Gas Mixtures for Excimer Lasers
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Advanced Excimer Laser Technologies Enable Green Semiconductor Manufacturing
PROCEEDINGS OF SPIE SPIEDigitalLibrary.org/conference-proceedings-of-spie Advanced excimer laser technologies enable green semiconductor manufacturing Hitomi Fukuda, Youngsun Yoo, Yuji Minegishi, Naoto Hisanaga, Tatsuo Enami Downloaded From: https://www.spiedigitallibrary.org/conference-proceedings-of-spie on 10/25/2017 Terms of Use: https://spiedigitallibrary.spie.org/ss/TermsOfUse.aspx Advanced Excimer Laser Technologies Enable Green Semiconductor Manufacturing Hitomi Fukuda*, Youngsun Yoo, Yuji Minegishi, Naoto Hisanaga and Tatsuo Enami Gigaphoton Inc., 400 Yokokura-Shinden, Oyama-shi, Tochigi, JAPAN 323-8558 ABSTRACT "Green" has fast become an important and pervasive topic throughout many industries worldwide. Many companies, especially in the manufacturing industries, have taken steps to integrate green initiatives into their high-level corporate strategies. Governments have also been active in implementing various initiatives designed to increase corporate responsibility and accountability towards environmental issues. In the semiconductor manufacturing industry, there are growing concerns over future environmental impact as enormous fabs expand and new generation of equipments become larger and more powerful. To address these concerns, Gigaphoton has implemented various green initiatives for many years under the EcoPhoton™ program. The objective of this program is to drive innovations in technology and services that enable manufacturers to significantly reduce both the financial and environmental “green cost” of laser operations in high-volume manufacturing environment (HVM) – primarily focusing on electricity, gas and heat management costs. One example of such innovation is Gigaphoton’s Injection-Lock system, which reduces electricity and gas utilization costs of the laser by up to 50%. Furthermore, to support the industry’s transition from 300mm to the next generation 450mm wafers, technologies are being developed to create lasers that offer double the output power from 60W to 120W, but reducing electricity and gas consumption by another 50%. -
Buffer Gas Experiments in Mercury (Hg+) Ion Clock
Buffer Gas Experiments in Mercury (Hg+) Ion Clock Sang K. Chung, John D. Prestage, Robert L. Tjoelker, Lute Maleki California Institute of Technology, Jet Propulsion Laboratory 4800 Oak Grove Drive, Bldg 298 Pasadena, CA 91109 Abstract—We report measured buffer gas collision shifts of the environment and stable helium pressure this system is not 40.507347996xx GHz mercury ion clock transition using inert sufficient to meet mass, power, size, and operability helium, neon, and argon gases and getterable molecular considerations of a space clock [6]. hydrogen and nitrogen gases. The frequency shift due to Two buffer gas / vacuum pump combination are currently methane was also examined. At low partial pressures methane being considered for possible operation of a small space-born gas did not impact the trapped ion number but was observed to strongly relax the population difference in the two hyperfine clock. One approach uses a small getter pump with a fixed clock states thereby reducing the clock resonance signal. A amount of inert buffer gas. Two issues that must be similar population relaxation was also observed for other understood are the long term buffer gas pressure stability and molecular buffer gases (N2, H2) but at much reduced rate. possible evolution of non-getterable gas that could potentially adversely affect clock stability or operation. A second approach is to use a miniature ion pump and a calibrated I. INTRODUCTION micro-leak buffer gas that is not inert (inert gas can shorten In recent years, mercury ion (199Hg+) clock technology has ion pump life very quickly). demonstrated excellent inherent stability, reaching ~3 x 10-16 long-term frequency stability with continuous, free running II. -
I. Excimer Fluorescence, II. Heavy-Atom Spin-Orbital Coupling Effect and Iii. the Electronic Spectra of Ferrocene." (1965)
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1965 Studies in Molecular Spectroscopy; I. Excimer Fluorescence, II. Heavy-Atom Spin-Orbital Coupling Effect and IIi. The lecE tronic Spectra of Ferrocene. Fred Jewel Smith Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Smith, Fred Jewel, "Studies in Molecular Spectroscopy; I. Excimer Fluorescence, II. Heavy-Atom Spin-Orbital Coupling Effect and IIi. The Electronic Spectra of Ferrocene." (1965). LSU Historical Dissertations and Theses. 1092. https://digitalcommons.lsu.edu/gradschool_disstheses/1092 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has bssn microfilmed exactly as received 6 6 -7 4 8 SMITH, Fred Jewel, 1939- STUDIES IN MOLECULAR SPECTROSCOPY} I. EXCIMER FLUORESCENCE, II. HEAVY- ATOM SPIN-ORBITAL COUPLING EFFECT AND HI. THE ELECTRONIC SPECTRA OF FERROCENE. Louisiana State University, Ph.D., 1965 Chemistry, physical University Microfilms, Inc., Ann Arbor, Michigan STUDIES IN MOLECULAR SPECTROSCOPY; I. EXCIMER FLUORESCENCE, II. HEAVY-ATOM SPIN-ORBITAL COUPLING EFFECT AND III . THE ELECTRONIC SPECTRA OF FERROCENE A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Chemistry by Fred Jewel Smith B.A., University of Southern Mississippi, 1960 August, 1965 ACKNOWLEDGMENT The author wishes to express his sincere appreciation to Dr. -
Development and Applications of Proton Transfer Reaction-Mass Spectrometry for Homeland Security: Trace Detection of Explosives
DEVELOPMENT AND APPLICATIONS OF PROTON TRANSFER REACTION-MASS SPECTROMETRY FOR HOMELAND SECURITY: TRACE DETECTION OF EXPLOSIVES by Ramón González-Méndez, MSc A thesis submitted to the University of Birmingham for the degree of DOCTOR OF PHILOSOPHY School of Physics and Astronomy The University of Birmingham, UK February 2017 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. Abstract This thesis investigates the challenging task of sensitive and selective trace detection of explosive compounds by means of proton transfer reaction mass spectrometry (PTR-MS). In order to address this, new analytical strategies and hardware improvements, leading to new methodologies and analytical tools, have been developed and tested. These are, in order of the Chapters presented in this thesis, the switching of reagent ions, the implementation of a novel thermal desorption unit, and the use of an ion funnel drift tube or fast reduced electric field switching to modify the ion chemistry. In addition to these, a more fundamental study has been undertaken to investigate the reactions of picric acid (PiA) with a number of different reagent ions. The novel approaches described in this thesis have improved the PTR-MS technique by making it more versatile in terms of its analytical performance, namely providing assignment of chemical compounds with high confidence. -
Enhanced Escape Rate for Hg 254Nm Resonance Radiation in Fluorescent Lamps
Home Search Collections Journals About Contact us My IOPscience Enhanced escape rate for Hg 254 nm resonance radiation in fluorescent lamps This content has been downloaded from IOPscience. Please scroll down to see the full text. 2013 J. Phys. D: Appl. Phys. 46 415204 (http://iopscience.iop.org/0022-3727/46/41/415204) View the table of contents for this issue, or go to the journal homepage for more Download details: IP Address: 128.104.46.196 This content was downloaded on 24/09/2013 at 02:20 Please note that terms and conditions apply. IOP PUBLISHING JOURNAL OF PHYSICS D: APPLIED PHYSICS J. Phys. D: Appl. Phys. 46 (2013) 415204 (8pp) doi:10.1088/0022-3727/46/41/415204 Enhanced escape rate for Hg 254 nm resonance radiation in fluorescent lamps James E Lawler1 and Mark G Raizen2 1 Department of Physics, University of Wisconsin, Madison, WI 53706, USA 2 Center for Nonlinear Dynamics and Department of Physics, University of Texas, Austin, TX 78712, USA Received 7 June 2013, in final form 7 August 2013 Published 23 September 2013 Online at stacks.iop.org/JPhysD/46/415204 Abstract The potential of the low-cost MAGIS isotopic separation method to improve fluorescent lamp efficacy is explored using resonance radiation transport simulations. New Hg isotopic mixes are discovered that yield escape rates for 254 nm Hg I resonance radiation equal to 117% to 122% of the rate for a natural isotopic mix under the same lamp conditions. (Some figures may appear in colour only in the online journal) 1. Introduction will represent over 75% of all lighting sales by 2030, resulting in an annual primary energy savings of 3.4 quads.’ Fluorescent lighting is the technology of choice for almost Even after inorganic LED and/or organic LED (OLED) all non-residential indoor lighting applications around the technology achieve competitive performance and cost levels, world. -
6 5 • Vacuum Ultraviolet Ar Excimer Emission Initiated by High Intensity Laser Produced Electrons
JP0050803 JAERI-Cont" 2000-006 6 5 • Vacuum Ultraviolet Ar Excimer Emission Initiated by High Intensity Laser Produced Electrons Shoichi Kubodera and Wataru Sasaki Department of Electrical and Electronic Engineering and Photon Science Center, Miyazaki University Gakuen Kibanadai Nishi 1-1, Miyazaki, 889-2192 Japan We have observed Ar2* emission using a tabletop femtosecond high intensity laser as an excitation source. High intensity laser produced electrons via an optical field induced ionization (OFI) process initiated the Ar2* production kinetics, which made themselves analogous to those produced in an electron beam produced plasma. A fast conductive cooling of the OFI plasma was found to be appropriate to initiate the excimer formation kinetics more efficiently. Keywords: Vacuum ultraviolet, Excimer molecule, Short pulse laser, Conductive cooling There have been considerable demands for the development of compact short wavelength lasers in the vacuum ultraviolet (VUV) spectral region. Such compact short wavelength lasers would be applicable to various scientific and industrial fields, such as photochemistry, biological science, and new types of materials processing. Currently available practical compact VUV lasers are the ArF excimer laser at 193 tun and the F2 laser at 157 run, both of which are excited by a compact discharge device. Recently more attention is paid to short wavelength lasers in the VUV in the future optical lithography industry. Rare gas excimers have long been one of the very few laser media in the VUV spectral region [1]. The emission wavelength of Ar2* is 126 run which is long enough to use transmission optical elements such as MgF2 and LiF. The Kr2* laser has an even longer emission wavelength centered at 147 mn which relaxes the conditions for optics and would become a competitor to the F2 laser at 157 run. -
Tungsten Electrode with Emitter
US 20060O87242A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2006/0087242 A1 Scholl et al. (43) Pub. Date: Apr. 27, 2006 (54) LOW-PRESSURE GAS DISCHARGE LAMP Publication Classification WITH ELECTRON EMITTER SUBSTANCES SMILAR TO BATO3 (51) Int. Cl. HOI. I7/04 (2006.01) (76) Inventors: Robert Peter Scholl, Roetgen (DE); HOI. 6L/04 (2006.01) Rainer Hilbig, Aachen (DE); Bernd (52) U.S. Cl. ..................... 313/633; 313/311; 313/346 R Rausenberger, Aachen (DE) Correspondence Address: (57) ABSTRACT PHILIPS INTELLECTUAL PROPERTY & A low-pressure gas discharge lamp is described, which is STANDARDS equipped with a gas-discharge vessel containing an inert gas P.O. BOX 3 OO1 filling as the buffer gas and an indium, thallium and/or BRIARCLIFF MANOR, NY 10510 (US) copper halide, and with electrodes and with means for Appl. No.: 10/526,923 generating and maintaining a low-pressure gas discharge, (21) which has as the electron emitter Substance a compound (22) PCT Fed: Aug. 29, 2003 selected from the group of ABO or ABO, ACOs, or ADO, wherein: A=an alkaline earth element or a mix (86) PCT No.: PCT/BO3/O3948 ture of several different alkaline earth elements, B=cerium, titanium, Zirconium, hafnium, or a mixture of these ele (30) Foreign Application Priority Data ments, C=vanadium, niobium, tantalum, or a mixture of these elements, D=Scandium, yttrium, lanthanum, a rare Sep. 12, 2002 (DE)..................................... 102-42-241.9 earth element, or a mixture of these elements. tungsten electrode With emitter discharge chamber with InBr Or similar Substances Patent Application Publication Apr. -
Energy Transfer Processes in Electron Beam Excited Mixtures of Laser Dye Vapors with Rare Gases G
Energy transfer processes in electron beam excited mixtures of laser dye vapors with rare gases G. Marowsky Max-Planck Institut fur Biophysikalische Chemie. D 3400 Gottingen. Federal Republic of Germany R. Cordray, F. Tittel, and B. Wilson Electrical Engineering Department, Rice University. Houston. Texas 77001 J. W. Keto Physics Department. University of Texas at Austin. Austin. Texas 78712 (Received 26 May 1977) The energy transfer mechanisms for electron beam excited N -92 dye vapor in various bU!fer gas mixtur.es have been examined. Optimum conditions for achieving intense dye vapor fluorescence with short duratIOn electron pulse excitation are reported. INTRODUCTION colliSional excitation from the metastable states of the Direct electrical excitation of dye vapor lasers has rare gas buffer atoms and molecules and electron im pact excitation appear to be the dominant processes for received considerable attention in recent years. l,Z Elec trical excitation offers the possibilities of overcoming coupling electron beam energy to the dye vapor. By op timizing the buffer gas composition, the total pressure, the inherent limitations in efficiency for optically pumped dye lasers, extending the present uv wavelength limit and the electron beam deposition it is possible to en hance the fluorescence yields of excited state populations of about 320 nm to shorter wavelengths, and scaling to of buffer gas-dye vapor mixtures. Due to the complex high power laser systems. In this paper we report re ity of these mixtures under high levels of eXCitation, no sults of a study to identify the optimum energy transfer quantitative measurements on kinetic parameters such conditions which produce efficient fluorescence yields as relevant rate constants and colliSional and radiative for electron beam excited high pressure buffer gas-dye lifetimes have been obtained as yet. -
APPLICATION NOTE LD20-05 Multidetek2 Gas Chromatograph with Plasmadetek2 & TCD Detectors Uses for the Analysis of Purity Xenon-Krypton-Neon
APPLICATION NOTE LD20-05 MultiDetek2 gas chromatograph with PlasmaDetek2 & TCD detectors uses for the analysis of purity Xenon-Krypton-Neon MultiDetek2 PlasmaDetek2 The noble gases also called inert gases or rare gases have several characteristics that make them important and unique as: low reactivity, low thermal conductivity and high stability, among others. Being at very low concentration in the earth’s atmosphere, it makes these gases very expensive to produce. The six naturally noble gases are Helium (He), Neon (Ne), Argon (Ar), Krypton (Kr), Xenon (Xe) and the radioactive Radon (Rn). The rarest gases of these are Xenon, Krypton and Neon making them very expensive to use for industrial applications. NEON/KRYPTON/XENON MAJOR APPLICATIONS: Aerospace: Xenon is used for the following aerospace applications: satellite programs, space travel, propulsion agent for spacecraft, satellite thruster and interplanetary probe. Electronics: These rare gases, can be used in many electronics applications such as: excimer lasers, buffer gas used in lasers for semiconductor manufacturing, deep trench etching of DRAM integrated circuits, focused etch process, and plasma panel display. Glass: Krypton is used as a filler in the production of double and triple-pane insulated windows. Major advantages of using krypton are reducing heat loss, increasing heat transfer resistance in the unit, and reducing levels of solar radiation. You can also increase the R-value or decrease the U-factor for window and door insulation with krypton, xenon and rare gas mixtures. Lasers: Neon-based excimer lasers are utilized for etching silicon wafers, LASIK eye surgery, micro-machining organic materials, UV lithography in integrated circuit fabrication, micro drilling, He/Ne mixes for optical readers, and wafer dicing. -
"The Buffer-Gas Positron Accumulator and Resonances in Positron
Written in conjunction with the symposium honoring the retirement of Dick Drachman and Aaron Temkin (NASA Goddard Space Flight Center, Greenbelt, MD; November 18, 2005); to be published by the NASA Conference Publication Service, A. Bhatia, ed. (2006). THE BUFFER-GAS POSITRON ACCUMULATOR AND RESONANCES IN POSITRON-MOLECULE INTERACTIONS C. M. Surko Department of Physics, University of California, San Diego, La Jolla CA 92093 ABSTRACT This is a personal account of the development of our buffer-gas positron trap and the new generation of cold beams that these traps enabled. Dick Drachman provided much appreciated advice to us from the time we started the project. The physics underlying trap operation is related to resonances (or apparent resonances) in positron- molecule interactions. Amusingly, experiments enabled by the trap allowed us to understand these processes. The positron-resonance “box score” to date is one resounding “yes,” namely vibrational Feshbach resonances in positron annihilation on hydrocarbons; a “probably” for positron-impact electronic excitation of CO and N2; and a “maybe” for vibrational excitation of selected molecules. Two of these processes enabled the efficient operation of the trap, and one almost killed it in infancy. We conclude with a brief overview of further applications of the trapping technology discussed here, such as “massive” positron storage and beams with meV energy resolution. IT ALL STARTED AT LUNCH WITH MARV Since this paper is written in conjunction with the symposium marking the retirement of Dick Drachman and Aaron Temkin, I depart from third-person style to relate a personal view of the development of the buffer-gas trap and the physics that has come from it. -
Laser Cooling of Dense Rubidium-Noble Gas Mixtures Via Collisional Redistribution of Radiation
Laser Cooling of Dense Rubidium-Noble Gas Mixtures via Collisional Redistribution of Radiation Ulrich Vogla,†, Anne Saßa and Martin Weitza a Institut f¨ur Angewandte Physik der Universit¨at Bonn, Wegelerstr. 8, 53115 Bonn, Germany ABSTRACT We describe experiments on the laser cooling of both helium-rubidium and argon-rubidium gas mixtures by collisional redistribution of radiation. Frequent alkali-noble gas collisions in the ultradense gas, with typically 200 bar of noble buffer gas pressure, shift a highly red detuned optical beam into resonance with a rubidium D- line transition, while spontaneous decay occurs close to the unshifted atomic resonance frequency. The technique allows for the laser cooling of macroscopic ensembles of gas atoms. The use of helium as a buffer gas leads to smaller temperature changes within the gas volume due to the high thermal conductivity of this buffer gas, as compared to the heavier argon noble gas, while the heat transfer within the cell is improved. Keywords: Laser cooling, optical refrigeration, collisional redistribution 1. INTRODUCTION The idea to cool matter with light can be traced back at least 80 years,1 but not until the invention of the laser viable proposals and experimental work has started. The greatest influence on further research in this area had the technique of Doppler cooling of atomic gases suggested by H¨ansch and Schawlow,2 which has lead to the extremely successful field of ultracold dilute atomic gases.3–5 In another approach for laser cooling, anti-Stokes processes in multilevel systems have been employed. Proof of principle experiments for this type of laser cooling 6, 7 8 have been carried out with CO2 gas and a dye-solution. -
Laser Induced Breakdown Spectroscopy for Elemental Analysis in Environmental, Cultural Heritage and Space Applications: a Review of Methods and Results
Sensors 2010, 10, 7434-7468; doi:10.3390/s100807434 OPEN ACCESS sensors ISSN 1424-8220 www.mdpi.com/journal/sensors Review Laser Induced Breakdown Spectroscopy for Elemental Analysis in Environmental, Cultural Heritage and Space Applications: A Review of Methods and Results Rosalba Gaudiuso 1,*, Marcella Dell’Aglio 2, Olga De Pascale 2, Giorgio S. Senesi 2 and Alessandro De Giacomo 1,2 1 Department of Chemistry, University of Bari, via Orabona 4, 79126, Bari, Italy; E-Mail: [email protected] 2 IMIP-CNR sec. Bari, via Amendola 122/D, 70126, Bari, Italy; E-Mails: [email protected] (M.D.A.); [email protected] (O.P.); [email protected] (G.S.S.) * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +39-080-5929522; +39-080-5929513; Fax: +39-080-5929520. Received: 7 April 2010; in revised form: 24 May 2010 / Accepted: 22 June 2010 / Published: 9 August 2010 Abstract: Analytical applications of Laser Induced Breakdown Spectroscopy (LIBS), namely optical emission spectroscopy of laser-induced plasmas, have been constantly growing thanks to its intrinsic conceptual simplicity and versatility. Qualitative and quantitative analysis can be performed by LIBS both by drawing calibration lines and by using calibration-free methods and some of its features, so as fast multi-elemental response, micro-destructiveness, instrumentation portability, have rendered it particularly suitable for analytical applications in the field of environmental science, space exploration and cultural heritage. This review reports and discusses LIBS achievements in these areas and results obtained for soils and aqueous samples, meteorites and terrestrial samples simulating extraterrestrial planets, and cultural heritage samples, including buildings and objects of various kinds.