Patent Application
20200005997
The present invention relates to permanent magnets, and more particularly, this invention relates to methods of producing permanent magnets using electrophoretic deposition techniques.
In modern technology, permanent magnets are essential for energy efficient, lightweight devices such as cell phones, ear buds, and laptops, and are essential in larger quantities (e.g. kilogram to ton quantities) for high efficiency and renewable energy applications such as wind turbines, electric drive, and hybrid motors. The use of permanent magnets in electric motors provides high efficiency in a significantly smaller mass and volume. In the United States, electric motors consume approximately 15% of total electricity usage. Thus, even small increases in electrical motor efficiency have a sizable impact on reduced energy costs and reduced CO2 emissions. For example, a 1% efficiency improvement may translate into savings of hundreds of millions of dollars and a reduction of 2.2 million metric tons of CO2 emissions per year.
Permanent magnets may be graded for merit according to a measure of (BH)max energy product which represents maximum usable energy stored in the magnet. The energy product is a combination of the remanent magnetization (Mr), the magnetism retained absent an external magnetic field (total magnetic moment divided by the volume of the magnet), and the coercivity (Hc), a measure of the resistance to becoming demagnetized. High coercivity at room temperature is important for motor applications because coercivity generally declines with temperature for conventional magnets. A magnet with high coercivity would retain a large energy product at elevated temperatures. Progress in magnetic materials over the past century has been ascribed to a mastery of coercivity.
The conventional magnets with the highest coercivity are composed of rare earth element-transition metal (RE-TM) materials, where electrons with unpaired spin in the 4f orbitals (4f electrons) from the RE provide high magnetocrystalline anisotropy and 3d electrons of the TM contribute high magnetization and Curie temperature (Tc). Typically, the realized coercivity of conventional magnets reach only 25-30% of the theoretical maximum coercivity, after a long optimization of the microstructure to improve magnetic behavior. Moreover, a magnetic material should ideally retain a high coercivity at working temperatures for motor applications which run at temperatures greater than 150° C.
Currently the highest performing magnets in terms of energy product (i.e. (BH)max in units of MG-Oe or energy density in units of kJ/m3) are sintered rare earth permanent magnets. For example, top quality Nd2Fe14B magnets can have a (BH)max that may exceed 50 MG-Oe (400 kJ/m3). Thus, Nd2Fe14B magnets, which may include Dy, Tb, and other rare earths, as well as samarium cobalt magnets (e.g. SmCo5 or Sm2Co17). Moreover, all these magnets may include iron (e.g. 5-10% Fe) and, often, vanadium (V), or other elements as minor components (<2%). Furthermore, the most valuable magnetic material is associated typically with high performing magnetic properties in terms of high energy product.
However, although the inexpensive material components of ferrite, an iron oxide based material including additional metallic elements, accounts for ferrite as a dominant permanent magnet material by volume, RE magnets outperform at room temperature all other magnets. Thus, RE permanent magnet materials are preferred in large quantities for hybrid and electric drive motors.
However, the critical materials, such as the rare earth elements (e.g. Sm, Nd, Dy, etc.), essential to these high performing permanent magnets are not easily or affordably obtained, and there are supply chain risks as most of the material is mined in China. Therefore, for reasons of national and economic security as well as general efficiency of manufacture, it would be desirable to improve manufacturing of the permanent magnets to reduce waste and consumption of the critical materials.
Conventional manufacturing of permanent magnets involves methods of compacting powder, for example, producing a desired alloy and turning the alloy into a powder (e.g. hydrogenation disproportionation desorption recombination (HDDR) or melt-spinning, either of which may be followed by jet milling). The powders are then compacted (e.g. by pressing) and sintered under inert atmospheres, followed by magnetization and dicing, grinding, etc. to achieve the appropriate size and shape. A final step may include coating the magnet to prevent corrosion of the magnet material.
There are several drawbacks for these current methods of manufacture of permanent magnets. In particular, for smaller magnets, particularly those under a few millimeters in size, the amount of waste (e.g. swarf, kerf, etc.) generated by these conventional manufacturing techniques may be as much as 80% of the total material volume. For example, much of the kerf generated by dicing becomes contaminated with cutting fluids, other impurities which make its reuse impractical. Magnets produced in this manner are also uniform in material concentration.
RE magnets are very brittle and readily chip, so precision machining of magnets to high tolerances significantly adds to production costs, including the costs of breakage during fabrication. Machining permanent magnets using a subtractive process results in significant waste of the valuable material.
Alternative conventional manufacturing techniques may involve producing bonded magnets using injection molding or similar techniques. These methods form bonded magnets that include a mixture of magnetic particles combined with a polymer binder such that this mixture is extruded, molded, or rolled into sheets and geometric shapes.
However, there are drawbacks with the methods of forming bonded magnets. In particular, the presence of the bonding agent (e.g. epoxy, thermoplastic, etc) in the final product causes the bonded magnets to have lower energy densities than sintered magnets. Moreover, bonded magnets typically function at modest temperatures because of the temperature sensitivity of the bonding agent present in the bonded magnets.
It would be desirable to develop efficient methods of additive manufacturing (AM) techniques for the manufacture of permanent magnets. However, AM methods prefer powders with particles that are spherical in shape that have high flowability. Anisotropic Nd—Fe—B powders having desirable magnetic properties include particles with sharp edges and high aspect ratios (length versus cross-section), but as such, have poor flowability. Additionally, many AM techniques apply directed energy methods to the powders wherein the materials are melted to create a part. The act of melting destroys the microstructure of the permanent magnet material, and effectively eliminates the coercivity necessary for high energy product magnets. Thus, methods for manufacturing permanent magnets with reduced waste (as typically generated by subtractive machining) and reduced loss of energy (as typically occurs with blending with polymers) have been elusive.
In one embodiment, a magnet includes a plurality of layers, each layer having a microstructure of sintered particles. The particles in at least one of the layers are characterized as having preferentially aligned magnetic orientations in a first direction.
In another embodiment, a product includes a part having a plurality of layers of sintered magnetic anisotropic particles, where the part is characterized by physical characteristics of formation by an electrophoretic deposition process.
In yet another embodiment, a method of forming a magnet includes forming a structure by electrophoretic deposition (EPD) and sintering the formed structure to form a magnet. The forming a structure by EPD includes adding a plurality of first particles having magnetic anisotropy to an electrophoretic deposition (EPD) chamber and applying a voltage differential across electrodes of the EPD chamber to create an electric field in the EPD chamber for causing electrophoretic deposition of the first particles above a first of the electrodes for forming a first layer comprising the first particles.
Other aspects and advantages of the present invention will become apparent from the following detailed description, which, when taken in conjunction with the drawings, illustrate by way of example the principles of the invention.
The following description is made for the purpose of illustrating the general principles of the present invention and is not meant to limit the inventive concepts claimed herein. Further, particular features described herein can be used in combination with other described features in each of the various possible combinations and permutations.
Unless otherwise specifically defined herein, all terms are to be given their broadest possible interpretation including meanings implied from the specification as well as meanings understood by those skilled in the art and/or as defined in dictionaries, treatises, etc.
It must also be noted that, as used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless otherwise specified.
The nanoscale is defined as between 1 nanometer and about 500 nanometers.
The following description discloses permanent magnets formed by electrophoretic deposition and/or related systems and methods.
In one general embodiment, a magnet includes a plurality of layers, each layer having a microstructure of sintered particles. The particles in at least one of the layers are characterized as having preferentially aligned magnetic orientations in a first direction.
In another general embodiment, a product includes a part having a plurality of layers of sintered magnetic anisotropic particles, where the part is characterized by physical characteristics of formation by an electrophoretic deposition process.
In yet another general embodiment, a method of forming a magnet includes forming a structure by electrophoretic deposition (EPD) and sintering the formed structure to form a magnet. The forming a structure by EPD includes adding a plurality of first particles having magnetic anisotropy to an electrophoretic deposition (EPD) chamber and applying a voltage differential across electrodes of the EPD chamber to create an electric field in the EPD chamber for causing electrophoretic deposition of the first particles above a first of the electrodes for forming a first layer comprising the first particles.
A list of acronyms used in the description is provided below.
Some embodiments described herein are directed to efficiently producing homogeneous magnets via electrophoretic deposition, while others are directed to producing magnets with specifically tailored properties. Producing functionally graded materials (FGM) that include gradients in composition, microstructure, and/or density may enhance bulk properties, which typically correspond to a combination of the precursor material properties. It would be desirable to use processing techniques to produce FGM magnets, with minimal waste and maximum cost efficiency. Various techniques described herein use electrophoretic deposition (EPD) technology to fabricate functionally graded, nanostructured magnetic materials tailored in three-dimensions that may be sintered to produce a permanent magnet with FGM and magnetism.
The EPD processes described herein may use methodology based on the techniques disclosed in U.S. patent application Ser. No. 13/085,405, which is incorporated by reference. Basically, the EPD process is an additive technique that allows virtually all material deposited to remain in the final product, thereby creating near net-shape parts. Moreover, material remaining in solution in the EPD chamber, that has not been deposited, may be reused in subsequent depositions thereby sharply reducing any generation of waste.
EPD is an additive manufacturing process that allows construction of near net shape materials with low levels of waste, and so may be useful for producing parts from expensive materials. Thus, in various embodiments described herein, EPD produces pre-defined shapes that are desirable for permanent magnets such as cylinders, arcs, parallelepipeds, etc.
Materials
Materials with magnetic properties, as understood herein, include materials and composites having magnetic properties as would be understood by one having ordinary skill in the art upon reading the present application.
Materials with magnetic anisotropy have a directional dependence of the magnetic properties of the materials. For example, the magnetic moment of the magnetically anisotropic materials as described herein aligns along an easy axis, which is an energetically favorable direction of spontaneous magnetization.
In addition, formulations that form a permanent magnet as understood herein include material that retains magnetization and creates a persistent magnetic field after an external magnetizing field has been removed.
According to various embodiments described herein, the formulations of permanent magnets may include magnetic material and non-magnetic material, and material with varying degrees of magnetism. As such, EPD can be used to deposit at least one component of the formulation, so long as the final product comprises a magnetic part, as would be understood by one having ordinary skill in the art upon reading the present descriptions. Additionally and/or alternatively, the synthesis of a final part may involve multiple steps, some of which do not employ EPD.
Materials conventionally used in permanent magnets may be used in various embodiments. Illustrative materials with magnetic anisotropy generally include Neodymium Iron Boride (Nd2Fe14B), samarium cobalt (SmCo5, Sm2Co17), ferrites, etc. In various embodiments described herein the material may include at least one of: neodymium, cobalt, samarium, iron, nickel, ferrite, boride, other rare earth elements, etc., and combinations thereof, as would be understood by one having ordinary skill in the art upon reading the present descriptions. In some approaches, the permanent magnet may include an alloy comprised of a combination of at least two materials. In some approaches, the permanent magnet may include a combination of materials. In some approaches the EPD process may be used with pre-cursor materials, such as oxides or fluorides of what will become the magnetic material.
In preferred approaches, the EPD process may be used to additively manufacture permanent magnets using powders of the starting materials. In particular powders having magnetic anisotropic properties (e.g. the particles having a magnetic moment that will align with an easy axis) have not been useful for conventional AM methods because anisotropic particles of magnetic powders (e.g. Nd—Fe—B powders) in solution have poor flowability. However, since EPD uses powders dispersed in a fluid, flowability may not be an essential parameter for the EPD process.
Thus, magnetic anisotropic powders having particles with high aspect ratios, such as Nd—Fe—B, may be suspended in solution and deposited in pre-defined three-dimensional (3D) shapes during the EPD process. In some approaches, magnetic structures may be formed by EPD with powders having a magnetic characteristic of being highly anisotropic.
In some approaches, the formulation of the permanent magnet may include non-magnetic materials deposited during the EPD process, for example, but not limited to aluminum (Al) for structural support, zinc (Zn) for corrosion resistance, etc. Additionally, or alternatively, these secondary materials may be added to tailor the magnetism of the permanent magnet in a manner that would become apparent to one having ordinary skill in the art upon reading the present descriptions, such as a soft magnetic material of a particular geometry to shape the magnetic field of the permanent (hard) magnet.
Moreover still, composites suitable for deposition by EPD and use in relevant applications described herein may additionally and/or alternatively include secondary agents for modifying electrochemical properties of the particles of the magnetic material(s) upon suspension in a dispersion liquid. Such agents might include: a second phase of magnetic material to create an exchange spring magnet, a material to improve strength and fracture toughness, a functional material to create a multiferroic device, etc. The primary advantage of including such secondary agents is to facilitate and/or confer electrophoretic mobility of the particles of the magnetic material by conveying and/or tuning the surface charge of the particles. Exemplary secondary agents include salts, acids, bases, ions, etc. In operation, secondary agents may convey, modify and/or tune particle surface charge by any suitable means as understood by skilled artisans, such as by modifying solution pH, salt concentration, ion concentration, etc. as would be understood by one having ordinary skill in the art upon reading the present descriptions.
In some embodiments, particles automatically acquire a surface charge upon suspension in the dispersion liquid, and in others, particles of the magnetic materials suspended in the dispersion liquid acquire a surface charge upon addition of one or more secondary agents and mixing of the secondary agent, magnetic material particles, and dispersion liquid as discussed herein.
Mixing and suspension of magnetic materials, secondary materials, and/or secondary agents in a dispersion liquid may be achieved by any suitable means appreciable by skilled artisans upon reading the present descriptions, including stirring, shaking, vortexing, applying ultrasonic energy, etc. Mixing should be performed in any manner sufficient to suspend the magnetic material particles in the dispersion liquid, and, while homogenous suspensions may confer advantages including enhanced deposition uniformity and/or efficiency, reduce deposition time necessary to achieve a particular deposition thickness, etc. as would be understood by one having ordinary skill in the art upon reading the present descriptions, the suspension need not be homogenous according to the present disclosure.
Dispersion liquids suitable for use within the scope of the present descriptions include any liquids capable of supporting a suspension of magnetic material particles, secondary materials, and/or secondary agents as described herein. The dispersion liquid may be an aqueous or organic solution. In preferred approaches, the solution is a nonpolar solution that may contain an effective amount of an aqueous solution to impart a charge on the particles in solution without providing an environment for hydrolysis. In preferred approaches, the solution in the EPD chamber is essentially free of hydrolysis reactions. The effective amount of an additive is an amount that imparts the desired function or result, and may be readily determined without undue experimentation following the teachings herein and varying the concentration of the additive, as would become apparent to one skilled in the art upon reading the present description. Exemplary approaches include solutions that include ethanol, carbonate, etc. as would be understood by one having ordinary skill in the art upon reading the present descriptions.
In general, the achievable thickness is dependent upon parameters such as the identity of a substrate material, if included, and the magnetic material(s), the strength of the electric field applied during deposition, the deposition time, etc. but may be difficult to predict without attempting experiments to determine the optimum deposition conditions. However, one skilled in the art, upon reading the present descriptions, would be able to make such determinations for various materials via experimentation, without resorting to undue experimentation.
Accordingly, it is possible to co-deposit materials of differing identity and/or composition provided that each material exhibits similar electrophoretic mobility and/or deposition behavior, enabling synthesis of complex combinations of energetic materials and/or binding agents, in various embodiments.
EPD Devices
As shown in
Thus, in one approach, a product may include a primarily nonconductive substrate having a conductive portion upon which at least one material with magnetic properties is electrophoretically deposited.
In another approach, the product may include a nonconductive structure, where at least one material with magnetic properties is positioned in and/or around the structure.
The EPD device 100, in some embodiments, may be used to deposit materials with magnetic properties on or above the first electrode 110 or a conductive substrate 112 positioned on a side of the electrode 110 exposed to a suspension 108 (e.g. dispersion) including the magnetic material as nanoparticles 102 in suspension 108, and/or particles 104 in suspension 108 to be deposited. By controlling certain characteristics of formation of structures in an EPD process, such as the precursor material composition (e.g., homogenous or heterogeneous nanoparticle solutions) and orientation (e.g., non-spherical nanoparticles), deposition rates (e.g., by controlling an electric field strength, using different solvents, etc.), particle self-assembly (e.g., controlling electric field strength, particle size, particle concentration, temperature, etc.), material layers and thicknesses (e.g., through use of an automated sample injection system and deposition time), and deposition patterns with each layer (e.g., via use of an electrode having an area corresponding to the desired pattern, via use of electrode each having an area corresponding to the desired portion of a pattern, dynamic electrode patterning, etc.), intricate and complex structures may be formed using EPD processes that may include a plurality of densities, microstructures, and/or compositions, according to embodiments described herein.
Now regarding
Turning to
As depicted in part (b) of
Other components and/or resulting products shown in
In another approach, the substrate and/or electrode may have a non-planar shape, e.g., it is cylindrical, polygonal, conical, etc.
Now referring to
As shown in
Of course,
In some embodiments the substrate may comprise an electrode, and in preferred embodiments may comprise a patterned electrode. In one embodiment, the substrate may be characterized as a planar substrate, while in another embodiment the substrate may be characterized as a non-planar substrate, such as a lattice. In even further embodiments, the substrate may be a porous structure.
Properties of Magnets Produced by EPD
Notably, the products producible by employing the presently described EPD process(es) include a composite of particles, at least some of which are magnetic, where the composite has physical characteristics of being formed by an EPD process. Such characteristics include, but are not limited to deposition conformal to a surface of a substrate, a tuned volumetric magnetic density, highly precise film thickness, highly precise particle packing density, a particular particle orientation, a particular deposition pattern (2D or 3D), etc. as would be understood by one having ordinary skill in the art upon reading the present descriptions. In preferred embodiments, each physical characteristic may be selected and/or customized by tuning deposition conditions.
Since EPD confers the ability to control the deposition of both material with magnetic properties and material without magnetic properties, it enables creation of highly controllable magnetic materials, in some approaches.
Equation 1 sets out the basic system-level model for electrophoretic deposition, where Wfilm is the mass of the deposition layer, μ is the electrophoretic mobility, E is the electric field, A is the area of the electrode substrate, C is the deposition particle mass concentration, and t is the deposition time.
W
film=∫t2t1μEACdt Equation 1
Combining these principles with dynamic patterning and sample delivery (which is described in more detail later), electrophoretic deposition may be employed to produce a diverse set of products with unique and/or difficult to obtain shapes, designs, and properties custom-fitted to any of a number of practical applications.
Now referring to
As shown in
Of course, the embodiments described herein are not meant to be limiting on the invention in any way. Also, the patterns are not limited to those shown in
In some embodiments described herein functionally graded structures may be formed by changing out the deposition solutions during the EPD process. Thus, deposition of an expensive material may be strategically used for a final product, e.g. a permanent magnet.
For example, and not meant to be limiting in any way, Dy is a desirable component of Nd—Fe—B magnets as Dy increases the coercivity and resistance to demagnetization, however, Dy also reduces the magnetic remanance and is very expensive. In some approaches of methods described herein, the EPD process may define locations for Dy in the permanent magnet where large demagnetizing fields occur. Thus, Dy in solution may be selectively deposited to a green body thereby improving overall performance of the magnet while reducing the material cost.
In some approaches, a Nd2Fe14B system may have layers of Dy rich Dy—Fe—B. In some approaches, DyF3 from a solution of DyF3 particles may be selectively deposited on the magnet in areas where large demagnetizing fields will be applied.
According to one embodiment, as shown in
In another embodiment, at least the first material 306 and/or the first layer 302 may have a characteristic of being deposited through an EPD process according to the first pattern. This characteristic may include, in some embodiments, smooth, gradual gradients between the materials in the first layer 302, abrupt transitions from the particles 308 of first material 306 to the particles 310 of a second material 312 in the first layer 302, regular patterning between the first material 306 and the second material 312, or any other characteristic of deposition through an EPD process as would be understood by one of skill in the art upon reading the present descriptions. In a further embodiment, at least the first material 306 may have a characteristic of being deposited through the EPD process above a non-planar electrode. For example, the non-planar electrode may have a cylindrical shape, a regular polygonal shape, a conical shape, a curved surface shape, or any other non-planar shape as would be understood by one of skill in the art upon reading the present descriptions. Illustrative non-planar electrodes are described in more detail above.
In another embodiment as shown in
In another embodiment, each layer may employ one or more unique patterns and/or materials, thereby creating a structure which, in the z-direction perpendicular to the x-y plane, may have differing arrangements of materials.
As would be understood by one of skill in the art upon reading the present descriptions, in some embodiments one or more additional layers may be arranged above the first layer 302 and the second layer 304, thereby forming a structure that may have complex layering and/or composition.
According to various embodiments, at least the first material, a second material, an nth-material, etc. of the first layer, second layer, nth layer may have a characteristic of being deposited through an EPD process. This characteristic may include, in some embodiments, smooth, gradual gradients between the materials in the first layer, abrupt transitions from the first material to the second material in the first layer and/or the second layer, regular patterning between the first material and the second material, or any other characteristic of deposition through an EPD process as would be understood by one of skill in the art upon reading the present descriptions. In a further embodiment, at least the first material may have a characteristic of being deposited through the EPD process above a non-planar electrode. For example, the non-planar electrode may have a cylindrical shape, a regular polygonal shape, a conical shape, a curved surface shape, or any other non-planar shape as would be understood by one of skill in the art upon reading the present descriptions.
In some approaches, a characteristic of deposition through an EPD process may include characteristics of the second material being deposited after the first material is deposited.
In various embodiments as illustrated in
In one embodiment, products incorporating magnetic materials as described herein may include a thin film containing particles of one or more magnetic materials, and the thin film may be disposed on one or more surfaces of a substrate. Importantly, the thin film of magnetic materials incorporated into such products may preferably exhibit one or more physical characteristics of electrophoretic deposition, as discussed in detail above.
Of course, the patterns shown in
In some approaches, the magnet 400 may have a gradient of composition, microstructure and/or density in a thickness direction of the layers.
In some approaches, the magnet 400 having a plurality of layers may include a first layer 402 and a second layer 404 formed above the first layer 402. As would be understood by one of skill in the art upon reading the present descriptions, one or more additional layers may be arranged above the first layer and the second layer, thereby forming a structure that may have complex layering and/or composition, with gradients possible in the x-y plane and the z-direction across some or all of the layers, in a plethora of combinations.
In some approaches, at least one of the layers of the magnet 400 may have a gradient in composition, microstructure and/or density in at least one direction, e.g., in the x-y plane and/or in the z direction. In some approaches, the magnet may have a plurality of layers that includes a first layer 402 and a second layer 404 formed above the first layer 402, where the first layer 402 and/or the second layer 404 have a gradient in composition, microstructure and/or density in a z-direction perpendicular to an x-y plane of the first layer 402.
The first and second layers 402, 404 may have a gradient that includes a transition from a first characteristic of the first layer 402 to a second characteristic of the second layer 404. Characteristics of the gradients may include composition, microstructure, and density. For example, in some approaches, a gradient may include a transition from the composition of the first layer to a composition of the second layer where the composition of the second layer is different from the composition of the first layer.
In some approaches, the gradient may include a transition from a microstructure of the first layer to a microstructure of the second layer where the microstructure of the second layer is different from the microstructure of the first layer.
In some approaches, the gradient may include a transition from a density of the first layer to a density of the second layer where the density of the second layer is different from the density of the first layer.
In some approaches, the second layer 404 may have a gradient in composition, microstructure and/or density in an x-y plane oriented parallel to a plane of deposition of the first layer 402. The gradient of the first and second layer 402, 404, according to various approaches, may be smooth, abrupt, or comprised of small, incremental steps, and combinations thereof.
This gradient in the z-direction may be used in addition to or in place of a gradient in the x-y plane of each layer based on patterns, e.g., and may be formed by changing solutions in an EPD chamber during EPD processing (see
Looking back to
Returning to
In other approaches, the second layer 404 may have different magnetic properties than the first layer 402. In some approaches, the particles of the second layer may be characterized as having a commonly aligned magnetic orientation in a second direction that is different from the first direction, for example different from a S to N direction (as shown in
In some approaches, the magnet may have coercivity greater than 10 kilo Oersteds (kOe) at temperatures of at least 300° C. In some approaches, the magnet may have coercivity of greater than 10 kOe at a temperature of about 300° C. In some approaches, the magnet may have coercivity of greater than 10 kOe at a temperature of about 400° C. In some approaches, the magnet may have a coercivity of greater than 40 kOe at temperatures above 100° C. In some approaches, the magnet may have coercivity above 50 kOe at room temperature (e.g. 300 K or in a range of about 20° C. to about 25° C.).
In some embodiments, the EPD system may be combined with a magnetic field generator such that the packing density and/or magnetic properties of the deposited material may be improved. In some approaches, the EPD flow cell may be placed in a magnetic field, preferably a uniform magnetic field, so that the particles are aligned in the magnetic field as the particles are deposited along the electric field lines. Looking to
By way of example, but not limited to the images shown, part (a) of
According to one embodiment, the magnet 400 is a permanent magnet. In some approaches, the permanent magnet may have a thickness in the z-direction in a range of greater than about 5 nanometers and less than about 1 centimeter.
In some approaches, a permanent magnet may be a thin film permanent magnet. In one approach, the thickness of the thin film permanent magnet may be about 3 atoms thick. In other approaches, the thin film permanent magnet may have a nanoscale thickness.
In various embodiments, a permanent magnet may have a plurality of layers having a physical characteristic of being deposited by an EPD process, as described earlier.
In some approaches, the plurality of layers of the permanent magnet may have a physical characteristic of being deposited above a non-planar electrode, e.g., as described for
In some approaches, each layer of the permanent magnet may individually include one or more of the following materials: neodymium, cobalt, samarium, iron, nickel, ferrite, boride, and a combination thereof. Accordingly, one layer may have one material and a second layer may have another material in combination with a third material. In some approaches, more than one layer may have the same material. For example, one layer of the permanent magnet may have iron, a second layer may have iron with neodymium, and a third layer may have samarium. In some approaches, any layer may include an alloy of more than one of the materials.
In some approaches, the first and second layers may include a same material in each respective composition, e.g., both layers include the same material along but each includes another material that is exclusive to that particular layer.
In one embodiment, a product includes a part having a plurality of layers of sintered magnetic anisotropic particles. The part may be characterized by physical characteristics of formation by an electrophoretic deposition process. In various approaches, the part is a permanent magnet.
In some approaches, the part may have a gradient of composition, microstructure and/or density in a thickness direction of the layers. In some approaches, the part may have a thickness in a range of greater than about 5 nanometers and less than about 1 millimeter.
In some approaches, each layer of the part individually includes at least one of the following materials: neodymium, cobalt, samarium, iron, nickel, ferrite, boride, or a combination thereof. Accordingly, one layer may include one material and a second layer may include a different material. Moreover, one layer may include an alloy of two materials and a second layer may include one of the materials. These examples are not exhaustive, and any combination of materials may be used for each layer, as would be understood by one skilled in the art reading this description.
A method 500 of forming a magnet includes a first operation 502 of forming a structure by EPD that may include a series of sub-operations 502a, and 502b, as shown in
Sub-operation 502a includes adding a plurality of first particles having magnetic anisotropy to an electrophoretic deposition (EPD) chamber. In some approaches, sub-operation 502a may include adding a solution of particles to the EPD chamber, where the solution includes a first material to be deposited onto a surface.
Sub-operation 502b includes applying a voltage differential across electrodes of the EPD chamber to create an electric field in the EPD chamber for causing electrophoretic deposition of the first particles above a first of the electrodes for forming a first layer comprising the first particles. Looking back to
In some approaches of method 500, operation 502 may include applying a magnetic field to the EPD chamber during the electrophoretic deposition for aligning magnetic orientations of the particles in a common direction. In some approaches, the magnetic field may be applied in a direction parallel to the electric field formed by the applied voltage differential in the EPD chamber. In other approaches, the magnetic field may be applied in a direction perpendicular to the electric field formed by the applied voltage differential in the EPD chamber.
In some approaches, at least one of the layers may include a plurality of particles of one material and a plurality of particles of a second material, where magnetic orientations of the particles of the first material and the particles of the second material are commonly aligned in a same direction.
In various approaches, the EPD chamber includes a solution having the first material to be deposited therein. In other approaches, the EPD chamber may include a solution having a first material of particles and a second material of particles.
In various approaches, the electric field between the electrodes in the EPD chamber causes the first particles to form a particle packing density gradient in a direction consistent with the electric field.
In some approaches, sub-operation 502b may include electrophoretically depositing the first material above a first electrode according to a first pattern for forming a first layer including the first material. The first layer may be defined by the first particles being commonly aligned in the magnetic field. In various approaches, as would be understood by one of skill in the art upon reading the present descriptions, one or more additional layers may be arranged above the first layer and the second layer, thereby forming a structure that may have complex layering and/or composition, with gradients possible in the x-y plane and/or the z-direction in and/or across some or all of the layers, e.g., as shown in
In various approaches, the formed structure of operation 502 may be a 3D structure. In other approaches, the formed structure of operation 502 may be a thin film.
In some embodiments, the first electrode 110 (as in
In other approaches of operation 502 of
In some approaches, introducing a solution having a second material into the EPD chamber may include expelling the solution having the first material from the EPD chamber prior to introducing the solution having the second material into the EPD chamber. In this way, more abrupt transitions from the electrophoretically deposited first material to the electrophoretically deposited second material may be made, whereas slowly introducing the second material (such as in a solution having the second material therein) into the EPD chamber while the first solution is still present may result in more gradual transitions from the first material to the second material in the green body.
In some approaches, the formed structure may have a plurality of layers; and include altering a condition in the EPD chamber for creating a gradient in composition, microstructure and/or density along the plane of deposition (x-y plane) and/or a thickness direction (z-direction) oriented perpendicular to the plane of deposition.
According to one embodiment, the structure 620 comprises a first layer 604 having a first composition, a first microstructure, and a first density and a second layer 608 above the first layer 604, the second layer 608 having at least one of: a second composition that is different than the first composition, a second microstructure that is different than the first microstructure, and a second density that is different than the first density. A gradient may exist between the first layer 604 and the second layer 608, and the first and second layers 604, 608 have a characteristic of being formed in an EPD chamber, as previously described. In some approaches, the gradient may exist in a z-direction perpendicular to the x-y plane between the first layer and the second layer formed above the first layer.
In one embodiment, the gradient may be a transition from at least one of: the first composition, the first microstructure, and the first density, to the at least one of: the second composition, the second microstructure, and the second density. That is to say, any of the composition, microstructure and/or density may change from the first layer 604 to the second layer 608, with any of the remaining properties being about the same, according to various embodiments.
For example, and not meant to be limiting to the invention in any way, an Nd—Fe—B magnet may include a first layer having a composition of Dy rich Dy—Fe—B and a second layer having a composition of DyF3. For example, a magnet as part of a motor or generator stator will experience a rotating magnetic field as the electrical coils of the rotor pass. This can create regions of high demagnetizing forces near corners and sharp edges. A magnet with Dy rich regions near the corners may include fewer expensive components than a magnet with uniform Dy throughout. In this example, two properties, composition and magnetic response change from the first layer to the second layer.
Moreover, a gradient may affect one property, two properties, three properties or even other properties, such as melting point, freezing point, conductivity, rigidity, or any other mechanical property, chemical property, electrical property, magnetism, etc., as would be understood by one of skill in the art upon reading the present descriptions.
In another embodiment, the gradient from the first layer 604 to the second layer 608 may be abrupt, gradual, in small incremental steps, etc., as would be understood by one of skill in the art upon reading the present descriptions.
According to another embodiment, the first layer 604 and the second layer 608 may have a characteristic of being deposited above a non-planar electrode, e.g., as is described in more detail in
In some approaches, the first particles 602 in a solution may form a first layer 604, and the second particles 603 in a solution 614 may form a second layer 608. In some approaches, the first particles 602 and the second particles 603 may be the same material but have different concentrations in a solution 614. In other approaches, the first particles 602 and the second particles 603 may be different.
In some approaches, forming the first pattern and/or the second pattern may be dynamically altered to modify a gradient in composition, microstructure and/or density in the z-direction across a plurality of layers.
In various approaches, each layer may have particles that individually include a first material, second material, nth material from a powder dispersed in the deposition solution, as previously described. The powder of the material may be derived from materials such as neodymium, cobalt, samarium, iron, nickel, ferrite, boride, alloys comprising a combination thereof, etc. Methods to produce powder include grinding, crushing, etc. as known to one skilled in the art.
In some approaches, a layer may have particles of one material, e.g. iron, and a second layer may have particles of nickel. In other approaches, the first and second layer includes particles of the same material, but the composition or density of the material may be different. In other approaches, the first layer may include an alloy of two materials and the second layer may include a single material of the alloy. These examples are provided to describe possible approaches, and are not meant to be limiting in any way.
In some approaches, the second material may include a plurality of second particles having magnetic anisotropy, where the first particles of the first material and the second particles of the second material may be commonly aligned in the magnetic field.
In one embodiment, EPD may be used in conjunction with controlled electric field 140 patterns to direct the composition of deposited material in an x-y plane parallel to a plane of deposition, including multilayer deposition of a single pattern as well as dynamically changing patterns as the particles build up in the z-direction, perpendicular to the x-y plane. This technique enables, for example, permanent Nd—Fe—B magnets with a controlled z-direction concentration of Dy material.
Conventional methods of forming permanent magnets tend to be limited to uniform composition profiles. However, in one embodiment, because the electrophoretic deposition occurs only where the field is applied, precisely patterned x-y concentration profiles are possible by modifying the electrode pattern in this plane. To enable this capability, one electrode in a typical EPD system may be replaced with a photoconductive layer (such as α-H:Si) and a transparent or semi-transparent electrode, e.g., of indium tin oxide (ITO) and illuminated in specific regions using any number of light sources and/or light altering devices or mechanisms, such as a static mask, a dynamic pattern from a light altering or emitting mechanism, etc.
Referring to
As shown in
In other embodiments, the light altering mechanism may be positioned near to the photoconductive layer (not shown). The light from the light source, in one embodiment, passes through the light altering mechanism prior to reaching the photoconductive layer. According to several approaches, the light altering mechanism may include a LCoS array, one or more filters, one or more patterned screens, or any other light altering mechanism as would be known to one of skill in the art that would be capable of providing one or more patterns to the light (e.g., to alter the light from the light source).
In these embodiments, dynamic altering of the light may be greatly enhanced, as the light altering mechanism may be programmed to change over time to allow light to reach the photoconductive layer as desired by a user.
The light source 622 may be any light source capable of providing sufficient light 624 to shine upon designated areas of the photoconductive layer 626, as would be understood by one of skill in the art upon reading the present descriptions.
Other components shown in
Looking back to
In some approaches, before the sintering of operation 504, the formed structure may be dried. Conventional drying techniques may used to dry the structure as would be understood by one having ordinary skill in the art upon reading the present descriptions, for example, supercritical drying, evaporation, etc.
In some approaches of operation 504, the formed structure produced by EPD may be sintered in a reducing atmosphere, such as forming gas, to produce a fully dense solid. The processing temperature for sintering of the formed structure may be significantly below the melting point of the solid. This avoids reduction of the magnetic properties, as would otherwise be seen at higher sintering temperatures. Moreover, the sintered solid may maintain the microstructure of the green body with an increased density, for example, the density may reach near 100% in the sintered solid magnet. Thus, the resultant permanent magnet may maintain a high coercivity represented in part by the microstructure of the solid and sintering at a temperature below the melting point of the material resists any melting of the solid that could sharply reduce the coercivity.
In some approaches, a temperature for sintering the green body may be less than a temperature of a melting point of the first material. For example, without intending to be limiting, a Fe—Ni green body may be sintered at about 50° C. under hydrogen gas for 30 minutes. In various approaches, the parameters of sintering of the green body may correlate to the conditions of thermal consolidation of the material as known by one skilled in the art.
Deposition and then sintering in this form may result in a highly anisotropic magnet which may have improved magnetic properties compared to a magnet produced from isotropic particles.
Conventional sintering methods are restrictive in designing a magnetic field shape using pole-pieces to produce permanent magnets since processing of isostatically pressed particles uses large magnetic fields to align the particles as they are pressed. In sharp contrast, the EPD process as described herein allows careful design of the magnetic field shape using pole-pieces to produce complex magnetic structures.
In some approaches, the functionally graded magnet formed from method 500 may be a permanent magnet.
Greenbodies of SmCo5 Magnets
Magnetic Properties
The greenbodies of SmCo5 magnets shown in
In Use
Various embodiments described herein use electrophoretic deposition to reduce the amount of raw materials used in magnet assembly. Permanent magnets are key elements of compact high power density motors and related actuators, as well as for sensors and transducers such as speakers. The techniques presented herein offer a methodology to make permanent rare earth magnets with much reduced waste material, and so is particularly valuable for producing small magnets, or magnets with novel or difficult to manufacture shapes.
The inventive concepts disclosed herein have been presented by way of example to illustrate the myriad features thereof in a plurality of illustrative scenarios, embodiments, and/or implementations. It should be appreciated that the concepts generally disclosed are to be considered as modular, and may be implemented in any combination, permutation, or synthesis thereof. In addition, any modification, alteration, or equivalent of the presently disclosed features, functions, and concepts that would be appreciated by a person having ordinary skill in the art upon reading the instant descriptions should also be considered within the scope of this disclosure.
While various embodiments have been described above, it should be understood that they have been presented by way of example only, and not limitation. Thus, the breadth and scope of an embodiment of the present invention should not be limited by any of the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents.
The United States Government has rights in this invention pursuant to Contract No. DE-AC52-07NA27344 between the United States Department of Energy and Lawrence Livermore National Security, LLC for the operation of Lawrence Livermore National Laboratory.
