Search results for "Picosecond"
showing 10 items of 88 documents
All-fiber spectral compression of picosecond pulses at telecommunication wavelength enhanced by amplitude shaping
2012
International audience; We demonstrate efficient spectral compression of picosecond pulses in an all-fiber configuration at telecommunication wavelengths. A spectral compression by a factor 12 is achieved. Performing temporal shaping with a parabolic pulse significantly improves the spectral compression with much lower substructures and an enhanced Strehl ratio.
Towards combined multispectral, FLIM and Raman imaging for skin diagnostics
2020
To explore challenges for further improvement of diagnostic performance, a project aimed at development of technology for tri-modal skin imaging by combining multispectral, fluorescence lifetime and Raman band imaging was initiated. In this study, each of the mentioned imaging modalities has been preliminary tested and updated. Four different multispectral imaging devices were tested on color standards. Picosecond laser-excited fluorescence lifetime imaging equipment was examined on ex-vivo skin samples. Finally, a new Raman spectroscopy setup with 785 nm laser was launched and tested on cell cultures and ex-vivo skin. Advantages and specific features of the tri-modal skin imaging are discu…
Concentration measurements in molecular gas mixtures with a two-pump pulse femtosecond polarization spectroscopy technique
2001
0021-9606; Recently, we have demonstrated the ability of the Raman-induced polarization spectroscopy (RIPS) technique to accurately determine concentration or polarizability anisotropy ratio in low-pressure binary molecular mixtures [E. Hertz, B. Lavorel, O. Faucher, and R. Chaux, J. Chem. Phys. 113, 6629 (2000)]. It has been also pointed out that macroscopic interference, occurring when two revivals associated to different molecules time overlap, can be used to achieve measurements with picosecond time resolution. The applicability of the technique is intrinsically limited to a concentration range where the signals of both molecules are of the same magnitude. In this paper, a two-pump puls…
Mesoscopic organization in ionic liquids.
2017
We discuss some published results and provide new observations concerning the high level of structural complexity that lies behind the nanoscale correlations in ionic liquids (ILs) and their mixtures with molecular liquids. It turns out that this organization is a consequence of the hierarchical construction on both spatial (from ångström to several nanometer) and temporal (from fraction of picosecond to hundreds of nanosecond) scales, which requires joint use of experimental and computational tools. © 2017, Springer International Publishing Switzerland.
Study of Structure–Third-Order Susceptibility Relation of Indandione Derivatives
2016
By using the Z-scan method we studied the third-order nonlinear optical parameters of several aminobenziliden-1,3-indandione (ABI) derivatives that have previously been shown to own second-order nonlinear optical properties. Measurements were carried out using two 1064 nm Nd:YAG lasers with picosecond (ps) and nanosecond (ns) pulse widths, respectively. When ns laser was employed in the Z-scan setup, a strong thermal lensing took place resulting in severe overestimation of optical Kerr coefficients. Due to this reason the ps laser was employed to evaluate correct magnitude of Kerr effect. For investigated organic molecules, experimental results show that two-photon absorption at 1064 nm is …
Structure and characteristics of laser crystallized thin amorphous Si films
2011
Abstract Pure amorphous Si thin films deposited on oxidized crystalline Si surface (111) were crystallized by picosecond UV laser pulses. The Raman scattering spectra show that pulse energy of 330 mJ/cm2 is enough to fully crystallize Si film and further increase of the energy does not improve crystallinity. A large grained polycrystalline Si was obtained as revealed by surface analysis. A significant increase in carrier mobility was observed after laser crystallization.
Picosecond Time Resolved Analysis of the Fast and Slow Reversible Non-Photochemical Chlorophyll Fluorescence Quenching
1998
Photosystem II, which is a potential target of adverse effects of supersaturating light, is strongly dependent on a mechanism, which allows to switch over between efficient photochemical energy conversion at limiting light intensity and efficient photothermal energy conversion under strong light. The mechanisms for the thermal dissipation of light absorbed in excess are reflected by the socalled non-photochemical quenching of chlorophyll fluorescence (NPQ). Under excessive illumination two major components contribute to the overall NPQ which can be distinguished by their different kinetics of dark relaxation. The fast reversible component is supposed to be linked to the light-induced format…
Picosecond energy relaxation in
2005
Abstract Investigating the reflectance response dynamics of La 0.67 Ca 0.33 MnO 3 thin films after excitation by femtosecond laser pulses, we identify for the first time a picosecond relaxation step which only exists below the Curie temperature T C . The relaxation time increases from zero at T C to several picoseconds at low temperatures. The data can be explained with the existence of a magnetization-related effective energy gap, and assuming relaxation between these states to be mediated by a Frohlich-type electron–lattice interaction.
Secondary relaxation in the glass-transition regime of ortho-terphenyl observed by incoherent neutron scattering.
1992
We report on incoherent-neutron-scattering measurements in the supercooled regime of the van der Waals liquid ortho-terphenyl. A secondary localized relaxational process on the picosecond time scale is found. In accordance with mode-coupling theories of the glass transition, the relaxational dynamics around a critical temperature ${\mathit{T}}_{\mathit{c}}$ decomposes into two time regimes.
Direct temporal reconstruction of picosecond pulse by cross-correlation in semiconductor device
2012
Cross-correlation measurements using the two-photon absorption process in a semiconductor is experimentally demonstrated for two pulses of different wavelengths (shifted by ~200 nm) and durations (20 times ratio). These measurements were found to be highly repeatable and fully suitable for the determination of the temporal intensity profile of picosecond (ps) pulses.