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A. Battistoni

Publications and source records attributed to A. Battistoni.

2 recordsLinked to original sources

A tilted pulse-front setup for femtosecond extreme ultraviolet transient grating spectroscopy in highly non-collinear geometries

We demonstrate a tilted pulse-front transient grating technique that allows to optimally utilize time-resolution as well as transient grating line density while probing under grazing incidence as typically done in extreme ultraviolet (EUV) or soft x-ray (SXR) experiments. Our optical setup adapts the pulse front tilt of the two pulses that create the transient grating to the relative tilt grazing incident pulse. We demonstrate the technique using all 800 nm femtosecond laser pulses for transient grating generation on a vanadium dioxide film. We probe that grating via diffraction of a third 800 nm pulse. The time resolution of 100 fs is an improvement by a factor 30 compared to our previous experiments on the same system (1,2). The scheme paves the way for EUV and SXR probing of optically induced transient gratings on any material.

physics.ins-det

Probing ultrafast ππ*/nπ* internal conversion in organic chromophores via K-edge resonant absorption

Organic chromophores with heteroatoms possess an important excited state relaxation channel from an optically allowed ππ* to a dark nπ*state. We exploit the element and site specificity of soft x-ray absorption spectroscopy to selectively follow the electronic change during the ππ*/nπ* internal conversion. As a hole forms in the n orbital during ππ*/nπ* internal conversion, the near edge x-ray absorption fine structure (NEXAFS) spectrum at the heteroatom K-edge exhibits an additional resonance. We demonstrate the concept with the nucleobase thymine, a prototypical heteroatomic chromophore. With the help of time resolved NEXAFS spectroscopy at the oxygen K-edge, we unambiguously show that ππ*/nπ* internal conversion takes place within (60 \pm 30) fs. High-level coupled cluster calculations on the isolated molecules used in the experiment confirm the superb electronic structure sensitivity of this new method for excited state investigations.

physics.chem-ph