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Full-Text Articles in Physics
Dissociative Excitation, Ionization, And Fragmentation Processes For Nitrogen, Oxygen, Methane, And Water Molecules By Electron Bombardment, M. Gochitashvili, R. Lomsazde, D. Kuparashvili, O. Taboridze, Roman Ya. Kezerashvili
Dissociative Excitation, Ionization, And Fragmentation Processes For Nitrogen, Oxygen, Methane, And Water Molecules By Electron Bombardment, M. Gochitashvili, R. Lomsazde, D. Kuparashvili, O. Taboridze, Roman Ya. Kezerashvili
Publications and Research
Electron–impact ionization and fragmentation of molecules are investigated by the chromatography mass-spectrometry device. While the excitation processes are investigated by an optical spectroscopy method. The spectral analysis is performed in the vacuum ultraviolet 50-130 nm spectral regions. The absolute value of the fragmentation cross-section in the dissociative ionization and excitation processes is determined. Measurements are performed in the electron energy range 25-120eV for ionization and 200-500eV for excitation processes respectively.
Quantum Interference In The Field Ionization Of Rydberg Atoms, Rachel Feynman, Jacob A. Hollingsworth, Michael Vennettilli, Tamas Budner, Ryan Zmiewski, Donald P. Fahey, Thomas J. Carroll, Michael W. Noel
Quantum Interference In The Field Ionization Of Rydberg Atoms, Rachel Feynman, Jacob A. Hollingsworth, Michael Vennettilli, Tamas Budner, Ryan Zmiewski, Donald P. Fahey, Thomas J. Carroll, Michael W. Noel
Physics and Astronomy Faculty Publications
We excite ultracold rubidium atoms in a magneto-optical trap to a coherent superposition of the three |mj | sublevels of the 37d5/2 Rydberg state. After some delay, during which the relative phases of the superposition components can evolve, we apply an electric field pulse to ionize the Rydberg electron and send it to a detector. The electron traverses many avoided crossings in the Stark levels as it ionizes. The net effect of the transitions at these crossings is to mix the amplitudes of the initial superposition into the same final states at ionization. Similar to a Mach-Zehnder interferometer, the three …
Imaging The Dipole-Dipole Energy Exchange Between Ultracold Rubidium Rydberg Atoms, Donald P. Fahey, Thomas J. Carroll, Michael W. Noel
Imaging The Dipole-Dipole Energy Exchange Between Ultracold Rubidium Rydberg Atoms, Donald P. Fahey, Thomas J. Carroll, Michael W. Noel
Physics and Astronomy Faculty Publications
The long-range, anisotropic nature of the interaction among atoms in an ultracold dipolar gas leads to a rich array of possibilities for studying many-body physics. In this work, an ultracold gas of highly excited atoms is used to study energy transport due to the long-range dipole-dipole interaction. A technique is developed to measure both the internal energy states of the interacting Rydberg atoms and their positions in space. This technique is demonstrated by observing energy exchange between two spatially separated groups of Rydberg atoms excited to two different internal states. Simulations confirm the general features of the energy transport in …
Ultrafast Intense-Field Photoionization And Photofragmentation Of Systematic Series Of Substituted Organic Molecules, Timothy D. Scarborough
Ultrafast Intense-Field Photoionization And Photofragmentation Of Systematic Series Of Substituted Organic Molecules, Timothy D. Scarborough
Department of Physics and Astronomy: Dissertations, Theses, and Student Research
The abundance and relevance of organic molecules similar to benzene makes their study important. Studying the interactions of such molecules with intense light fields has implications for the generation of short-wavelength radiation, attosecond science, high-harmonic generation, and many other fields. However, the computing power necessary to complete fully ab initio calculations describing molecules of this size does not exist; this leaves theoretical studies to rely on assumptions and approximations just to calculate the energies of the ground state. Including any sort of dynamics in these calculations is prohibitively complicated, and this makes experimental observations important. Since many organic molecules are …
Observation And Identification Of Metastable Excited States In Ultrafast Laser-Ionized Pyridine, David B. Foote, Timothy D. Scarborough, Cornelis J. Uiterwaal
Observation And Identification Of Metastable Excited States In Ultrafast Laser-Ionized Pyridine, David B. Foote, Timothy D. Scarborough, Cornelis J. Uiterwaal
C.J.G.J. Uiterwaal Publications
We report on the fragmentation of ionized pyridine (C5H5N) molecules by focused 50 fs, 800 nm laser pulses. Such ionization produces several metastable ionic states that fragment within the field-free drift region of a reflectron- type time of flight mass spectrometer, with one particular metastable dissociation being the leading fragmentation process. Because the time of flight is no longer dependent in a simple way on the mass of the ion, the metastable decay is manifested as an unfocused peak on the mass spectrum that appears at a time of flight not corresponding to an integer mass. …
Partial Ion Yield Sspectroscopy Around The Cl 2p And C 1s Ionization Thresholds In Cf3cl, D. Ceolin, Maria Novella Piancastelli, Wayne C. Stolte, Dennis W. Lindle
Partial Ion Yield Sspectroscopy Around The Cl 2p And C 1s Ionization Thresholds In Cf3cl, D. Ceolin, Maria Novella Piancastelli, Wayne C. Stolte, Dennis W. Lindle
Chemistry and Biochemistry Faculty Research
We present a partial ion yield experiment on freon 13, CF3Cl, excited in the vicinity of the C 1s and Cl 2p ionization thresholds. We have collected a large amount of cationic fragments and a few anionic fragments at both edges. We have observed a strong intensity dependence of Rydberg transitions with ion fragment size for the CFnCl+ and CFn+/F+ (n=0–3) series at both the Cl 2p and C 1s ionization edges. Selectivity in the fragmentation processes involving the C–Cl and C–F bonds are highlighted by the intensities of the C …
Electron Heating In Atmospheric Pressure Glow Discharges, Robert H. Stark, Karl H. Schoenbach
Electron Heating In Atmospheric Pressure Glow Discharges, Robert H. Stark, Karl H. Schoenbach
Bioelectrics Publications
The application of nanosecond voltage pulses to weakly ionized atmospheric pressure plasmas allows heating the electrons without considerably increasing the gas temperature, provided that the duration of the pulses is less than the critical time for the development of glow-to-arc transitions. The shift in the electron energy distribution towards higher energies causes a temporary increase in the ionization rate, and consequently a strong rise in electron density. This increase in electron density is reflected in an increased decay time of the plasma after the pulse application. Experiments in atmospheric pressure air glow discharges with gas temperatures of approximately 2000 K …
Photofragmentation Of Third-Row Hydrides Following Photoexcitation At Deep-Core Levels, D. L. Hansen, M. E. Arrasate, J. Cotter, G. R. Fisher, Oliver Hemmers, K. T. Leung, Jon C. Levin, R. Martin, Paul Neill, Rupert C. Perera, I. A. Sellin, Marc Simon, Y. Uehara, B. Vanderford, S. B. Whitfield, Dennis W. Lindle
Photofragmentation Of Third-Row Hydrides Following Photoexcitation At Deep-Core Levels, D. L. Hansen, M. E. Arrasate, J. Cotter, G. R. Fisher, Oliver Hemmers, K. T. Leung, Jon C. Levin, R. Martin, Paul Neill, Rupert C. Perera, I. A. Sellin, Marc Simon, Y. Uehara, B. Vanderford, S. B. Whitfield, Dennis W. Lindle
X-Ray Atomic and Molecular Science Program
The relaxation dynamics of HCl, DCl, H2S, and D2S following photoexcitation in the vicinities of the Cl and S K-shell thresholds (~2.8 keV for Cl, ~2.5 keV for S) were studied by means of ion time-of-flight mass spectroscopy. In all cases, the onset of pre-edge core-shell photoionization precedes the formation on resonance of a significant amount of neutral hydrogen as well as postcollision-interaction effects above threshold. Examination of the width of the H+ peak in spectra taken with the analyzer parallel and perpendicular to the polarization vector of the incident light indicates that on resonance, …
Auger Resonance Decay Process In Ar 2p Shell Excitation And Ionization, Y. Lu, Wayne C. Stolte, J.A. R. Samson
Auger Resonance Decay Process In Ar 2p Shell Excitation And Ionization, Y. Lu, Wayne C. Stolte, J.A. R. Samson
Chemistry and Biochemistry Faculty Research
The production and subsequent autoionization of the Ar+ (1D2)6d1 satellite state that is formed either by shake-up or recapture during the Auger decay of a 2p vacancy in Ar has been studied by photoelectron spectroscopy in the energy region from 243 to 256 eV. The creation of near zero energy electrons below and immediately above the Ar 2p ionization threshold is discussed. Some ambiguous points in previous studies are clarified.
Double Photoionization Of Helium, James A.R. Samson, Wayne C. Stolte, Z. X. He, Y. Lu, J. N. Cutler, R. J. Bartlett
Double Photoionization Of Helium, James A.R. Samson, Wayne C. Stolte, Z. X. He, Y. Lu, J. N. Cutler, R. J. Bartlett
Chemistry and Biochemistry Faculty Research
The cross sections for double photoionization of helium and the ratios of double to single ionization have been measured from the double-ionization threshold to 820 eV. The results are in very good agreement with several recent calculations.
Molecular-Orbital Studies Via Satellite-Free X-Ray Fluorescence: Cl-K Absorption And K–Valence-Level Emission Spectra Of Chlorofluoromethanes, Rupert C. Perera, P. L. Cowan, Dennis W. Lindle, R. E. Lavilla, T. Jach, R. D. Deslattes
Molecular-Orbital Studies Via Satellite-Free X-Ray Fluorescence: Cl-K Absorption And K–Valence-Level Emission Spectra Of Chlorofluoromethanes, Rupert C. Perera, P. L. Cowan, Dennis W. Lindle, R. E. Lavilla, T. Jach, R. D. Deslattes
Chemistry and Biochemistry Faculty Research
X-ray absorption and emission measurements in the vicinity of the chlorine K edge of the three chlorofluoromethanes have been made using monochromatic synchrotron radiation as the source of excitation. By selectively tuning the incident radiation to just above the Cl 1s single-electron ionization threshold for each molecule, less complex x-ray-emission spectra are obtained. This reduction in complexity is attributed to the elimination of multielectron transitions in the Cl K shell, which commonly produce satellite features in x-ray emission. The resulting "satellite-free" x-ray-emission spectra exhibit peaks due only to electrons in valence molecular orbitals filling a single Cl 1s vacancy. These …
Argon-Photoion–Auger-Electron Coincidence Measurements Following K-Shell Excitation By Synchrotron Radiation, Jon C. Levin, C. Biedermann, N. Keller, L. Liljeby, C.-S. O, R. T. Short, Ivan A. Sellin, Dennis W. Lindle
Argon-Photoion–Auger-Electron Coincidence Measurements Following K-Shell Excitation By Synchrotron Radiation, Jon C. Levin, C. Biedermann, N. Keller, L. Liljeby, C.-S. O, R. T. Short, Ivan A. Sellin, Dennis W. Lindle
Chemistry and Biochemistry Faculty Research
Argon photoion spectra have been obtained for the first time in coincidence with K-LL and K-LM Auger electrons, as a function of photon energy. The simplified charge distributions which result exhibit a much more pronounced photon-energy dependence than do the more complicated noncoincident spectra. In the near-K-threshold region, Rydberg shakeoff of np levels, populated by resonant excitation of K electrons, occurs with significant probability, as do double-Auger processes and recapture of the K photoelectron through postcollision interaction.