The combination of fiber Bragg grating inscription with femtosecond laser sources and the usage of the Talbot interferometer setup not only gives access to the fabrication of Bragg gratings in new types of materials but also allows, at the same time, to keep the high flexibility of an interferometric setup in choosing the Bragg grating wavelength. Since the spatial and temporal coherence properties of the femtosecond laser source differ strongly from those of conventional laser sources, specific limits and tolerances in the interferometric setup have to be considered. Such limits are investigated on the basis of an analytical ray tracing model. The results are applied to tolerance measurements of fiber Bragg grating reflections recorded with a DUV sub-picosecond laser source at 262 nm. Additionally we demonstrate the wavelength versatility of the two-beam interferometer setup for femtosecond inscription over a 40 nm wavelength band. Inscription experiments in Al/Yb doped silica glasses are demonstrated as a prove for the access to non-photosensitive fibers.

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Plasmas were generated by 400 fs KrF laser pulses at intensities of ~~10 17 Wcm -2 on aluminum targets. Reflectivity and x-ray emission were measured as a function of laser polarization, angle of incidence, and intensity. For the same absorbed intensity, p-polarized laser light is up to a factor of 5 more efficient in generating x rays ( > 0.5 keV) than s-polarized light. These results show the importance of an additional absorption process, besides collisional absorption, for short scale length plasmas that is effective for /^-polarized light only and has the characteristics of resonance absorption.

The manipulation of polymers and biological molecules or the control of chemical reactions on a nanometer scale by means of laser pulses shows great promise for applications in modern nanotechnology, biotechnology, molecular medicine or chemistry. A controllable, parallel, highly efficient and very local heat conversion of the incident laser light into metal nanoparticles without ablation or fragmentation provides the means for a tool like a 'nanoreactor', a 'nanowelder', a 'nanocrystallizer' or a 'nanodesorber'. In this paper we explain theoretically and show experimentally the interaction of laser radiation with gold nanoparticles on a polymethylmethacrylate (PMMA) layer (one-photon excitation) by means of different laser pulse lengths, wavelengths and pulse repetition rates. To the best of our knowledge this is the first report showing the possibility of highly local (in a 40 nm range) regulated heat insertion into the nanoparticle and its surroundings without ablation of the gold nanoparticles. In an earlier paper we showed that near-infrared femtosecond irradiation can cut labeled DNA sequences in metaphase chromosomes below the diffraction-limited spot size. Now, we use gold as well as silver-enhanced gold nanoparticles on DNA (also within chromosomes) as energy coupling objects for femtosecond laser irradiation with single-and two-photon excitation. We show the results of highly localized destruction effects on DNA that occur only nearby the nanoparticles.

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