The present invention relates to magnetic structures, to methods of fabricating the structures, and to devices incorporating such structures.
The micro-magnets commonly used in micro-magnetic devices are bulk rare earth magnets, including elements of Niobium Iron Boron (Nd-Fe-B) and Samarium Cobalt (SmCo) individually micro-machined using wire electrodischarge machining [1]. However, this fabrication method is not compatible with full integration or batch fabrication since the magnets have to be manually assembled.
Electrochemical processes including electroplating and electrolysis deposition are well-suited to fulfill the requirements of high yield and cost effective processes, but the resulting magnetic properties of electroplated rare earth materials are very much inferior to their bulk counterparts [2, 3]. The main reason for this is the difficulty in effecting electrolytic co-deposition of rare earth metals in pure metallic states from the electrolyte, due to the low equilibrium potential of the rare earth elements [3].
Cobalt platinum (CoPt) is a class of promising hard magnetic films which can be electroplated with relatively good magnetic properties. Theoretically, ordered phases of Co50Pt50 could show a very high coercivity of >10 kOe [4]. However, it is known that when the thickness of a CoPt film exceeds ˜1 μm, its inherently high perpendicular magnetic anisotropy (PMA) rapidly deteriorates with increasing thickness [5]. This is a major drawback for the application of this material in micro-devices since thick films or microstructures are often required for generation of a sufficiently high absolute magnetic field for-micro-actuation purposes.
In a previous patent application (Singapore patent application 200504005-5, filed 24 Jun. 2005, claiming priority from Singapore patent application no. 200503561-3 filed 3 Jun. 2005, neither of which applications had been published by the priority date of the present application) two of the present inventors proposed, among other materials, a magnetic structure for use in a MEMS device and having multiple electroplated layers of Co-Pt-P.
The present invention aims to provide a magnetic structure suitable for use in a micro-magnetic device, as well as micro-magnetic devices incorporating the structure. It further aims to provide methods for producing the structure.
In general terms the invention proposes that a magnetic structure is formed by electrodeposition onto substrate of a CoPt layer, with additive tungsten W and phosphorus P (hereafter denoted as CoPtWP).
Preferred values for the composition are 45-95 atomic % cobalt, 0.5-50 atomic % platinum, 0.5-20 atomic % tungsten, and 0.5-10 atomic % phosphorus.
As discussed below in detail, certain embodiments of the invention are magnetic films having high magnetization and coercivity. Specifically, a magnetic film of CoPtWP has been successfully fabricated by an electroplating process under selected process conditions.
In one embodiment of the invention, a multi-layered structure comprising thin individual CoPtWP layers spaced by non-magnetic electrically-conducting layers was fabricated. This makes it possible to achieve higher remnant magnetization, and further makes it possible to avoid the degradation in Hc after annealing which is observed for the case of a thick single layer film. Hence, the embodiment makes possible the use of a thick CoPtWP film (in the form of a multi-layered structure) to generate a sufficiently high absolute magnetization field with high coercivity properties for application in magnetic micro-devices.
Preferably, the thickness of each CoPtWP layer is kept to a maximum of 1.5 μm, more preferably no more than 1 μm, and typically about 0.5 μm.
Preferred features of the invention will now be described, for the sake of illustration only, with reference to the following figures in which:
a is a graph showing the variation of out-of-plane coercivity Hc with film thickness for CoPtP and CoPtWP films.
b is a graph showing the variation of out-of-plane absolute magnetization Mr with film thickness for CoPtP and CoPtWP films.
c is a graph showing the variation of out-of-plane squareness S with film film thickness for CoPtP and CoPtWP films.
a is a graph showing the variation of out-of-plane coercivity Hc with film thickness before and after annealing in air at 320° C. for 2 hrs for a CoPtWP film.
b is a graph showing the variation of out-of-plane absolute magnetization Mr with film thickness before and after annealing in air at 320° C. for 2 hrs for a CoPtWP film.
c is a graph showing the variation of out-of-plane squareness S with film thickness before and after annealing in air at 320° C. for 2 hrs for a CoPtWP film.
a is a graph showing the variation of out-of-plane coercivity Hc with annealing time at 320° C. in air for 5 samples of CoPtWP films each with about 0.5 μm thickness.
b is a graph showing the variation of out-of-plane absolute magnetization Mr with annealing time at 320° C. in air for 5 samples of coPtWP films each with about 0.5 μm thickness.
c is a graph showing the variation of out-of-plane squareness S with annealing time at 320° C. in air for 5 samples of CoPtWP films each with about 0.5 μm thickness.
a is the hysteresis curve of the embodiment of
b is the hysteresis curve of the embodiment of
A method of fabricating a magnetic structure which is an embodiment of the invention will now be described.
In a first step, seedlayers of Cr/Au (20/200 nm) were formed by sputtering on a glass substrate. After activation of the seedlayer with concentrated H2SO4 (for about 3 minutes), electrodeposition was carried using a rotating disk electrode (RDE) system via a galvanostat/potentiostat. Ag/KCI was used as the reference electrode while pure platinum wire was used as the anode, to produce a single layer of magnetic material.
In the case of the embodiment, the electrolyte contained tungsten (W). However, a control experiment was performed, as a comparative example, in which exactly the same process was carried out using an electrolyte composition not containing tungsten, thereby producing a layer of Cobalt-Platinum-Phosphorus (“CoPtP”). The composition of the two electrolyte solutions is shown in Table 1. The properties of the electrolyte in the case of the embodiment are given in the third column of the table (“Co-Pt-P-W”), while the properties of the electrolyte in the comparative example are shown in the second column (“Co-Pt-P”). Each of the solutions were adjusted to a pH of 4.5 using NaOH and H2SO4. The electroplating conditions of current density and agitation speed are summarized in Table 1.
An out-of-plane hysteresis curve of the comparative example, using CoPtP electroplated for 3 min, is shown as the solid curve 1 in
By contrast, a typical hysteresis curve of the embodiment of the invention is shown by the curve 2 in
The effect of additive W in the CoPtP system was further investigated as a function of film thickness as shown in FIGS. 2(a), 2(b) and 2(c). Out-of-plane Hc and S decrease with increasing film thickness for both CoPtP and CoPtWP. Nevertheless, at all film thicknesses, CoPtWP exhibits a higher Hc and S than CoPtP. As expected, absolute Mr (as well as Ms) increases with film thickness since there are more magnetic materials with thicker films. However, the increase in absolute Mr seems to reach a plateau beyond a film thickness of about 1 μm as shown in
FIGS. 4(a), 4(b) and 4(c) show the thermal stability of CoPtWP as a function of film thickness upon annealing at 320° C. for 2 hrs in air atmosphere. The results shown in
The effect of prolonged annealing time at the same temperature is shown in FIGS. 5(a) to 5(c) for 5 separate samples processed with parameters shown in Table 1 under the same conditions i.e. a plating time of 3 min. For each sample, experimental points are given for each of a number of annealing times, and a respective line is provided interpolating those points. Further improvement in Hc and S continue to be observed until beyond about 6 hrs upon which a decrease in magnetic properties were observed. Due to inevitable oxidation caused by annealing in air, Ms continues to drop as the annealing time increases until when it dropped below the original unannealed Mr level beyond which Mr is greatly affected. From
To summarize, it was possible to produce a single layer of CoPtWP, due to grain decoupling caused by the formation of non-magnetic metallic oxides at grain boundaries, exhibiting an Hc improved to ˜4211-4619 Oe with absolute Mr of ˜7.0-8.4 memu, and S of ˜0.68-0.85, after annealing at 320° C.
Although higher absolute remnant magnetic flux (i.e. Mr) could be achieved with thicker films, a thick CoPtWP film suffers drastic magnetic degradation after annealing at 320° C. Hence, with the aims of increasing Mr and avoiding the annealing degradation, the effects of performing annealing during the formation of the multilayer structure was studied experimentally. For a preliminary study, a 3-layered multilayered structure with Au interlayers was fabricated. Specifically, in a second embodiment of the invention a first layer of CoPtWP is deposited by the steps described above in relation to the first embodiment of the invention, but following the deposition of the CoPtWP magnetic layer, in this second experiment a layer of gold (Au) was plated over the magnetic layer. A non-cyanide Au electrolyte solution was used for plating the Au interlayer at a current density of 25 mA/cm2, pH 4.5 and an agitation speed of 500 rpm. Under these plating conditions, the film thickness of each Au interlayer was about 200 nm. As in the case of the sputtered Au seedlayer, each plated Au interlayer was activated by concentrated H2SO4 (for about 3 minutes) before plating onto it of an additional magnetic CoPtWP layer (or, in the case of the comparative example, a CoPtP magnetic layer). This process was repeated, to form a multi-layered structure comprising three layers of magnetic CoPtWP interleaved by two layers of plated gold (Au). This structure is as shown schematically in
The annealing study was carried out in air at 320° C. via two different approaches. One of the approaches was a one-time annealing of the 3-layered structure at 320° C. for 3 hrs, while the other approach was to anneal separately the individual CoPtWP film at 320° C. for 1 hr after each was plated on and before the subsequent plating of the next layer.
References
Number | Date | Country | Kind |
---|---|---|---|
200507703 | Dec 2005 | SG | national |