RUGGED, SINGLE CRYSTAL WIDE-BAND-GAP-MATERIAL SCANNING-TUNNELING-MICROSCOPY/LITHOGRAPHY TIPS
20210263069 · 2021-08-26
Inventors
- Steven R.J. Brueck (Albuquerque, NM)
- Daniel FEEZELL (Albuquerque, NM, US)
- John RANDALL (Albuquerque, NM, US)
- Tito BUSANI (Albuquerque, NM, US)
- Joshua B. BALLARD (Albuquerque, NM, US)
- Mahmoud BEHZADIRAD (Albuquerque, NM, US)
- Ashwin Krishnan RISHINARAMANGALAM (Albuquerque, NM, US)
Cpc classification
G01Q60/16
PHYSICS
G01Q80/00
PHYSICS
B82B3/0004
PERFORMING OPERATIONS; TRANSPORTING
International classification
G01Q60/16
PHYSICS
B82B3/00
PERFORMING OPERATIONS; TRANSPORTING
G01Q80/00
PHYSICS
Abstract
Provided is a composite metal-wide-bandgap semiconductor tip for scanning tunneling microscopy and/or scanning tunneling lithography, a method of forming, and a method for using the composite metal-wide-bandgap semiconductor tip.
Claims
1. A method of forming a composite tip for a scanning tunneling microscope (“STM”), comprising: using a nanomanipulator to select a single crystal wide-band-gap semiconductor from an array of formed single crystal wide-band-gap semiconductors epitaxially grown selectively on a crystalline substrate; preparing an electrically conductive wire to provide a substantially flat end surface that is substantially perpendicular to the wire length direction; transferring the single crystal wide-band-gap semiconductor from the growth substrate to the substantially flat end surface of the electrically conductive wire; and affixing the single crystal wide-band-gap semiconductor to the substantially flat end surface of the electrically conductive wire to form the composite tip.
2. The method of claim 1, wherein the affixing comprises welding using a Pt ion source.
3. The method of claim 1, wherein the single crystal wide-band-gap semiconductor comprises a group III-N nanowire wherein the group III composition comprises one or more of Ga, In, or Al.
4. The method of claim 1, wherein the composite tip has dimensions that are from about a length of 0.5 to 4 μm, with a faceted diameter of about 0.1 to 1 μm, a tip radius of about or less than about 2 nm, and with a controlled doping to provide a resistivity of about 10.sup.−2 Ohm-cm.
5. The method of claim 1, wherein the electrically conductive wire comprises platinum, iridium, tungsten, and doped silicon and combinations thereof.
6. The method of claim 1, wherein the electrically conductive wire and the tip is affixed having a common orientation within about ±1°.
7. A method of forming an array of composite tips for use in scanning tunneling microscopy, comprising: preparing an array of scanning tunneling microscope tip precursors on a crystalline substrate; providing an area for selective area growth of a wide bandgap semiconducting material on each tip precursor; growing a III-N wide bandgap material nanowire on each selective growth area wherein the nanowire has a faceted diameter of about 0.1 to 0.5 μm, a tip radius of about or less than about 2 nm, and with a controlled doping to provide a resistivity of about 10.sup.−2 Ohm-cm; separating the array of scanning tunneling tip precursors into subarrays wherein each subarray contains at least one scanning tunneling tip; and mounting the at least one of the subarrays of scanning tunneling microscope tip precursors for use in a scanning tunneling microscope.
8. The method of claim 7, wherein the wide bandgap material is one of GaN, AlN, InN, or alloys thereof.
9. The method of claim 7, wherein the growth technique is metal organic chemical vapor deposition and the growth is controlled to provide the sharp tip of the nanowire with a radius of less than about 2 nm without further processing.
10. The method of claim 7, wherein a sub-array contains only a single scanning tunneling tip precursor.
11. The method of claim 7, wherein a sub-array contains more than one scanning tunneling tip precursor and means is provided for relative motion between the multiple scanning tunneling tips to allow for a degree of parallel application in a scanning tunneling microscope.
12. A method of forming a composite tip for a scanning tunneling microscope (“STM”), comprising: using a nanomanipulator to select a single crystal wide-band-gap semiconductor from an array of formed single crystal wide-band-gap semiconductors epitaxially grown selectively on a crystalline substrate; preparing an electrically conductive wire to provide a substantially flat end surface that is substantially perpendicular to the wire length direction; transferring the single crystal wide-band-gap semiconductor from the growth substrate to the substantially flat end surface of the electrically conductive wire; and affixing the single crystal wide-band-gap semiconductor to the substantially flat end surface of the electrically conductive wire to form the composite tip, wherein the electrically conductive wire comprises a substantially cylindrical body and a distal end tapered to a diameter larger than the single crystal wide-band-gap semiconductor and terminated with a flat surface that is approximately perpendicular to a transverse axis of the electrically conductive wire.
13. The method of claim 12, wherein the single crystal wide-band-gap semiconductor comprises a group III-N material.
14. The method of claim 13, wherein the group III material comprises one or more of Ga, In, or Al.
15. The method of claim 12, wherein the body of the single crystal wide-band-gap semiconductor has a substantially constant diameter and is bounded by a surface with a diameter ranging from about 0.1 to 1.0 micrometer and the surface comprising a first set of facets corresponding to natural crystal planes of the single crystal wide-band-gap semiconductor.
16. The method of claim 15, wherein a tip of the single crystal wide-band-gap semiconductor tapers to a radius of 2 nm or less, and wherein the surface of the tip comprises additional crystal facets of the wide-band-gap semiconductor.
17. The method of claim 12, wherein the electrically conductive wire comprises platinum, iridium, tungsten, and doped silicon and combinations thereof.
18. The method of claim 12, wherein the electrically conductive wire and the tip is affixed having a common orientation within about ±1°.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the present teachings and together with the description, serve to explain the principles of the disclosure.
[0018]
[0019]
[0020]
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
DESCRIPTION OF THE EMBODIMENTS
[0035] Reference will now be made in detail to the present embodiments, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
[0036] Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the embodiments are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Moreover, all ranges disclosed herein are to be understood to encompass any and all sub-ranges subsumed therein. For example, a range of “less than 10” can include any and all sub-ranges between (and including) the minimum value of zero and the maximum value of 10, that is, any and all sub-ranges having a minimum value of equal to or greater than zero and a maximum value of equal to or less than 10, e.g., 1 to 5. In certain cases, the numerical values as stated for the parameter can take on negative values. In this case, the example value of range stated as “less that 10” can assume negative values, e.g. −1, −2, −3, −10, −20, −30, etc.
[0037] The following embodiments are described for illustrative purposes only with reference to the Figures. Those of skill in the art will appreciate that the following description is exemplary in nature, and that various modifications to the parameters set forth herein could be made without departing from the scope of the present embodiments. It is intended that the specification and examples be considered as examples only. The various embodiments are not necessarily mutually exclusive, as some embodiments can be combined with one or more other embodiments to form new embodiments.
[0038] Generally speaking, examples of the present disclosure provides a composite tip for a scanning tunneling microscope (“STM”), methods of making the composite tip, and various uses for the composite tip. The composite tip comprises an electrically conductive wire and a tip affixed to the electrically conductive wire, wherein the tip comprises a single crystal wide-band-gap semiconductor. The single crystal wide-band-gap semiconductor can comprise a group III-N nanowire, wherein the group III-N nanowire can comprise GaN, AlN, InN, InGaN, AlGaN, or AlInGaN. Other materials as disclosed herein can also be used for the single crystal wide-band-gap semiconductor. The wide-bandgap semiconductor material can be formed into a single crystal nanowire. In one example, the single crystal nanowire tip is grown epitaxially with a controlled dopant distribution to provide a controlled resistivity, and with a faceted crystal shape that provides a tip with a radius of less than about 2 nm without requiring tip sharpening as do the metal tips. The electrically conductive wire can be composed of materials, including but are not limited to: platinum; iridium; tungsten; doped semiconductors; and combinations thereof.
[0039] As used herein, the term “nanowire” generally refers to any elongated conductive or semiconductive material that includes at least one minor dimension, for example, one of the cross-sectional dimensions such as width or diameter, of less than or equal to about 1000 nm. In various embodiments, the minor dimension can be less than about 100 nm. In various other embodiments, the minor dimension can be less than about 10 nm. In various examples, the diameter can be about 0.1 to 1 μm. The nanowires can have an aspect ratio (e.g., length:width and/or major dimension:minor dimension) of about 100 or greater. In various embodiments, the aspect ratio can be about 200 or greater. In various other embodiments, the aspect ratio can be about 2000 or greater. In an exemplary embodiment, the cross-section of the nanowire can be highly asymmetric such that in one direction of the cross-sectional dimension can be much less than 1000 nm and in an orthogonal direction the dimension can be substantially greater than 1000 nm.
[0040] It is also intended that the term “nanowires” also encompass other elongated structures of like dimensions including, but not limited to, nanoshafts, nanopillars, nanoneedles, nanorods, and nanotubes (e.g., single wall nanotubes, or multiwall nanotubes).
[0041] The nanowires can have various cross-sectional shapes, such as, for example, rectangular, hexagonal, polygonal, square, oval, or circular. Accordingly, the nanowires can have cylindrical and/or cone-like three dimensional (3-D) shapes. In various embodiments, a plurality of nanowires can be, for example, substantially parallel with respect to each other.
[0042] Metallic bonds largely ionic and bond angles are not strongly sterically limited, allowing W atoms to move on the surface, while the covalent bonds of WBS materials provide a more significant steric hindrance to motion of individual atoms along a surface. Covalent bonds and their sensitivity to bond angle results in a lower surface mobility than for ionic metal bonds. This is the primary advantage to the use of covalently bonded materials for STM and/or STL applications as opposed to the use of metallic materials with comparable bond strengths. For example, surface Si atoms (at least ones that are dimerized or are part of an island) are stable at room temperature, while W atoms will move from island edges to lower surface energy facets at room temperature, supporting the proposition that GaN will be more stable than W as an STM tip. As such, STM tips made of GaN or related wide band gap semiconductors tend to be more robust than W tips. Also, GaN can be grown with a sharp tip not requiring any additional processing. In contrast, an initially single crystal tungsten material must be machined/milled/etched/etc. into a tip shape leaving complex faceting and adatoms that are probably not incorporated into the lattice.
[0043] An additional advantage of the current invention is that the tip shape is actually known. Not only at the apex but over the entire physical range of the tip that contributes to the imaging and lithography modes of operation. For imaging this range is very small (on the order of a nm distance from the apex), but for lithography in the high bias mode where the tip is effectively a cold field emitter of electrons, the portion of the tip that controls the emission is on the order of a micrometer from the tip apex. The WBS tips have a well-defined shape that will give far more reproducible lithographic results in the high-bias mode. In contrast the tip shape for metal tips is almost never known.
[0044] According to examples, the composite tip is constructed to have one or more of the following attributes in order to overcome the issues of the conventional tips, as described above. First, the composite tip can be conductive in order to support the tunneling current. Second, the composite tip can have a sharp apex, possibly ending with a well-defined atomic arrangement determined by the local atomic structure and bonding. Within the context of this disclosure, the term “sharp” will mean a tip with a radius of less than about 2 nm, for example, a radius between about 1 nm and about 2 nm. Third, the composite tip can have atomic bonds stronger than the atomic bonds that need to be broken on the surface of the sample where the pattern is to be created. Fourth, the composite tip can be manufactured in a very clean environment, as is known in the art.
[0045] Compared to crystalline, polycrystalline, or amorphous metals, single crystal nitrides tend to have exceptionally strong bonds and they can be readily grown in a single crystal with a sharp termination defined by natural crystal planes. The process also allows control, at the nm scale, of the x, y, z dimensions of the tip, as well the doping of the tip (i.e. its resistivity) in order to regulate the current flow between the STM tip and the sample.
[0046] In order to meet these requirements, example composite tips were made and tested by the inventors that were fabricated using single crystalline nanowire GaN bonded to PtIr wire holders. Although the direct growth of single crystalline GaN nanowire tips on substrates suitable for use in a STM apparatus is discussed further below, a composite tip comprising Group III-N nanowires bonded to metallic wires can be used as discussed herein.
[0047] As known in the art, nanowires can be formed using a variety of methods. For examples, the nanowires can be formed using any of the method disclosed in the following references: S. D. Hersee et al. GaN nanowire light emitting diodes based on templated and scalable growth process. Electronic Letters. Vol. 45. No. 1 (Jan. 1, 2009); A. K. Rishinaramangalam et al. Controlled Growth of Ordered III-Nitride Core-Shell Nanostructure Arrays for Visible Optoelectronic Devices. Journal of Electronic Materials. (Oct. 21, 2014) (doi: 10.1007/s11664-014-3456-z); M. Nami et al. Tailoring the morphology and luminescence of GaN/InGaN core-shell nanowires using bottom-up selective-area epitaxy. Nanotechnology 28 (Dec. 2, 2016) (doi: 10.1088/0957-4484/28/2/025202); and S. D. Hersee et al. The Controlled Growth of GaN Nanowires. Nano Letters. Vol. 6, No. 8., 1808-1811 (2006).
[0048] In one example as described in U.S. Pat. No. 8,410,496 titled “Pulsed Growth of Catalyst-Free Growth of GaN Nanowires and Application in Group III Nitride Semiconductor Bulk Material,” issued on Apr. 2, 2013, which can be used to form the present nanowires, the nanowires can be formed on/from a support, which can include selected surface regions where the nanowires can be connected to and extend (e.g., be grown) from. The support of the nanowires can also include a substrate formed from a variety of materials including Si, SiC, sapphire, III-V semiconductor compounds such as GaN, or GaAs and related compounds. The support of the nanowires can also include a selective growth mask formed on the substrate. In various examples, the support of the nanowires can further include a buffer layer disposed between the selective growth mask and the substrate.
[0049] In various examples, the nanowires and/or nanowire arrays can be formed using a III-V compound semiconductor materials system, for example, the group III-N compound materials system. Examples of the group III elements can include Ga, In, or Al, which can be formed from exemplary group III precursors, such as trimethylgallium (TMGa) or triethylgallium (TEGa), trimethylindium (TMln) or trimethylaluminum (TMAl). Exemplary N precursors can be, for example, ammonia (NH.sub.3). Other group V elements can also be used, for example, P or As, with exemplary group V precursors, such as tertiarybutylphoshine (TBP), or arsine (AsH.sub.3).
[0050] In the following description, group III-N semiconductor alloy compositions can be described by the combination of group III-N elements, such as, for example, GaN, AlN, InN, InGaN, AlGaN, or AlInGaN. Generally, the elements in a composition can be combined with various molar fractions. For example, the semiconductor alloy composition InGaN can stand for In.sub.xGa.sub.1-xN, where the molar fraction, x, can be any number less than 1.00. In addition, depending on the molar fraction value, various active devices can be made by similar compositions.
[0051] In various embodiments, the nanowires and/or nanowire arrays can include a dopant from a group consisting of: a p-type dopant from Group II of the periodic table, for example, Mg, Zn, Cd and Hg; a p-type dopant from Group IV of the periodic table, for example, C; or an n-type dopant selected from a group consisting of: Si, Ge, Sn, S, Se and Te.
[0052] In various embodiments, the nanowires and/or nanowire arrays can have high-quality heterogeneous structures and be formed by various crystal growth techniques including, but not limited to, metal-organic chemical vapor deposition (MOCVD) (also known as organometallic vapor phase epitaxy (OMVPE)), molecular-beam epitaxy (MBE), gas source MBE (GSMBE), metal-organic MBE (MOMBE), atomic layer epitaxy (ALE), or hydride vapor phase epitaxy (HVPE).
[0053] In various embodiments, a multiple-phase growth mode, for example, a two-phase growth mode, can be used for the high-quality crystal growth of nanowires and/or nanowire arrays. For example, a first phase growth mode such as a selective growth mode can be used to provide a condition for growth selectivity and nucleation of the nanowires and/or nanowire arrays. In the selective growth mode, standard crystal growth methods, for example, standard MOCVD, can be used to nucleate the growth of the nanowires with a desired thickness of, for example, about 10 nm or more.
[0054] The second phase growth mode can create a process to continue the growth of each nanowire and maintain its cross-sectional features from the first growth mode, and also provide an arbitrary desired length. The second phase growth mode can be applied by a growth-mode-transition, which can terminate the first phase growth mode. In the second phase growth mode, a pulsed growth mode, for example, a pulsed MOCVD growth, can be used.
[0055] As used herein, the term “pulsed growth mode” refers to a process in which the group III and group V precursor gases are introduced alternately in a crystal growth reactor with a designed sequence. For example, TMGa and NH.sub.3 can be used as the precursors for an exemplary formation of GaN nanowires and/or nanowire arrays. In the pulsed growth mode, TMGa and NH.sub.3 can be introduced alternately in a sequence that introduces TMGa with a designed flow rate (e.g., about 10 sccm) for a certain period of time (e.g., about 20 seconds) followed by introducing NH.sub.3 with a designed flow rate (e.g., about 1500 sccm) for a time period (e.g., about 30 seconds). In various embodiments, one or more sequence loops can be conducted (e.g., repeated) for a designed length of each nanowire. In various embodiments, the growth rate of each nanowire can be orientation dependent.
[0056] Additional growth phases can be used, for example, the growth can be switched from pulsed growth to continuous growth to encourage the formation of a sharp tip at the later stages of growth.
[0057] In various embodiments, dielectric materials can be involved in formation of the disclosed nanowires and/or nanowire arrays. For example, the selective growth mask can be made of dielectric materials during the formation of the plurality of nanowires and/or nanowire arrays. As used herein, the dielectric materials can include, but are not limited to, silicon dioxide (SiO.sub.2), silicon nitride (Si.sub.3N.sub.4), silicon oxynitride (SiON), fluorinated silicon dioxide (SiOF), silicon oxycarbide (SiOC), hafnium oxide (HfO.sub.2), hafnium-silicate (HfSiO), nitride hafnium-silicate (HfSiON), zirconium oxide (ZrO.sub.2), aluminum oxide (Al.sub.2O.sub.3), barium strontium titanate (BST), lead zirconate titanate (PZT), zirconium silicate (ZrSiO.sub.2), tantalum oxide (TaO.sub.2) or other insulating materials. According to various other embodiments, a conducting metal growth mask, such as, for example, tungsten can be used for selective growth of the disclosed nanowires.
[0058]
[0059]
[0060] In experiments conducted by the inventors, a single crystalline, p-type, Si (100) wafer was used to test, both imaging and writing modes using the STM, e.g., STM 200 with the GaN tip 205. The native oxide of the Si wafer was removed using an HF solution.
[0061] According to some examples, the composite tips can be grown directly on Si pedestals, which simplifies the fabrication process allowing large scale fabrication. According to some examples, a linear array of independently controlled tips can be mounted to allow parallel writing capabilities. According to some examples, a material with a larger bond strength can be used to provide additional robustness, such as MN with a bond strength of 11.5 eV/atom.
[0062] According to examples of the present disclosure, a composite tip for scanning tunneling microscopy and scanning tunneling lithography is provided, which comprises a single crystal GaN tip with dimensions of ˜2 μm long and 0.5 μm faceted diameter coming to a sharp tip with a tip radius of <2 nm and a conductivity of −10.sup.−4 ohm-cm; and the GaN tip welded to a metal wire for use in an STM apparatus.
[0063] According to examples of the present disclosure, a method of forming a composite tip for scanning tunneling microscopy and scanning tunneling lithography is provided. The method can comprise growing an array of GaN tips by selective-area metal-organic chemical vapor deposition with dimensions of more or less a length of 2 μm, a faceted diameter of 0.5 micron, coming to a tip radius of <−2 nm, and with a controlled doping to provide a resistivity of <10.sup.−2 Ohm-cm; selecting a single GaN nanowire from the array with a nanomanipulator; transferring the single GaN nanowire from the growth substrate to a wire prepared for scanning tunneling microscopy and milled off to provide a more or less flat surface perpendicular to the wire direction; and welding the single GaN nanowire to the milled off surface of the STM wire using an organometallic Pt source.
[0064] According to examples of the present disclosure, a method of forming multiple composite tips for scanning tunneling microscopy and scanning tunneling lithography is provided. The method can comprise preparing an array of GaN (or other semiconductor) STM tips with 3D silicon manufacturing techniques; protecting all but selective growth areas of the Si STM tips with a dielectric film; using selective area MOCVD to grow GaN nanowires from the selective areas; wherein the dimensions of the GaN nanowires are more or less 2 μm long and a faceted diameter of 0.5 μm with a tip radius of more or less 2 nm and doped to provide a resistivity of <10.sup.−2 Ohm-cm; separating the individual silicon-GaN structures for use in scanning tunneling microscopy or scanning tunneling lithography apparatus.
[0065]
[0066] It will be understood that there are many variants of the process illustrated in
[0067] According to examples of the present disclosure, the formation of an array of independently addressed composite tips for parallel applications of scanning tunneling microscopy and scanning tunneling lithography is provided. The formation can comprise forming a 3D silicon structure with a linear array of independently addressable structures that can be individually bent out of the plane of the Si with applied fields; protecting all but selective growth areas of the Si structures with a dielectric film; using selective area MOCVD to grow GaN nanowire from the selective areas; wherein the dimensions of the GaN nanowires are more or less 2 μm long and a faceted diameter of 0.1 to 1 μm coming to a tip radius of more or less 2 nm and doped to provide a resistivity of <10.sup.−2 Ohm-cm; providing individually addressable electrical contacts to each element of the array; and mounting the array in a scanning tunneling microscopy or scanning tunneling lithography apparatus.
[0068] According to examples, the use of the array of composite tips for scanning tunneling microscopy or scanning tunneling lithography, wherein: each composite tip is individually addressed to provide a lithographic capability; the entire array is scanned in the surface directions (x and y) of the substrate: and individual tips are moved in the z-direction essentially perpendicular to the surface to maintain a constant tunneling current and to write individual pixels.
[0069] According to examples, the composite tips can be used for scanning tunneling microscopy and scanning tunneling lithography under ultrahigh vacuum conditions.
[0070] While the embodiments have been illustrated respect to one or more implementations, alterations and/or modifications can be made to the illustrated examples without departing from the spirit and scope of the appended claims. In addition, while a particular feature of the embodiments may have been disclosed with respect to only one of several implementations, such feature may be combined with one or more other features of the other implementations as may be desired and advantageous for any given or particular function.
[0071] Furthermore, to the extent that the terms “including”, “includes”, “having”, “has”, “with”, or variants thereof are used in either the detailed description and the claims, such terms are intended to be inclusive in a manner similar to the term “comprising.” As used herein, the phrase “one or more of”, for example, A, B, and C means any of the following: either A, B, or C alone; or combinations of two, such as A and B, B and C, and A and C; or combinations of three A, B and C.
[0072] Other embodiments will be apparent to those skilled in the art from consideration of the specification and practice of the descriptions disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the embodiments being indicated by the following claims.