the solution to occur, and draining off excess liquid after the resting. In some embodiments, forming the gel includes using a centrifuge. In some embodiments, forming the gel includes a drying process to remove excess liquid.

(24) At block 708, particles to be coated are mixed into the gel. In various embodiments, the particles are particles of active electrode material, particles of ionically conductive material, particles of electrically conductive material, and combinations thereof. At block 710, the mixture is stirred and heated to about 60-80° C. until the solvent is at least substantially evaporated away. In some embodiments, the solvent is completely evaporated away. At block 712, the resulting mixture is heated to at about 650-850° C. for about 24-48 hours to form particles that are each at least partially coated with the isolation coating. In some embodiments, the particles are at least substantially coated with the isolation coating. In some embodiments, the particles are completely coated with the isolation coating. In some embodiments, the particles are completely coated with the isolation coating. In some embodiments, the coating on the particles is substantially uniform. The method ends at block 714.

(25) FIG. 8 depicts a flow diagram of another exemplary method 800 for producing particles with an isolation coating on each particle via a pulsed laser deposition process. The method starts at block 802. At block 804, precursor solutes for forming an isolation coating are added with a cross-linking agent to a solvent to form a solution. At block 806, the solution is formed into a gel. At block 808, the solution is stirred and heated to about 60-80° C. until the solvent is completely evaporated away. At block 810, the resulting mixture is heated to at about 650-850° C. for 24-48 hours to form a fine powder. At block 812, the powder is pressed into pellets and sintered at 1000° C. for 1 hour. At block 814, the resulting sintered pellets are used as targets to prepare an isolation coating on particles using a pulsed-laser-deposition process to form an isolation coating on the particles. In various embodiments, the particles are particles of active electrode material, particles of ionically conductive material, particles of electrically conductive material, or combinations thereof. In some embodiments, the particles are at least substantially coated with the isolation coating. In some embodiments, the particles are completely coated with the isolation coating. In some embodiments, the particles are completely coated with the isolation coating. In some embodiments, the coating on the particles is substantially uniform. The method ends at block 816.

(26) Other methods to apply the isolation coating to the particles of active electrode material are also contemplated in other embodiments, such as atomic layer deposition, chemical vapor deposition, and sputtering, for example.

(27) FIG. 9 depicts an exemplary embodiment of a method 900 for forming an electrode that includes particles with an isolation coating. The method begins at block 902. At block 904, particles of active electrode material and particles of ionically conductive material, at least one of which has an isolation coating, are mixed together with particles of an electronic conductor. In some embodiments, the electronic conductor is graphite. In some embodiments, the particles of the electronic conductor also have an isolation coating. At block 906, the mixture is formed into a film via a tape-casting process. In some embodiments, the tape-casting process is binder free. At block 908, the film is sintered at a temperature greater than 600° C. to form an electrode. The method ends at block 910.

(28) FIG. 10 depicts another exemplary embodiment of a method 1000 for forming an electrode that includes particles with an isolation coating. The method starts at block 1002. At block 1004, particles of active electrode material and particles of ionically conductive material, at least one of which has an isolation coating, are mixed together with a polymer binder and particles of an electronically conductive oxide such as, for example, TiO.sub.2, SnO.sub.2, In.sub.2O.sub.3, ZnO, and ITO, or combinations thereof. In some embodiments, the particles of the electronically conductive material also include an isolation coating. At block 1006, the mixture is formed into a film via a tape-casting process. At block 1008, the film is heated to 500° C. or greater in an oxygen containing atmosphere until the polymer binder is at least substantially burned off. At block 1010, the film is sintered at a temperate greater than 600° C. to form an electrode. The method ends at block 1012.

(29) FIG. 11 depicts a cell 1100 that includes an electrode 1102 similar in structure to one of the electrode embodiments from FIGS. 3, 5, and 6. In other words, the electrode 1102 is a composite electrode including particles of active electrode material and particles of ionically conductive material, at least one of which has an isolation coating, as well as particles of an electronic conductor. The cell 1100 additionally includes a first current collector 1104, a solid electrolyte layer 1106, a second electrode 1108, and a second current collector 1110.

(30) The electrode 1102 is disposed between the first current collector 1104 and the solid electrolyte layer 1106. The solid electrolyte layer 1106 separates the electrode 1102 from the second electrode 1108. The second electrode 1108 is disposed between the solid electrolyte layer 1106 and the second current collector 1110.

(31) Any acceptable current collector is usable as the first current collector 1104 or the second current collector 1110 such as, for example a metal grid or foil. Any acceptable material is usable to form such a collector such as, for example, aluminum, lithium, steel, copper, iron-nickel alloy, or combinations thereof.

(32) In this embodiment, the solid electrolyte layer 1106 is formed from particles of the same type of material forming the ionically conductive particles in the electrode 1102. Using the same types of materials for the ionically conductive particles in the electrode 1102 and the solid electrolyte layer 1106 enables a homogeneous solid-solid interface between the ionically conductive particles in the electrode 1102 and similar particles in the solid electrolyte layer 1106. In some embodiments, the material or materials forming the solid electrolyte layer 1106 are different from the ionically conductive particles in the electrode 1102.

(33) In some embodiments, two or more of the electrode 1002, solid electrolyte layer 1106, and second electrode 1108 are co-sintered. In some embodiments, materials for the electrode 1102, solid electrolyte layer 1106, and second electrode 1108 are assembled between the current collectors 1104 and 1110, and the assembly is then sintered to form the cell 1100. In some embodiments, one or more of the electrode 1102, solid electrolyte layer 1106, and second electrode 1108 are separately produced and assembled together to form the cell 1100 by any acceptable process such as, for example, a cold-press process.

(34) In some embodiments, the electrode 1102 is a positive electrode, and the second electrode 1108 is a negative electrode. In some embodiments, the electrode 1102 is a negative electrode, and the second electrode 1108 is a positive electrode. In some embodiments, the second electrode 1108 is a composite electrode similar to the electrode 1102. In some embodiments, the second electrode 1108 is not a composite electrode, whereby any acceptable electrode is usable such as, for example, a lithium-based electrode as a negative electrode.

(35) It will be appreciated that variants of the above-described and other features and functions, or alternatives thereof, may be desirably combined into many other different systems, applications or methods. Various presently unforeseen or unanticipated alternatives, modifications, variations or improvements may be subsequently made by those skilled in the art that are also intended to be encompassed by the foregoing disclosure.