1. Field of the Invention
The present invention relates generally to a technology for fabricating an optical fiber or an optical device, and more particularly to a method of fabricating an optical fiber or an optical device doped with reduced metal ion(s) and/or rare earth ion(s).
2. Description of the Related Art
An optical fiber containing metal ion and/or rare earth ion is brought under a special optical fiber, since it can be variously applied to an optical amplifier or an optical switching device etc. Therefore, much of the research in this area has been performed.
One of the research projects is a technique of reducing doped metal ion and/or rare earth ion, Generally, an atom has a different energy level distribution depending on its valence, and therefore has different spectroscopic characteristics such as light absorption and light emission. Accordingly, a little more diverse light absorption and light emission can be obtained by utilizing the change of valence and thereby the optical fiber and the optical device having various optical amplification and optical switching characteristics can be obtained.
As an example, let us consider rare earth ions, when a rare earth ion has the valence of 3+, the light absorption characteristic due to electronic transition between 4ƒ electron orbit and 5d electron orbit occurs only in an ultraviolet wavelength region, whereas when the valence of the rare earth ion changes to 2+ ion, such an light absorption characteristic occurs in both visible and infrared wavelength regions. For this reason, a technique of making doped metal ion and rare earth ion with desired valences, respectively is required. Furthermore, every atom has its own valence states in which the atom is mainly existed in nature and thus a specific process is required in order to transfer the valence into another valences.
For example, most of the rare earth ions have the valence of 3+. In order to stably transfer the valence of 3+ into the valence of 2+, 1+ or 0, it is necessary to reduce the rare earth ions. There have been proposed various reduction treatment methods as described below.
Firstly, there is a method of applying gamma rays to the rare earth metal ion having the valence of 3+. For example, it is reported that Tm2+ can be obtained, if the gamma rays is applied to a CaF2 crystal containing Tm3+.
However, in this method, there is a problem that a gamma ray source is dangerous to handle and the cost required in handling it safely is thus expensive.
Secondly, there is another method in which an aerosol type material is utilized. In this method, a MCVD (modified chemical vapor deposition) process is indispensable. In other words, this method includes the MCVD process in which a glass layer containing rare earth ions is deposited in a quartz glass tube, using material having aerosol formulation which generates carbon, together with a powder which generates rare earth ion and glass when fired. Then, processes of removing the carbon and OH radical, sintering the glass and collapsing the glass tube are, in turn, performed to thus obtain an optical fiber preform. For example, in a glass optical fiber having SiO2—Al2O3 components, Eu2+ and SM2+ are reduced from Eu3+ and Sm3+, respectively.
To date, this method which utilizes the material having aerosol formulation is performed through only the MCVD process. A desired rare earth ion material having aerosol formulation and an additional apparatus for supplying material having aerosol formulation are needed.
Further, there is a method of injecting a mixture of H2 and Ar gases and obtaining the reduced rare earth ion during melting of glass. For example, in a glass having SiO2—Al2O3 components or SiO2—B2O3 components, Sm2+ is reduced from Sm3+.
In this method, there is a problem that processes of fabricating the optical fiber preform are complicated in comparison with the conventional processes and are not yet commercialized.
Therefore, it is an object of the present invention to provide a method of fabricating an optical fiber or an optical device, in which metal ion and/or rare earth ion safely and facilely reduced, in comparison with the prior art methods, together with the utilization of the prior art processes of fabricating the optical fiber and/or the optical device.
To achieve the aforementioned object of the present invention, a method according to the present invention is characterized by forming a partially-sintered fine structure in a base material for fabricating an optical fiber or an optical device and soaking the fine structure into a doping solution containing a reducing agent together with metal ion and/or rare earth ion during a selected time, thus doping the fine structure with the metal ion and/or rare earth ion together with the reducing agent. Therefore, reduced metal ion and/or rare earth ion through the reducing agent is obtained.
One method according to the present invention of fabricating an optical fiber or an optical device doped with reduced metal ion and/or rare earth ion comprising the steps of: forming a partially-sintered fine structure in a base material for fabricating the optical fiber or the optical device; soaking the fine structure into a doping solution containing a reducing agent together with metal ion and rare earth ion during a selected time; drying the fine structure in which the metal ion and rare ion is soaked; and heating the fine structure such that the fine structure is sintered.
Another method of fabricating an optical fiber or an optical device doped with reduced metal particle and/or rare earth element, comprising steps of: forming a partially-sintered fine structure in a base material for fabricating the optical fiber or the optical device; soaking the fine structure into a doping solution containing a reducing agent having strong reduction potential together with metal ion and rare earth ion during a selected time; drying the fine structure in which the metal ion and/or the rare earth ion is/are soaked; and heating the fine structure such that the fine structure is sintered, thereby forming the metal particle and/or the rare earth elements.
Preferably, the reducing agent is hydrocarbon compounds. Glucose, sucrose, glycerine, dextrin, benzene, phenol, hexane, toluene, stylene, naphthalene, and the like are exemplified.
In addition, the reducing agent is alkoxide compounds. TEOS (tetraethyl orthosilicate), TMOS (tetramethyl orthosilicate), TEOC (tetraethyl orthocarbonate), TMOC (tetamethyl orthocarbonate) and the like are exemplified.
Preferably, the metal ion and/or rare earth ion is at least one ion selected from the group consisting of Ce, Pr, Nd, Pm, Sm, Eu, Gd, Th, Dy, Ho, Br, Tm, Yb, Lu, Al, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sn, Hf, Ta, W, Re, Os, Ir, Pt, Au, Tl, Pb, Bi and a mixture thereof.
Further, the base material for fabricating the optical fiber or the optical device has a basic composition comprising a silicon oxide or a composite oxide of a silicone oxide and an oxide; in which the oxide is at least one selected from the group consisting of germanium oxide (GeO2), boron oxide (B2O3), phosphorous oxide P2O5), and titanium oxide (TiO2).
Preferably, the base material for fabricating the optical fiber or the optical device has a basic composition selected from silica (SiO2), germa osilicate (SiO2—GeO2), phosphorosilicate (SiO2—P2O5), phosphorogermanosilicate (SiO2—GeO2—P2O5), borosilicate (SiO2—B2O3), borophosphorosilicate (SiO2—P2O5—B2O3), borogermanosilicate (SiO2—GeO2—B2O3), titanosilicate (SiO2—TiO2), phosphorotitanosilicate (SiO2—TiO2—P2O5), or borotitanosilicate (SiO2—TiO2—B2O3).
Preferably, the step of forming the partially-sintered fine structure in the base material for fabricating the optical fiber or the optical device is performed by a process selected from MCVD (modified chemical vapor deposition), VAD (vapor-phase axial deposition), VOD (outside vapor deposition), FHD (flame hydrolysis deposition), etc.
The optical device in the present invention includes a planar optical amplifier, an optical communication laser, and a planar optical switch device, and the like.
The above objects and another advantages of the present invention will become more apparent by describing in detail preferred embodiments thereof with reference to the attached drawings in which:
Now, preferred embodiments of the present invention will be described in detail with reference to the annexed drawings.
A method of the present invention comprises a step of forming a partially-sintered fine structure in a base material for fabricating an optical fiber or an optical device, and a step of soaking the fine structure in a doping solution containing a hydrocarbon compound as a reducing agent together with metal ion and/or rare earth ion for 1 to 1.5 hours. That is, the fine structure of the base material is doped with the reducing agent together with metal ion and/or rare earth ion and the metal ion and/or rare earth ion reduced by the doped reducing agent is thereby obtained.
The method of the present invention is a modification of a solution doping technique for adding the rare earth ion and/or metal ion to the optical fiber or the optical device. This solution doping technique is a method of doping the metal ion or the rare earth ion in an optical fiber core, which can be utilized with any of conventional methods of fabricating an optical fiber preform, such as MCVD (modified chemical vapor deposition), VAD (vapor-phase axial deposition), OVD (outside vapor deposition), etc. The solution doping technique is also used as the technique which may dope all of the rare earth ion and/or the metal ion, capable of being formed into a solution type, even in a method of fabricating a plane glass optical device through a FHD (flame hydrolysis deposition) process.
For example, the solution doping technique please refer to J. E. Townsend, et al. “Solution for fabrication of rare earth doped optical fibers”, Electron, Lett., Vol. 23, p.p. 329-331, 1987) through the MCVD process is as follows. Herein, in order to obtain reduced rare earth ion, an aqueous solution in which sucrose as a strong reducing agent is dissolved together with rare earth chloride is used as a doping solution. First, a core layer partially sintered and then having a plurality of pores is formed in a silica tube using the conventional MCVD process (please refer to MacChesney et. al., “Optical fiber fabrication and resulting product”, U.S. Patent, 1997). Then, the silica tube is filled with the aqueous solution in which the sucrose is dissolved together with the rare earth chloride. The aqueous solution is hold for 1 to 1.5 hours in order for the solution to be sufficiently permeated into the pores of the core layer and is then discharged. As a result, the doping solution remains in the pores. The core layer doped with the aqueous solution is dried while the silica tube is hold at a temperature of 100 to 250° C. with the passage of an inert gas such as helium gas only, using the MCVD process. At this time, ethanol and moisture is removed. Sequentially, using hydrogen-oxygen flames, the core layer is heated at a high temperature of 2000° C. until carbon generated from the sucrose is removed and the core layer is then completely sintered (referring to M. F. Yan, et al., “Sintering of optical wave-guide glasses”, J. of Mater. Sci., p.p. 1371-1378, 1980). After that, the optical fiber preform is fabricated through a collapsing step in which the tube is heated to more than 2200° C. with the continuous purging of the inert gas, using the hydrogen-oxygen flames. The optical fiber preform is drawn to produce the optical fiber doped with the reduced rare earth ion.
The sucrose contained in the doping solution is composed of C, H and O components. During the above drying step, most of the H and O components among the above components are removed and only the carbon (C) is remained. The carbon (C) is combined with Oxygen (O2) remained at the high temperature of about 2000° C. to form carbon monoxide (CO), and thus carbon monoxide reduces the doped rare earth ion. At this time, the reaction temperature at which the carbon monoxide (CO) is formed is decided within the possible range of reduction of the rare earth ion, using an Ellingham Diagram. At the same time, a strong reduction atmosphere is created by injecting only the inert gas into the silica glass tube, so that the carbon (C) can be fully participated in the reduction reaction of rare earth ion. Further, preferably, the inert gas only is also passed through during the collapsing step for fabricating the optical fiber preform, thereby creating a reduction atmosphere at its maximum.
First, thulium chloride hexahydrate (TmCl3.6H2O) of 0.04M and sucrose (C12H22O11) of 2.17M are dissolved in deionized water to prepare a doping solution containing rare earth ion (Tm3+) and the sucrose as a reducing agent. Herein, a hydrocarbon compound or an alkoxide compound is used as the reducing agent.
As shown in
Then, the above sintering step and collapsing step are repeatedly performed 8 times and 15 times, respectively, at a temperature of 2000° C., thereby obtaining the optical fiber preform doped with Tm2+ ion. The optical fiber preform is drawn to fabricate the optical fiber. Herein, even when a sintering step is carried out at a temperature of 1600 to 2200° C., the same result is also obtained.
A light absorption spectrum of the optical fiber fabricated using the doping solution containing the sucrose as a reducing agent is shown in
Thulium chloride hexahydrate (TmCl3.6H2O) of 0.04M and aluminum chloride hexahydrate (AlCl3.6H2O) of 0.19M are dissolved in ethanol to prepare a doping solution without containing the sucrose as the reducing agent.
A core layer having a porous fine structure is formed at an inner wall of a silica glass tube in the same method as the embodiment 1. The fabricated doping solution is injected into the glass tube and then discharged after 1 hour. Then, the core layer is dried together with the purge of helium, oxygen and chlorine through the tube.
Then, the above sintering step and collapsing step are repeatedly performed 3 times and 7 times, respectively, at a temperature of 2000° C., thereby obtaining the optical fiber preform doped with Tm3+ ion. The optical fiber preform is drawn to fabricate the optical fiber.
A light absorption spectrum of the optical fiber fabricated by using the doping solution without containing the sucrose as the reducing agent is shown in
Europium chloride (EuCl3.xH2O) of 0.097M and sucrose (C12H22O11) of 0.518M are dissolved in deionized water to prepare a doping solution containing rare earth ion (Eu3+) and the sucrose as a reducing agent.
Then, the optical fiber doped with Eu2+ ion is fabricated by the same processes as in the embodiment 1.
A light absorption spectrum of the optical fiber fabricated by using the doping solution containing the sucrose as the reducing agent is shown in
Europium chloride hydrate (EuCl3.xH2O) of 0.097M and aluminum chloride hexahyrate (AlCl3 6H2O) of 0.518M are dissolved in ethanol to prepare a doping solution without containing the sucrose as the reducing agent.
Then, the optical fiber doped with Eu3+ ion is fabricated by the same processes as in the comparative 1.
A light absorption spectrum of the optical fiber fabricated by using the doping solution without containing the sucrose as the reducing agent is shown in
The above embodiments 1 and 2 illustrate that the optical fibers perform doped with Tm2+ ion and Eu+2 ion, respectively, by the doping solutions containing the reducing agents are obtained. Depending on the intensity of reduction potential which the reducing agent has, it is confirmed that metal ion or rare earth ion having 3+ valence is changed to 2+ valence or 1+, in some cases to “0” valence. When the metal ion or rare the earth ion is reduced to “0” valence, an optical fiber preform or an optical device preform doped with metal particle or rare earth element is formed.
As described above, the present invention can fabricate an optical device doped with reduced metal ion and/or rare earth ion having a desire valence by a facile solution doping technique.
According to the present invention, an optical fiber or an optical device doped with metal ion and/or rare earth ion reduced by the facile solution doping technique, with no need to change the conventional MCVD, VAD, OVD processes, etc. may be fabricated.
While the present invention has been described in detail, it should be understood that various changes, substitutions and alterations can be made hereto without departing from the spirit and scope of the invention as defined by the appended claims.