The present invention relates generally to the field of lasers and more particularly to an optical oxygen laser and method.
Singlet delta oxygen has a number of uses in lasers, medicine, bio-decontamination and high temperature superconductors. One method of producing singlet delta oxygen in high percentages relative to ground state oxygen is a chemical generation process. This method is commonly associated with chemical lasers where iodine is used to extract energy stored in the singlet delta oxygen and is the optically active species in the laser. The lasing wavelength for this laser is 1315 nm in a region of the spectrum which presents a potential eye hazard and limitations on propagation through the atmosphere.
Thus there exists a need for a system and method producing high densities of singlet delta oxygen that does not require large weight and volume devices, does not consume large quantities of explosive and toxic chemicals, and operates as a laser in a region of the spectrum which has a greater degree of eye safety and propagates well through the atmosphere. A device which produces high densities of singlet delta oxygen enables the generation of laser light on one of the optical transitions in the oxygen at 1580 nm which is a wavelength that is relatively eye safe and propagates through the atmosphere.
An optical oxygen laser includes a source of oxygen. A cryoreactor has an input connected to the source of oxygen. An optical pump is coupled to the cryoreactor. The optical pump excites the source of oxygen to form an excited state of oxygen. An optical resonator cavity receives the excited state oxygen and has a laser output.
In one embodiment, the source of oxygen is a liquid oxygen. In another embodiment, the source of oxygen is a supercritical oxygen. The source of oxygen is pressurized. The pressure of the source of oxygen is between two and ninety atmospheres.
In one embodiment, the optical pump source is a diode array. The diode array is coupled through an optical element to an optical fiber. In one embodiment, the diode array is bathed in the source of oxygen.
In one embodiment, the cryoreactor includes an intake manifold, a waveguide and an exhaust manifold. The waveguide has an optical input. An exhaust pipe is coupled to the exhaust manifold. The pressure in the exhaust pipe is less than a pressure of the source of oxygen.
In one embodiment, a method of operating an optical oxygen laser includes the steps of illuminating a volume of oxygen with an optical pump source in a reactor to form an excited state of oxygen. Placing the excited state of oxygen in an optical resonant cavity which has a laser output. Exhausting a decayed state of oxygen from the optical resonant cavity. In one embodiment, the step of illuminating includes powering a ytterbium doped fiber laser. In another embodiment, the step of illuminating includes powering a Raman fiber laser.
In one embodiment, the method of operating an optical oxygen laser includes cooling the optical pump with a source of oxygen.
In one embodiment, an optical oxygen laser includes an optical pump. A reactor is coupled to a source oxygen. The reactor combines a volume of oxygen from the source of oxygen with a light from the optical pump to form an excited state of oxygen. An optical resonant cavity receives the excited state of oxygen and has a laser output. In one embodiment, the reactor has a waveguide where the light and the volume of oxygen are combined. A pair of mirrors are placed at each end of the waveguide.
In one embodiment, the optical pump includes a laser diode array.
An optical oxygen laser includes a source of high density molecular oxygen. A portion of the ground state, molecular oxygen, O2(X3_), is excited by an optical source to the so called singlet delta state, O2(a1_). A state of population inversion then exists between the O2(a1_), v′=0 (zeroth vibrational level) and O2(X3_), v″=1 (first vibrational level) states. Stimulated emission on the transition between these two states produces coherent light output at 1580 nm. Bottlenecking on the lower laser level is eliminated by (1) vibrational relaxation with He or another rapid deactivator of this state or (2) flow of the molecules in this state out of the active region of the resonator. In its liquid state oxygen has a substantial heat of vaporization. This vaporization energy can be employed for laser waste heat thermal control as well as optical source temperature stabilization and waste heat elimination. The laser, therefore, has a unique property of dual use of its optically active medium as its coolant.
Because of molecular oxygen's small cross section for absorption of light and low stimulated emission cross section, high densities of oxygen are required to achieve gains necessary for efficient laser operation and power extraction. High densities of oxygen can be obtained by high pressure in combination with temperatures below room temperature (supercritical oxygen) or pressure below atmospheric in combination with cryogenic temperatures (liquid oxygen). In these cases, an oxygen density greater than 1022/cm3 can be obtained.
With an adequate density of oxygen, light resonant with optical transitions in molecular oxygen can efficiently convert ground state oxygen, O2(X3_), to singlet delta oxygen, O2(a1_). Transitions which couple the ground state to the excited state exist at a variety of wavelengths including 635 nm, 1065 nm, and 1270 nm. The linewidth of these transitions is typically greater than 10 nm. At high density, both mono- and bi-molecular transitions can participate in the production of singlet delta oxygen.
At liquid oxygen densities, absorption lengths on these transitions are about one centimeter. Therefore, light sources such as diodes (635 nm), fiber lasers (1067 nm) and Raman fiber lasers (1270 nm) offer ideal high intensity optical pump sources.
To promote about 1% of the oxygen to the singlet delta state in a typical excitation time period of 10 microseconds, a light intensity of 10 MW/cm2 is needed. Therefore, high intensity light sources are key to enabling laser operation. One-percent singlet delta oxygen at liquid oxygen density results in a gain of about 1%/cm on the optical transition at 1580 nm and an extractable power of about 32 J/cm3.
This is the first molecular oxygen laser ever designed. Because of its high power operation, extremely compact nature, excellent atmospheric propagation, and eye safe wavelength, it may find many uses in material processing, oil well drilling, and directed energy applications.
An optical oxygen laser requires generating an excited state of oxygen.
O2(3Σ, v″=0) O2(3Σ, v″=0)→O2(1Δ, v′=0) O2(1Δ, v′=0) Heat released from the reaction along with heat from the diode array provides the necessary heat to convert the liquid to a gas. The gas phase O2(1Δ) is allowed to expand into a volume sized to achieve an operating pressure of several atmospheres. This high pressure is used to drive a supersonic expansion through the nozzle 50. Molecular iodine 52 is mixed with the excited oxygen at the nozzle 50. The molecular iodine dissociates in the presence of the oxygen by collisions with the singlet sigma or singlet delta oxygen. A population inversion is obtained by the iodine atom collisions with the singlet delta oxygen and the resulting energy transfer reactions. An optical resonator 54 is placed across the output of the nozzle 50 and extracts optical energy from the gas flow by stimulated emission. A condenser 56 is used to collect the oxygen and nitrogen for reuse. In one embodiment, the light source is a Nd:YAG laser operating at 1060 nm or a ytterbium doped fiber laser.
The method of operating the optical oxygen laser is: First, a volume of oxygen is illuminated with an optical pump source 116 in a reactor 122 to form an excited state of oxygen. Second, the excited state of oxygen is placed in an optical resonant cavity 126 having a laser output 136. Last, the decayed state of oxygen is exhausted from the optical resonant cavity. To achieve adequate gain for high power operation an oxygen density greater than 8×10ˆ21/cmˆ3 is necessary. Additionally an optical excitation intensity of greater than 5 MW/cmˆ2 is needed with an oxygen illumination time of approximately 10 microseconds to achieve the gain necessary for high power operation. Output powers of about a kilojoule per cubic centimeter of active oxygen liquid can be expected. Waste heat release into the optical medium is taken up as phase change energy in the liquid oxygen. The amount of heat release per unit volume is substantially below the amount of energy required for liquid vaporization and therefore the exhaust remains as a cryogenic fluid which vaporizes on contact with the air.
Thus there has been described an optical oxygen laser and method. In one embodiment, the laser uses the pressure differential inherent in device to flow liquid oxygen through the laser continuously. In addition, the system uses the liquid oxygen to cool the pump laser and related optics. This is the first optical oxygen laser ever designed. This is the first molecular oxygen laser ever designed. Because of its high power operation, extremely compact nature, and eye safe wavelength, it may find many uses in material processing, oil well drilling, and directed energy applications
While the invention has been described in conjunction with specific embodiments thereof, it is evident that many alterations, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alterations, modifications, and variations in the appended claims.
This patent claims priority from and is a continuation-in-part of the U.S. patent application entitled “System for Producing Singlet Delta Oxygen Laser”, filed on Jul. 18, 2002 and having application Ser. No. 10/198,594 and assigned to the same assignee as the present application.
This invention was made with Government support under contract DAS60-0-C-0025 awarded by U.S. Army Space and Missile Defense Command. The Government has certain rights in the invention
Number | Date | Country | |
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Parent | 10198594 | Jul 2002 | US |
Child | 10670689 | Sep 2003 | US |