Patent Application
20110274850
1. Field of the Invention
Embodiments of the present invention relate generally to lithium-ion batteries, and more specifically, to a method of fabricating such batteries using thin-film deposition processes.
2. Description of the Related Art
Fast-charging, high-capacity energy storage devices, such as supercapacitors and lithium (Li) ion batteries, are used in a growing number of applications, including portable electronics, medical devices, transportation, grid-connected large energy storage, renewable energy storage, and uninterruptible power supplies (UPS). In modern rechargeable energy storage devices, the current collector is made of an electric conductor. Examples of materials for the positive current collector (the cathode) include aluminum, stainless steel, and nickel. Such collectors can be in the form of a foil, a film, or a thin plate, having a thickness that generally ranges from about 6 to 50 μm.
The active electrode material in the positive electrode of a Li-ion battery is typically selected from lithium transition metal oxides, such as LiFePO4, LiMn2O4, LiCoO2, LiNiO2, or combinations of Li, Ni, Mn, and Co oxides and includes electroconductive particles, such as carbon black or graphite, and a binder material. Such positive electrode material is considered to be a lithium-intercalation compound, in which the quantity of conductive material is in the range from 0.1% to 15% by weight.
The active materials are dispersed in a polymeric binder matrix and then applied to the current collector. The polymers for the binder matrix are made of thermoplastic polymers including polymers with rubber elasticity. The polymeric binder serves to bind together the cathode active materials to preclude crack formation and prevent disintegration of the active materials on the surface of the current collector. The quantity of polymeric binder is in the range of 0.5% to 30% by weight.
Current manufacturing techniques for forming cathodes are both energy and time consuming. The synthesis of active material in present methods requires high temperature and harsh reaction conditions. Synthesis of the active material may also take several hours to several days to complete. Once synthesis of the active material is complete, the active material is combined with conductive additives, binders, and toxic and expensive solvents to make a slurry. The slurry is then deposited onto the positive current collector. The slurry coated on the current collector needs to go through a long and energy intensive drying process. Drying lines created to complete the drying of the slurry can be quite long depending on the output of the synthesis and deposition processes.
Accordingly, there is a need in the art for systems and methods which can quickly and more energy efficiently produce cathodes for energy storage devices.
In one embodiment, an apparatus for continuously forming an electrochemical film on a substrate is disclosed. The apparatus generally includes at least one precursor supply, a reaction chamber, and a spray chamber. The reaction chamber generally includes a chamber tube having an inlet fluidly coupled to the at least one precursor supply, an energy applicator positioned to operatively energize precursors in the chamber tube, and an energy source coupled to the energy applicator. The spray chamber is fluidly coupled to an outlet of the chamber tube.
In another embodiment, a method of continuously forming a layer on a substrate is disclosed. The method generally includes flowing one or more precursors into a reactor chamber continuously, coupling energy with the one or more precursors continuously to form crystals of active material, continuously passing a substrate through a spray chamber, and spraying the active material continuously into the spray chamber to deposit a layer of the active material onto the substrate.
So that the manner in which the above-recited features of the present inventions can be understood in detail, a more particular description of the inventions, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings. It is to be noted, however, that the appended drawings illustrate only typical embodiments of these inventions and are therefore not to be considered limiting of its scope, for the inventions may admit to other equally effective embodiments.
To facilitate understanding, identical reference numerals have been used, where possible, to designate identical elements that are common to the figures. It is contemplated that elements disclosed in one embodiment may be beneficially utilized on other embodiments without specific recitation.
Embodiments disclosed herein generally provide methods and apparatus for continuously forming a film on a substrate. In one embodiment, the film may be an electrochemical film for a thin-film battery, such as a Li-ion battery. Other applications include fuel cell manufacturing, semiconductor manufacturing, and solar cell manufacturing. A precursor or mixture of precursors of specific compounds is provided to a reactor chamber where energy is applied to carry out reactions. The specific compounds, when reacted, become an electrochemically active material. The precursors may be particles suspended in a carrier medium or dissolved solutions. The active material synthesis produces nano- or micro-crystals, which may then be sprayed to form a layer or film on the substrate surface.
The anode structure 102 and the cathode structure 103 each serve as a half-cell of the Li-ion battery 100 and together form a complete working cell of the Li-ion battery 100. The anode structure 102 includes the current collector 111, or negative electrode, and a material layer 110, such as a carbon-based intercalation host material for hosting lithium ions. Similarly, the cathode structure 103 includes the current collector 113, or positive electrode, and a second material layer 112, such as a metal oxide, consisting of an electrochemically active material combined with other conductive materials which are suspended in a binder. The material layer 112 may also be a host for lithium ions since lithium ions may pass from the anode structure 102 to the cathode structure 103 during discharging of the Li-ion battery 100. The current collectors 111 and 113 are made of electrically conductive material, such as a metal. The separator layer 104, which is electron insulating, porous, and fluid-permeable, is used to prevent direct electrical contact between the components in the anode structure 102 and the cathode structure 103.
The electrochemically active material of the material layer 112 in the cathode structure 103 may be made from layered oxides, such as lithium cobalt oxide, an olivine, such as lithium iron phosphate, or a spinel, such as lithium manganese oxide, or a mixture thereof. In non-lithium embodiments, an exemplary cathode may be made from TiS2 (titanium disulfide). Exemplary lithium-containing oxides may be layered lithium cobalt oxide, or a mixed metal oxide, such as LiNixCO1-2xMnO2, where x is in a range between 0 and 0.5, or a spinel such as LiMn2O4. Other exemplary mixed metal oxides are LiNi0.8CO0.15Al0.05O2 and LiNixMnyCOzO2, where x, y, and z are between 0 and 1. Exemplary phosphates may be iron olivine (LiFePO4) and its variants (such as LiFe1-xMgPO4, where x is in a range between 0 and 1), LiMoPO4, LiCoPO4, LiNiPO4, Li3V2(PO4)3, LiVOPO4, LiMP2O7, or LiFe1.5P2O7. Exemplary fluorophosphates may be LiVPO4F, LiAlPO4F, Li5V(PO4)2F2, Li5Cr(PO4)2F2, Li2CoPO4F, or Li2NiPO4F. Exemplary silicates may be Li2FeSiO4, Li2MnSiO4, or Li2VOSiO4. An exemplary non-lithium compound is Na5V2(PO4)2F3.
The material layer 110 in the anode structure 102 may be made from graphitic microbeads dispersed in a polymer matrix. Additionally, microbeads or alloys of silicon, tin, or lithium titanate (Li4Ti5O12) may be used with, or instead of, graphitic microbeads to provide the conductive core anode material.
Referring additionally to
The precursor and carrying medium mixture, hereafter “slurry”, is supplied from the mixer 303 to a reaction chamber 319 at box 202 of the method 200. The reaction chamber 319 may include a chamber tube 304, having an inlet 322 and an outlet 323, surrounded by an energy applicator 305, as seen in
At box 203 of the method 200, the slurry is energized to synthesize an active material. The energy excites thermal motion of atoms in the particles dispersed in the slurry causing them to move to preferentially find lower energy crystal lattice positions. The active material may be, but is not limited to, any of the active materials for the material layers 110, 112 listed above. Energy source 306 supplies energy to the energy applicator 305 which evenly distributes the energy across the chamber tube 304. The supplied energy may be microwave energy, ultrasonic energy, DC voltage, RF energy, or combinations thereof. The energy may be applied in two phases. For example, RF energy may be applied in a first phase, and then microwave energy may be applied in a second phase. The energy may be applied through a combination of means, such as electrical and thermal means. Conditions within the chamber tube 304 during energization of the slurry may need to be varied. A regulator valve 312 may be utilized to maintain the pressure within the chamber tube 304 between a range of 10 bar and 100 bar, for example, between 20 bar and 80 bar, to prevent damage to the chamber tube 304 due to expansion of the slurry while heating.
Particles of active material may be synthesized at box 203 of the method 200 to be of a controlled size and morphology. The size and morphology of the active particles may be controlled by controlling at least on of the slurry flow rate into the chamber tube 304, the pressure inside the chamber tube 304, the amount of energy provided by the energy source 306 to the slurry, or other variables, such as carbon content in the slurry, for example. The precursor combination or concentration of each precursor and the carrying medium may also be varied to achieve different targets in size of the particles or composition of the active material. Slurry passing through the chamber tube 304 may be energized continuously so as to provide a continuous production of activate material for use in the method 200. The particles of active material, which may be nano- or micro-particles or crystals, may have a flake or needle shape, and have a size between about 10 nm and 20000 nm, for example between about 75 nm and 750 nm, or between about 90 nm and 500 nm. The particles of active material may optionally have a [020] crystal surface texture. The particles of active material may also have a conductive coating, such as a carbon coating, upon exiting the chamber tube 304. The carbon coating may be between 1 nm and 25 nm thick, such as for example between 5 nm and 10 nm thick. The active material synthesized may be one of the exemplary electrolyte containing materials described above.
In one embodiment, an optional binding agent may be supplied from a binder supply 307 to a mixer 308, for example by one of the pumps 360, where the binding agent is mixed with the active material mixture exiting the chamber tube 304, as seen in
At box 204 of the method 200, the active material may be sprayed toward a substrate 310 to form a layer of the active materials thereon. If a binder material is used, the active material and binder are both deposited onto the substrate, and the binder material is evenly distributed within the active material. The substrate 310 may consist of a sheet or roll of current collecting material, such as for example copper or aluminum. The substrate 310 may also have raised structures, such as a mesh, to enhance the interface between the active materials and the substrate 310. The substrate 310 may be transported through a spray chamber 309 and under a spray nozzle 318 on rollers (not shown). The substrate 310 may be on a roll (not shown) and may be placed on another roll (not shown) after passing through the spray chamber. The spray nozzle 318 may be attached to an upper portion of a chamber body 321 of the spray chamber 309. In one embodiment, the spraying method employed is that of a plasma spray, such as a DC plasma spray or an RF inductive plasma spray, where the material is carried by a jet of plasma toward the substrate and deposited.
During the spray process, the added carbon-containing material may be bonded to the crystals of active material and form a thin carbon layer. The thin carbon layer may assist in creating a conductive connection to the substrate 310 and may be between 5 nm and 10 nm thick. The crystals of active material may also be at least partially coated in a thin carbon layer after exiting the reaction chamber 319 if a carbon-containing compound is added to the carrying medium. The layer of active material deposited onto the substrate 310 may contain crystals of active material where each crystal of active material coated in a thin carbon film. The crystals may be in contact with each other and at least a portion of the crystals, and the thin carbon film, are in contact with the substrate 310. The layer of active material may also contain a binder material distributed between the active material crystals to bind the crystals of active material together and to bind the layer of active material to the substrate. The binder material may be distributed in such a way as to allow contact between the crystals of active material and to allow contact of the crystals of active material with the substrate 310.
The carrying medium in the active material mixture may be a liquid that is atomized upon entering the spray chamber 309. The carrying medium may also be selected to nucleate around the active material particles to reduce attachment to the walls of the spray chamber 309. The substrate 310 may optionally pass through the spray chamber 309 a second time to coat the opposite side of the substrate 310 with the active materials.
The spray nozzle 318 may consist of one or more spray nozzles arranged in an array. The array may be configured to effectively cover a width of the passing substrate 310 by placing multiple nozzles side by side in a direction perpendicular to the direction of travel of the substrate 310. It may be beneficial to build multiple or thicker layers of active material onto the substrate 310. The spray nozzle 318 may consist of one or more nozzles positioned one behind the other in a direction parallel to the direction of travel of the substrate 310 in order to deposit a thicker layer of the active materials. The rate at which the substrate 310 travels through the spray chamber 309 may also be varied to alter the thickness of the active material layer being deposited onto the substrate 310. In another embodiment, a second spray nozzle (not shown) or nozzle array may be positioned within the spray chamber 309 and underneath the substrate 310 in order to spray the bottom of the substrate 310.
The use of a second spray nozzle 320, in combination with the spray nozzle 318, may allow for simultaneous spraying of the top and bottom of the substrate as it passes through the spray chamber 309, as seen in
The active material mixture may be sprayed at a rate between 1 ml/min and 5000 ml/min, such as for example between 1 ml/min and 15 ml/min, or between about 2 ml/min and 10 ml/min, from spray nozzle 318 or each spray nozzle in the array of spray nozzles. The conditions within the spray chamber may be controlled such that the pressure within the chamber is between 1 Torr and 125 Torr, such as for example between 5 Torr and 100 Torr, and the temperature is between 100° C. and 1500° C., such as for example between 200° C. and 1000° C.
Optionally, as seen in
The active material synthesis methods described effectively and efficiently produce active materials for the creation of energy storage devices.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow.
This application claims benefit of U.S. provisional patent application Ser. No. 61/331,635 (Attorney Docket No. 15013L), filed May 5, 2010, which is herein incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61331635 | May 2010 | US |
