Nanorods are nanoscopic rods or fibers that have an aspect ratio (e.g. diameter versus length) greater than, less than, or equal to one, but relatively small overall dimensions (e.g. under 1000 nanometers). Nanorods have been relatively difficult to fabricate. The choices of materials for nanorods has been limited. Nanorods have been fabricated such that they are not tethered to a surface or substrate. These limitations further limit the practicality and implantation of nanorods.
Embodiments relate to an apparatus (and a method of making the apparatus) that includes a substrate (e.g. a conductive and/or non-conductive material) and a plurality of nanorods tethered to the substrate. In embodiments, the nanorods may be synthesized by forming the substrate on a mold (e.g. a membrane having a plurality of pores) and then depositing material on the substrate inside of the mold. In embodiments, since the deposited material has a relatively low interaction with the mold and a relatively high interaction with the substrate, nanorods may be formed. After the nanorods are formed inside of the mold, the mold may be removed (e.g. by chemical or mechanical means) in a manner allowing the nanorods to remain tethered to the substrate.
In embodiments, the nanorods may be fabricated by self assembly or other methods. Due to the relative flexibility of materials that may be used to fabricate nanorods and/or the ability of nanorods to be tethered to a substrate, many applications of nanorods may be implemented, in accordance with embodiments. For example, tethered nanorods may be implemented in high surface area applications (e.g. biosensors, heat sinks, or catalytic applications). As another example, tethered nanorods may be implemented in surface-to-surface conformation (e.g. gecko feet applications). In embodiments, self assembled (or partially self assembled nanorods) may have multi-functionality (e.g. adhesion functions, mechanical functions, thermal functions, electrical functions, conduction function, and/or optical functions). Further, in embodiments, tethered nanorods may be fabricated to have substantially predetermined dimensions (e.g. length) based on a self assembly process.
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Example
Substrate 10 represents a broad class of surfaces. For example, substrate 10 may be a conductive material or a non-conductive material. Substrate 10 may be part of a previously existing structure. The materials of substrate 10 and nanorods 12 may be such that nanorods 12 can be formed on substrate 10 and tethered (e.g. bonded) to substrate 10. In embodiments, the materials of substrate 10 and nanorods 12 may be the same or different materials. A collection of nanorods 12 on substrate 10 may be referred to as a nanorod forest or nanorod array.
The spatial distribution and dimensions of nanorods illustrated in all of the Figures is intended for illustration purposes only. One of ordinary skill in the art would appreciate other dimensions, in accordance with embodiments.
Example Figure Sets 2-4 illustrate a fabrication process of nanorods 12 tethered to substrate 10, in accordance with embodiments. Example
As illustrated in example
Example
In embodiments, when depositing material that forms the nanorods 12, external stimulation may be utilized to promote contact and/or interaction with the deposited nanorod material and substrate 10. For example, electrical stimulation may be used to promote interaction (e.g. electrochemical deposition and/or electrophoresis). For example, applied pressure deposition (e.g. applied water and/or air pressure) may be used to promote interaction.
In embodiments, nanorods 12 may be formed by electrochemical deposition and/or electrophoresis. In electrochemical deposition and/or electrophoresis embodiments, substrate 10 and/or nanorods 12 may include a conductive material. A voltage potential and/or electrical current may be applied to a conductive substrate to promote migration of conductive material to be formed on substrate 10 inside pores 16. The length of nanorods 12 may be formed to a substantially predetermined length by control of the parameters of an electrochemical deposition and/or electrophoresis process, in accordance with embodiments.
In embodiments, nanorods 12 may be formed by a self assembly process. U.S. patent application Ser. No. 10/774,683 (filed Feb. 10, 2004 and titled “RAPIDLY SELF-ASSEMBLED THIN FILMS AND FUNCTIONAL DECALS”) is hereby incorporated by reference in its entirety. U.S. patent application Ser. No. 10/774,683 discloses self-assembly of nano-particles and nano-layers, in accordance with embodiments. In embodiments, the size (i.e. diameter or substantial diameter) of the nano-particles may be less than approximately 1000 nanometers. In embodiments, the size of the nano-particles may be less than approximately 50 nanometers. In embodiments, nano-particles may be gold and/or gold clusters. However, in other embodiments, nano-particles may be other metals (e.g. silver, palladium, copper, or other similar metal) and/or metal clusters. In embodiments, nano-particles may include metals, metal oxides, inorganic materials, organic materials, ceramics, and/or mixtures of different types of materials. In embodiments, nano-particles may be semiconductor materials.
Through self assembly, nano-particles may be substantially uniformally and/or spatially dispersed during deposition to form a self assembled film, in accordance with embodiments. In embodiments, a self assembled film may be deposited in pores 16 to formed a layered nanorod 12. The self assembly of nano-particles may utilize electrostatic and/or covalent bonding of the individual nano-particles to a host layer (e.g. a linking agent material layer and/or a flexible base material). A host layer (e.g. substrate 10) may be polarized in order to allow for the nano-particles to bond to the host layer, in accordance with embodiments. Since the deposition of the nano-particles may be dependent on individual bonding of the nano-particles to the host layer, a nano-particle material layer may have a thickness that is approximately the diameter of the individual nano-particles. Through a self-assembly deposition method, nano-particles that do not bond to a host layer may be removed, so that a nano-particles material layer is formed that is relatively uniform in thickness and material distribution.
Linking agent material layer(s) may be a material that is capable of covalently and/or electrostaticly bonding to nano-particles, in accordance with embodiments. U.S. patent application Ser. No. 10/774,683 (which is incorporated by reference above) discloses examples of materials which may be included in linking agent material layer(s). Linking agent material layer(s) may include polymer material. In embodiments, the polymer material may include poly(urethane), poly(etherurethane), poly(esterurethane), poly(urethane)-co-(siloxane), poly(dimethyl-co-methylhydrido-co-3-cyanopropyl, methyl) siloxane, and/or other similar materials. Linking agent material layer(s) may include materials that are polarized, in order for bonding with nano-particles, in accordance with embodiments.
In embodiments, since self assembly of nanorods 12 can form multi-layered nanorods having substantially predetermined thickness and material attributes, nanorods 12 may be fabricated with multi-functional attributes. For example, nanorods 12 may have various combinations of adhesion functions, mechanical functions, thermal functions, electrical functions, conduction functions, and/or optical functions. For example, nanorods 12 may be utilized as a heat sink due to high surface area and heat conduction attributes of engineered nanorods. Those skilled in the art would appreciate other applications, in accordance with embodiments.
In embodiments, nanorods 12 may be formed by delivering material of the nanorods to the substrate using a liquid as a delivery agent. For example, in electrochemical deposition and/or electrophoresis embodiments, conductive materials may be incorporated in a liquid that fills pores 16. For example, in a self assembly process, materials to be deposited may be dispersed in a liquid. Embodiments also relate to material deposition processes aside from electrochemical deposition, eletrophoretics, and/or self-assembly or a combination of deposition methods.
Example
Example
Example
Example Figure Sets 9-11 illustrate using a mask 18 on mold 14, in accordance with embodiments. Example
In embodiments, nanorods 12 may be processed after being formed. Example
Example
Although embodiments have been described herein, it should be understood that numerous other modifications and embodiments can be devised by those skilled in the art that will fall within the spirit and scope of the principles of this disclosure. More particularly, various variations and modifications are possible in the component parts and/or arrangements of the subject combination arrangement within the scope of the disclosure, the drawings and the appended claims. In addition to variations and modifications in the component parts and/or arrangements, alternative uses will also be apparent to those skilled in the art.
The present application claims priority to U.S. Provisional Patent Application No. 60/884,540 (filed Mar. 28, 2007), which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
---|---|---|---|
60884540 | Mar 2007 | US |