arXiv subjects

Niranjan Shivaram

Publications and source records attributed to Niranjan Shivaram.

21 records · Page 2Linked to original sources

arXiv2015

Attosecond Quantum-Beat Spectroscopy in Helium

The evolution of electron wavepackets determines the course of many physical and chemical phenomena and attosecond spectroscopy aims to measure and control such dynamics in real-time. Here, we investigate radial electron wavepacket motion in Helium by using an XUV attosecond pulse train to prepare a coherent superposition of excited states and a delayed femtosecond IR pulse to ionize them. Quantum beat signals observed in the high resolution photoelectron spectrogram allow us to follow the field-free evolution of the bound electron wavepacket and determine the time-dependent ionization dynamics of the low-lying 2p state.

physics.atom-ph↗

arXiv2012

Ultrafast dynamics of neutral superexcited Oxygen: A direct measurement of the competition between autoionization and predissociation

Using ultrafast extreme ultraviolet pulses, we performed a direct measurement of the relaxation dynamics of neutral superexcited states corresponding to the nlσ_g(c^4Σ_u^-) Rydberg series of O_2. An XUV attosecond pulse train was used to create a temporally localized Rydberg wavepacket and the ensuing electronic and nuclear dynamics were probed using a time-delayed femtosecond near-infrared pulse. We investigated the competing predissociation and autoionization mechanisms for superexcited molecules and found that autoionization is dominant for the low n Rydberg states. We measured an autoionization lifetime of 92+/-6 fs and 180+/-10 fs for (5s,4d)σ_g and (6s,5d)σ_g Rydberg state groups respectively. We determine that the disputed neutral dissociation lifetime for the ν=0 vibrational level of the Rydberg series is 1100+/-100fs.

physics.chem-ph↗

arXiv2011

Real-time evolution of a laser-dressed Helium atom: Attosecond-resolved two-color photoionization study

Using extreme-ultraviolet attosecond-pulse-trains, we investigate the photoionization dynamics of a Helium atom in the presence of moderately-strong (~10^12 W/cm^2) femtosecond laser pulses. The electronic structure of a laser-dressed atom is traced in real-time through precision measurements of ion-yields and photo-electron angular distributions. Quantum interferences between photo-excitation paths are interpreted using the Floquet formalism. As the laser pulse intensity ramps on femtosecond timescales, we observe transitions between ionization channels mediated by different atomic resonances. The quantum phase of interfering paths is extracted for each channel and compared with simulations. Our results elucidate photoionization mechanisms in strong-fields and open the doors for photo-absorption/ionization control schemes.

physics.atom-ph↗