| Itzik Ben-Itzhak |
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| Professor | ||
| Address: | 306 Cardwell Hall | |
| Phone: | (785) 532-1636 | |
| E-mail: | ibi@phys.ksu.edu | |
| Group Webpage | ||
| Ph.D. The Technion, Haifa, Israel 1986 | ||
Research Area
Experimental Atomic, Molecular
& Optical Physics
The focus of our research is the interaction of
intense ultrashort laser pulses with molecular ions. The molecular ion beams, at
a few keV, originating from an ion source (ECR), are crossed by the Kansas Light
Source (KLS) laser beam. The resulting fragments are measured in coincidence by
a 3-dimensional momentum imaging system, which allows for direct separation of
the ionization and dissociation channels. These measurements provide the
complete angular distribution of the molecular breakup around the laser
polarization vector as well as the kinetic energy release (KER) upon
dissociation with sufficient resolution to identify the vibrational states of H2
+. During this year we have modified the experimental setup and imaging
technique to allow measurements of dissociation with zero kinetic
energy release (KER→0).
Taking advantage of the improved energy resolution and extended energy range we
explored the dissociation of H2 + in intense ultrashort laser pulses.
In one example, the improved energy resolution allowed us to provide experimental evidence for the reduction in dissociation probability of the v=12 vibrational state that has been predicted by Esrys group. This suppressed dissociation was attributed in the past to vibrational trapping in the light induced potential well. However, the present calculations including nuclear rotation indicate that there is no vibrational trapping. The observed suppression in H2 + dissociation is caused by the small magnitude of the transition dipole moments and not by vibrational trapping, as has been commonly believed5.
In another example, the ability to measure H2 + dissociation with zero KER provided clear experimental evidence for zero photon dissociation (ZPD) namely dissociation with net absorption of zero photons. Also in this case, vibrational trapping has been a key ingredient of the mechanism suggested in the past to explain ZPD, but the theoretical work of Esrys group suggests that there is no vibrational trapping. The alternative mechanism we suggest to explain ZPD involves the absorption of a slightly more energetic photon followed by the stimulated emission of a less energetic photon, both photons within the spectral bandwidth of the laser pulse that is a Raman scattering process.
Research Support
Recent Selected Publications
Tracing the photodissociation probability of H2+ in intense fields using chirped laser pulses, Vaibhav S. Prabhudesai, Uri Lev, Adi Natan, Barry D. Bruner, Adi Diner, Oded Heber, Daniel Strasser, D. Schwalm, Itzik Ben-Itzhak, J.J. Hua, B.D. Esry, Yaron Silberberg, and Daniel Zajfman, Phys. Rev. A 81, 023401 (2010).
Benchmark measurements of H3+ nonlinear dynamics in intense ultrashort laser pulses, J. McKenna, A.M. Sayler, B. Gaire, Nora G. Johnson, K.D. Carnes, B.D. Esry, and I. Ben-Itzhak, Phys. Rev. Lett. 103, 103004 (2009).
Suppressed dissociation of H2+ vibrational states by reduced dipole coupling, J. McKenna, F. Anis, B. Gaire, Nora G. Johnson, M. Zohrabi, K.D. Carnes, B.D. Esry, and I. Ben-Itzhak, Phys. Rev. Lett. 103, 103006 (2009).
Rapid Formation of H3+ from ammonia and methane following 4 MeV proton impact, Bethany Jochim, Amy Lueking, Laura Doshier, Sharayah Carey, E. Wells, Eli Parke, M. Leonard, K.D. Carnes, and I. Ben-Itzhak J. Phys. B: At. Mol. Opt. Phys. 42, 091002 (2009) Fast Track Communication.
Enhancing high-order above-threshold dissociation of H2+ beams with few-cycle laser pulses, J. McKenna, A.M. Sayler, F. Anis, B. Gaire, Nora G. Johnson, E. Parke, J.J. Hua, H. Mashiko, C.M. Nakamura, E. Moon, Z. Chang, K.D. Carnes, B.D. Esry, and I. Ben-Itzhak, Phys. Rev. Lett. 100, 133001 (2008).