1. Field
The present application relates generally to the fabrication and utilization of micron or nano scale structures. More particularly, this application relates to using a compliant base to increase contact for micro- or nano-fibers.
2. Related Art
There is an ongoing need for improved adhesives. Improved adhesives have applications ranging from everyday aspects of life (e.g., tape, fasteners, and toys) to high technology (e.g., removal of microscopic particles from semiconductor wafers, transporting fiber optic devices, and assembly of sub-mm mechanisms, particularly those including micro-fabricated components, or components that cannot tolerate grippers, adhesives, or vacuum manipulators).
Adhesive mechanisms in nature have been studied, but have not been fully understood or exploited. For example, Geckos are exceptional in their ability to rapidly climb up smooth vertical surfaces. The mechanism of adhesion used in Geckos, Anolis lizards, some skinks, and some insects, has been debated for nearly a century.
While some prior work has identified the morphology of seta used by Geckos and other insects, this prior work does not identify how the seta operates. In addition, this prior work fails to identify how to use a seta to perform useful work.
It would be highly desirable to identify and exploit the adhesive force mechanism utilized by Geckos and other insects. Such information could result in the utilization of new adhesive microstructures and the fabrication of such structures.
In one exemplary embodiment, a fabricated microstructure includes a substrate, a primary fiber, and a plurality of base fibers. The primary fiber has a width less than about 5 microns. Each base fiber of the plurality of base fibers has a first end attached to the primary fiber and a second end attached to the substrate. Each base fiber has a width less than the width of the primary fiber.
The present application can be best understood by reference to the following description taken in conjunction with the accompanying drawing figures, in which like parts may be referred to by like numerals:
The following description sets forth numerous specific configurations, parameters, and the like. It should be recognized, however, that such description is not intended as a limitation on the scope of the present invention or applications thereof, but instead provides examples and illustrations.
With reference to
As depicted in
In the present exemplary embodiment, assume that fiber 104 has a length L, radius R, elastic modulus E, and work of adhesion w per unit length of contact with contact surface 108. The width of fiber 104 (i.e., 2×R) is less than about 5 microns. As depicted in
In accordance with one analytic approach, fiber 104 is treated as an elastica, i.e., an elastic rod that is subject to large deflections in a plane. See, J. M. Gere and S. P. Timoshenko, Mechanics of Materials 2nd ed., PWS-KENT Publishing Company, 1984, which is incorporated herein by reference in its entirety. It is assumed that fiber 104 can slide freely with respect to contact surface 108 prior to side contact. Side contact begins when the tip of fiber 104 is oriented laterally, i.e., θ(L)=π/2.
Assume that fiber 104 is pulled away from the substrate by a force T in the direction normal to contact surface 108. The peel strength is defined as the maximum normal force applied to fiber 104 prior to complete detachment of fiber 104 from contact surface 108. From fracture mechanics, the normal force is determined as the critical load at which the work of adhesion is equal to the path independent J-integral calculated near the crack tip, i.e., the edge of the contacting interface. For an elastica, the J-integral is evaluated as:
J=(2Ma2)/(πER4)
where Ma=M(a) is the internal moment acting near the crack tip. See, N. J. Glassmaker and C. Y. Hui, Elastica Solution for a Nanotube Formed by Self-Adhesion of a Folded Thin Film, Journal of Applied Physics, v. 96, 3429-3434 (2004), which is incorporated herein by reference in its entirety.
The following analyses will demonstrate the dependence of peel strength on the support conditions at the base of fiber 104, i.e., where fiber 104 attaches to substrate 106. For the purpose of these analyses, it is convenient to express the peel strength (Tnd) and work of adhesion parameters (wnd) in the non-dimensional forms:
T
nd=(4TL2)/(πER4) and
w
nd=(4wL2)/(πER4),
respectively.
First, consider the case in which fiber 104 is constrained both rotationally and laterally at its base.
For this system, side contact begins when the tip displaces laterally by an amount 0.763L. See, S. T. Timoshenko and J. M. Gere, Theory of Elastic Stability, 2nd ed., McGraw-Hill Book Company, pg. 79 (1961), which is incorporated herein by reference in its entirety. As depicted in
By the constitutive law for an elastica, the internal moment (M) is related to the fiber curvature by the equation:
M(s)=(πER4/4)(dθ/ds).
Hence, the equilibrium condition J=w implies (dθ/ds)s=a=(1/L)(2wnd)1/2. Fiber 104 is also subject to the additional boundary conditions θ(0)=0 and θ(a)=π/2 and the governing equation:
(πER4/4)d2θ/ds2=T sin(θ)+V cos(θ).
Moreover, the reaction force V must satisfy the fourth boundary condition that the integral of sin(θ) over the entire length of fiber 104 should be equal to 0.763L. Numerically solving the governing equation and four boundary conditions fOr θ(s), V, and a yields a one-to-one relationship between the normal load T and the non-contact length a. According to this relationship, T increases monotonically with a, and so the peel strength corresponds with the value of T at a=L. The predicted peel strength for various values of wnd is given below in Table 1.
Next, consider the case in which the base of fiber 104 is fixed to be vertical but free to translate laterally.
The method for determining peel strength is similar to the laterally constrained case above except that V=0 since substrate 106 cannot supply any reaction in the lateral direction. Hence, the governing equation reduces to:
(πER4/4)d2θ/ds2=T sin(θ)
subject only to the boundary conditions θ(0)=0, θ(a)=π/2 and (dθ/ds)s=a=(1/L)(2wnd)1/2. Solving for θ(s) and a yields the equilibrium relationship:
a/L=[2/(wnd−Tnd)]1/2F(π/4, [2/(1−wnd/Tnd)]1/2)
where F(u,k) is the Jacobi integral of the first kind. As in the laterally constrained case, Pnd increases monotonically with a, and so the peel strength is the solution to:
1=[2/(wnd−Tnd)]1/2F(π/4, [2/(1−wnd/Tnd)]1/2).
The predicted peel strength for various values of wnd is given below in Table 1.
Lastly, consider the case in which fiber 104 is allowed to rotate freely at its base.
Following the assumption that fiber 104 can slide with respect to contract surface 108 prior to side contact, fiber 104 can orient itself to make full contact (i.e., a=0) during initial attachment. For this system, M=T*a, and so the equilibrium condition J=w implies:
T
nd=(L/a)(2wnd)1/2.
From this expression, T is found to decrease monotonically with a, which suggests that T is smallest when a=L. The predicted peel strength for various values of wnd is given below in Table 1 assuming an initial crack that is five percent of the total fiber length.
With reference again to
with corresponding contact width:
The system is converted to non-dimensional coordinates to simplify analysis. The relevant parameters for the present discussion are:
where {circumflex over (P)} is the non-dimensional load, and {circumflex over (ω)} is the non-dimensional adhesion parameter.
Also, a is the length of fiber not in contact with contact surface 108, and L-a is the length of fiber in contact with contact surface 108. So, â is the non-dimensional non-contact length and 1−â is the non-dimensional contact length. The shear force required to detach a contact can be approximated as V=τAr, where τ is the shear strength of the interface and Ar is the real area of contact. The real area of contact for a fiber is the contact length times the contact width. Thus contact length gives an approximation of the shear force required to detach a fiber (when pulling in the appropriate direction).
In particular,
With reference to
In the present exemplary embodiment, primary fiber 104 has a width that is greater than width of each base fiber 704. The width of primary fiber 104 is preferably at least 10 times greater than the width of each base fiber 704. The width of base fibers 704 can be the same or different.
For example,
With reference to
Although
With reference to
With reference to
The double-cantilever structures can be fabricated using stereolithography. See, K. Ikuta, K. Hirowatari, and T. Ogata, “Three Dimensional Micro Integrated Fluid Systems (MIFS) Fabricated by Stereo Lithography”, Proc. IEEE Micro Electro Mechanical Systems, pp. 1-6, Oiso, Japan Jan. 25-28, 1994, which is incorporated herein by reference in its entirety. It should be recognized, however, that the double-cantilever structure can be fabricated using various fabrication techniques, such as by casting into a mold fabricated with deep reactive ion etching.
With reference to
The coiled spring structure can be fashioned using stereolithography. See, K. Ikuta, K. Hirowatari, and T. Ogata, “Three Dimensional Micro Integrated Fluid Systems (MIFS) Fabricated by Stereo Lithography”, Proc. IEEE Micro Electro Mechanical Systems, pp. 1-6, Oiso, Japan Jan. 25-28, 1994), which is incorporated herein by reference in its entirety. It should be recognized, however, that the coiled spring structure can be fabricated using various fabrication techniques, such as chemical vapor deposition. See, Sean Pursel, Mark W. Horn, Melik C. Demirel and Akhlesh Lakhtakia, “Growth of sculptured polymer submicronwire assemblies by vapor deposition,” Polymer, v. 46, pg. 9544-9548, 2005, which is incorporated herein by reference in its entirety.
With reference to
As also depicted in
With reference to
As depicted in
Template 1602 can be an array of pores, such as a Whatman Anodisc nanopore array with 200 nm holes and 60 micron thickness. Template 1602 can also be filter or porous membranes, such as nanochannel alumina, track etched poly carbonate membranes, and the like. When a nanopore array is used, care should be taken when inserting the nanopore array into layer of silicone adhesive 1606 to not force the silicone adhesive all the way through the nanopore array.
As depicted in
As depicted in
As depicted in
After drying, the array of fibers 104 is not very adhesive since fibers 104 are sticking straight up. By applying a shear stress, such as by dragging the array on glass in one direction, or grooming fibers 104 with a cotton swab, fibers 104 can be oriented on their sides. Fibers can then engage a smooth surface, such as glass.
The foregoing description, for purposes of explanation, used specific nomenclature to provide a thorough understanding of the invention. However, it will be apparent to one skilled in the art that the specific details are not required in order to practice the invention. Thus, the foregoing descriptions of specific embodiments of the present invention are presented for purposes of illustration and description. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed, obviously many modifications and variations are possible in view of the above teachings. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications, to thereby enable others skilled in the art to best utilize the invention and various embodiments with various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.
The present application claims the benefit of U.S. Provisional Application Ser. No. 60/737,939, filed Nov. 18, 2006, which is incorporated herein by reference in its entirety.
This invention was made with Government support under Grant (contract) Nos. N66001-00-C-8047 and N6600101-C-8072 awarded by the US Defense Advanced Research Project Agency and Grant (contract) No. EEC-0304730 awarded by the National Science Foundation. The Government has certain rights in this invention.
Number | Date | Country | |
---|---|---|---|
60737939 | Nov 2005 | US |