1. Field of the Invention
The invention relates to rare-earth doped phosphate laser glasses and methods of generating pulses of laser light in a laser system using such laser glasses.
2. Background of the Invention
It was first recognized that neodymium (Nd) doped laser glass could serve as a lasering material or gain medium over forty years ago (E. Snitzer, “Optical Maser Action in Barium Crown Glass,” Physical Review Letters 7, 444 (1961)). The Nd-doped glass is energized with a pump source, such as a flashlamp of other laser components such as laser diodes, so that the material exhibits gain near the lasing wavelength. For example, in the case of Nd-doped barium crown glass the lasing wavelength is 1054 nm. In this way, it is possible to amplify or generate laser light within the gain medium, i.e., the laser glass.
Following the recognition that Nd-doped glass was a useful gain medium, there were numerous developments in the area of laser glass in which particular formulations and compositions were developed with properties specifically tailored to match individual applications. Phosphate glasses were one area that received particular attention from the scientific community. The first Nd-doped phosphate laser glass patents focused solely on the composition of the glass material itself (DePaolis et al., U.S. Pat. No. 3,250,721). Later, Deutschbein et al. disclosed Nd-doped phosphate laser glass compositions having low thermal expansion and negative temperature coefficient of refractive index (dn/dT) making possible the design of solid-state laser systems with optical pathlength nearly independent of changes in device temperature (see U.S. Pat. No. 4,022,707).
Alexeev et al., in U.S. Pat. No. 3,979,322, combined the use of negative dn/dT values along with higher values for stimulated emission of laser light (σemm), and claimed more limited phosphate glass compositions specific for Nd-lasers. Later patents disclosed Nd-doped laser glass compositions that provide for: reduced glass transition temperature, the temperature at which glass properties such as refractive index are subsequently influenced by exposure to high temperature (U.S. Pat. No. 4,996,172 by Beall et al.); improved thermal shock resistance (e.g., high fracture toughness) in combination with good laser properties (U.S. Pat. No. 4,929,387 by Hayden et al., U.S. Pat. No. 5,053,165 by Toratani et al., and U.S. Pat. No. 5,032,315 of Hayden et al.); chemical strengthening techniques (U.S. Pat. No. 5,164,343 by Myers); a desirable athermal behavior (U.S. Pat. No. 4,075,120 and U.S. Pat. Nos. 4,333,848 by Myers et al. and 4,108,673 by Izumitani et al.); sensitized laser glasses (U.S. Pat. No. 4,770,811 by Myers); glasses with reduced concentration quenching behavior (U.S. Pat. No. 4,371,965 by Limpicki et al., U.S. Pat. No. 4,470,922 by Denker et al., and U.S. Pat. No. 4,661,284 by Cook et al.); glasses characterized by low values of emission cross section σemm (U.S. Pat. No. 5,173,456 by Hayden et al.); and glasses with properties enhanced for manufacturing yield in combination with improved performance in high peak energy laser systems (U.S. Pat. No. 5,526,369 by Hayden et al.). In addition, U.S. Pat. No. 4,820,662 by Izumitani et al., discloses phosphate glass compositions that contain SiO2 as a required additive which also contain rare-earths (specifically neodymium) up to 12 mol % on an oxide basis. The aforementioned patents are cases where rare-earth-doped, in particular neodymium-doped, glass compositions were tailored to offer properties favorable for specific laser application examples.
The current invention relates to the use of a particular type of rare-earth containing glass in a laser system to generate or amplify laser light where the high rare-earth contents are utilized.
Accordingly, an object of the invention is to provide improved laser systems that employ highly doped rare-earth phosphate laser glasses as the active material.
A further object of the invention is to provide improved laser systems that employ a phosphate glass composed primarily of P2O5, Al2O3, alkali earth oxides, and alkaline earth oxides, that contains high concentrations of rare earth ions and possesses other properties such as physical and thermal properties that are compatible with melting and manufacturing methods.
A further object of the invention is to provide improved laser systems in which a highly doped rare earth containing phosphate laser glass, in the form of rod or slab shaped component or in waveguide or film structures prepared by structuring technologies such as ion exchange and femtosecond laser writing and/or by sputtering, is employed as the active material.
Upon further study of the specification and appended claims, further objects and advantages of this invention will become apparent to those skilled in the art.
The present invention entails the means of generating or amplifying laser light pulses by utilizing a highly doped rare earth containing phosphate glass as the preferred gain medium. The invention involves the recognition that certain levels of rare earth content, higher than those used in the prior art, are desirable in certain laser system designs. Such levels were thought to be previously prohibitive, either because of manufacturing difficulties associated with solubility issues of rare earth materials in glass or because of decreased laser performance due to issues of self quenching of rare earth excited states involved in the laser transition when rare earth concentration levels achieve a critical value, called concentration quenching. See, e.g. U.S. Pat. No. 4,239,645 which discloses that high Nd2O3-contents cause difficulties in oscillating and amplifying the laser glass due to quenching.
Laser glasses of the present invention comprise P2O5, Al2O3, alkali earth oxides, and alkaline earth oxides. Preferably, the glass contains a maximum of 4 weight percent, especially a maximum of 2 weight percent, of conventional additives or impurities, such as refining agents (e.g., As2O3), antisolarants (e.g., Nb2O5) and SiO2 which can enter the glass through dissolution of the melting vessel. The inventive glasses are doped with lanthanide oxides (oxides of elements 57-71) or rare earth oxides (lanthanide oxides and oxides of Sc and Y) in an amount exceeding 8 mol %, preferably exceeding 12 mol %. Exemplary lanthanide/rare earth oxides are La2O3, Ce2O3, Pr2O3, Nd2O3, Sm2O3, Eu2O3, Gd3O3, Tb2O3, Dy2O3, Ho2O3, Er2O3, Tm2O3, and Yb2O3. The laser glasses according to the invention are highly doped with preferably neodymium, ytterbium and/or erbium. In the glasses, the oxygen in the metal oxides can optionally be replaced by fluorine up to 90%.
In general, the glasses have a P2O5 content of 50 to 75 mol %, for example, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74 mol %. Further preference is given to glasses having a P2O5 content above 60 mol %, more preferably above 65 mol %, even more preferably above 70 mol %, and especially preferably above 71 mol %.
In addition, in general, the glasses have a Al2O3 content of 3 to 15 mol %, for example, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 mol %. Preference is given to glasses having an Al2O3 content above 5 mol %, more preferably above 8 mol %, and even more preferably over 10 mol %, and particularly more preferably over 12 mol %.
The alkali metal oxides used in the inventive glasses are Na2O, K2O, Li2O, Rb2O and Cs2O, preferably Na2O, Li2O, K2O and Cs2O, and especially Li2O, K2O and Na2O. The amount of combined alkali metal oxides is, for example, 2.5 to 35 mol %, for example, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34 mol %, preferably 5 to 30 mol %.
The alkaline metal oxide used in the inventive glasses are MgO, CaO, SrO and BaO. However, ZnO can be used interchangeably for these alkaline metal oxides. Preferably MgO, BaO and ZnO are the employed metal oxides at levels of, for example, 0 to 35 mol %, for example, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34 mol %, preferably 0 to 30 mol %, especially 5 to 30 mol %.
In accordance with one embodiment, the glasses contain Nd2O3 in an amount of more than 8 mol %, for example, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 mol %, etc., preferably more than 12 mol %. In accordance with another embodiment, the glasses have a combined ytterbium and erbium content in an amount exceeding 8 mol %, for example, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 mol %, etc., preferably exceeding 12 mol %. Preference is given to glasses doped with erbium in an amount exceeding 0.15 mol %, for example, 0.20, 0.25, 0.30, 0.40, 0.45, 0.50, 0.55, 0.60, 0.65, 0.70, 0.75 mol %, etc.
Laser glasses of the present invention can also contain refining agents, such as As2O3, and Sb2O3, and antisolarant additives, such as Nb2O5, as well as small levels of additional components, such as SiO2, that are present in the glass from dissolution of the melting equipment used to manufacture the glass. The combined levels of these other additives normally do not exceed 4 percent on a weight basis.
Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The following preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.
In the foregoing and in the following examples, all temperatures are set forth uncorrected in degrees Celsius and, all parts and percentages are by weight, unless otherwise indicated.
Examples of the highly doped rare earth containing phosphate laser glass of the present invention are disclosed in Table 1.
Properties of the glasses in Table 1 are detailed in Table 2.
The absorption spectrum of the neodymium, erbium, and/or ytterbium containing phosphate glasses (hereafter referred to as “HDG-1”) pictured in FIG. 1 and
The main luminescence band employed in neodymium doped laser systems is the well-known band at 1054 nm. In the case of ytterbium, the emission is centered near 1.02 μm and in the case of erbium the fluorescence emission is centered near 1.54 μm. The fluorescence lifetime of these features is known to be a strong function of the doping concentration. This is exemplified in
τemm=τo[1−NNd/q]
whereτo and q are fitting parameters that are typically arrived at by mathematical fitting of actual measured fluorescence lifetime values,τemm, for various neodymium concentrations in the glass, NNd. As can be seen in the above fitting formula, as well as in
The data in
σe(ν)=σa(ν) exp[(ε−hv)/kT]
where ν is the frequency of interest (=c/λ where c is the speed of light in vacuum and λ is the wavelength of interest), k is Boltzmann's constant, T the temperature in units of Kelvin, and ε is a temperature dependent excitation energy described as that required to excite one Er3+ ion from the 4I15/2 ground state to the 4I13/2 excited state at temperature T. The 4I15/2 ground state and the 4I13/2 excited state are the two electronic energy levels involved in the main laser transition of erbium at 1.54 μm. It can be seen in
A laser system of this invention can be constructed in a number of ways.
The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.
The entire disclosures of all applications, patents and publications, cited above or below, is hereby incorporated by reference.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.
Number | Name | Date | Kind |
---|---|---|---|
3979322 | Alexeev et al. | Sep 1976 | A |
4022707 | Deutschbein et al. | May 1977 | A |
4075120 | Myers et al. | Feb 1978 | A |
4076541 | Rapp | Feb 1978 | A |
4108673 | Toratani et al. | Aug 1978 | A |
4239645 | Izumitani et al. | Dec 1980 | A |
4248732 | Myers et al. | Feb 1981 | A |
4333848 | Myers et al. | Jun 1982 | A |
4371965 | Lempicki et al. | Feb 1983 | A |
4470922 | Denker et al. | Sep 1984 | A |
4661284 | Cook et al. | Apr 1987 | A |
4770811 | Myers | Sep 1988 | A |
4820662 | Izumitani et al. | Apr 1989 | A |
4929387 | Hayden et al. | May 1990 | A |
4962067 | Myers | Oct 1990 | A |
5032315 | Hayden et al. | Jul 1991 | A |
5053165 | Toratani et al. | Oct 1991 | A |
5164343 | Myers | Nov 1992 | A |
5173456 | Hayden et al. | Dec 1992 | A |
5322820 | Myers et al. | Jun 1994 | A |
5334559 | Hayden | Aug 1994 | A |
5526369 | Hayden et al. | Jun 1996 | A |
5607886 | Onozawa | Mar 1997 | A |
5663972 | Payne et al. | Sep 1997 | A |
Number | Date | Country | |
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20040042515 A1 | Mar 2004 | US |