We have determined the time-dependent displacement fields in molecular sub-micrometer thin films as response to femtosecond and picosecond laser pulse heating by time-resolved X-ray diffraction. This method allows a direct absolute determination of the molecular displacements induced by electron-phonon interactions, which are crucial for, for example, charge transport in organic electronic devices. We demonstrate that two different modes of coherent shear motion can be photoexcited in a thin film of organic molecules by careful tuning of the laser penetration depth relative to the thickness of the film.
View Article and Find Full Text PDFIn this work we presented a compact femtosecond laser system based on Yb doped fiber seed laser and efficient Yb:YAG crystal rod power amplifier. Matched pair of chirped fiber Bragg grating stretcher and chirped volume Bragg grating compressor were used to obtain high fidelity - Strehl ratio 76%, pulses of 764 fs duration, 104 µJ energy at 200 kHz repetition rate at the output of the laser system.
View Article and Find Full Text PDFIn this work, a compact fiber chirped pulse amplification system exploiting a tandem of a chirped fiber Bragg grating stretcher and a chirped volume Bragg grating compressor with matched chromatic dispersion is presented. Chirped pulses of 230 ps duration were amplified in a Yb-doped fiber amplifier and re-compressed to 208 fs duration with good fidelity. The compressed pulse duration was fine-tuned by temperature gradient along the fiber Bragg grating stretcher.
View Article and Find Full Text PDFWe report on the developed front-end/pump system for optical parametric chirped pulse amplifiers. The system is based on a dual output fiber oscillator/power amplifier which seeds and assures all-optical synchronization of femtosecond Yb and picosecond Nd laser amplifiers operating at a central wavelength of 1030 nm and 1064 nm, respectively. At the central wavelength of 1030 nm, the fiber oscillator generates partially stretched 4 ps pulses with the spectrum supporting a <120 fs pulse duration and pulse energy of 0.
View Article and Find Full Text PDFThe photoelectron spectrum shows that multiphoton ionization of amyl nitrite, C(5)H(11)ONO, using ultrafast laser pulses deposits up to 3.7 eV of energy into internal degrees of freedom. As a result, the molecules fragment to produce various daughter ions of masses 87, 71, 60, 57, 41, 30, 29, and 27.
View Article and Find Full Text PDFWe have investigated the processes induced by femtosecond laser pulses in chloroamines, with a focus on the generation and observation of a highly reactive radical and on the involvement and general importance of excited-state ions in time-resolved mass spectrometry investigations of gaseous molecules. We have found that 280 nm femtosecond pulses lead to an ultrafast breakage of the N-Cl bond on the repulsive S1 surface, and that resulting radical is long-lived. When exposing the molecule to 420 nm photons a multiphoton ionization takes place to generate ions; these ions can then be excited with a 280 nm photon.
View Article and Find Full Text PDFWe have performed ab initio calculations to examine the potential energy along the normal modes of ground-state HCHO and along the reaction coordinates for loss of H2 and atomic hydrogen, respectively. This exploration showed that there are no specific features that will lead to reaction on the excited-state surfaces for excitations that are relevant to the troposphere and stratosphere. The calculations did however lead to the localization of a conical intersection point through which a specific loss of H2 could take place.
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