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Author: F. Fleming Crim Publisher: ISBN: Category : Languages : en Pages : 6
Book Description
Combining the techniques of direct excitation of overtone vibrations and time resolved spectroscopic detection permits detailed measurements of the vibrational and rotational relaxation of highly vibrationally excited molecules. Using this technique, we have measured vibrational and rotational relaxation in HF(v=3,4,5,). By observing near-infrared fluorescence, we determine the self-relaxation probabilities for HF(v=3,4,5) to be 0.19, 0.47, and 0.97, respectively, and find that the rates decrease more rapidly with temperature in these high levels than for v=1. Using laser double resonance to probe individual rotational states, we find phenomenological rotational relaxation rate constants which decrease montonically with rotational energy change in the vibrationally excited molecule. (Author).
Author: F. Fleming Crim Publisher: ISBN: Category : Languages : en Pages : 6
Book Description
Combining the techniques of direct excitation of overtone vibrations and time resolved spectroscopic detection permits detailed measurements of the vibrational and rotational relaxation of highly vibrationally excited molecules. Using this technique, we have measured vibrational and rotational relaxation in HF(v=3,4,5,). By observing near-infrared fluorescence, we determine the self-relaxation probabilities for HF(v=3,4,5) to be 0.19, 0.47, and 0.97, respectively, and find that the rates decrease more rapidly with temperature in these high levels than for v=1. Using laser double resonance to probe individual rotational states, we find phenomenological rotational relaxation rate constants which decrease montonically with rotational energy change in the vibrationally excited molecule. (Author).
Author: Publisher: ISBN: Category : Languages : en Pages : 17
Book Description
The transfer of energy in isolated or colliding molecules is a fundamental process with practical consequences for complex phenomena occurring in atmospheric chemistry, combustion, molecular lasers, plasmas, and a host of other environments containing energetic species. We have developed a technique that combines vibrational overtone excitation, to prepare highly vibrationally excited initial states, and time-resolved spectroscopic detection, to probe the evolution of the prepared state, for studying energy transfer in vibrationally energized molecules. We have used this approach to determine directly, for the first time, the frequencies of the three ungerade vibrations in the first electronically excited state of acetylene. Using this information we have characterized highly vibrationally excited states of acetylene and directly the frequencies and rotational constants of the perturbing vibrational states at these energies. Combining these spectroscopic insights on the vibrationally and electronically excited states of acetylene has allowed us to determine the energy transfer rates and pathways in the collisional relaxation of a polyatomic molecule containing 10,000 cm-1 of vibrational energy, Rotational energy transfer is very rapid, occurring on about every other collision, but is essentially unaffected by the identity of the vibrational state in which the rotational relaxation occurs.
Author: F. F. Crim Publisher: ISBN: Category : Languages : en Pages : 22
Book Description
The three objectives of this work are to determine the nature of highly vibrationally excited polyatomic molecule, to determine the rate constants and pathways for the collisional relaxation of these molecules, and to probe the electronic spectroscopy of these molecules. We have created and implemented approaches for accomplishing these objectives and have demonstrated their feasibility by studying the collisional energy transfer in highly vibrational excited acetylene. We have found that the collisional self relaxation rates of single angular momentum states with 10,000/cm of vibrational energy are a substantial fraction of the gas kinetic collision rates. The rate constant is about a factor of two smaller for relaxation by atomic partners. Molecular energy transfer, Vibrational energy transfer. (MJM).
Author: Trevor C. Brown Publisher: ISBN: Category : Languages : en Pages : 338
Book Description
This thesis describes the studies made on several unimolecular reaction systems in order to obtain collisional energy transfer information on highly excited polyatomic molecules. Pressure-dependant very low-pressure pyrolysis (VLPP) and infrared multiphoton decomposition (IRMPD) experimental techniques are used.
Author: Kilyoung Kim Publisher: ISBN: Category : Languages : en Pages : 216
Book Description
This research is focused on single-collision energy transfer events between highly vibrationally excited benzene-like donor molecules and small bath molecules, CO2 and N2O in the vibrational ground level. Measuring how much energy is transferred from donors to bath molecules was accomplished by probing bath molecules scattered into specific-rotational states using a tunable dv=0.0003 cm-1 solid state diode laser. The normalized energy transfer probability distribution function, P(E,E'), determined from energy gain information, is very useful in comparing collisional energy transfer efficiency between various collision systems. P(E,E') is also used to investigate the effects of donor and bath physical properties on collisional energy transfer. The first chapter details the C6H5F-CO2 system, which is the basis of a study on the effect of donor fluorination on strong collision energy transfer. The second chapter is about all fluorobenzene-CO2 systems, which investigates the effect of excess vibrational excitation energy of donors on supercollision energy transfer efficiency as well as donor fluorination effect. The third chapter focuses on how the physical properties of bath molecules affect supercollision energy transfer by measuring state-specific energy gain of N2O scattered into 0000, J=59-75. Instead of CO2, N2O was used as a bath molecule with a pyrazine donor to compare energy gain results of bath molecules with somewhat different physical properties. N2O and CO2 are isoelectronic and have similar mass, but N2O has a small dipole moment. Comparison of P(E,E') obtained from pyrazine-CO2, -N2O, -DCl, and -H2O systems helps to elucidate the effect of the bath physical properties on supercollision energy transfer efficiency. The last chapter is dedicated to the extension of the measurement range of N2O energy gain to the mid J states (J=37-75). In this chapter I discuss reliability of P(E,E') obtained from only high J tail as well as the correction of overall energy transfer rate constant.
Author: I. Oref Publisher: ISBN: Category : Languages : en Pages : 35
Book Description
A statistical collisional energy transfer probability related to Boltzmann forms is assumed. Single collisions between vibrationally excited substrate molecules with heat bath molecules are considered. The dependence of the average energy per collision transferred up, down and overall on the initial energy content, on the temperature and on the size of the bath and substrate molecules is calculated and compared with data in the literature. (Author).
Author: Kilyoung Kim Publisher: ISBN: Category : Languages : en Pages : 0
Book Description
This research is focused on single-collision energy transfer events between highly vibrationally excited benzene-like donor molecules and small bath molecules, CO2 and N2O in the vibrational ground level. Measuring how much energy is transferred from donors to bath molecules was accomplished by probing bath molecules scattered into specific-rotational states using a tunable dv=0.0003 cm-1 solid state diode laser. The normalized energy transfer probability distribution function, P(E, E'), determined from energy gain information, is very useful in comparing collisional energy transfer efficiency between various collision systems. P(E, E') is also used to investigate the effects of donor and bath physical properties on collisional energy transfer. The first chapter details the C6H5F-CO2 system, which is the basis of a study on the effect of donor fluorination on strong collision energy transfer. The second chapter is about all fluorobenzene-CO2 systems, which investigates the effect of excess vibrational excitation energy of donors on supercollision energy transfer efficiency as well as donor fluorination effect. The third chapter focuses on how the physical properties of bath molecules affect supercollision energy transfer by measuring state-specific energy gain of N2O scattered into 0000, J=59-75. Instead of CO2, N2O was used as a bath molecule with a pyrazine donor to compare energy gain results of bath molecules with somewhat different physical properties. N2O and CO2 are isoelectronic and have similar mass, but N2O has a small dipole moment. Comparison of P(E, E') obtained from pyrazine-CO2, -N2O, -DCl, and -H2O systems helps to elucidate the effect of the bath physical properties on supercollision energy transfer efficiency. The last chapter is dedicated to the extension of the measurement range of N2O energy gain to the mid J states (J=37-75). In this chapter I discuss reliability of P(E, E') obtained from only high J tail as well as the correction of overall energy transfer rate constant.
Author: F. Fleming Crim
Author: F. Fleming Crim
Author: 
Author: F. F. Crim
Author: Trevor C. Brown
Author: Kieran Fergus Lim
Author: Chris Arthur Michaels
Author: Kilyoung Kim
Author: Pamela Mei-Ying Chu
Author: I. Oref
Author: Kilyoung Kim