Browsing by Subject "Electron spectroscopy"
Now showing 1 - 2 of 2
Results Per Page
Sort Options
Item Quantum state resolved studies of copper-H₂ system and electronic spectroscopy of Cu(100)(2009-08) Uka, Arban; Sitz, Greg OrmanHydrogen quantum state resolved energy losses upon scattering from copper are studied using molecular beam techniques and quantum state-specific detection methods. Also clean copper and hydrogen and oxygen covered copper surfaces were studied using electron spectroscopy. There are many questions about the nature of molecule-surface dynamics and the processes. The relative role of the different degrees of freedom in the reaction and the importance of non-adiabatic effects have been two of these questions. These two questions motivated this work. Energy loss in the elastic scattering of H₂(v=1. J=1) and H₂(v=0, J=1) molecular quantum states is measured as a function of incident translational energy at two surface temperatures. The energy loss process is shown to agree to the Baule classical model for energy ranges 74-150 meV for the excited vibrationally state and 74-125 for the ground vibrational state. Results suggest that translational energy is more effective that vibrational energy in the observed process. Theoretical models have been able to explain several processes using nonadiabatic models where friction coefficient tensor is included. Results in this thesis suggest that the energy loss in the elastic scattering is a nonadiabatic one. Electron spectroscopy studies showed that the surface plasmon intensity is very sensitive to surface contamination. Using this property, surface-only sensitive virtual temperature programmed desorption (VTPD) is developed. A better understanding of unique behavior of hydrogen covered Cu(100) was gained.Item Ultrafast delocalization, excited-state chemistry and spectroscopy of the hydrated electron(2003-08) Kee, Tak Wee, 1975-; Barbara, P. F. (Paul F.), 1953-Femtosecond spectroscopic measurements are reported on the delocalization, electron transfer reactions, solvation dynamics, and spectroscopy of the hydrated electron (eaq- ). The eaq- is an excess electron trapped in water and it has been under intense investigations for decades, e.g. for its charge transfer reactions, and nonadiabatic electronic transition. In the research presented in this dissertation, we choose to study eaq- because it is a unique prototype for studying localization and delocalization of a charge in water, electron transfer kinetics, solvation dynamics, and spectroscopy involving a highly delocalized excited state. First, the delocalization of eaq- is observed using a novel spatially sensitive technique which involves monitoring the effect of photo-excitation on the electron/hole geminate recombination following photoionization of neat water. vi The results indicate that excitation to the highly delocalized conduction band (CB) state produces significant suppression of geminate recombination, whereas excitation to the localized excited state (p-state) does not. The results show that the spatial extent of CB has a lower limit of 30 Å. Secondly, the electron transfer reactions, which correspond to scavenging of the various delocalized excited and precursor states of the hydrated electron by localized electron acceptors such as Cd2+, are studied. The rate constant of electron transfer per scavenger is found to inversely proportional to the volume of the specific state. Thirdly, the solvation dynamics of the different precursors and excited states of eaq- are investigated. The results show that the timescale of solvation depends on the initial degree of delocalization of the specific state. Fourthly, using the spatially sensitive technique with multi-color excitation, the broad and featureless absorption spectrum of eaq- is decomposed into two contributions. The first contribution involves the transition from the localized ground state (s-state) to the p-state and the second contribution corresponds to the transition from the s-state to CB. Finally, in order to obtain further insights on the spatial extent of CB, photodetachment experiments are performed on the hydrated electron trapped in the water pool of a reverse micelle (RM) with a radius ranging from 18 to 45 Å. The results indicate that the spatial extent of CB is comparable to the sizes of RM.