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Multiphoton ionization (MPI) of alkyl iodides (RI, R = CnH2n+1, n = 1–4) has been investigated with femtosecond laser pulses centered at 800 and 400 nm along with photoelectron imaging detection. In addition, the ultraviolet (UV)–vacuum ultraviolet (VUV) absorption spectra of gas-phase RIs have been measured in the photon energy range of 5–11 eV using the VUV Fourier transform spectrometer at the VUV DESIRS beamline of the synchrotron SOLEIL facility. The use of high-laser-field strengths in matter–radiation interaction generates highly non-linear phenomena, such as the Stark shift effect, which distorts the potential energy surfaces of molecules by varying both the energy of electronic and rovibrational states and their ionization energies. The Stark shift can then generate resonances between intermediate states and an integer number of laser photons of a given wavelength, which are commonly known as Freeman resonances. Here, we study how the molecular structure of linear and branched alkyl iodides affects the UV–VUV absorption spectrum, the MPI process, and the generation of Freeman resonances. The obtained results reveal a dominant resonance in the experiments at 800 nm, which counter-intuitively appears at the same photoelectron kinetic energy in the whole alkyl iodide series. The ionization pathways of this resonance strongly involve the 6p(2E3/2) Rydberg state with different degrees of vibrational excitation, revealing an energy compensation effect as the R-chain complexity increases. [ABSTRACT FROM AUTHOR]

In this work, laser‐induced periodic surface structures (LIPSS) are generated on the surface of thin films of poly(trimethylene terephthalate) (PTT) fabricated by spin coating on silicon. Previous studies have shown the appearance of LIPSS in this type of materials with femtosecond laser pulses in the near‐infrared region of the spectrum, despite the extremely low absorption of the polymer. The present work consists of an exploration of the effect of adding complexity to the femtosecond laser fields employed for irradiation. Changes in the repetition rate of the pulse train, the pulse duration, and the pulse temporal chirp are explored, and conditions for optimum LIPSS formation are identified. The effects of these modifications on the polymer surface topography, assessed by atomic force microscopy, are described and discussed. [ABSTRACT FROM AUTHOR]

Multiphoton ionization (MPI) of methyl iodide, CH3I, has been investigated with the photoelectron imaging (PEI) technique, using high intensity femtosecond laser pulses at different central wavelengths. The use of high laser field strengths alters the way in which matter–radiation interaction takes place. This generates highly nonlinear phenomena, among which we can highlight the Stark shift effect. It can distort the potential energy surfaces of atoms and molecules, varying both the energy of electronic and rovibrational states of these systems and their ionization potentials. In this way, the Stark shift can generate resonances between intermediate states and an integer number of laser photons of a given wavelength, which would be absent in the low intensity regime. The main purpose of this work is the generation, detection and characterization of resonances produced by the Stark shift, commonly known as Freeman resonances, induced by multiphoton ionization of gas-phase CH3I at different laser wavelengths. The results obtained reveal that a multitude of resonances are induced in the ionization of CH3I in the range of intensities employed, involving several Rydberg states. Ionization pathways associated with different degrees of vibrational excitation in both the intermediate states and the molecular cation generated in each of the experiments are proposed. [ABSTRACT FROM AUTHOR]

Multiphoton ionization (MPI) of methyl iodide, CH 3 I, has been investigated with the photoelectron imaging (PEI) technique, using high intensity femtosecond laser pulses at different central wavelengths. The use of high laser field strengths alters the way in which matter-radiation interaction takes place. This generates highly nonlinear phenomena, among which we can highlight the Stark shift effect. It can distort the potential energy surfaces of atoms and molecules, varying both the energy of electronic and rovibrational states of these systems and their ionization potentials. In this way, the Stark shift can generate resonances between intermediate states and an integer number of laser photons of a given wavelength, which would be absent in the low intensity regime. The main purpose of this work is the generation, detection and characterization of resonances produced by the Stark shift, commonly known as Freeman resonances, induced by multiphoton ionization of gas-phase CH 3 I at different laser wavelengths. The results obtained reveal that a multitude of resonances are induced in the ionization of CH 3 I in the range of intensities employed, involving several Rydberg states. Ionization pathways associated with different degrees of vibrational excitation in both the intermediate states and the molecular cation generated in each of the experiments are proposed.