Optical waveguides – With optical coupler – Switch
Reexamination Certificate
2002-07-01
2004-03-02
Ullah, Akm Enayet (Department: 2874)
Optical waveguides
With optical coupler
Switch
C385S040000
Reexamination Certificate
active
06701035
ABSTRACT:
The present application is an improvement over the foregoing applications in that it is directed to classes of molecules that provide switching from one state to a different state, characterized by a change in the optical properties, including color, of the molecules. In the case of color switching, the present invention turns ink or dye molecules into active opto-electronic devices that can be switched with an external electric field.
The present application is related to application Ser. No. 09/759,438, filed Jan. 12, 2001, which is directed to bistable molecular mechanical devices with an appended rotor activated by an electric field for electronic switching, gating, and memory applications. The class of molecules disclosed in that application have been found to be useful in the optical switching devices of the present application.
TECHNICAL FIELD
The present invention relates generally to optical devices whose functional length scales are measured in nanometers, and, more particularly, to classes of molecules that provide optical switching. Optical devices both of micrometer and nanometer scale may be constructed in accordance with the teachings herein.
BACKGROUND ART
The area of molecular electronics is in its infancy. To date, there have been two convincing demonstrations of molecules as electronic switches published in the technical literature; see, C. P. Collier et al., Science, Vol. 285, pp. 391-394 (Jul. 16, 1999) and C. P. Collier et al., Science, Vol. 289, pp. 1172-1175 (Aug. 18, 2000), but there is a great deal of speculation and interest within the scientific community surrounding this topic. In the published work, a molecule called a rotaxane or a catenane was trapped between two metal electrodes and caused to switch from an ON state to an OFF state by the application of a positive bias across the molecule. The ON and OFF states differed in resistivity by about a factor of 100 and 5, respectively, for the rotaxane and catenane.
The primary problem with the rotaxane was that it is an irreversible switch. It can only be toggled once. Thus, it can be used in a programmable read-only memory (PROM), but not in a RAM-like (random access memory) device nor in a reconfigurable system, such as a defect-tolerant communications and logic network. In addition, the rotaxane requires an oxidation and/or reduction reaction to occur before the switch can be toggled. This requires the expenditure of a significant amount of energy to toggle the switch. In addition, the large and complex nature of rotaxanes and related compounds potentially makes the switching times of the molecules slow. The primary problems with the catenanes are small ON-to-OFF ratio and a slow switching time.
Currently, there are a wide variety of known chromogenic materials that can provide optical switching in thin film form. These materials and their applications have been reviewed recently by C. B. Greenberg,
Thin Solid Films,
Vol. 251, pp. 81-93 (1994); R. J. Mortimer,
Chemical Society Reviews,
Vol. 26, pp. 147-156 (1997); and S. A. Agnihotry,
Bulletin of Electrochemistry,
Vol. 12, pp. 707-712 (1996). These materials are currently being studied for several applications, including active darkening of sunglasses, active darkening of windows for intelligent light and thermal management of buildings, and various types of optical displays, such as heads-up displays on the inside of windshields of automobiles or airplanes and eyeglass displays.
Despite their long history of great promise, there are very few photon gating devices made from the existing classes of electrochromic materials. This is because most of them require an oxidation-reduction reaction that involves the transport of ions, such as H
+
, Li
+
, or Na
+
through some type of liquid or solid electrolyte. Finding the appropriate electrolyte is a major problem, as is the slow speed of any device that requires transport of ions. Furthermore, such reactions are extremely sensitive to background contamination, such as oxygen or other species, and thus degradation of the chromogenic electrodes is a major limitation.
In fact, for photonic switching applications such as a crossbar switch router for a fiber optic communications network, the lack of a suitable chromogenic material has forced companies to use very different approaches: (a) transform the optical signal into an electronic signal, perform the switching operation, and then transform back to an optical signal before launching into a fiber (this is the most frequent solution used today, but it is very inefficient and the electronics have a hard time keeping up with the data rates of the optical system); (b) use a moving-mirror array made by micro-electromechanical (MEM) processing to switch optical data packets (this has the disadvantage that extremely high tolerances are required for the device, which makes it very expensive); and (c) using ink jet technology to push bubbles into a chamber to create a mirror to deflect an optical beam (this approach again requires precision manufacturing and the switching time is slow).
Thus, what is needed is a molecular system that avoids chemical oxidation and/or reduction, permits reasonably rapid switching from a first state to a second, and can be used in a variety of optical devices.
DISCLOSURE OF INVENTION
In accordance with embodiments disclosed herein, a molecular system is provided for optical switching. The molecular system has an electric field induced band gap change that occurs via a molecular conformation change or an isomerization. Changing of extended conjugation via chemical bonding change to change the band gap is accomplished by providing the molecular system with one rotating portion (rotor) and two stationary portions (stators), between which the rotor is attached.
The embodiments disclosed herein are suitably employed in the fabrication of, for example, optical switches that can be assembled easily to make displays, electronic books, rewrittable media, electronic lenses, electrically-controlled tinting for windows and mirrors, optical crossbar switches for fiber optic communications, and more. Such applications are discussed elsewhere, and are not germane to the present invention, except to the extent that the optical switch of the present invention is employed in the construction of apparatus of such applications.
The bistable molecules evidence high switching speed. Such molecules are essentially stable against switching due to thermal fluctuations. These molecules are useful for optical switches, in which the molecules change color when changing state. This property can be used for a wide variety of display devices or any other application enabled by a material that can change color or transform from transparent to colored.
Thus, the molecule is not oxidized nor reduced in the toggling of the switch. Also, the part of the molecule that moves is quite small, so the switching time should be very fast. Also, the molecules are much simpler and thus easier and cheaper to make than the rotaxanes, catenanes, and related compounds.
REFERENCES:
patent: 5655038 (1997-08-01), Schilling
patent: 6198655 (2001-03-01), Heath et al.
patent: 6470105 (2002-10-01), Baney et al.
Collier, C.P. et al, “Electronically Configurable Molecular-Based Logic Gates”, Science, vol. 285, Jul. 16, 1999, pp. 391-394.
Collier, Charles P. et al, “A [2] Catenane-Based Solid State Electronically Reconfigurable Switch”, Science, vol. 289, Aug. 18, 2000, pp. 1172-1175.
Agnihotry, S.A., “Electrochromic Devices: Presnet and Forthcoming Technology”, Bulletin of Electrochemistry, 12 (11-12) Nov.-Dec. 1996, pp. 707-712.
Greenberg, Charles B., “Optically Switchable Thin Films: A Review”, Thin Solid Films, 251 (1994), pp. 81-93.
Mortimer, Roger J., “Electrochromic Materials”, Chemical Society Reviews, vol. 26, 1997, pp. 147-156.
Vincent Kent D.
Williams R. Stanley
Zhang Xiao-An
Hewlett--Packard Development Company, L.P.
Rahll Jerry T
Ullah Akm Enayet
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