1. Field of the Invention
The present invention relates in general to the photonics field and, in particular, to a fiber array and a method for fabricating the fiber array which is coupled to a lens array to form a collimator array.
2. Description of Related Art
In the photonics field, one of the most significant design challenges today involves the development of a new and improved collimator array that can function properly over a broad range of temperatures. Referring to
The traditional collimator array 100 in order to work properly should have optical fibers 140 that are aligned with the lenses 130 and remain aligned with the lenses 130 regardless of the environmental temperature. Unfortunately, the traditional collimator array 100 has optical fibers 140 that do not remain aligned with the lenses 130 when there is a change in the environmental temperature. This is because the traditional fiber array 120 is made from a material that does not have the same coefficient of thermal expansion (CTE) as the material used to make the traditional lens array 110. If the traditional fiber array 120 has a different CTE than the traditional lens array 110, then as the temperature changes the traditional fiber array 120 contracts and expands differently than the traditional lens array 110 which adversely affects the alignment between the lenses 130 and the optical fibers 140 (see
The present invention includes a collimator array, a fiber array and a method for fabricating the fiber array. In one embodiment, that fiber array includes a plurality of optical fibers and a glass plate with a plurality of holes in each of which there is secured one of the optical fibers, wherein the holes were formed by etching away a plurality of opal regions within an exposed and heated photosensitive glass which after the etching became the glass plate. In another embodiment, the fiber array includes a plurality of optical fibers and a glass plate with a plurality of holes in each of which there is secured one of the optical fibers, wherein the holes were formed by etching away a plurality of opal regions within an exposed and heated photosensitive glass which after the etching became the glass plate that included a plurality of oversized holes which were filled with a moldable material that was then drilled to form the holes.
A more complete understanding of the present invention may be had by reference to the following detailed description when taken in conjunction with the accompanying drawings wherein:
Referring to
Referring to
Like the traditional collimator array 100, the collimator array 200 includes a lens array 210 and a fiber array 220. The lens array 210 (e.g., plano-convex microlens array 210) has formed therein an array of lenses 230 (see
Unlike the traditional collimator array 100, the collimator array 200 has optical fibers 240 that are aligned with the lenses 230 and remain aligned with the lenses 230 regardless of the environmental temperature. In particular, the collimator array 200 has optical fibers 240 that remain aligned with the lenses 230 in a temperature range of between −40° C. and 100° C. This is possible because the fiber array 220 is made from a material that has the same CTE as the material used to make the lens array 210. If the fiber array 220 has the same CTE as the lens array 210, then as the temperature changes the fiber array 220 contracts and expands in the same manner as the lens array 210. Thus, the alignment between the lenses 230 and the optical fibers 240 is not lost during a change in the temperature as it is between the lenses 130 and the optical fibers 140 in the traditional collimator array 100 (compare
To ensure that the fiber array 220 and the lens array 210 have matching CTEs, the fiber array 220 can be made from the same material used to make the lens array 210. Today some commercially available lens arrays 210 are made from a photosensitive glass plate which is subjected to an ultraviolet light exposure step and a heat treatment step in accordance with the SMILE® process (see, e.g., U.S. Pat. Nos. 4,572,611, 4,518,222 and 5,062,877). As such, the material used to make the fiber array 220 can be a photosensitive glass plate. In the preferred embodiment, the photosensitive glass plate is a photonucleable, crystallizable lithium-silicate glass body marketed by Coming Incorporated under the brand name of FOTOFORM® glass. A more detailed discussion about the composition of FOTOFORM® glass is provided in U.S. Pat. Nos. 2,326,012, 2,422,472, 2,515,936, 2,515,938, 2,515,275, 2,515,942 and 2,515,943 the contents of which are incorporated herein by reference.
Basically in the preferred embodiment, the fiber array 220 is a glass plate that has formed therein a series of holes in each of which is secured an optical fiber 240. The glass plate is originally a photosensitive glass plate (e.g., FOTOFORM® glass plate) that is subjected to one of the two processes described below with respect to methods 300 and 1200 (see
Referring to FIGS. 3 and 4A–4E, there are respectively illustrated a flowchart of the preferred method 300 for making the first embodiment of the fiber array 220′ and various cross-sectional side views and top views of the fiber array 220′ at different steps in the preferred method 300. Beginning at step 302, a photomask 402 is placed in contact with a photosensitive glass plate 404 (see
The contact can be an air interface 403 between the photomask 402 and the photosensitive glass plate 404. Instead of having the air interface 403, an oil closely matching the index of glass such as glycerin can be used as a medium between the photomask 402 and the photosensitive glass plate 404 to help eliminate the air gap 403 and the resulting reflection and/or scattering of light that can result from the air gap 403.
At step 304, the photomask 402 and selected regions of the photosensitive glass plate 404 are exposed to an ultraviolet light 406 (see
The exposure step 304 can be performed by any method that is capable of producing an ultraviolet light or shortwave radiation with sufficient energy to nucleate the opal phase (future opal regions 406) in the photosensitive glass plate 404 and with sufficient collimation so that the exposure is well defined through the photosensitive glass plate 404. For example, a 100 W UV Xenon lamp (e.g., Hanovia L 5179 or ORIEL 6271) can be used to expose the photosensitive glass plate 404. In this example, the light power applied to the photomask 402 and the photosensitive glass plate 404 is 1.06 Lux with an exposure of 240–400 nm (most preferable 300–350 nm) for 12 minutes, where deviations from this range result in longer exposure times. After the exposure step 304, the photomask 402 is separated from the exposed photosensitive glass plate 404. If needed, the exposed photosensitive glass plate 404 is washed with soap and water to remove dust, contaminants, residue etc..
It should be understood that the photosensitive glass plate 404 needs to be protected, at all stages prior to the heat treatment step 306, from ambient ultraviolet exposure (e.g., sunlight, unfiltered artificial light) to prevent trace amounts of opal formation in areas where glass regions 408 are desired in the final product.
At step 306, the exposed photosensitive glass plate 404 is heated to form therein the opal regions 406 (shown as shaded regions) and the glass regions 408 (shown as clear regions)(see
The annealing oven heats the exposed photosensitive glass plate 404 in accordance with a predetermined thermal cycle. Table 1 shows an exemplary thermal cycle that can be used to heat the exposed photosensitive glass plate 404:
Reference is made to
In the event, the photosensitive glass plate 404 is FOTOFORM® glass 404 then the heated photosensitive glass plate 404 could be produced by exposing the FOTOFORM® glass 404 to ultraviolet light with a wavelength of 240–400 nm (most preferable 300–350 nm) and then heat treating the exposed FOTOFORM® glass 404 to form the opal regions 406 and the glass regions 408. The opal regions 406 have ceramic particles and as such they have a greater density than the glass regions 408. The mechanism for formation of nuclei that enables the growth of the ceramic particles in the opal regions 406 starts when cerium III (Ce3+) in the FOTOFORM® glass 404 absorbs the ultraviolet light and converts to cerium IV (Ce4+) which results in the release of an electron. The electron is absorbed by metal ions, for example silver ions (Ag1+), in the FOTOFORM® glass 404 and converts these ions to metal (e.g., Ago). Alternative metal ions include gold, copper and palladium.
At step 308, the heated photosensitive glass plate 404 is etched until the opal regions 406 (shown as shaded regions) are etched away to form holes 410 (see
Referring to
Referring to
It should be understood that the etching time is variable depending on the diameter of the etched holes 410, the plate 404 thickness, the HF concentration and the glass-ceramic microstructure as dictated by the thermal treatment. For example, holes with a 140 μm diameter etch faster than holes with a 250 μm diameter.
It should also be understood that the fiber array 220′ can be coupled to a lens array to form a collimator array that can be used to perform a variety of signal processing steps including multiplexing, switching, filtering, polarizing and demultiplexing. Following is a brief list of some of other photonic applications that can use a collimator array:
Referring to FIGS. 12 and 13A–13G, there are respectively illustrated a flowchart of the preferred method 1200 for making the second embodiment of the fiber array 220″ and various cross-sectional side views and top views of the fiber array 220″ at different steps in the preferred method 1200. Beginning at step 1202, a photomask 1302 is placed in contact with a photosensitive glass plate 1304 (see
The contact can be an air interface 403 between the photomask 402 and the photosensitive glass plate 404. Instead of having the air interface 403, an oil closely matching the index of glass such as glycerin can be used as a medium between the photomask 402 and the photosensitive glass plate 404 to help eliminate the air gap 403 and the resulting reflection and/or scattering of light that can result from the air gap 403.
At step 1204, the photomask 1302 and selected regions of the photosensitive glass plate 1304 are exposed to an ultraviolet light 1306 (see
The exposure step 1204 can be performed by any method that is capable of producing an ultraviolet light or shortwave radiation with sufficient energy to nucleate the opal phase (future opal regions 1306) in the photosensitive glass plate 1304 and with sufficient collimation so that the exposure is well defined through the photosensitive glass plate 1304. For example, an ultraviolet light with an intensity of 5.5 to 7.5 mW/cm2 for 1–10 minutes can be used to expose the photosensitive glass plate 1304.
After the exposure step 1204, the photomask 1302 is separated from the exposed photosensitive glass plate 1304. If needed, the exposed photosensitive glass plate 404 is washed with soap and water to remove dust, contaminants, residue etc.. It should be understood that the photosensitive glass plate 404 needs to be protected, at all stages prior to the heat treatment step 306, from ambient ultraviolet exposure (e.g., sunlight, unfiltered artificial light) to prevent trace amounts of opal formation in areas where glass regions 408 are desired in the final product.
At step 1206, the exposed photosensitive glass plate 1304 is heated to form therein the opal regions 1306 (shown as shaded regions) and the glass regions 1308 (shown as clear regions)(see
In the event, the photosensitive glass plate 1304 is FOTOFORM® glass 1304 then the heated photosensitive glass plate 1304 could be produced by exposing the FOTOFORM® glass 1304 to ultraviolet light with wavelengths between 240–400 nm (most preferable 300–350 nm) and then heat treating the exposed FOTOFORM® glass 1304 to form the opal regions 1306 and the glass regions 1308. The opal regions 1306 have ceramic particles and as such they have a greater density than the glass regions 1308. The mechanism for formation of nuclei that enables the growth of the ceramic particles in the opal regions 1306 starts when cerium III (Ce3+) in the FOTOFORM® glass 1304 absorbs the ultraviolet light and converts to cerium IV (Ce4+) which results in the release of an electron. The electron is absorbed by metal ions, for example silver ions (Ag1+), in the FOTOFORM® glass 1304 and converts these ions to metal (e.g., Ago). Alternative metal ions include gold, copper and palladium. A more detailed discussion about the composition of FOTOFORM® glass is provided in U.S. Pat. Nos. 2,326,012, 2,422,472, 2,515,936, 2,515,938, 2,515,275, 2,515,942 and 2,515,943 the contents of which are incorporated herein by reference.
At step 1208, the heated photosensitive glass plate 1304 is etched until the opal regions 1306 (shown as shaded regions) are etched away to form oversized holes 1310 (see
At step 1210, the oversized holes 1310 in the etched glass plate 1304 are filled or infiltrated with a moldable material 1312 (see
An adhesive known as MCA-80 adhesive which is manufactured and sold by Coming Incorporated is one example of a moldable material 1312 that can be used to fill the oversized holes 1310 in the etched glass plate 1304. The MCA-80 adhesive happens to have a CTE that matches the CTE of the etched glass plate 1304 that is made from FOTOFORM® glass. Below are listed some of the physical properties of the MCA-80 adhesive:
At step 1212, a precision drill is used to drill the moldable material 1312 in each of the oversized holes 1310 to form holes 1314 (see
Like fiber array 220′, this fiber array 220″ can be coupled to a lens array to form a collimator array that can be used to perform a variety of signal processing steps including multiplexing, switching, filtering, polarizing and demultiplexing. Following is a brief list of some of other photonic applications that can use a collimator array:
It should be understood that the material used to make the fiber array 220′ and 220″ does not necessarily need to have the exact CTE as the material used to make the lens array. However, the material used to make the fiber array 220′ and 220″ should have a CTE that is relatively close to the CTE of the material used to make the lens array. In particular, the CTE match of the moldable material 1312 (if used), the fiber arrays 220′ and 220″ and the lens array should allow for sufficient alignment over the temperature range of −40° C.–100° C.
Although only two embodiments of the present invention have been illustrated in the accompanying Drawings and described in the foregoing Detailed Description, it should be understood that the invention is not limited to the embodiments disclosed, but is capable of numerous rearrangements, modifications and substitutions without departing from the spirit of the invention as set forth and defined by the following claims.
This application claims the benefit of U.S. Provisional Patent Application No. 60/364,700, filed Mar. 14, 2002, entitled Fiber Array And Methods For Fabricating The Fiber Array.
Number | Name | Date | Kind |
---|---|---|---|
2326012 | Dalton | Aug 1943 | A |
2515275 | Stookey | Jul 1950 | A |
2515936 | Houston | Jul 1950 | A |
2515938 | Stookey | Jul 1950 | A |
2515942 | Stookey | Jul 1950 | A |
2515943 | Stookey | Jul 1950 | A |
4518222 | Borrelli et al. | May 1985 | A |
4572611 | Bellman et al. | Feb 1986 | A |
4609259 | Suemitsu et al. | Sep 1986 | A |
4727047 | Bozler et al. | Feb 1988 | A |
4976148 | Migliori et al. | Dec 1990 | A |
5062877 | Borrelli et al. | Nov 1991 | A |
5074649 | Hamanaka | Dec 1991 | A |
5104435 | Oikawa et al. | Apr 1992 | A |
5121459 | Chiang | Jun 1992 | A |
5126863 | Otsuka et al. | Jun 1992 | A |
5135590 | Basavanhally et al. | Aug 1992 | A |
5345529 | Sizer, II et al. | Sep 1994 | A |
5346583 | Basavanhally | Sep 1994 | A |
5430819 | Sizer, II et al. | Jul 1995 | A |
5482800 | Gal | Jan 1996 | A |
5552092 | Francis et al. | Sep 1996 | A |
6328482 | Jian | Dec 2001 | B1 |
6436265 | Shimada et al. | Aug 2002 | B1 |
20020097957 | Kikuchi et al. | Jul 2002 | A1 |
20030068153 | Suzuki | Apr 2003 | A1 |
Number | Date | Country |
---|---|---|
5-215934 | Aug 1993 | JP |
WO0020899 | Apr 2000 | WO |
Number | Date | Country | |
---|---|---|---|
20030174944 A1 | Sep 2003 | US |
Number | Date | Country | |
---|---|---|---|
60364700 | Mar 2002 | US |