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Advances in Physical Chemistry

Stimulated Raman Adiabatic Passage in a Dense Medium

Boris D. Fainberg, B. N. Levinsky

Published Dec 22, 2010• 6 citations
Publisher

Abstract

We have considered a coherent population transfer to a higher excited singlet state ( S2 ) of molecules with anomalous fluorescence in molecular assemblies (e.g., a dense medium). A direct excitation to S2 requires light in the UV region. Because of this, the transition is conveniently realized by a two-step (two-photon) process: S0→S1→S2 , where transitions S0→S1 and S1→S2 correspond to the optical region. We have shown that efficient stimulated Raman adiabatic passage (STIRAP) in the ladder configuration can be realized in this case, using suitably chirped pulses, to compensate a change of the two-photon transition frequency in time, induced by the pulses themselves, due to near dipole-dipole interactions. We have provided a reduced state formulation of the optical control process. Chirping the “pump” pulse that excites transition S0→S1 is nonequivalent to chirping the “Stokes” pulse that excites transition S1→S2 , with respect to the population of the intermediate state ( S1 ) in the pulse nonadiabatic regime. We have also shown that with suitably chirped pulses, efficient STIRAP still persists even for a rather large decay of the intermediate state.

DOI
10.1155/2010/798419

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We have considered a coherent population transfer to a higher excited singlet state ( S2 ) of molecules with anomalous fluorescence in molecular assemblies (e.g., a dense medium). A direct excitation to S2 requires light in the UV region. Because of this, the transition is conveniently realized by a two-step (two-photon) process: S0→S1→S2 , where transitions S0→S1 and S1→S2 correspond to the optical region. We have shown that efficient stimulated Raman adiabatic passage (STIRAP) in the ladder configuration can be realized in this case, using suitably chirped pulses, to compensate a change of the two-photon transition frequency in time, induced by the pulses themselves, due to near dipole-dipole interactions. We have provided a reduced state formulation of the optical control process. Chirping the “pump” pulse that excites transition S0→S1 is nonequivalent to chirping the “Stokes” pulse that excites transition S1→S2 , with respect to the population of the intermediate state ( S1 ) in the pulse nonadiabatic regime. We have also shown that with suitably chirped pulses, efficient STIRAP still persists even for a rather large decay of the intermediate state.
Four-photon stimulated Raman adiabatic passage--like (STIRAP-like) processes in the frame of the D1{D}_{1}D1​ optical transition line of atomic 39K^{39}\mathrm{K}39K are investigated theoretically by means of a rigorous model that takes into account all the atomic states involved in the interaction with the pump and Stokes light fields and is valid for any field intensities. The same sequential up-down-up-down transition involving two pump (up) and two Stokes (down) photons, going from the initial ground state $|F=2,M=+2\ensuremath{\rangle}$ to the final ground state $|F=1,M=0\ensuremath{\rangle}$, which was proven in the past to be very convenient for two-photon amplification and lasing, is considered here. The fact that two atomic states, one with F=1F=1F=1 and another with F=2F=2F=2, participate at each intermediate step of the multiphoton process makes the existence of an ideal unique adiabatic transfer state impossible, and at exact four-photon resonance the population-transfer efficiency to the final atomic state is low (below 60% in general, 80% in the best conditions). Nevertheless, it is shown that by choosing appropriate static detunings for the pump and Stokes fields with respect to the atomic transitions the system follows, sequentially, two adiabatic states, connected by an efficient diabatic passage, so that population-transfer efficiency asymptotically approaching 100% for increasing field amplitudes can be reached. These results are quite robust and suggest the possibility of using STIRAP (or STIRAP-like) pumping to, among other applications, increase the (presently very low) efficiency of two-photon amplification and lasing, a so far unfulfilled goal in quantum and nonlinear optics.
The rovibrational dynamics of an extended ladder stimulated Raman adiabatic passage (STIRAP) system through permanent dipole moment transitions is investigated theoretically using the time-dependent quantum-wave-packet method for the ground electronic state of the HF molecule. The calculated results show that nearly 100% of the population can be transferred to the target state through (1+2), (1+3), and (2+2) STIRAP schemes. By choosing a suitable excitation pathway, the effects of the background states on the final population of the target state can be removed. For the multiphoton STIRAP process, the one-photon overtone pump scheme is more efficient than the two-photon pump scheme in controlling the population transfer to the target state.
The population transfer of stimulated Raman adiabatic passage (STIRAP) is investigated using a time-dependent quantum wave packet method. The population is transferred from an initial state to a target state through the interaction of the external laser field with the permanent dipole moment and the transition dipole moment. The laser field is composed of an infrared pulse and a near ultraviolet pulse. The two pulses with small detunings are more efficient to achieve the STIRAP transition. The process of STIRAP is sensitive to the detunings of the two pulses. When the two detunings are the same in a Λ transition or the positive detuning of the pump pulse is equal to the negative detuning of the Stokes pulse in a ladder transition, the final population in the intermediate state can be eliminated and the target population is increased.
Abstract The population transfer of a NaH molecule from the ground state X 1 Σ + to the target state A 1 Σ + via stimulated Raman adiabatic passage (STIRAP) is investigated. The results show that the intensity, delay time and detuning have a significant effect on population transfer. A large population transfer is observed with increased pump and Stokes intensity, especially when the pump and Stokes intensity match. Population transfer also depends on the delay time between the pump laser pulse and the Stokes laser pulse. The detuning of the two pulses influences the population transfer. Efficient population transfer can be realized under the resonant or two-photon resonant condition.
The technique of stimulated Raman adiabatic passage (STIRAP) is a highly efficient tool for coherent population transfer in a chainwise-connected three-state quantum system. It is widely accepted that the two-photon resonance between the two end states of the chain is a crucial condition for STIRAP. This assumption is indeed correct when the two driving fields, pump and Stokes, produce nearly equal couplings for their respective transitions. We show analytically, supported by numeric examples, that when the pump and Stokes couplings differ significantly, the two-photon population transfer profile is distorted and its center is shifted away from the two-photon resonance; hence, the optimal operation of STIRAP demands a two-photon detuning. We derive simple analytic estimates for the center and the width of the two-photon profile. The results are of potential importance in situations when the pump and Stokes fields are of different physical natures (e.g., laser and cavity fields) or when two-photon resonance is unwanted (e.g., in the presence of residual light).
We have developed a new type of stimulated Raman adiabatic passage (STIRAP) that is applicable to a degenerated reaction system. The direction of the photon polarization vector is the adiabatic parameter in the STIRAP. The molecular handedness of H2POSH, a preoriented phosphinotioic acid that has two stable configurations, L and R enantiomers, is used as a model system. The control of molecular handedness in both pure and mixed state cases are considered. In the case of a pure state, a STIRAP with a linearly polarized single laser allows an almost complete transfer from an L (R) enantiomer to the other by adiabatically changing its polarization direction. The adiabatic criterion for changing the polarization direction is clarified. In the case of a mixed state, a STIRAP with two linearly polarized laser pulses allows a selective preparation of pure enantiomers from its racemic mixture. In the low temperature limit, a five-level model reduces a three-level model by setting the direction of the polarization of the pump and Stokes pulses in such a way that only the forward transfer is allowed, while the reverse is forbidden. Furthermore, in the case of mixed state, relaxation effects originating from vibrational mode couplings are taken into account, and the influence of the population decay from intermediate states on the STIRAP is compared with that by a π-pulse approach.