This application claims priority to International Application PCT/US2014/021313 titled “Ultraviolet Triply-Optically-Pumped Atomic Lasers (TOPAL) filed in the U.S. Receiving Office on Mar. 6, 2014 which claims the benefit of U.S. Provisional Patent Application No. 61/851,369 tided “Ultraviolet Triply-Optically-Pumped Atomic Lasers (TOPAL),” filed Mar. 7, 2013, incorporated herein by reference.
1. Field of the Invention
The present invention relates generally to continuous wave (CW) lasers and more specifically it relates to continuous wave lasers operating in the deep UV that do not require nonlinear optical crystal frequency convertors exposed to deep ultraviolet radiation with wavelengths less than ˜370 nm.
2. Description of Related Art
An important application carried out with the aid of laser radiation is the detection and classification of small defects inadvertently produced in the fabrication of semiconductor chips. Generally, the smaller the defect, the shorter the laser wavelength must be. Historically, this laser application was accomplished using a continuous wave (CW) argon ion gas laser emitting its radiation at a wavelength of 514 nm or 488 nm as a primary source. To achieve adequately short deep ultraviolet wavelengths of radiation for commercially viable defect detection, the 514 nm or 488 nm output radiation from an argon ion gas laser is converted to second harmonic wavelengths of 257 nm or 244 nm, respectively, by interaction with a nonlinear optical (NLO) crystal, Wavelengths shorter than 370 am are designated herein as “deep ultraviolet wavelengths”, or DUV. This type of deep UV source generally provides low output power (<1 watt), is extremely inefficient (<0.01%), requires extensive electrical power conditioning and active cooling, and is physically bulky. The utilized NLO crystal degrades during use and must be refurbished frequently (see more discussion below). The stressing physical operating conditions within an argon ion gas laser generally limit its operating lifetime to <10,000 hours. Thus, there is a need to develop CW deep ultraviolet laser sources that are more than an order of magnitude more powerful and efficient (i.e., multi-watt, >1%), whose reliabilities are not compromised by NLO crystal degradation due to exposure to DUV irradiation, are much more compact, and that require only comparably benign utilities.
In an attempt to overcome some of the limitations of this above described prior art, DUN lasers based on infrared-emitting, diode-pumped solid-state lasers (DPSSLs), combined with nonlinear harmonic generation, have been developed. These lasers possess performance features that are substantially superior to awn ion gas laser based solutions. Generally, this type of laser comprises a diode-pumped solid-state gain medium (such as Nd:YAG, Nd:YVO4 or Yb fiber) emitting “fundamental” radiation in the near infrared spectral region (i.e., λIR=1064 nm), and two or more harmonic nonlinear optical (NLO) crystal converters. The NLO elements convert the fundamental IR radiation into radiation of shorter “harmonic” wavelengths: λIR/2, λIR/3, λIR/4, etc (i.e., 532 nm, 355 nm, 266 nm, respectively). Practically efficient harmonic conversion requires of the NLO crystal that: 1) its birefringence is such that the NLO conversion process is “phase-matched” (i.e., the indices of refraction at both fundamental and harmonic wavelengths are equal); 2) its nonlinearity is adequately large; 3) it is adequately transparent at all present wavelengths; and 4) its intensity threshold for optical damage substantially exceeds that of the drive intensity needed for efficient NLO conversion.
Long sustained searches for practical NLO crystals have resulted in the identification and commercial development of several NLO crystals capable of enabling practical use at output wavelengths >˜370 nm, but only a few NLO crystals possessing properties suitable for harmonic generation at wavelengths lying in the deep ultraviolet spectral region <˜370 nm. Among these latter crystals are lithium borate (LBO), beta-meta-borate (BBO), and cesium-lithium borate (CLBO).
Because the efficiency of such non-linear conversion processes scales rapidly with the intensity of the drive laser, and is degraded by poor beam quality, the drive lasers must irradiate a NLO crystal with a good spatial quality beam at intensities in the 100-1000 MW cm−2range for efficient harmonic conversion. These intensities are readily realized by pulsed solid state lasers but are a significant challenge for CW lasers. At such intensities, nonlinear optical materials tend to degrade during operation due to optical damage. This is particularly so for NLO crystals operating with output wavelengths below 370 nm. Thus, 355 nm and 266 nm lasers based on the use of NLO crystals tend to degrade with operating time, so that their relatively short operating times before refurbishment or replacement becomes a cost driver for users. To be commercially viable, complicated and expensive defensive measures have been adopted, such as translating the nonlinear optical crystal transverse to the drive laser beam to operate in an undamaged region of the crystal.
For some inspection applications a purely continuous wave (i.e., not repetitively pulsed) optical laser source is required to avoid optical damage to the specimen being inspected. A prior art purely CW 266 nm source of laser radiation has been based on fourth harmonic generation of the 1064 nm fundamental radiation from a diode-pumped solid state laser Suedmeyer, Optics Express, 16 (3) 1546 (2008)1.
This type of laser consists of three major subsystems: 1) a CW, high-power 1064 nm Master-Oscillator-Power-Amplifier (MOPA) drive laser: 2) a second harmonic converter subsystem comprising, a first optical cavity containing a first non-linear crystal operating in the visible spectral region; and 3) a fourth harmonic converter subsystem comprising a second optical cavity and a second nonlinear crystal operating in the DIN spectral region, To respond to the need for high drive laser intensities at the nonlinear crystal to achieve practically high conversion efficiencies, it is necessary to resonate the drive radiation within each optical cavity containing a NLO crystal, to build up the drive intensity within the cavity. To stabilize the intra-cavity intensities, the length of each coupled optical cavity must be controlled to a fraction of its drive wavelength. The drive wavelength and the optical cavity length fluctuate due to thermal and to mechanical motion effects in the environment, so these effects Must be monitored and actively counteracted using feedback mechanisms. While a single stage of frequency conversion can be achieved stably and efficiently, the stability requirements for a second stage are extremely challenging. While this type of CW DUV laser is more than an order of magnitude more efficient and powerful than the earlier prior art based on the argon-ion gas laser, the requirement of controlling the lengths of the coupled optical cavities to a fraction of the drive wavelengths greatly increases the complexity and cost, and greatly lowers operational availability of this type of source. As with the prior art based on the argon ion gas laser , the solid state based DUV CW 266 nm laser source is subject to degradation of the NLO crystals being exposed to short DUV 266 nm wavelength, high intra-cavity intensity radiation. Thus the need persists for a practical, powerful (multi-watt), efficient (>1%) reliable CW DUV source, not subject to the 266 nm-caused degradation of a NLO crystal of the prior art.
To avoid the most deleterious aspects of the above-mentioned intrinsic limitations of NLO based approaches to CW DUV laser sources, several prior art methods have been described wherein the energies of several longer wavelength laser photons are combined, by various means described below, thereby creating DIN wavelength laser photons.
In discussing, these various means, it is important to differentiate several distinct types of multiple photon processes. Herein we use the following terminology:
(A) Sequential photon energy “summing,” or “summation” refers to the incoherent, time successive absorption of two or more photons from two or more drive pump lasers by a neutral atom, in winch as valence electron is promoted from the ground electronic level successively to higher-lying real (non-virtual) electronic levels via on-resonance, parity-allowed, electric dipole transitions. The resulting electron population densities in the real electronic levels do not depend on any fixed relationships between the phases of electro-magnetic waves of the drive pump lasers.
(B) “Multi-photon-adding” refers to the coherent simultaneous absorption of two or more photons by a neutral atom, in which a valence electron is promoted from the ground electronic, level to an excited electronic level of the same parity, via virtual. parity-allowed electric-dipole transitions. This multi-photon energy adding mechanism may occur in one of two types: 1) the involved virtual parity-allowed intermediate electronic levels lie in energy well away from any of the input photon energies; and 2) the input photon energies are detuned in energy from the resonance energy of a parity-allowed electric dipole transition between electronic levels of the atom being excited. The resulting electron population densities in real electronic levels depend on fixed phase relationships between the phases of electro-magnetic waves of the drive pump lasers.
In the related prior art shown in
in related prior art shown in
In this laser scheme the Doppler peak cross-section of a purely 2-photon transition is proportional to the intensity of the drive laser. At the drive intensities of practical interest (˜10's of kW/cm2) this peak cross-section is generally orders of magnitude smaller than the typical peak Doppler cross-section of a parity-allowed electric dipole transition, (10−18 cm2 vs 10−11 cm2, respectively). Thus to achieve practical degrees of drive photon absorption in such 2-photon pumped devices, the operating atom density generally needs to be higher, (requiring higher operating temperatures) and the gain cell lengths need to be longer, than for devices based on successive 1-photon absorption parity allowed electric dipole transitions. Again, employing two infrared drive photons only, output wavelengths are limited to the visible spectral region (i.e., 400-450 nm) in this related prior art.
Extending the coherent multi-photon excitation process to more than 2 photons was disclosed in the prior art (
The present invention provides a practical means for the efficient production of continuous wave deep ultraviolet radiation at a number of specific wavelengths in the ˜230 to ˜370 nm spectral region without utilizing NLO crystals subject to irradiation at wavelengths shorter than ˜370 nm, a wavelength below which NLO crystal converters tend to lose their practical effectiveness. The present invention teaches how certain atomic vapors of the periodic table of the elements can be utilized to efficiently and incoherently “sum” the output powers of three “drive” pump lasers whose output wavelengths are resonant with or matched to (are substantially equal to) the wavelengths of certain parity-allowed electric dipole transitions of the atomic vapor atoms, when the atomic vapor is mixed with an appropriate buffer gas (or gases) forming a gain mixture and placed within a laser resonator cavity that has sufficiently high reflectivity (or Q-factors) at an appropriate specified ultraviolet wavelength. This type of laser device is referred to herein as a continuous-wave (CW), ultraviolet triply-optically-pumped atomic laser (TOPAL). A drive pump wavelength is said herein to be “resonant with”, “matched to”, or “substantially equal to” the wavelength of a transition when the pump wavelength is within about the spectral half-width of the transition. Due to the large pump transition dipole strengths of the selected atomic transition dipoles involved in the TOPAL incoherent photon energy summing process, the typical operating pump drive intensities are orders of magnitude lower than those found in conventional lasers using NLO crystal converters (i.e., 10's of kW cm−2 vs. 100-1000 MW cm−2), and generally significantly lower than those predicted for the prior art. coherent multi-photon enemy adding schemes. At the same time, in a TOPAL there is no requirement for “phase-matching” the drive pumps and output laser beams, since the energy-summing process itself is incoherent, and describable in terms of simple electron population density rate equations (as opposed to the density-matrix formulation necessary for the Goldstone prior art). Analysis also shows that, because of the relatively large cross-sections and relatively low corresponding saturation intensities of the selected transitions employed, TOPALs can efficiently generate ultraviolet laser power with a purely continuous-wave temporal waveform. Therefore, the life-limiting optical degradation and damage processes present in conventional NW wavelength converters at wavelengths shorter than ˜370 nm are absent in this type of radiation converter, providing for long-lived power conversion in the UV spectral region ˜230-˜370 nm. Critical to the efficient functioning of a DUV TOPAL is rendering its gain cell in appropriate multiple segments that provide control and restraint of potentially deleterious amplified-spontaneous-emission (ASE) transitions that would deplete energy that otherwise would be available to the DIN output laser beam, or even prevent the desired population inversion with respect to the ground electronic level.
The present inventive new class of TOPALs differs essentially from the prior art described above by utilizing three specific “drive” pump lasers whose wavelengths are resonant with specific strong parity-allowed electric-dipole transitions of a neutral atomic atom, and used to irradiate as laser gain mixture of neutral atomic atoms and one or more buffer gases, TOPALs further differ essentially from the prior art by the approximate summing of the photon energies of the three “drive” pump lasers, producing a population inversion density between the ground 2S1/2 level and a highly lying level connected by a parity-allowed electric dipole transition lying in the ultraviolet (˜370-˜230 nm) spectral region. TOPALs differ from the Goldstone prior art at least in that (a) the lasers are all fully resonant with atomic transitions, and. not detuned, (b) a buffer gas is used to cause non-radiative atomic transitions between certain electronic level pair(s) in addition to those levels directly driven by the drive lasers, (c) no relatively consistent phase relation must be maintained between the drive lasers and (d) efficient operation is achieved at the 10's of kW/cm2 scale drive laser intensities. Further. TOPAL gain cells and associated optical elements are designed in a manner that provides for control and restraint of any potentially deleterious ASE transitions, facilitating efficient operation of the TOPAL at a DUV-wavelength output.
In view of the foregoing disadvantages inherent in the known types of deep ultraviolet lasers, and particularly continuous wave (CW) deep ultraviolet lasers present. in the prior art, the present invention provides a practical means to realize a family of CW, deep ultraviolet atomic vapor lasers that are incoherently, triply-optically-pumped, and rendered efficient by controlling and/or suppressing deleterious competing generally-infrared wavelength ASE transitions.
Many atoms of the periodic table may be considered for use as the laser active spicie in a TOPAL, From a practical standpoint, however, attention is naturally directed to those atoms possessing relatively high vapor pressures, in particular: 1) the neutral alkali atoms (Li, Na, K, Rb, Cs) that possess a single valence electron and a 2S1/2 ground electronic configuration; and 2) the elements Thallium (Tl), Indium (In) and Gallium (Ga) that possess a single valence electron and 2P1/2 ground electronic configuration. Below, we discuss in turn TOPALs based on these two types of atoms.
A TOPAL of the present invention generally comprises a gaseous laser gain medium formed by a mixture of neutral atomic vapor and one or more buffer gases. The buffer gases comprise the rare gases (He, Ar, Kr, Ne, and Xe) and/or small molecules, such as the hydrocarbon molecules ethane or methane, or small molecules such as NH3, NF3 or CF4 The gain medium mixture is placed within a segmented gain cell which in turn is placed within an optical cavity whose cavity mirrors provide a high quality factor, Q, at the desired DUV output wavelength,
First consider TOPALs based on the use of alkali atoms. The desired DUV output radiation occurs on a transition that terminates on the 2S1/2 ground electronic level of the alkali atom, and originates on a specified high lying (third or greater) 2P1/2 electronic level of the alkali atom. Radiation from three “drive” laser pump sources, with three specific selected visible and/or IR wavelengths that are resonant with three specific parity-allowed transitions of the alkali atoms in the gain mixture, is directed into the laser cavity containing the alkali atomic vapor and buffer gas(es) laser gain mixture, and is absorbed by the alkali atoms. This excitation process induces a population inversion between a high lying (third or greater) 2P1/2 electronic level and the 2S1/2 ground electronic level, causing continuous wave laser action to occur at an ultraviolet wavelength of the so-pumped alkali atoms. The gain cell may be axially segmented into multiple sub-cells that are adjoined with suitable optical filtering elements that control and restrain the local intensities of potentially deleterious ASE radiation within the optical cavity.
Second consider TOPALs based on the use of the atoms of thallium, indium, or gallium. The desired DUV output radiation occurs on a transition that terminates on the 2P1/2 ground electronic level of the selected atom, and originates on a specified high lying (third or greater) 2S1/2 electronic level of the atom. Radiation from three “drive” laser pump sources, with three specific selected visible and/or IR wavelengths that are resonant with wavelengths of three specific parity-allowed transitions of the atoms in the gain mixture, is directed into the laser cavity containing the atomic vapor and buffer gas(es) laser gain mixture, and is absorbed by the atoms. This excitation process induces a population inversion between a high lying (second or greater) 2S1/2 electronic level and the 2P1/2 ground electronic level, causing continuous wave laser action to occur at an ultraviolet wavelength of the so-pumped atom. The gain cell may be axially segmented into multiple sub-cells that are adjoined with suitable optical filtering elements that control and restrain the local intensities of potentially deleterious ASE radiation within the optical cavity.
There has thus been outlined, rather broadly, the more important features of the invention in order that the detailed description thereof may be better understood, and in order that the present contribution to the art may be better appreciated. There are additional features of the invention that will be described hereinafter,
In this respect, before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not limited in its application to the details of construction and to the arrangements of the components set forth in the following description or illustrated in the drawings. The invention is capable of other embodiments and of being practiced and carried out in various ways. Also, it is to be understood that the phraseology and terminology employed herein are for the purpose of the description and should not be regarded as limiting.
The present invention include a triply optically pumped atomic laser (TOPAL) device emitting continuously at a deep ultraviolet wavelength, overcoming the shortcomings of the prior art devices.
The present invention also includes efficient sources of ultraviolet radiation at numerous discrete wavelengths in the spectral range from 230 nm to 370 nm.
Other advantages of the present invention will become obvious to the reader and it is intended that these objects and advantages are within the scope of the present invention. To achieve the benefits of the invention, the invention may be embodied in the form illustrated in the accompanying drawings, attention being called to the fact, however, that the drawings are illustrative only, and that changes may be made in the specific construction illustrated.
The precise technical meanings of the words ASE and laser, as utilized in this provisional application, are crucial to the understanding of the inventive differences between the present invention and prior art.
To elucidate the precise technical meanings of these key words it is instructive to refer to
If the ray 14 is trapped within a laser resonator, as shown with mirrors 16 and 18, which contains cell 12, as shown in
The accompanying Figures, which are incorporated into and form a part of the disclosure, illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention.
First consider TOPALs employing neutral alkali atoms. Each neutral alkali atom possesses a single valance electron. Each electronic energy level available to this valance electron is distinguished by values of the four “good” quantum numbers: n, S, L and J=L±S (principle spin, orbital, and total angular momentum, respectively), and is labeled by n(2S+1)L(2J+1). Further, since for a single valance electron all levels have S=1/2 alkali atom electronic levels are labeled by n 2L(2J+1). The quantum number L can take values of 0, 1, 2 etc. When L=0, J=1/2, and such electronic levels are labeled n 2S1/2. When L=1, J=1/2, or 3/2, and such levels are labeled n 2P1/2 or n 2P3/2. When L=2, J=J=3/2, or 5/2, and such levels are labeled a n 2D3/2 or n 2D5/2 . As the mass of the alkali atom increases monotonically in its column of the Periodic Table, the electron shells are progressively filled and the value of n assumes a minimum value: Li, n≧2; Na, n≧3; K, n≧4; Rb, n≧5; Cs, n≧6, (Note this rule is suspended for D levels in Cs and Rb). Transitions between electronic levels for which ΔL=±1, and ΔJ=0, ±1 are parity-allowed electric dipole transitions and are relatively strong, resulting in relatively large transition cross-sections compared to transitions for which these selection rules do not obtain, in TOPALs, all selected transitions are parity-allowed electric dipole allowed.
For all alkali atom based TOPALs the first drive pump laser wavelength is set to match the wavelength of the so-called D2 transition between the 2S1/2 ground electronic level and the energetically lowest lying 2P3/2 level. For all alkali atom based TOPALs the second drive pump laser wavelength is set to match the wavelength of allowed electric dipole transition originating the energetically lowest lying 2P1/2 level. in a TOPAL this level is populated with electrons transferred non-radiatively from the pumped 2P3/2 level as a result of collisions with buffer gas(es). Ideally, this non-radiative relaxation process is sufficient fast so that the electron population densities in this excited pair of 2P levels attains a Boltzmann distribution at the gas mixture temperature. However, regarding the second and third drive pump lasers, there are two generic types of alkali atom TOPAL energy level schemes, as discussed in detail below.
The basic TOPAL device configuration, and preferred embodiment (
There are variations of this preferred embodiment. such as axially pumping the gain cell from both ends enabled by the use of resonator end mirrors coated with appropriate dichroic thin films, well know in the state of the art. There are other configurations of pump lasers besides axial pumping, notably transverse pumping. Typically transverse pumping enables greater CW output power. Managing waste heat produced in the gain cell by flowing the gain medium can increase the CW laser output power without limit, except for the laser power of the pumps and the damage thresholds of the optics.
Consider in more detail. TOPALs pumped via levels as illustrated in
The second excitation is produced by the second drive pump, with a power P2, having a wavelength λpump2. This second step excitation always originates on the n 2P1/2 level and terminates on a 2S1/2 level whose principle quantum number is n+1, or n+2, etc., that is, the second pump transitions are a 2P1/2→(n+1) 2S1/2, or 2P1/2→(n+2) 2S1/2, etc. These transitions also satisfy the selection rules: ΔL=±1, ΔJ=0, ±1, and are also parity allowed electric-dipole transitions.
The third excitation step is produced by the third drive pump, with a power P3, having a wavelength λpump3. This third excitation step originates on the terminal level of the second step excitation and terminates on a 2P3/2 level lying higher in energy than the terminal level of the second step excitation: that is, if the terminal level of the second step excitation has a principle quantum number (n+1), then the principle quantum number of terminal level of the third step excitation is, generally, ≧(n+1). The third step transition also satisfies the selection rules: ΔL=±1, ΔJ=0, ±1, and is a parity-allowed electric dipole transition,
In a TOPAL, the 2P3/2 electron populations driven by the first and third drive pump lasers are necessarily relaxed by collisions with buffer gas atoms or molecules to their respective, paired lower-lying 2P1/2 levels, Let the respective energy splitting of these pairs be ΔE1 and ΔE3. If these collisional relaxation rates are sufficiently fast (generally proportional to the buffer gas number density), and the three drive pump laser intensities are sufficiently high (see below), then the electron population of the 2P1/2 level paired with the terminal level of the third excitation step is inverted with respect to the electron population in the n 2S1/2 ground level. Laser action on the corresponding UV transition terminating on the ground level, with a wavelength λlaser, is enabled when the optical cavity losses at this UV wavelength are rendered sufficient small.
In addition to the aforementioned population inversion established to permit DUV laser emission, population inversions will also be created between 2P3/2 and 2P1/2 levels excited by the third drive pump laser and lower-lying electronic levels of opposite parity that are not directly excited by first and. second pumps, and therefore nominally unpopulated. For efficient DUV laser extraction of atom excitation energy, it is necessary to substantially limit the degree of amplified spontaneous emission (ASE) on these parity-allowed electric dipole transitions. Generally, it is the longest wavelength of these ASE transitions that are most deleterious to efficient DUV laser emission because the magnitude of the emission cross-section scales as the square of the transition wavelength. ASE on such transitions will have no significant deleterious effect on the efficiency of DUV energy extraction if the degree of ASE growth is limited to approximately ≦10 nepers. This need to limit ASE growth is addressed in the present invention by segmenting the gain cell, as shown schematically in
Next, consider in more detail the type of alkali TOPAL that is pumped via a second excitation step that terminates on a 2D3/2 level (see
In this second alkali TOPAL type, however, the second excitation step originates on the n 2P1/2 level but terminates on one of the in 2D3/2 levels lying higher in energy, where in n−1 for Cesium, Rubidium, and Potassium; in n for Sodium; and m=n+1 for lithium. The quantum numbers of this second step transition satisfy the selection rules: ΔL=±1, ΔJ=0, ±1, and is a parity-allowed electric dipole transition,
In this second alkali TOPAL type, the third excitation step originates on either the m 2D3/2 or the m 2D5/2 level (whichever lies lower in energy) of the second step transition, and terminates on a higher lying 2P3/2 level. The third step transition also satisfies the selection rules: ΔL=±1, ΔJ=0, ±1, and is as parity-allowed electric dipole transition.
Note that for Cesium, Rubidium, and Lithium, the m 2D5/2 level lies higher in energy than its pair companion m 2D3/2 level, whereas for Potassium and Sodium the 2D3/2 levels lie above the 2D5/2 levels.
The 2P3/2 and 2D1 level electron populations driven by the first, second, and third drive pump lasers are relaxed by collisions with buffer gas atoms or molecules to their respective, paired lower-lying 2P1/2 and 2DJ levels. Let the respective enemy splittings of these level pairs be ΔE1, ΔE2, and ΔE3). If these collisional relaxation rates are sufficiently fast (generally proportional to the buffer gas number density), and the three drive pump laser intensities are sufficiently high (see below), then the electron population density of the 2P1/2 level paired with the terminal level of the third excitation step is inverted with respect to the electron population density in the n 2S1/2 ground level. Laser action on the corresponding UV transition terminating on the ground level, with a wavelength λlaser, is enabled when the optical cavity losses at this UV wavelength are rendered sufficiently small.
Again, in addition to the aforementioned desired population inversion densities established to permit DUV laser emission, population inversions densities will also be created between 2P3/2 and 2P1/2 levels excited by the third drive pump laser and lower-lying electronic levels of opposite parity that are not directly excited by first and second pumps, and therefore nominally unpopulated. For efficient DUV laser extraction of atom excitation energy, it is necessary to substantially limit the degree of amplified spontaneous emission (ASE) on these parity-allowed electric dipole transitions. Generally, it is the longest wavelength of these “ASE” transitions that are most deleterious to efficient DUV laser emission because the magnitude of the emission cross-section scales as the square of the transition wavelength. ASE on such transitions will have no significant deleterious effect on the efficiency of DUV energy extraction if the degree of ASE growth is limited to approximately ≦10 nepers above the spontaneous emission intensity. This need to so limit ASE growth is addressed in the present invention by segmenting the gain cell, as shown schematically in
A single segment of a cell 120 is shown in
When, in an alkali TOPAL, the three external drive pump laser intensities are sufficiently large, and the collisional mixing rates are sufficiently large to bring pairs of 2PJ and 2DJ levels significantly toward a Boltzmann equilibrium, and threatening ASE transitions are limited to less than ≦10 nepers of gain in a segmented gain sub-cell by selective spectral filtering, a maximum population inversion density, Δnmax, is produced between the high-lying, third-step excited 2P1/2 level and the 2S1/2 ground level (assuming no stimulated emission due to this population inversion). Let the total alkali atom density be N0. This maximum population inversion density, normalized to the total alkali atom density, Δnmax/N0, depends only on the temperature, T, and the appropriate energy splittings of the 2P3 levels (for an alkali TOPAL pumped via a 2S1/2 level), or of the 2PJ and 2DJ levels (for an alkali TOPAL pumped via a 2D3/2 level).
For an alkali TOPAL pumped via a 2S1/2 level, the maximum normalized population inversion density is given by:
Δnmax/N0={I/γ1−I/γ2}×{4+3γ2+I/γ2}−1 (1)
where γ1=1.44 ΔE1/T (2)
and γ2=1.44 ΔE2/T (3)
where ΔE1 is the energy splitting of the (n+1) 2PJ level pair, and ΔE2 is the energy splitting of the 2PJ level pair excited in the third step excitation. (The ΔE and T units in (2) and (3) are, respectively, cm−1 and ° K.)
As an example and a TOPAL preferred embodiment, consider the characteristics and projected performance of a Sodium (Na) 2S1/2 TOPAL type operating at 330 nm in the 4 2P1/2→3 S1/2 transition (the energy level scheme is shown in
The normalized maximum population inversion densities for 2D3/2 TOPAL types on be calculated by expressions: similar to Eq. (1).
To project alkali TOPAL performance of a 330 nm Sodium 2S1/2 type TOPAL type laser, and to illustrate a preferred technique for limiting the degree of ASE of threatening transitions in the TOPAL, a rate-equation model was constructed for this TOPAL, assuming the end-pumping geometry shown schematically in
This alkali TOPAL code treats the electron populations of up to 14 active levels, the photon fluxes of the three external drive pump lasers, as well as the photon flux of the output deep UV laser, and optionally photon fluxes of ASE from the vapor. The code assumes ID geometry and plane waves for all of the laser fluxes. It links electron populations and fluxes through a set of rate equations, including pooling processes. Collision broadened transition cross-sections are calculated using calculated transition moments and measured collisional broadening parameters. For this Na TOPAL, the 3 2PJ collisional mixing cross-section for helium buffer gas was taken from the literature, and the mixing rate in the code was set by the assumed He buffer pressure. The code was used to project the performance of a 330 nm Sodium TOPAL. In these calculations assumed device parameters are listed in
Together,
Additionally, given the higher normalized maximum population inversion densities for Cesium, Rubidium, and Potassium (compared to Sodium) it is anticipated that TOPALs utilizing the former alkali atoms will manifest even higher performance levels.
The simulation of the 330 nm Sodium TOPAL, point design indicates that dominant threatening ASE transition is the 4p 2P3/2→3d 2D5/2 transition with a wavelength near ˜9.1 microns (see
An example of a suitable filter to suppress and control axial ASE is a thin plate of silica glass.
α(λ)=4πκ(λ)/λ (4)
Next, we turn to the use of Thallium, Indium, or Gallium atomic vapor as the gain specie in a different type of TOPAL. These neutral atoms, like alkali atoms, possess but a single valance electron. However, in these atoms the ground state is a 2P1/2 level rather than 2S1/2. Nonetheless the principles of TOPALs elucidated herein can be readily applied to atoms with this ground state. We now illustrate the principles of TOPALs for a specie with a 2P1/2 ground state by considering in detail a 258 nm TOPAL using atomic Thallium as the active gain specie.
The one preferred embodiment the small hydro-carbon molecule methane, (CH4), is used as a buffer gas to collisionally relax the pumped 7p 2P3/2 electronic level to the 7p 2P1/2 electronic level, enabling a CW population inversion density between the Ss 2S1/2 upper laser level and the 6p 2P1/2 ground electronic level. In a second preferred embodiment the small molecule ammonia (NH3) is used as a buffer gas.
In this TOPAL scheme, the parity-allowed, electric-dipole 8s 2S1/2→6p 2P3.2 transition at a wavelength of 323.07 nm would superficially appear to be a deleterious ASE transition since the population in the 6p 2P3.2 level is zero as pumping begins. Fluorescence and ASE from the 8s 2S1/2 level will populate this level and eventually ASE will self terminate as the population inversion density approaches zero.
To model the performance of a Thallium TOPAL we utilized the rate equation code described previously, but adapted with spectroscopic and kinetic data appropriate to the Thallium atom (the code was also rendered for projecting the performance of a 256 inn Indium TOPAL). The performance of a 258 nm Thallium TOPAL device was projected using the device parameters listed in
Simulation of the Thallium TOPAL shows that all emission transitions (save the desired 258 nm output laser transition) experience net loss in propagation through the full 3 cm long cell, and therefore no segmentation of the gain cell is required to maintain power flow from the pump lasers to the 258 nm output laser beam.
In this point design of a. Thallium TOPAL the total pump intensity is 16 kW/cm2 at visible and infrared wavelengths. The output laser intensity at 258 nm is 6.5 kW/cm2. Since the laser resonator out-coupled power fraction is 2.5% in this design, the circulating intensity at 258 nm is 260 kW/cm2. Of course, there is no NLO crystal subjected to this flux at this wavelength. It should be noted that this point design has not been optimized in terms of the myriad design parameters: temperature, cavity length, ratios of various pump intensities with respect to each other, out-coupling fraction, etc, improved performance compared to that of the point design presented above can reasonably be anticipated.
As noted earlier, the requirement for resonant pumping is critical to the operation of TOPALs. For TOPAL's to operate most effectively, each drive pump laser wavelength should be such as to maximize the laser-induced transition rate of the atomic specie between the two levels connected by the drive pump laser. Thus the drive pump wavelength is set ideally at the spectral peak of transition to which it couples, under the conditions of temperature, buffer gas(es) and pressure pertaining to the gain medium. For practical purposes, herein a drive pump is considered resonant with, matched to, or substantially equal to the wavelength of a transition when the drive pump wavelength lies within about the spectral half-width of the spectral peak wavelength (λLC) of the transition. Both the pump wavelength and the pump bandwidth is ideally constrained by this condition.
Practitioners of the art of lasers will readily appreciate that the spectral linewidth of a transition has both a Doppler component and a collisional component, which scale differently with the wavelength of the transitions. However, under the conditions of the 258 nm Thallium TOPAL laser described herein, a typical spectral frequency linewidth of the three pumped transitions is approximately 1-3 GHz. Under the conditions of the (higher pressure) 330 nm Sodium TOPAL, laser described, herein, a typical spectral linewidth for the three pumped transitions is approximately 5-20 GHz, and somewhat greater for IR transitions emitting ASE. The wavelength and bandwidth of a drive pump are therefore lie ideally in the range λLC−δλ<λ<λLC+δλ where λLC is the actual spectral peak wavelength. Typically, in the visible spectral region, δλ/λLC˜10−4 for the (hive pumps of the 258 nm Thallium TOPAL laser and 10−3 fur the 330 nm Sodium TOPAL laser. Given the collisional literature data and operating conditions of a TOPAL, it is straightforward to estimate the Voigt integrals and the wavelength and bandwidth tolerances for each pump laser in the TOPAL.
As to a further discussion of the manner of usage and operation of the present invention, the same should be apparent from the above description. Accordingly, no further discussion relating to the manner of usage and operation will be provided.
With respect to the above description then, it is to be realized that the optimum dimensional relationships for the parts of the invention, to include variations in size, materials, shape, form, function and manner of operation, assembly and use, are deemed readily apparent and obvious to one skilled in the art, and all equivalent relationships to those illustrated in the drawings and described in the specification are intended to be encompassed by the present invention.
Therefore, the foregoing is considered as illustrative only of the principles of the invention. Further, since numerous modifications and changes will readily occur to those skilled in the art, it is not desired to limit the invention to the exact construction and operation shown and described, and accordingly, all suitable modifications and equivalents may be resorted to, falling within the scope of the invention.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US2014/021313 | 3/6/2014 | WO | 00 |
Number | Date | Country | |
---|---|---|---|
61851369 | Mar 2013 | US |