This invention relates generally to periodic layered structures and methods for fabricating and using such periodic layered structures.
Industrial interest in materials having structural and functional features with nanoscale dimensions has been growing rapidly. Nano-structures have been fabricated by semiconductor processing techniques including patterning techniques such as photolithography, electron-beam lithography, ion-beam lithography, X-ray lithography, and the like. Other nano-structures have also been fabricated utilizing structures formed by self-ordering processes.
Some devices for manipulating optical signals have incorporated nanostructures, often including periodic structures such as photonic crystals, for example. Fabrication of optical devices, including macroscopic, microscopic, and nanoscopic elements, has usually used glasses such as silica glasses, transparent crystals, or polymeric materials.
Nanostructures have been applied to display devices, magnetic recording media, quantum-well devices, molecular and gas sensors, optical devices, electroluminescent devices, and electrochromic devices, for example. Periodic layered structures such as superlattice structures may be used in many such applications. Efficient, reproducible, low-cost methods for making periodic layered structures are therefore needed.
The features and advantages of the disclosure will readily be appreciated by persons skilled in the art from the following detailed description when read in conjunction with the drawings, wherein:
For clarity of the description, the drawings are not drawn to a uniform scale. In particular, vertical and horizontal scales may differ from each other and may vary from one drawing to another. In this regard, directional terminology, such as “top,” “bottom,” “front,” “back,” “leading,” “trailing,” etc., is used with reference to the orientation of the drawing figure(s) being described. Because components of the invention can be positioned in a number of different orientations, the directional terminology is used for purposes of illustration and is in no way limiting.
The term “anodization” is used in this specification and the appended claims to mean electrochemical oxidation of an oxidizable material (such as an oxidizable metal) by employing the oxidizable material as an anode in an electrolytic cell and by operating the electrolytic cell with voltage and current suitable to partially or fully oxidize the material of the anode. An “anodic oxide” is the oxide thus formed. An “anodizable material” is a material that can be oxidized in that manner. “Partial anodization” refers to oxidation of less than the entire thickness of a metal layer; i.e., some thickness of unoxidized metal remains after partial anodization, unless full anodization is explicitly specified. “Full anodization” refers to oxidation of the entire thickness of a metal layer. References herein to a layer of electrochemically oxidizable metal are intended to include semiconductor materials such as silicon which, with respect to their anodization, behave like the electrochemically oxidizable metals.
One aspect of the invention provides embodiments of a periodic layered structure having physical and chemical properties varying periodically at least along a direction perpendicular to its layers. The periodicity (pitch) of the layered structure may be characterized by a nanoscale dimension. Throughout this specification and the appended claims, the term “nanoscale” refers to a length of scale corresponding generally to the scale in the definition of U.S. Patent Class 977, generally less than about 100 nanometers (nm).
The term “superlattice” has been used to denote structures such as periodic heterojunctions having a periodicity longer than that of the characteristic crystal lattice of a base material, e.g., due to lattice mismatch. The term “superlattice” has also been used more generally to denote periodic structures constructed from other crystalline, polycrystalline, or non-crystalline materials. “Superlattice” is used in this more general sense in the present specification and claims.
An embodiment of a periodic layered structure may be made by providing a substrate, depositing a quantity of non-porous electrochemically oxidizable material such as a metal over the substrate, anodizing the non-porous electrochemically oxidizable material (partially or fully), and repeating similar steps until a layered structure having a desired periodicity and a desired total structure thickness is completed. The thickness of each layer and/or the periodicity of the periodic layered structure may be nanoscopic. Thus, another aspect of the invention provides methods for fabricating embodiments of periodic layered structures, including structures whose layers have nanoscale dimensions and periodic structures with nanoscale pitch.
One embodiment of a method for fabricating a periodic layered structure (having physical and chemical properties varying periodically at least along a direction perpendicular to its layers) employs steps of providing a substrate, depositing a quantity of non-porous electrochemically oxidizable material over the substrate to form an electrochemically oxidizable layer, anodizing the non-porous electrochemically oxidizable material until a layer of oxide is formed, and repeating alternately the depositing and anodizing steps until a periodic layered structure having a desired periodicity and a desired total thickness is completed. The periodic layered structure may be one of the types known as a superlattice. The non-porous electrochemically oxidizable material is anodized until a layer of oxide having a desired thickness is formed. In some cases, that anodization may be a partial anodization, i.e., less than the entire thickness of the electrochemically oxidizable material is oxidized.
Many electrochemically oxidizable materials are known, including the metals aluminum (Al), tantalum (Ta), niobium (Nb), tungsten (W), bismuth (Bi), antimony (Sb), silver (Ag), cadmium (Cd), iron (Fe), magnesium (Mg), tin (Sn), zinc (Zn), titanium (Ti), copper (Cu), molybdenum (Mo), hafnium (Hf), zirconium (Zr), titanium (Ti), vanadium (V), gold (Au), and chromium (Cr), along with their electrochemically oxidizable alloys, mixtures, and combinations, all of which are suitable for use in this method. Another suitable material is non-porous silicon (Si), although it is not classified as a metal, but as a semiconductor. Thus, references herein to a layer of non-porous electrochemically oxidizable material or metal are intended to include non-porous semiconductor materials such as non-porous silicon which, with respect to their anodization, behave like the non-porous electrochemically oxidizable metals. To simplify the description and drawings, embodiments using metals for a non-porous electrochemically oxidizable material will be described. Those skilled in the art will understand that any non-porous electrochemically oxidizable material may be substituted wherever “metal” is mentioned, except where the metal is explicitly described as not being electrochemically oxidizable.
While porous oxides have been formed by anodization, control of the thickness of oxides thus formed can be problematical. However, the thickness of dense oxide films (with densities comparable to theoretical oxide densities) formed by electrochemical oxidation of non-porous electrochemically oxidizable material is precisely controllable by controlling the anodization voltage, as described in more detail hereinbelow.
Suitable non-porous electrochemically oxidizable materials include the “valve metals,” defined in the review paper by M. M. Lohrengel, “Thin anodic oxide layers on aluminium and other valve metals: high field regime,” Materials Science and Engineering Vol. R11 (1993) pp. 243-294, for example. As described in the review paper by Lohrengel, valve metals may be defined to be in accordance with i=i0*exp(β*E), where i is the oxide formation current, i0 and β are material-dependent constants, and E is the electric field strength in the oxide. Lohrengel goes on to list various properties typical of a valve metal: The surface of an (electro-) polished electrode is covered with 2-5 nanometers of oxide from air or electrolyte passivation. This corresponds to an open circuit potential of about zero V (vs. a hydrogen electrode in the same solution). The thickness of the oxide layer increases during anodization. In a galvanostatic experiment the potential increases almost linearly with time; in a potential sweep experiment with constant potential sweep the current is almost constant. These are equivalent and correspond to a constant charge and, therefore, a constant increase of thickness for a given potential change. The oxide layer is not reduced by (moderate) cathodic currents. Further oxide growth is only observed when the potential exceeds the previous formation potential. The ionic conductivity is small (steady state conditions or at potentials smaller than the formation potential). The electronic conductivity (of undoped oxides) and, hence, oxygen evolution are negligible. An addition of redox systems to the electrolyte causes no additional currents. Corrosion is small at moderate pH values. The oxide grows independently of the composition of the electrolyte. A (possible) incorporation of anions from the electrolyte, for example, causes no fundamental changes of the layer properties. The combination of the low oxide electrode potential (and, therefore, air passivation), negligible electronic conductivity, and the lack of oxygen evolution is not accidental, as the oxide electrode potential depends almost linearly on the band gap. Valve metals are usually covered by oxide films of the barrier type. An ideal barrier oxide “. . . is a nonporous, thin oxide layer possessing electronic and ionic conductivity at high electric field strength.”
Returning now to the description of a method embodiment for fabricating a periodic layered structure, the layer of non-porous electrochemically oxidizable metal (or, in the case of silicon, for example, non-porous electrochemically oxidizable semiconductor) may be deposited by any suitable conventional deposition method, such as evaporation, sputtering, plating, electroplating, atomic layer deposition (ALD), or chemical vapor deposition (CVD). The metal layer may have a thickness of about two nanometers (2 nm) or greater, for example, with essentially no theoretical upper limit, but limited only by practical considerations such as anodizing voltage, application requirements, etc.
In practice, the metal layer may be made thinner on a smooth, substantially planar substrate than on a substrate which is not smooth and planar. The substrate may be prepared by polishing to a smooth planar surface before depositing the metal layer. Also, the metal layer may be planarized after its deposition, e.g., by mechanical polishing, chemical polishing, electrochemical polishing, chemical mechanical polishing (CMP), or other planarization technique.
The desired periodicity of structures that are made by such a method depends on the intended application of the periodic layered structure. For example, a periodic layered structure to be used as a photonic crystal may require a periodicity determined by the wavelength of the electromagnetic radiation that is to be processed by the photonic crystal. Method embodiments performed in accordance with the present invention may make periodic layered structures having periodicities (pitch) of about five nanometers (nm) or greater.
When the metal layer is anodized, the total thickness typically increases. The volume ratio of oxide to consumed metal is typically greater than one. For example, a five-nanometer-thick aluminum layer may be converted by anodization to about six and a half nanometers of aluminum oxide if the full thickness of aluminum is anodized, and a partially anodized layer (the entire film, aluminum and alumina together) has a thickness intermediate between five and about 6.5 nanometers. Similarly, partial anodization of a five nanometer film of tantalum results in a tantalum oxide film having a thickness intermediate between zero (or none) and about 11.5 nanometers (the entire film having thickness intermediate between 5 and 11.5 nanometers).
Thus, another aspect of the invention provides embodiments of a method for fabricating a periodic layered structure by employing the steps of providing a substrate, depositing a quantity of a first metal, anodizing the first metal until a desired thickness of first oxide is formed, depositing a quantity of a second metal over the first oxide, anodizing the second metal until a desired thickness of second oxide is formed, and repeating the preceding four steps a number of times until a layered structure having a desired periodicity and a desired total structure thickness is completed.
The first and second metals may be distinct and different metals, or they may be the same metal. As in embodiments described above, each of the metals may be a material selected from among Al, Ta, Nb, W, Bi, Sb, Ag, Cd, Fe, Mg, Si, Sn, Zn, Ti, Cu, Mo, Hf, Zr, Ti, V, Au, and Cr, and their alloys, mixtures, and combinations. Some embodiments worth mentioning specifically are those in which the first metal comprises aluminum or tantalum, and those in which the second metal comprises aluminum or tantalum. Examples of such embodiments are described in more detail hereinbelow.
Those skilled in the art will recognize that the number of distinct metals and their corresponding oxides may also be more than two, as illustrated in
(
If the second metal and third metals deposited in steps S120 and S140 are different from each other and different from the first metal as deposited in steps S100 and S130, the completion of anodization step S150 serves to provide one composite layer 95, i.e., one period, of the periodic layered structure. For some applications the series of steps S100-S150 is then repeated until the desired periodic layered structure is complete, as determined in decision step S160.
Thus, when the structure is complete after a suitable number of repetitions, completion of anodization step S150 ends the process. The structure is determined to be complete if the total structure thickness has reached the desired thickness and/or if the total number of layers provided is the desired total number. If the periodic layered structure is not complete, suitable steps S100, S110, S120, S130, S140, and S150 are repeated until the desired periodic layered structure is complete. If the first, second, and third metals shown in
As shown by the dashed line in
Also, both the second metal deposited and anodized in steps S110 and S120 and the third metal deposited and anodized in steps S140 and S150 may be the same as the first metal as deposited in steps S100 and S130. In that case, if the corresponding thicknesses are also made equal, the completion of step S150 serves to provide three composite periodic layers, i.e., three periods of the periodic layered structure. Again, if the structure is complete as determined in decision step S160, this ends the process. Otherwise, suitable steps are repeated until the structure is complete. The structure is determined to be complete if the total structure thickness has reached the desired thickness and/or if the total number of layers provided is the desired total number.
In another example, an embodiment may be made that is related to the embodiments illustrated by
Those skilled in the art will recognize that various suitable electrolytes and various suitable conditions of anodization may be used for different non-porous electrochemically oxidizable materials. For example, dense anodic oxide films on Al and Ta may be prepared in electrolytes based on citric acid, boric acid, ammonium tartrate, ammonium borate, and many others. Tungsten may be oxidized in sulfuric-acid-based electrolyte, for example, and zinc may be oxidized in NaOH and K2Cr2O7, etc. In general, electrolytes may also include other surfactants and/or buffer materials.
Additional embodiments related to the embodiments illustrated by
Thus, another aspect of the invention provides a method for fabricating a periodic layered structure including the steps of providing a substrate, depositing a quantity of a first metal over the substrate to form a first metal layer, depositing a quantity of a second metal over the first metal layer to form a second metal layer, anodizing both the first and second metal layers until a composite layer of first and second oxides is formed, and repeating the three steps (two depositions and one combined anodization) a number of times until a layered structure having a desired periodicity and a desired structure thickness is completed.
In all the embodiments illustrated in
The method embodiments illustrated by
All of the periodic layered structure embodiments made by the methods described herein may be one of the types of layered structure known as a superlattice. The periodicities (pitch) of the periodic layered structures may be comparable to the thickness of native oxides commonly formed on metals that are electrochemically oxidizable, e.g., about 5 nanometers or greater.
It was mentioned above that a first metal in an embodiment of a periodic layered structure may comprise a metal, such as platinum, that is not readily oxidizable electrochemically. More generally, one or more of the layers of the periodic layered structure may comprise such a metal, e.g., platinum, palladium, or rhodium, while one or more other layers comprise a material that is readily oxidizable electrochemically.
Of the known electrochemically oxidizable metals, the anodization processes of tantalum and aluminum, especially, have been extensively studied. Thus, specific embodiments in which a first metal comprises aluminum or tantalum, and those in which a second metal comprises aluminum or tantalum (and the corresponding oxides formed are aluminum oxide and tantalum oxide respectively) provide good examples.
At least some of the method embodiments described herein are believed to operate in accordance with a common regime for electrochemical oxidation of metals such as tantalum (Ta), aluminum (Al), and other metals to produce dense oxides, including two major stages: galvanostatic and potentiostatic. During the galvanostatic stage, characterized by constant current density, steady state oxidation of metal occurs. During the potentiostatic stage, characterized by constant cell voltage, generally there is no more metal consumption, but the oxide layer thickness is still increasing due to diffusion of oxygen ions into the oxide matrix. However, the invention should not be construed as being limited to the consequences of any particular theory of operation.
As illustrated by
A second metal layer is deposited over the first-metal oxide, forming a second-metal layer 20 having a second-metal edge. Similarly to the other embodiments described hereinabove, the first-metal depositing, anodizing, and second-metal depositing steps are repeated alternately until a periodic layered structure having a desired periodicity and a desired structure thickness is completed (as shown in
Thus, another aspect of the invention provides embodiments of a method for fabricating an imprinting stamp for lithography (such as nano-lithography), comprising steps of providing a substrate, depositing a quantity of a first metal over the substrate to form a first metal layer having a first-layer thickness, anodizing the first metal until a desired thickness of first oxide is formed, depositing a quantity of a second metal over the first oxide, whereby a second metal layer having a second-metal layer edge is formed, repeating the previous three steps a number of times until a layered structure having a desired periodicity and a desired structure thickness is completed, selectively anodizing each second-metal layer edge until a desired thickness of second oxide is formed, and selectively etching back one of the two different oxides (the first oxide and second oxide), thus forming an imprinting stamp having the desired periodicity. The imprinting stamp has salient portions of one of the two oxides, separated by recesses where the other oxide has been etched back.
For this method embodiment, the first and second metals should comprise different metals, at least one of which can be electrochemically oxidized, such as Al, Ta, Nb, W, Bi, Sb, Ag, Cd, Fe, Mg, Si, Sn, Zn, Ti, Cu, Mo, Hf, Zr, Ti, V, Au, and Cr, or their alloys, mixtures, or combinations.
For example, in
A suitable etchant, for example, has about 5-40 wt. %,of H3PO4, about 2-15 wt. %, of CrO3, and etching temperature of 80-100° C. This etchant does not appreciably etch the aluminum or tantalum oxide. When the aluminum oxide has been etched out, remaining recesses 105 have reproducible profiles and dimensions suitable for use as an imprinting stamp. The salient portions composed of tantalum oxide also have suitable reproducible profiles and dimensions.
Another embodiment of an imprinting stamp also has alternate layers of metal and oxide. To fabricate such an embodiment, a suitable substrate is provided, a quantity of metal is deposited over the substrate to form a metal layer having a metal edge, and the metal is anodized until a second-layer thickness of oxide is formed. As in other embodiments described hereinabove, the depositing and anodizing steps are repeated alternately until a periodic layered structure having a desired periodicity and a desired structure thickness is completed. Then the metal edge of each metal layer is selectively etched back to form a recess, whereby an imprinting stamp having the desired periodicity is formed. Alternatively, in principle, the edges of the oxide layers could be selectively etched using a suitably selective etchant, leaving salient portions of the metal layers. This etching may be performed for a predetermined time.
The method embodiments described above for fabricating an imprinting stamp for lithography are specific examples of a more general method for fabricating an imprinting stamp. The more general method includes steps of providing a periodic layered structure comprising layers of at least two materials differing in etch rate, and of selectively etching back the edge of at least one of the at least two materials to form recesses separated by salient portions, thereby making an imprinting stamp having the periodicity of the periodic layered structure. In the imprinting stamp embodiments disclosed herein, the periodic layered structure is provided by methods using electrochemical oxidation as described above.
The periodic layered structures of
Methods performed in accordance with the invention are useful for fabricating imprinting stamps for lithography. Structures made in accordance with the invention may also be used for photonic-crystal applications and, more generally, for many other applications requiring superlattices or other periodic layered structures.
Although the foregoing has been a description and illustration of specific embodiments of the invention, various modifications and changes thereto can be made by persons skilled in the art without departing from the scope and spirit of the invention as defined by the following claims. For example, the steps of the various method embodiments may be performed in the order recited, or the order of steps may be varied somewhat. Functionally equivalent materials may be substituted for materials described in this specification and the claims. It is not intended that the methods and the resulting structures described should exclude from the periodic layered structures incorporation of layers that are not anodized. Thus, for example, an insulating layer that is not formed by electrochemical oxidation may be included in the stack of layers of the periodic layered structure. For specific examples of this, a metal or semiconductor layer may be thermally oxidized, or a layer of silicon oxide, silicon nitride, or diamond may be periodically deposited as one or more sublayers of the stack if desired for a particular application.
This application is related to co-pending and commonly assigned application Ser. No. 10/817,729, filed Apr. 2, 2004 (attorney docket no. 200311571), the entire disclosure of which is incorporated herein by reference, and is related to co-pending and commonly assigned applications Ser. No. ______ (attorney docket no. 200401845) and Ser. No. ______ (attorney docket no. 200406118).