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Bulletin of the American Physical Society

Four-Photon Stark Induced Ladder Climbing Prepares Large Ensemble of H$_{\mathrm{2\thinspace }}$in Selected High Lying Vibrational Levels

Nandini Mukherjee, William E. Perreault, Richard N. Zare

Published Jun 6, 2017• 0 citations
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Abstract We present a multi-color ladder excitation scheme that exploits Stark-induced adiabatic Raman passage to selectively populate a highly excited vibrational level of a molecule. We suggest that this multi-color coherent ladder excitation provides a practical way of accessing levels near the vibrational dissociation limit as well as the dissociative continuum, which would allow the generation of an entangled pair of fragments with near-zero relative kinetic energy. Specifically, we consider four- and six-photon coherent excitation of molecular hydrogen to high vibrational levels via intermediate vibrational levels, which are pairwise coupled by two-photon resonant interaction. Using a sequence of three partially overlapping, single-mode, nanosecond laser pulses we show that the sixth vibrational level of H 2 , which is too weakly coupled to be easily accessed by direct two-photon Raman excitation from the ground vibrational level, can be efficiently populated without leaving any population stranded in the intermediate level. Furthermore, we show that the fourteenth vibrational level of H 2 , which is the highest vibrational level in the ground electronic state with a binding energy of 22 meV, can be efficiently and selectively populated using a sequence of four pulses. The present technique offers the unique possibility of preparing entangled quantum states of H atoms without resorting to an ultracold system.

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Optimizing Raman Ladder Climbing: Theory and Application in Na2

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The theory of vibrational ladder climbing excitation by coherent stimulated nonresonant Raman using chirped laser pulses is developed. We analytically obtain the conditions for inverting the population to a final preselected vibrational state and the restrictions that apply in the linear chirp regime. By controlling both the shape of the laser pulses and the chirp profile, the ladder climbing process can be accelerated without reducing the yield of the selective excitation. Numerical results are presented for selection of moderately excited vibrational levels in Na 2, where the important contribution of several excited electronic states is also clarified.

The Journal of Physical Chemistry A•Sep 6, 2001•7 citations
Four-Photon Stark Induced Ladder Climbing Prepares Large Ensemble of H2 _{\mathrm{2\thinspace }}2​in Selected High Lying Vibrational Levels
Preparation of Vibrationally Excited H2_{\mathrm{2}}2​ in a Coherent Superposition of MMM-States Using Stark Induced Adiabatic Raman Passage (SARP)
Abstract We present a multi-color ladder excitation scheme that exploits Stark-induced adiabatic Raman passage to selectively populate a highly excited vibrational level of a molecule. We suggest that this multi-color coherent ladder excitation provides a practical way of accessing levels near the vibrational dissociation limit as well as the dissociative continuum, which would allow the generation of an entangled pair of fragments with near-zero relative kinetic energy. Specifically, we consider four- and six-photon coherent excitation of molecular hydrogen to high vibrational levels via intermediate vibrational levels, which are pairwise coupled by two-photon resonant interaction. Using a sequence of three partially overlapping, single-mode, nanosecond laser pulses we show that the sixth vibrational level of H 2 , which is too weakly coupled to be easily accessed by direct two-photon Raman excitation from the ground vibrational level, can be efficiently populated without leaving any population stranded in the intermediate level. Furthermore, we show that the fourteenth vibrational level of H 2 , which is the highest vibrational level in the ground electronic state with a binding energy of 22 meV, can be efficiently and selectively populated using a sequence of four pulses. The present technique offers the unique possibility of preparing entangled quantum states of H atoms without resorting to an ultracold system.
The theory of vibrational ladder climbing excitation by coherent stimulated nonresonant Raman using chirped laser pulses is developed. We analytically obtain the conditions for inverting the population to a final preselected vibrational state and the restrictions that apply in the linear chirp regime. By controlling both the shape of the laser pulses and the chirp profile, the ladder climbing process can be accelerated without reducing the yield of the selective excitation. Numerical results are presented for selection of moderately excited vibrational levels in Na 2, where the important contribution of several excited electronic states is also clarified.