Alkaloid halogen-doped sulfide glasses for optical amplifier and fabricating method thereof

Abstract

There is provided alkaloid halogen-doped sulfide glasses for an optical amplifier and a fabricating method thereof. An alkaloid halogen-doped sulfide glass is formed of silica doped with a Ge-Ga-S three-component system, Pr3+, and an alkaloid halogen. To fabricate the alkaloid halogen-doped sulfide glass for an optical amplifier, silica doped with Ge, Ga, S, Pr3+, and an alkaloid halogen as a starting material is filled into a container. The container is sealed in a vacuum and the starting material in the container is fused by heating the container. The container is cooled and the starting material is sintered by heating the container at a glass transition temperature.

Description

BACKGROUND OF THE INVENTION

[0001] 1. Field of the Invention

[0002] The present invention relates generally to sulfide glasses and a fabricating method thereof. More particularly, the present invention relates to sulfide glasses used as an optical amplifier and the fabricating method thereof.

[0003] 2. Description of the Related Art

[0004] The following list of literature reference is indicative of the extensive research conducted in recent years in the field of sulfide-containing glasses.

[0005] References

[0006] 1. “High-Gain Rare Earth Doped Fiber Amplifier Operating at 1.54 μm”, in Tech. Digest of Conference on Optical Fiber Communication, Reno Nevada (Optical Society of America. Washington, D.C.), W12, 167 (1987) by R. J. Mears, L. Leekie, I. M. Jauncey, and D. N. Payne.

[0007] 2. “Amplification and Lasing at 1350 nm in Neodymium Doped Fluorozirconate Fiber”, Electron. Lett. 24, 438 (1988) by M. C. Brierley and C. A. Millar.

[0008] 3. “Pr3+—doped Fluoride Fibre Amplifier Operating at 1.31 μm”, Opt. Lett. 16, 1747 (1991) by Y. Ohoshi, T. Kanamori, T. Kitagawa, S. Takahashi, E. Snitzer, and G. H. Sigel, Jr.

[0009] 4. “Amplification at 1.3 μm in a Pr3+—Doped Single Mode Fluorozirconate Fibre”, Electronics Letters vol. 27, no. 8, 628 (1991) by S. F. Carter, D. Szebesta, S. T. Davey, R. Wyatt, M. C. Brierley, and P. W. France.

[0010] 5. “Pr3+: La-Ga-S Glass: A Promising Material for 1.3 μm Fiber Amplification”, in Tech. Digest of Topical Meeting Optical Amplifiers and their Applications. PDP5 (1992) by P. C. Becker, M. M. Broer, V. C. Lambrecht, A. J. Bruce, and C. Nykolak.

[0011] 6. “Pr3+—Doped Ge-Ga-S Glasses for 1.3 μm Optical Fiber Amplifiers”, J. Non-Cryst. Solids, 182, 257 (1995) by K. Wei, D. P. Macherwirth, J. Wenzel, E. Snitzer, and G. H. Sigel, Jr.

[0012] 7. Spectroscopy and Quantum Efficiency of Halide-Modified Gallium-Lanthanium Sulfide Glasses Doped with Praseodymium”, J. Non-Cryst. Solids, 239, 176 (1998) by J. R. Hector, J. Wang, D. Brady, M. Kluth, D. W. Hewak, W. S. Brocklesby, and D. N. Payne.

[0013] In general, an optical communication system operates at the zero dispersion wavelength band, 1.31 μm, and a minimum loss wavelength band, 1.5 μm of silica glass, as an optical wave-guide material [See reference 1]. Particularly in the 1.31 μm wavelength band, the rare-earth ions of Nd3+, Dy3+, and Pr3+exhibit fluorescence transition. Efforts have been made toward utilization of these rare-earth ions.

[0014] With reference to Nd3+, the central wavelength of fluorescence resulting from transition from the energy level of 4F3/2 to 4F13/2 is 1.35 μm, which is different from the zero dispersion wavelength band of silica glass. Moreover, the probability of fluorescence emission at 1.31 μm is only one fifth of the fluorescence emission probability at 0.89 μm and 1.064 μm that are simultaneously generated at 4F3/2. The gain at 1.31 μm drops due to a strong, excited state absorption [See reference 2].

[0015] Dy3+produces fluorescence at 1.31 μm across an induced emission area that is four times larger than Pr3+, and has a high branching ratio relative to other rare-earth elements. Despite these advantages, Dy3+has a very narrow energy difference, about 1800 cm−1 between the fluorescence levels of 1.31 μm, 4F11/2 or 6H9/2, and the nearest lower energy level 6H11/2s. Here, the resulting multiphonon relaxation leads to energy loss. Consequently, Dy3+has only 10% of the fluorescence lifetime of Pr3+, which are low fluorescence efficiency and a low gain coefficient needed for light amplification.

[0016] While Pr3+ induces fluorescence at 1.31 μm utilizing transition 1G4 to 3H5 and has a much higher 1.3 1 μm fluorescence transition probability than other fluorescence transition probabilities, it also has a narrow energy difference, 3000 cm−1 between 1G4 and 3F4. Thus, when an oxide glass having a phonon energy of 800 cm−1 or above is used as a base material, it is highly probable that the energy of Pr3+ ions excited to 1G4 experiences radiation-less transition due to the multiphonon relaxation, which results in the decrease of optical amplification efficiency. To solve the problem, a fluoride glass or a sulfide glass that has low phonon energy was suggested as a base material. However, the use of the fluoride glass as a base material can not produce high optical amplification efficiency because its quantum efficiency is very low, 4%. The sulfide glass as a base material is not effective in achieving high optical amplification efficiency due to its short fluorescence lifetime, 300 μs at 1G4 [See references 3 to 7].

[0017] FIG. 1 illustrates the multiphonon relaxation of Pr3+ between energy levels, and the energy transfer between Pr3+ ion. The 1.31 μm fluorescence lifetime and the optical amplification efficiency of Pr3+ at 1G4 are much influenced by radiation-less transition in which energy excited to 1G4 is consumed in a form other than light. The radiation-less transition refers to the multiphonon relaxation of phonon energy, as indicated reference character a, and the energy transfer between adjacent Pr3+ ions, as indicated by reference character b in FIG. 1. The multiphonon relaxation is a dominant factor that decreases the optical amplification efficiency.

SUMMARY OF THE INVENTION

[0018] The present invention provides alkaloid halogen-doped sulfide glasses to be used as an optical amplifier and its fabricating method to extend fluorescence lifetime by eliminating the multiphonon relaxation, thus increasing the optical amplification efficiency of the optical amplifier.

[0019] The present invention can be achieved by providing alkaloid halogen-doped sulfide glasses for an optical amplifier and a fabricating method thereof. An alkaloid halogen-doped sulfide glass is formed of silica doped with a Ge-Ga-S three-component system, Pr3+, and an alkaloid halogen. To fabricate the alkaloid halogen-doped sulfide glass for an optical amplifier, silica doped with Ge, Ga, S, Pr3+, and an alkaloid halogen as a starting material is filled into a container. The container is sealed in a vacuum and the starting material in the container is fused by heating the container. The container is cooled and the starting material is sintered by heating the container at a glass transition temperature.

[0020] According to one aspect of the present invention, the Pr3+ and alkaloid halogen-doped sulfide comprises a mixture of GeGaS and CsBr, expressed in terms of mole percent on the sulfide basis, and is selected from the group consisting of 90-92% (Ge0.25Ga0.10S0.65) and 8-10% (CsBr); 94.5-96.0 % (Ge0.29Ga0.05S0.66) and 4-5.5% (CsBr); and, 84.2-85.25% (Ge0.18Ga0.18S0.64) and 14.75-15.75% (CsBr).

[0021] According to another aspect of the invention, the Pr3+ and alkaloid halogen-doped sulfide glass comprises a mixture of GeGaS and KBr, expressed in terms of mole percent on the sulfide basis, and comprises 90.91% (Ge0.25Ga0.10S0.65) and 9.09% (KBr).

[0022] According to a further aspect of the invention, the Pr3+ and alkaloid halogen-doped sulfide glass comprises a mixture of GeAsGaS and CsBr, expressed in terms of mole percent on the sulfide basis, and comprises 98% (Ge0.30As0.06Ga0.028S0.62) and 2%(CsBr).

[0023] Preferably, the alkaloid halogen is CsBr or Kbr.

BRIEF DESCRIPTION OF THE DRAWINGS

[0024] The above and other features and advantages of the present invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings in which:

[0025] FIG. 1 illustrates the multiphonon relaxation of Pr3+ between the energy levels and an energy transfer between Pr3+ ions;

[0026] FIG. 2 is a flowchart illustrating a flow chart for fabricating alkaloid halogen-doped sulfide glasses for an optical amplifier according to the present invention;

[0027] FIGS. 3 to 8 are graphs showing the fluorescence spectrums of the sulfide glasses fabricated according to various preferred embodiments of the present invention; and,

[0028] FIGS. 9 and 10 are graphs showing changes of the fluorescence intensity of sulfide glasses fabricated according to a few preferred embodiments of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0029] Preferred embodiments of the present invention will be described hereinbelow with reference to the accompanying drawings. For the purpose of clarity, well-known functions or constructions are not described in detail as they would obscure the invention in unnecessary detail.

[0030] Alkaloid halogen-doped sulfide glass for an optical amplifier according to the present invention is formed of a rare-earth element Pr3+, a three-component system Ge-Ga-S showing high solubility with respect to Pr3+, and an alkaloid halogen CsBr or KBr for decreasing the multiphonon relaxation of Pr3+. Also, in the embodiment of the present invention, it can be contemplated that the Ge-Ga-S three-component system is further doped with As.

[0031] With reference to FIG. 1, the alkaloid halogen, CsBr or KBr, serves to decrease the multiphonon relaxation rate of Pr3+ from 1G4 to lower levels 3F4 and 3F3. By decreasing the multiphonon relaxation through the provision of the alkaloid halogen in the sulfide glass, the present invention is able to provide higher optical amplification efficiency to the sulfide glass.

[0032] FIG. 2 is a flowchart illustrating a method of fabricating alkaloid halogen-doped sulfide glasses to be used as an optical amplifier according to the present invention. The sulfide glass fabricating method mainly includes the steps of filling (step 100), sealing (step 200), fusion (step 300), cooling (step 400), and sintering (step 500).

[0033] In step 100, silica doped with Ge, Ga, S, and Pr3+ or Ge, Ga, As, S, and Pr3+ and an alkaloid halogen as a starting material is filled in a container. As shown in FIG. 2, a first starting material 110 is silica doped with the Ge-Ga-S three component-system 112, Pr3+114, and the alkaloid halogen 116, and a second starting material 120 is silica doped with the Ge-Ga-As-S four-component system 122, Pr3+124, and the alkaloid halogen 126.

[0034] The composition of the Ge-Ga-S 112 is preferably Ge0.25Ga0.10S0.65, Ge0.29Ga0.05S0.66, or Ge0.18Ga0.18S0.64. The composition of Ge-As-Ga-S 122 is preferably Ge0.30As0.06Ga0.02S0.62. Here, the composition is expressed in terms of mole fraction. Preferably, CsBr or KBr is used as the alkaloid halogen 116 and 126. In the embodiment of the present invention, the alkaloid halogen 116 and 126 increase the fluorescence lifetime of sulfide glass by drastically decreasing the multiphonon relaxation rate of Pr3+ from 1G4 to 3F4 and 3F3. The filling step 100 is preferably performed at an Ar atmosphere and the container is a silicon ampule.

[0035] In step 200, the container having the starting material is sealed in a vacuum, and the starting material is fused by heating the sealed container in step 300.

[0036] The container filled with the fused starting material is cooled in a water tank in step 400, and the cooled starting material is melted by heating the container at a glass transition temperature in step 500.

[0037] Embodiment 1

[0038] The starting material includes the Ge-Ga-S three-component system of 99.999% in purity, CsBr of 99.9% in purity, and Pr ions. In the first embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.92[Ge0.25Ga0.10S0.65]-0.08CsBr, and Pr is 300 ppm (parts per million). 7 g of the starting material is measured out at the Ar atmosphere in a glove box, filled into a silica ampule, and sealed in vacuum. The silica ampule is fused at 950° C. for 12 hours in an agitator, water-cooled, and then sintered at a glass transition temperature for about one hour. Through the above process, the inventive optical amplifier glass is formed.

[0039] The fluorescence lifetime of a conventional Ge0.25Ga0.10S0.65 glass doped with 300 ppm of Pr is 335 μs, while the fluorescence lifetime of the sulfide glass according to the first embodiment of the present invention is 345 μs, as shown in Table 1 below. A longer fluorescence lifetime is achieved by minimizing the multiphonon relaxation rate of Pr from 1G4 to 3F4 through the provision of the alkaloid halogen CsBr. FIG. 3 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the first embodiment of the present invention.

	TABLE 1
	floures-
	cence
	doped ratio:	life-
embod-			compar-	CsBr	time
iments	composition	Ga (%)	ison	(%)	(μs)
1	Ge0.25Ga0.10S0.65	9.2	>	8	345
2	Ge0.25Ga0.10S0.65	9.091	=	9.091	1155
3	Ge0.25Ga0.10S0.65	9	<	10	1169
4	Ge0.29Ga0.05S0.66	4.8	>	4	378
5	Ge0.29Ga0.05S0.66	4.762	=	4.762	739
6	Ge0.29Ga0.05S0.66	4.725	<	5.5	1106
7	Ge0.18Ga0.18S0.64	15.345	>	14.75	973
8	Ge0.18Ga0.18S0.64	15.254	=	15.254	1188
9	Ge0.18Ga0.18S0.64	15.165	<	15.75	1261
10	Ge0.30As0.06Ga0.028S0.62	1.96	<	2	465

[0040] Table 1 lists compositions of starting materials, doped rations of Ga and an alkaloid halogen and the fluorescence lifetime of the resulting sulfide glasses in the embodiments of the present invention using CsBr as the alkaloid halogen.

[0041] Embodiment 2

[0042] According to a second embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.9091[Ge0.25Ga0.10S0.65]-0.0909CsBr with Ga/CsBr=1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 4 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the second embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the second embodiment of the present invention is 1155 μs.

[0043] Embodiment 3

[0044] According to a third embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.90[Ge0.25Ga0.10S0.65]-0.10CsBr with Ga/CsBr<1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention.

[0045] FIG. 4 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the third embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the third embodiment of the present invention is 1169 μs. The sulfide glass according to the third embodiment of the present invention has the longest fluorescence lifetime of all the sulfide glasses according to the embodiments of the present invention, because CsBr drastically decreases the multiphonon relaxation rate of Pr from 1G4 to lower levels 3F4 and 3F3. As more CsBr is doped, the peak of the 1.34-μm fluorescence spectrum of Pr3+ at 1G4 branches into two parts. Here, the central frequencies of the two peaks are 1310 nm and 1360 nm, respectively.

[0046] Embodiment 4

[0047] According to a fourth embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.96[Ge0.29Ga0.05S0.66]-0.04CsBr with Ga/CsBr>1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 5 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the fourth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the fourth embodiment of the present invention is 378 μs.

[0048] Embodiment 5

[0049] According to a fifth embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.95238[Ge0.29Ga0.05S0.66]-0.04762CsBr with Ga/CsBr=1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 5 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the fifth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the fifth embodiment of the present invention is 739 μs.

[0050] Embodiment 6

[0051] According to a sixth embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.945[Ge0.29Ga0.05S0.66]-0.055CsBr with Ga/CsBr<1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 5 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the sixth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the sixth embodiment of the present invention is 1106 μs.

[0052] Embodiment 7

[0053] According to a seventh embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.8525[Ge0.18Ga0.18S0.64]-0.1475CsBr with Ga/CsBr>1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 6 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the seventh embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the seventh embodiment of the present invention is 973 μs.

[0054] Embodiment 8

[0055] According to an eighth embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.84746[Ge0.18Ga0.18S0.64]-0.15254CsBr with Ga/CsBr=1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 6 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the eighth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the eighth embodiment of the present invention is 1188 μs.

[0056] Embodiment 9

[0057] According to a ninth embodiment of the present invention, the composition ratio of the three-component system and CsBr is set to 0.8425[Ge0.18Ga0.18S0.64]-0.1575CsBr with Ga/CsBr<1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 6 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the ninth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the ninth embodiment of the present invention is 1261 μs.

[0058] Embodiment 10

[0059] In the tenth embodiment of the present invention, the starting material includes the Ge-As-Ga-S four-component system of 99.999% in purity, CsBr of 99.9% in purity, and Pr. The composition ratio of the four-component system and CsBr is set to 0.98[Ge0.30As0.06Ga0.02S0.62]-0.02CsBr with Ga/CsBr<1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 7 and Table 1 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the tenth embodiment of the present invention. As shown in Table 1, the measured fluorescence lifetime of the sulfide glass according to the tenth embodiment of the present invention is 465 μs.

[0060] Embodiment 11

[0061] In the eleventh embodiment of the present invention, the starting material includes the Ge-Ga-S three-component system of 99.999% in purity, KBr of 99.9% in purity, and Pr. The composition ratio of the three-component system and KBr is set to 0.9091 [Ge0.25Ga0.10S0.65]-0.0909KBr with Ga/KBr=1 and the amount of Pr is 300 ppm. An optical amplifier glass is formed in the same manner as in the first embodiment of the present invention. FIG. 8 and Table 2 illustrate the fluorescence spectrum and fluorescence lifetime of the sulfide glass for an optical amplifier according to the eleventh embodiment of the present invention. As shown in Table 2 below, the measured fluorescence lifetime of the sulfide glass according to the eleventh embodiment of the present invention is 479 μs.

	TABLE 2
	doped ratio of
embo-			com-		fluorescence
diment	composition	Ga (%)	parison	CsBr (%)	lifetime (μs)
11	Ge0.25Ga0.10S0.65	9.091	=	9.091	479

[0062] Table 2 lists the composition of a starting material, doping ratios of Ga and an alkaloid halogen, and the fluorescence lifetime of the resulting sulfide glass in the embodiment of the present invention using KBr as the alkaloid halogen.

[0063] FIGS. 3 to 8 illustrate the fluorescence spectrums of the sulfide glasses for an optical amplifier fabricated according to the conventional technology and according to the preferred embodiments of the present invention. FIG. 3 illustrates the fluorescence spectrum of the sulfide glass for an optical amplifier according to the first embodiment of the present invention. FIG. 4 illustrates the fluorescence spectrums of the sulfide glasses for an optical amplifier according to the second and third embodiments of the present invention. FIG. 5 illustrates the fluorescence spectrums of the sulfide glasses for an optical amplifier according to the fourth, fifth, and sixth embodiments of the present invention. FIG. 6 illustrates the fluorescence spectrums of the sulfide glasses for an optical amplifier according to the seventh, eighth, and ninth embodiments of the present invention. FIG. 7 illustrates the fluorescence spectrums of the sulfide glass for an optical amplifier according to the tenth embodiment of the present invention. FIG. 8 illustrates the fluorescence spectrums of the sulfide glass for an optical amplifier according to the eleventh embodiment of the present invention. To measure the fluorescence spectrums according to the present invention, a 1014-nm Ti-sapphire laser driven by an Ar+ laser was used as an exciting light source. Pr3+ in the sulfide glasses were excited to 1G4 using the exciting light source. Fluorescence at the excited state was sensed with an InGaAs-PIN sensor at wavelengths identified with a ⅛-m monochromator. The sensed fluorescence was analyzed by a lock-in amplifier connected to a computer.

[0064] FIGS. 9 and 10 are graphs showing the fluorescence changes of sulfide glasses for an optical amplifier fabricated according to preferred embodiments of the present invention. FIG. 9 illustrates a comparison in fluorescence decrease between a conventional three-component system sulfide glass for an optical amplifier and a three-component system sulfide glass for an optical amplifier according to the embodiments of the present invention. FIG. 10 illustrates a comparison in fluorescence decrease between a conventional four-component system sulfide glass for an optical amplifier and a four-component system sulfide glass for an optical amplifier according to the embodiment of the present invention.

[0065] The fluorescence decrease curves were drawn with the decrements of fluorescence intensity measured by a digital oscilloscope versus time. The fluorescence lifetime is defined as time at which fluorescence intensity is a 1/eth of an initial value.

[0066] As described above, the alkaloid halogen-doped sulfide glasses and the fabricating method thereof according to the embodiments of the present invention alleviate multiphonon relaxation, increasing the lifetime of fluorescence. Therefore, the sulfide glasses have high optical amplification efficiency.

[0067] While the invention has been shown and described with reference to certain preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and the scope of the invention as defined by the appended claims.

Claims

1. An alkaloid halogen-doped sulfide glass for an optical amplifier, comprising: a three-component system of Ge-Ga-S, said three-component doped with a Pr3+ and an alkaloid halogen.

2. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 1, wherein said three-component system comprises a mixture of GeGaS and CsBr, expressed in terms of mole percent on the sulfide basis, and wherein said mixture is selected from the group consisting of 90-92% (Ge0.25Ga0.10S0.65) and 8-10% (CsBr); 94.5-96.0% (Ge0.29Ga0.05S0.66) and 4-5.5% (CsBr); and, 84.2-85.25% (Ge0.18Ga0.18S0.64) and 14.75-15.75% (CsBr).

3. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 1, wherein the three-component system comprises a mixture of GeGaS and KBr, expressed in terms of mole percent on the sulfide basis, and wherein said mixture comprises 90.91% (Ge0.25Ga0.10S0.65) and 9.09% (KBr).

4. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 1, wherein the three-component system comprises a mixture of GeAsGaS and CsBr, expressed in terms of mole percent on the sulfide basis, and wherein said mixture comprises 98% (Ge0.30As0.06Ga0.028S0.62) and 2%(CsBr).

5. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 1, wherein the alkaloid halogen is CsBr.

6. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 1, wherein the alkaloid halogen is KBr.

7. An alkaloid halogen-doped sulfide glass for an optical amplifier, comprising: a three-component system of Ge-Ga-S, said three-component doped with a Pr3+, an alkaloid halogen, and an As.

8. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 7, wherein the alkaloid halogen is CsBr.

9. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 7, wherein the alkaloid halogen is KBr.

10. The Pr3+ and alkaloid halogen-doped sulfide glass of claim 7, wherein the three-component system comprises a mixture of GeAsGaS and CsBr, expressed in terms of mole percent on the sulfide basis, and said mixture comprises 98% (Ge0.30As0.06Ga0.028S0.62) and 2% (CsBr).

11. A method for fabricating an alkaloid halogen-doped sulfide glass for use as an optical amplifier, the method comprising the steps of: filling silica doped with Ge, Ga, S, Pr3+, and an alkaloid halogen as a starting material into a container; sealing the container in a vacuum; fusing the starting material in the container by heating the container; cooling the container; and, sintering the starting material by heating the container at a glass transition temperature.

12. The method of claim 11, wherein the alkaloid halogen is CsBr.

13. The method of claim 11, wherein the alkaloid halogen is KBr.

14. The method of claim 11, wherein the starting material further includes As.

15. The method of claim 11, wherein the filling step is performed at an As atmosphere.