NANOMAGNETIC INDUCTOR CORES, INDUCTORS AND DEVICES INCORPORATING SUCH CORES, AND ASSOCIATED MANUFACTURING METHODS
20220189675 · 2022-06-16
Inventors
- Frédéric Voiron (Barraux, FR)
- Mohamed Mehdi JATLAOUI (Colleville-Montgomery, FR)
- Julien El Sabahy (Grenoble, FR)
Cpc classification
H01F17/0033
ELECTRICITY
International classification
Abstract
A nanomagnetic inductor core that includes: a porous, electrically-insulating template having high-permeability material in the pores thereof to constitute elongated nanowires, and wherein the elongated nanowires are segmented along their axial direction; and a segment of dielectric material interposed between adjacent segments of the high-permeability material along the axial direction of the nanowire; wherein each segment of the high-permeability material has a length, in the axial direction of the nanowire, no greater than a size of a single magnetic domain, and wherein a maximal cross-sectional dimension of the nanowire is no greater than the size of the single magnetic domain. Inductors and LC interposers using such nanomagnetic inductor cores, as well as associated fabrication methods.
Claims
1. A nanomagnetic inductor core comprising: a porous, electrically-insulating template having high-permeability material in the pores thereof to constitute elongated nanowires, wherein the elongated nanowires are segmented along their axial direction; and a segment of dielectric material interposed between adjacent segments of the high-permeability material along the axial direction of the nanowire, wherein each segment of the high-permeability material has a length, in the axial direction of the nanowire, no greater than a size of a single magnetic domain, and wherein a maximal cross-sectional dimension of the nanowire is no greater than the size of the single magnetic domain.
2. The nanomagnetic inductor core according to claim 1, wherein the segments of high-permeability material include segments made of one or more materials selected in the group of Zn, Fe, Ni, Co, Mn, Cr, mixtures and alloys thereof, permalloy, ZrO and CoZr.
3. The nanomagnetic inductor core according to claim 1, wherein the porous, electrically-insulating template is made of porous anodic aluminum oxide or another porous dielectric material.
4. The nanomagnetic inductor core according to claim 1, wherein the porous, electrically-insulating template is made of a porous dielectric material.
5. An inductor comprising: a first conductor; a second conductor; and the nanomagnetic inductor core according to claim 1, wherein the first conductor and the second conductor are electrically interconnected to encircle the nanomagnetic inductor core.
6. The inductor according to claim 5, wherein the nanomagnetic inductor core is sandwiched between the first conductor and the second conductor, and the first conductor and the second conductor are electrically interconnected by via-hole conductors traversing the nanomagnetic inductor core.
7. An inductor comprising a three-dimensional coil wound around the nanomagnetic inductor core according to claim 1.
8. An inductor comprising: the nanomagnetic inductor core according to claim 1; and a two-dimensional coil on a surface of the nanomagnetic inductor coil.
9. An inductor comprising: a first nanomagnetic inductor core comprising the nanomagnetic inductor core according to claim 1; a two-dimensional coil on a surface of the first nanomagnetic inductor core; and a second nanomagnetic inductor core on the two-dimensional coil at a side thereof remote from the first nanomagnetic inductor core.
10. An LC interposer comprising: a substrate; a capacitor comprising a nanoscale capacitive structure in pores of a first region within the substrate; and an inductor according to claim 5, wherein the nanowires of the nanocomposite inductor core are in pores of a second region in the substrate.
11. A method of fabricating a nanomagnetic inductor core, the method comprising: forming elongated nanowires comprising high-permeability material in pores of an electrically-insulating porous template, the nanowires being segmented along their axial direction; and interposing a segment of dielectric material between adjacent segments of the high-permeability material along the axial direction of the nanowire, wherein each segment of the high-permeability material has a length, in the axial direction of the nanowire, no greater than a size of a single magnetic domain, wherein a maximal cross-sectional dimension of the nanowire is no greater than the size of a single magnetic domain.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0027] Further features and advantages of the present invention will become apparent from the following description of certain embodiments thereof, given by way of illustration only, not limitation, with reference to the accompanying drawings in which:
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0041] The present invention relates to the fabrication of an inductance using a magnetic core built out of a functionalized porous matrix, wherein the dimensions of the deposited magnetic material are controlled in three dimensions. This new way of controlling the shape of the magnetic material produces confinement of the magnetic field and results in a nanomagnetic inductor core having excellent performance, including low losses. The distances between adjacent domain walls can be made small compared to magnetic domains (e.g. typ. <100 nm), in all three spatial dimensions. Thus, the magnetic losses are reduced (μ″). Very high efficiency is expected. Eddy currents are reduced because the nanowire's textured structure does not allow current loops in the X/Y plane, and also not in the Z direction given that the segmentation along the Z direction comprises dielectric material. Furthermore, the real part of permeability (μ′) is stable over higher frequency range.
[0042] A nanomagnetic inductor core according to an embodiment of the invention will now be described with reference to
[0043] As can be seen from the partial, enlarged view shown in
[0044] The porous matrix 2 is formed of an electrically-insulating material. The electrically-insulating material may be AAO, another porous anodic oxide, or another porous dielectric. If desired, a nanoporous polymer membrane may be used. An advantage of AAO is that various production techniques have been developed which process aluminum to create a self-organized AAO structure comprising large numbers of nanoscale elongated pores extending substantially parallel to each other in a regular array, with a high degree of controllability of the properties of the porous material (e.g. in terms of pore diameter, inter-pore distance, etc.). One example production method is the “one-step” anodizing process described in the above-mentioned Hsu et al. document. Another production method is the so-called “two-step” process in which a first oxide film (formed in a first anodizing step) is removed but pre-patterns the substrate so that a second oxide film (formed in a second anodizing step) has a much more regular structure. Such production techniques are known and so shall not be described in detail here. It will just be noted that the production techniques may include ancillary processes additional to anodization, such as, for example, etching to increase pore diameter.
[0045]
[0046] The diameter D of the pores 2a limits the dimensions, in the x and y directions, of each segment 4a/4b of high-permeability material, and diameter D is less than 1 μm so that the relevant segment dimensions do not exceed the size of a magnetic domain. Typically, the diameter D of the pores 2a is set in the range of 15 nm-250 nm. Particularly good results are obtained in the case where the diameter D of the pores is no greater than 100 nm. References here to pore diameter refer to the average diameter of the pores.
[0047] Typically, the inter-pore distance d is set in the range of 30 nm-500 nm. In the case of a porous template 2 consisting of a porous anodic oxide, the dimensions D and d may be regulated by control of the voltage applied, and of the acid used, during the anodization process. Dimension D can also be further tailored by introducing a step of etching to enlarge pores.
[0048] In the case of using a porous template which has pores that are not circular, the dimensions, in the x and y directions, of each segment 4a/4b of high-permeability material, may be suitably limited by ensuring that the maximal dimension of the pore in cross-section is no greater than the size of one magnetic domain.
[0049] The length S.sub.L of the nanowire segments 4a, 4b made of high-permeability material in the axial direction of the nanowire is typically less than 100 nm and so the segment dimension in the z-direction does not exceed the size of a magnetic domain. Typically, the length S.sub.L of the nanowire segments 4a, 4b made of high-permeability material is set comparable to the pore diameter D.
[0050] Various different types of high-permeability material may be used in the nanowires, including but not limited to: Zn, Fe, Ni, Co, Mn, Cr, mixtures and alloys of different elements, permalloy, ZrO, CoZr, etc. In a given nanowire, all of the segments made of high-permeability material may be made of the same material (homogeneous nanowire), or the nanowire may include segments made of different high-permeability materials.
[0051] Various different types of dielectric material may be used in the nanowires. However, it is convenient to form the dielectric material by oxidation of the material in an earlier-deposited segment of high-permeability material. Thus, in the latter case the dielectric segments will consist of one or more oxides of the high-permeability material(s) used in the nanowires.
[0052] In view of maximizing the permeability (i.e. to maximize the volume fraction of magnetic material compared to dielectric material), it is preferred to set the length S.sub.N of the nanowire segments 5 made of dielectric material approximately the same as or below the width IP of the dielectric matrix material interposed between adjacent pores.
[0053] The length SN of the nanowire segments 5 made of dielectric material in the axial direction of the nanowire is preferably less than 100 nm and more preferably in the order of 10 nm. In principle, the thickness SN of the dielectric layer can be even lower, e.g. a few nanometers, provided that it is sufficient to ensure continuity and isolation, i.e. a continuous insulation layer preventing conduction in the axial direction of the nanowire.
[0054] Various techniques may be used to deposit material in the pores 2a of the porous template 2 to form the segments 4a, 4b of the nanowires/nanotubes 3. Processes for depositing material in pores of a porous template are well-known and will not be described in detail here. However, as a non-limiting example, we will mention electrochemical deposition. For example, a conductive seed consisting of Ni may be deposited into the pores 2a by an electrolytic deposition process and then segmented wires may be co-grown by ECD in the porous template using one or more Watts-type baths, until the pores are completely filled. Complete filling of the pores ensures that the highest possible value of permeability may be obtained.
[0055] In various embodiments of the invention, the porous template 2 illustrated in
[0056] Nanomagnetic inductor cores according to the invention may be used in various configurations of inductor.
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[0058] One or more lateral isolation regions 1A are provided to surround the nanomagnetic inductor core 1. In this example, the nanomagnetic core is surrounded by a lateral isolation region 1A which is also made of AAO. Nanowires may be provided in at least some of the pores of the AAO in the lateral isolation region 1A, see below. In such a case the lateral isolation region 1A can be produced in a common anodization step with the AAO template that will house the nanowires, reducing the number of steps required for fabrication of the structure. However, in other embodiments the lateral isolation region(s) may be made in a separate step after the nanowires have been grown (e.g. by implementing another hard mask with the same hard masking process as that described below).
[0059] In this example the base substrate 10 is made of high-resistivity silicon, but other materials may be used. In this example the high-resistivity silicon substrate 10 is 10-50 microns thick. A first insulating layer 11 is formed on the substrate 10 so as to provide DC isolation to the substrate (i.e. symmetrical to layer 12 discussed below) and a first conductor (implemented in this example as an electrically-conductive layer 13 formed on the first insulating layer 11) is interposed between the substrate and one side of the nanomagnetic inductor core 1. In this example the first insulating layer 11 is made of an oxide (e.g. SiO.sub.2), but other insulating materials may be used. In this example the conductive layer 13 is made of aluminum, but other conductive materials may be used.
[0060] In the case of a nanomagnetic core formed by an “underpath last” process of the type described below in relation to
[0061] Returning to description of the structure according to the example illustrated in
[0062] An insulator layer 12 is formed on the other side of the nanomagnetic inductor core 1 (i.e. on the top surface of the core 1 in the orientation represented in
[0063] Via-hole conductors 15a traverse the nanomagnetic inductor core 1 and are connected to via-hole conductors 15b which traverse the insulator layer 12. The via-hole conductors 15a, 15b electrically connect the underpath (strip 51 of the first conductor) to the second conductor 14, encircling a region R of the nanomagnetic inductor core 1. In the example illustrated in
[0064] As an example, the thickness of the first conductor 13 may be set in the range 1 μm-3 μm, the thickness of the insulating layer 12 may be set in the range from hundreds of nanometers up to a few microns and the thickness of the second conductor 14 may be set relatively high in order to reduce the equivalent series resistance (ESR). As an example, a typical thickness value for layer 14 when that layer is formed of Cu and it is desired to reduce ESR may be 10 μm or greater.
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[0068] In the example illustrated in
[0069] Various advantages arise in a case where the L component 70 and the C component 72 both include porous templates made of the same material. For example, in this case both components have the same thermal coefficient of expansion and thus thermal stresses in the structure are reduced. Furthermore, co-integration of the components is facilitated because the same process steps can be used for both components during fabrication.
[0070] Depending on the manner in which the connection pads P.sub.L and P.sub.C are interconnected, the stacked components 70, 72 can implement the different equivalent circuits illustrated in
[0071]
[0072] In the method illustrated in
[0073] In this example method, a thick anodizable layer is deposited on top of the barrier layer (S3). As an example, the anodizable layer may be made of aluminum. Typically, an Al anodizable layer is deposited by a physical vapor deposition process and the layer is formed to have thickness of the order of 4-8 μm (usually no thicker than approximately 10 μm). A selected region of the anodizable layer is defined using a hard mask (not shown) made of a resistant material such as SiO.sub.2 which may, for example, be of the order of 1 μm thick, and then the selected region is anodized (S4) to obtain a nanoscale oriented tubular structure-made, for example, of AAO.
[0074] It will be understood that processes S1-S4 form a porous template on a wafer bearing the patterned layers which will serve as an underpath. Although specific processes have been described (e.g. anodization, photolithography) it will be understood that other processes may be adopted to form a porous template on a wafer+underpath, as desired. Moreover, in architectures that do not employ an underpath the porous template may be formed directly on a support substrate (e.g. a wafer).
[0075] Typically, in the present example method, the wafer is of the order of 10 μm thick, the thick conductive layer deposited on the wafer, under the anodic-etch barrier layer, is from 100 nm-1 μm thick and the anodic etch-barrier layer is of the order of 300 nm thick.
[0076] According to the example illustrated in
[0081] If homogenous nanowires are desired, in sub-steps a) and c) the same high-permeability material may be the deposited (i.e. material 1=material 2).
[0082] If it is desired to form nanowires comprising more than two different high-permeability materials, the sequence of deposition and oxidation processes may be adjusted to produce the desired pattern of layers.
[0083] In the above-described example, the fabrication process is simplified by virtue of the fact that the dielectric segments are formed by oxidation of earlier-deposited high-permeability material. However, it is not mandatory to form the dielectric segments by oxidizing the previously-deposited high-permeability material: if desired, dielectric segments may be formed by depositing a selected dielectric material in the pores.
[0084] It will be understood that processes S5-S6 form segmented nanowires in the pores of the porous template. Although specific processes have been described, it will be understood that other processes may be adopted to form segmented nanowires in the porous template, as desired and as appropriate to the materials being deposited as well as the material forming the porous template.
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[0086] Thus, in the method illustrated in
[0087] A thick anodizable layer 8 is deposited on top of the etch-barrier layer (S13) to form the structure illustrated schematically in
[0088] Multi-segmented wires are then co-grown bottom-up by ECD in the tubular structure using one or more Watts-type baths until the pores are filled (S15) as illustrated in
[0089] According to the example illustrated in
[0090] If desired, the above-described method may be varied so that steps S13 to S15 are repeated, over an insulating layer instead of a conductive layer (step S), so as to have nanowires consisting of a lower magnetic segment and an upper magnetic segment separated by an insulating layer.
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[0092] In the method illustrated by
[0093] After the passivation 17 has been formed (as illustrated in
[0094] Although the present invention has been described above with reference to certain specific embodiments, it will be understood that the invention is not limited by the particularities of the specific embodiments. Numerous variations, modifications and developments may be made in the specified embodiments within the scope of the appended claims.