Biomedical subjects

S A Aseyev

Publications and source records attributed to S A Aseyev.

4 recordsLinked to original sources

PubMed2003

Attosecond angle-resolved photoelectron spectroscopy.

We report experiments on the characterization of a train of attosecond pulses obtained by high-harmonic generation, using mixed-color (XUV+IR) atomic two-photon ionization and electron detection on a velocity map imaging detector. We demonstrate that the relative phase of the harmonics is encoded both in the photoelectron yield and the angular distribution as a function of XUV-IR time delay, thus making the technique suitable for the detection of single attosecond pulses. The timing of the attosecond pulse with respect to the field oscillation of the driving laser critically depends on the target gas used to generate the harmonics.

Photons↗

PubMed2003

Photodetachment of He- in the vicinity of the two-electron escape threshold.

Recording the yield of He(1snl(3)L) Rydberg states for n=11-14, we measure the photodetachment cross sections of metastable He-(1s2s2p(4)P(o)) ions in the vicinity of the two-electron escape threshold. We observe a large number of double Rydberg He- quartet state resonances and report energies and widths of intrashell states in the n=13-15 manifolds. Sharp thresholds are measured at He((3)P(o)) and He((3)D(e)) Rydberg states with preference for population of the former, whereas the He((3)S(e)) states are not populated, in agreement with qualitative theoretical arguments.

Journal Article↗

PubMed2001

Few cycle dynamics of multiphoton double ionization.

In intense field ionization, an electron removed from the atomic core oscillates in the combined fields of the laser and the parent ion. This oscillation forces repeated revivals of its spatial correlation with the bound electrons. The total probability of double ionization depends on the number of returns and therefore on the number of optical periods in the laser pulse. We observed the yield of Ne(2+) relative to Ne(+) with 12 fs pulses to be clearly less compared to 50 fs pulses in qualitative agreement with our theoretical model.

Journal Article↗

PubMed2000

Forced molecular rotation in an optical centrifuge.

Intense linearly polarized light induces a dipole force that aligns an anisotropic molecule to the direction of the field polarization. Rotating the polarization causes the molecule to rotate. Using femtosecond laser technology, we accelerate the rate of rotation from 0 to 6 THz in 50 ps, spinning chlorine molecules from near rest up to angular momentum states J approximately 420. At the highest spinning rate, the molecular bond is broken and the molecule dissociates.

Journal Article↗