Thesis (M.S.)--West Virginia University, 2005. / Title from document title page. Document formatted into pages; contains xii, 96 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 56-59).

The study of photovoltaic materials is important so as to develop new solar energy technologies: in particular, quantum-confined semiconductors could offer increased quantum efficiencies at a much lower manufacture cost. This thesis contains results from a number of pump-probe experiments designed to probe the carrier dynamics in bulk and quantum-confined photovoltaics. A THz time-domain spectrometer was designed, built and commissioned. The THz refractive indices and absorption coefficients of toluene and hexane were determined, and the spectrometer was benchmarked using a photoexcited GaAs wafer. Results are presented of time-resolved THz spectroscopy of photoexcited bulk InP as a function of laser excitation wavelength. These data were used to extract the quantum efficiency of bulk InP in order to compare with recent results for InP quantum dots. The quantum efficiency in quantum dots increases when the incident photon energy is at least twice the band gap energy, whereasthe efficiency of the bulk material is found to decrease. This is because of surface recombination, and these measurements therefore verify the potential superiority of quantum dot materials over bulk materials for use in solar energy applications. Initial measurements of quantum dots using THz spectroscopy highlighted the various experimental challenges involved and the upgrades required to study such samples in the future.The time-dependence of the photoinduced surface photovoltage (SPV) in Si was studied on nanosecond timescales by synchronizing an ultrafast laser system to a synchrotron radiation source (the SRS at Daresbury, UK), and measuring the resulting shift in the photoelectron spectrum. The equilibrium band bending was determined, and the decay of the SPV was attributed to the recombination of charge carriers across the band gap. Results are presented for the SPV in bulk ZnO and for PbS quantum dot chemically attached to ZnO. The fact that the PbS quantum dots were chemically attached to the surface without becoming oxidized was verified using X-ray photoelectron spectroscopy (XPS). The changes caused by photoexcitation occur on much longer timescales in ZnO than Si (sub-milliseconds rather than nanoseconds), and these timescales were conveniently accessed using the time-resolved XPS facility at the TEMPO beamline at Synchrotron SOLEIL (Paris, France). This is due to oxygen adsorption and desorption processes at the ZnO surface affectingthe transfer of charge carriers. The addition of PbS quantum dots to the ZnO surface was found to increase the speed of this charge transfer due to injection of carriers directly from the PbS quantum dot to the bulk ZnO conduction band.

No description available.

The objective of the present dissertation is to advance the science and engineering of metal-dielectric thin-film structures for ultrafast all-optical applications. The research presented consists of three parts: first, the linear and nonlinear optical (NLO) properties of Au and Ag/Au bilayer metallic thin films are comprehensively studied; then the design and properties of a novel nonlinear device structure are presented and finally an ultrafast all-optical shutter is developed and applications are discussed. In the first part, this study describes the linear and NLO properties of bilayer metallic films and shows that they can be tuned by controlling the mass-thickness ratio between Au and Ag. The combined properties of these bilayers are attractive for active plasmonic applications and nonlinear optical filters. Detailed physical models describing the linear and NLO response of Au and Ag/Au bilayers are presented and compared with experiments. In the second part, these models are used to optimize the NLO response of a novel Au-based NLO device. With only four layers, this novel device strongly amplifies the NLO response of the component Au thin film. NLO devices with broad spectral and angular bandwidths in the visible spectral region are demonstrated. The narrow band dependent NLO response of the NLO device is shown to lead to all-optical controls of high peak-power optical signal pulses. Finally, the NLO device technology is integrated into a novel ultrafast all-optical shutter, which allows temporal opening windows (the time shutter remains open) as short as a few ps. Ultrafast all-optical shutter potentially can temporally shape high peak-power nanosecond optical pulses, which could benefit biomedical and micromachining applications. Other possible optical applications such as short electron, X-ray pulse generations, ultrafast photography, and biomedical imaging will also be discussed.

Der erste Teil der Arbeit beschäftigt sich mit ultraschnellen Relaxationsprozessen in quasi-eindimensionalen organischen Molekülkristallen. Als Modellsystem wird das Perylenderivat MePTCDI untersucht. Mit verschiedenen Methoden der optischen Ultrakurzzeit-Spektroskopie werden Prozesse der Exzitonen- und Phononenrelaxation in der Zeit-Domäne untersucht. Die dafür aufgebauten Experimente erreichen eine Zeitauflösung von 20 Femtosekunden. Durch optische Anregung der niedrigsten elektronischen Übergänge werden in einem organischen Molekülkristall freie Exzitonen mit Wellenvektor k=0 gebildet. Dabei werden gleichzeitig zahlreiche intramolekulare und intermolekulare Schwingungsfreiheitsgrade angeregt. Die Anregung mit fs-Laserpulsen führt zum Aufbau kohärenter Schwingungswellenpakete. Es werden sowohl hochenergetische Oszillationen intramolekularer Vibrationen beobachtet, als auch erstmalig niedrigenergetische Oszillationen, die von Gittervibrationen (Phononen) stammen. Die kohärenten Vibrationen im elektronischen Grundzustand klingen bei Raumtemperatur im Bereich einiger Pikosekunden ab. Durch die optische Anregung mit fs-Laserpulsen wird nicht nur phononische Kohärenz, sondern auch elektronische Kohärenz der optischen Übergänge induziert. Die elektronische Kohärenz klingt mit der Dephasierungszeit T2 ab. Trotz der hohen Zeitauflösung war es letztendlich nicht möglich, die Dephasierung des niedrigsten exzitonischen Übergangs zeitlich aufzulösen - sie liegt jedoch im Bereich 17fs < T2 < 52fs. Die energetische Relaxation der freien Exzitonen zu den relaxierten, emittierenden Exzitonenzuständen erfolgt mit einer Zeitkonstante von ca. 50fs. Von diesen relaxierten Zuständen erfolgt die energetische Abregung in den elektronischen Grundzustand im ns-Bereich. Im zweiten Teil der Arbeit werden Untersuchungen an selbst-assemblierten Monoschichten (SAM) photochromer Moleküle vorgestellt. Als Modellsystem dienen Azobenzen-funktionalisierte Thiole auf Gold (111). Es konnten hochgeordnete Monoschichten dieser photochromen Moleküle erzielt werden, allerdings sind die bisherigen Schichten aufgrund der dichten Packung nicht photoaktivierbar. Mit Hilfe von Raster-Mikroskopie und Infrarot-Spektroskopie werden diese ultradünnen Schichten strukturell untersucht. Es wird ein kommensurates Wachstum mit zwei Molekülen in der nahezu rechteckigen Einheitszelle beobachtet, wobei die laubbaumförmigen Moleküle nahezu senkrecht auf der Oberfläche stehen. Als weitere Methode wurde die Generation der zweiten Harmonischen (Second Harmonic Generation, SHG) angewendet. Diese Technik eröffnet prinzipiell die Möglichkeit, photostimuliertes Schalten der Schicht zeitaufgelöst zu untersuchen. / The first part of this thesis is devoted to ultrafast relaxation processes in quasi-one-dimensional organic molecular crystals. Crystalline samples of the perylene derivative MePTCDI are employed as a model system. Processes concerning the excitonic and phononic relaxation are investigated in time domain using various experimental techniques of optical ultrafast spectroscopy. The experimental setups attain a time-resolution of 20 femtoseconds. Free excitons at wavevector k=0 are formed in a molecular crystal by optical excitation of the lowest electronic transitions. Thereby, various intramolecular and intermolecular vibrational degrees of freedom are excited simultaneously. The excitation by fs-laser pulses results in the composition of coherent vibrational wave packets. Both, higher-energetic oscillations caused by intramolecular vibrations (internal phonons) and, for the first time in a quasi-one-dimensional organic system, lower-energetic modulations which are related to coherent lattice phonons (external phonons) are observed. The coherence of both types of phonons in the electronic ground state is damped at room temperature within a few ps. Besides phononic coherence, optical excitation by fs-laser pulses additionally induces electronic coherence of the optical transitions. The electronic coherence decays with the dephasing time T2. In spite of the high time-resolution, finally it was not possible to time resolve the dephasing of the lowest excitonic transition - however, we can estimated it to be in the range of 17fs < T2 < 52fs. The energetic relaxation of free excitons to the relaxed, emitting exciton states takes place with a time constant of approx. 50fs. The subsequent energetic relaxation to the electronic ground state occurs on a ns-time scale. In the second part, investigations of self-assembled monolayers (SAM) of photochromic molecules are presented. Azobenzene-functionalized thiols on gold (111) are employed as a model system. Highly ordered monolayers of these photochromic molecules could be realized. However, these layers are not photoactive because of dense packing. By use of scanning tunneling microscopy and infra-red spectroscopy the structural properties of these ultrathin layers are investigated. A commensurate growth, yielding a lattice with two molecules within the nearly rectangular unit cell is observed. The molecules, shaped like a broad-leafed tree, are found to stand nearly upright on the surface. Second harmonic generation (SHG) is applied as another experimental method. This technique allows to time resolve photo-stimulated conformational changes of the layers in principle.