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ACS symposium series

Prospects for All-Optical Alignment and Quantum State Control of Nonpolar Molecules

A. M. Lyyra, F. C. Spano, Jun Qi, Teodora Kirova

Published Jun 21, 2002• 1 citation
Publisher

Abstract

We have demonstrated Autler-Townes splitting in molecular lithium using continuous wave triple resonance spectroscopy. The Autler-Townes split double resonance lineshape consists of a superposition of several narrower twin peaks, one for each | M j |. The splitting is proportional to | M j | enabling separation of the individual Mj peaks. Thus, excitation of an individual magnetic sublevel can be used to align the angular momentum of nonpolar molecules all-optically. We also propose a novel quantum control scheme based on using a coupling laser to create dressed states of controllable molecular character. Preliminary calculations are presented for variable singlet triplet character.

DOI
10.1021/bk-2002-0821.ch020

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We have demonstrated Autler-Townes splitting in molecular lithium using continuous wave triple resonance spectroscopy. The Autler-Townes split double resonance lineshape consists of a superposition of several narrower twin peaks, one for each | M j |. The splitting is proportional to | M j | enabling separation of the individual Mj peaks. Thus, excitation of an individual magnetic sublevel can be used to align the angular momentum of nonpolar molecules all-optically. We also propose a novel quantum control scheme based on using a coupling laser to create dressed states of controllable molecular character. Preliminary calculations are presented for variable singlet triplet character.
This paper describes an extension of the familiar coherence effects from atomic systems to the molecular regime. Such effects are inherent in the interaction of multiple laser fields with molecular systems. We have observed Autler–Townes splitting and the AC Stark shift in diatomic Lithium using the continuous wave all-optical triple resonance (AOTR) techniques. By using the Autler–Townes effect, we have partially resolved the magnetic sublevels of a molecular rovibrational level in a Doppler broadened sample, allowing all-optical alignment of the angular momentum in excited states of nonpolar molecules. The Autler–Townes effect in a molecular system extends the rovibrational state selectivity of the AOTR excitation technique to magnetic sublevels. PACS Nos.: 33.40tf, 42.50Hz
In recent years, coherent effects in atomic and molecular systems have been studied extensively, especially in several new classes of effects, such as lasing without inversion (LWI), electromagnetically induced transparency (EIT), coherent population trapping (CPT), AC Stark effect and Autler-Townes (AT) splitting in multilevel systems. The AC stark effect and Autler-Townes splitting in molecules have only been investigated recently. We demonstrate AC stark effect and Autler-Townes (AT) splitting in a lithium molecule using cw multi-photon spectroscopy. The excited upper level of the G1PigG^{1}\\Pi_{g}G1Pig​ is prepared by the optical-optical double resonance (OODR) excitation. The OODR line is split in the presence of a third coupling laser, which couples the upper level to an another intermediate level when the coupling laser is on or near resonance transition. The AT line shape consists of the superposition of ∣MJ∣|M_{J}|∣MJ​∣ components which have been resolved for G1Pig(v=12,J=3,f)G^{1}\\Pi_{g}(v=12, J=3,f)G1Pig​(v=12,J=3,f). We find that the AT splittingis linearly proportional to ∣MJ∣|M_{J}|∣MJ​∣, which allows the excitation of molecules with a selected ∣MJ∣|M_{J}|∣MJ​∣ level. The AC Stark shift of the OODR line is observed when the coupling laser is detuned from the resonance transition.
In recent years, quantum optics has been expanded from atomic to molecular systems despite much weaker oscillator strengths and complex relaxation pathways that have presented serious challenges in the past. The richness of molecular excitation pathways and the variety of molecular interactions has made it possible to develop novel applications in this field. We have demonstrated how the Autler–Townes effect can be used to control molecular angular momentum alignment and how the Autler–Townes split line shape, combined with accurate control-laser electric field amplitude measurement, can be used to map the absolute magnitude of the molecular internuclear distance dependent electronic transition dipole moment function. In addition, the electric field amplitude in the control laser Rabi frequency can be used as a ‘tuning’ mechanism for the mixing coefficients of energy levels that are weakly perturbed by the spin–orbit interaction, i.e. to control the valence electron spin polarization and the spin multipli...
Control of molecular angular momentum orientation enables state-resolved studies of molecular interactions and provides a basis for quantum information processing. Here we propose all-optical Autler-Townes state-selective adiabatic passage (ASAP) to prepare molecules in a single ∣J,M⟩|J,M\rangle∣J,M⟩ sublevel. An Autler-Townes branch created by a strong coupling field is selectively populated and adiabatically mapped onto the target vibrational state. We resolve detuning-dependent rovibrational Autler-Townes splitting in 13^{13}13CO2_22​, establishing the spectroscopic basis for the selective excitation of the target dressed branch. The density-matrix model calibrated by these spectra predicts transfer approaching 90\%. The scheme can exploit millisecond vibrational radiative lifetimes within the electronic ground state and extend to polar and nonpolar molecules with infrared-active vibrational modes.
We have demonstrated quantum control of the spin-orbit interaction based on the Autler-Townes (ac-Stark) effect in a molecular system using a cw optical field. We show that the enhancement of the spin-orbit interaction between a pair of weakly interacting singlet-triplet rovibrational levels, G (1)Π(g)(v=12,J=21,f)-1 (3)Σ(g)(-)(v=1,N=21,f), separated by 750 MHz in the lithium dimer, depends on the Rabi frequency (laser power) of the control laser. The increase in the spin-orbit interaction due to the control field is observed as a change in the spin character of the individual components of the perturbed pair.