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Poster Session

Poster Session I (4pm-6pm CDT)

4:00 pm – 6:00 pm, Tuesday June 4 Session D00
Topics:

Channel-selective analysis of strong-field-induced nuclear wave packet in sulfur dioxide

Poster 34
Presenter: Sanduni Kudagama (Kansas State University)
Authors: Huynh Van Sa Lam (Kansas State University), Anbu Venkatachalam (Kansas State University), Van-Hung Hoang (Kansas State University), Sina Jacob (Goethe-Universität Frankfurt am Main), Surjendu Bhattacharyya (Kansas State University), Keyu Chen (Kansas State University), Tu Thanh Nguyen (Kansas State University), Vinod Kumarappan (Kansas State University), Uwe Thumm (Kansas State University), Daniel Rolles (Kansas State University), Artem Rudenko (Kansas State University)

The temporal evolution of vibrational wave packets in sulfur dioxide molecules irradiated by intense 800 nm laser pulses is studied employing momentum-resolved ion spectroscopy and channel-selective Fourier analysis. We map the wave-packet dynamics created by laser ionization or excitation of the molecule using two different probe schemes: weak-field excitation by a 300 nm laser pulse and strong-field excitation or ionization by a second 800 nm pulse. The 300 nm pulse exclusively probes bending vibrations in the ground state of the SO2+ ion by a one-photon resonant coupling to a single repulsive excited state. In contrast, the 800 nm probe pulse can map the dynamics via a broad range of singly, doubly or multiply charged final states, either bound or dissociative. While the signal in all channels is dominated by the ionic-state bending vibrations, the Fourier analysis of delay-dependent ion yields also reveals the signatures of the same vibrational mode in the ground state of the neutral SO2 molecule. We discuss how the choice of the final state populated by the probe pulse influences the Fourier spectra and the phase of the observed oscillations, and compare the experimental results to the predictions of the theoretical model simulating the wave packet propagation in SO2 neutral and ionic ground states. 

Funding acknowledgement

Supported by the Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, US Department of Energy under Awards No. DE-FG02-86ER13491 and by the National Science Foundation grant no. PHYS-1753324 (ASV).

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