Alignment structures of rotational wavepacket created by two strong femtosecond laser pulses
نویسندگان
چکیده
منابع مشابه
Diffractive imaging of a rotational wavepacket in nitrogen molecules with femtosecond megaelectronvolt electron pulses
Imaging changes in molecular geometries on their natural femtosecond timescale with sub-Angström spatial precision is one of the critical challenges in the chemical sciences, as the nuclear geometry changes determine the molecular reactivity. For photoexcited molecules, the nuclear dynamics determine the photoenergy conversion path and efficiency. Here we report a gas-phase electron diffraction...
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Single-color illumination of a copper surface by a red or an ultraviolet femtosecond laser pulse yields a threephoton (red) or a two-photon (UV) photoemission process. A multicolor, multiphoton process is generated when the red and the UV pulses overlap both in space and in time on the photocathode. It is shown that this emission process results from the absorption by an electron of one red and...
متن کاملPhotoluminescence from voids created by femtosecond-laser pulses inside cubic-BN.
Photoluminescence (PL) from femtosecond-laser-modified regions inside cubic-boron nitride (c-BN) was measured under UV and visible light excitation. Bright PL at the red spectral range was observed, with a typical excited state lifetime of ∼4 ns. Sharp emission lines are consistent with PL of intrinsic vibronic defects linked to the nitrogen vacancy formation (via Frenkel pair) observed earlie...
متن کاملTwo-color two-photon excitation using femtosecond laser pulses.
The use of two-color two-photon (2c2p) excitation easily extends the wavelength range of Ti:sapphire lasers to the UV, widening the scope of its applications especially in biological sciences. We report observation of 2c2p excitation fluorescence of p-terphenyl (PTP), 2-methyl-5-t-butyl-p-quaterphenyl (DMQ) and tryptophan upon excitation with 400 and 800 nm wavelengths using the second harmonic...
متن کاملPhotoelectron imaging on time-dependent molecular alignment created by a femtosecond laser pulse.
Rotational wave packet revivals on an excited electronic state have been measured by femtosecond time-resolved photoelectron imaging for the first time. The first full revival at 82 ps of S1 (n,pi*) pyrazine was clearly observed in the time dependencies of the photoelectron intensity and the photoelectron angular distribution (PAD). The PAD, measured for laser aligned pyrazine, clearly reflects...
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ژورنال
عنوان ژورنال: Optics Express
سال: 2010
ISSN: 1094-4087
DOI: 10.1364/oe.18.008990