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Physical Review A

Selective photochemistry via adiabatic passage: An extension of stimulated Raman adiabatic passage for degenerate final states

Mark N. Kobrak, Stuart A. Rice

Published Apr 1, 1998• 85 citations
Publisher

Abstract

In this paper we extend the existing theory of stimulated Raman adiabatic passage (StiRAP) in three-level systems to examine the nature of selective photoexcitation using counterintuitively ordered pulses. Our goal is to develop a version of StiRAP that permits control of product selectivity in a chemical reaction. We analyze the case of selective excitation to one state in a pair of degenerate target states in a four-level system, and find that one cannot control the ratio of the populations in the two states in a resonant two-photon process. However, the extension of the system to include a fifth state and a third laser field makes selective excitation to one of the degenerate states possible. It is found that, subject to reasonable restrictions, one may accomplish complete population transfer to a single target state of a degenerate pair of states in a five-level system.

DOI
10.1103/physreva.57.2885

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In this paper we extend the existing theory of stimulated Raman adiabatic passage (StiRAP) in three-level systems to examine the nature of selective photoexcitation using counterintuitively ordered pulses. Our goal is to develop a version of StiRAP that permits control of product selectivity in a chemical reaction. We analyze the case of selective excitation to one state in a pair of degenerate target states in a four-level system, and find that one cannot control the ratio of the populations in the two states in a resonant two-photon process. However, the extension of the system to include a fifth state and a third laser field makes selective excitation to one of the degenerate states possible. It is found that, subject to reasonable restrictions, one may accomplish complete population transfer to a single target state of a degenerate pair of states in a five-level system.
Two-pulse selective photochemistry that exploits population transfer via adiabatic passage is considered for the case that there are degenerate product states with different lifetimes. As an example, a four-level model system with a complex symmetric Hamiltonian is constructed. Analytical and numerical studies of this model system demonstrate that extensive control over the product branching ratio can be achieved by detuning either the pump pulse or the Stokes pulse while maintaining negligible population in the intermediate state. This control approach represents a significant simplification of both the Kobrak-Rice extended stimulated Raman adiabatic passage scheme and the Chen-Shapiro-Brumer strong-field control scheme.
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.
We describe the exploitation of adiabatic transfer of population between selected states of a molecule as a means for the control of product selectivity in a branching unimolecular reaction. The particular procedures employed to achieve that adiabatic transfer of population depend on the character of the spectrum of states of the molecule; the ones we consider are either extensions of, or are illuminated by, the STIRAP method. The results of studies of efficient selective population of one of a pair of nearly degenerate states in the thiophosgene molecule, and of efficient promotion of the HCN → CNH isomerization reaction, are reported. In the former case the adiabatic population transfer is achieved by use of the Kobrak-Rice extended STIRAP method, while in the latter case it is achieved by use of consecutive STIRAP processes. In both cases the efficiency of selective population transfer is shown to be insensitive to radiative
A five-level four-pulse phase-sensitive extended stimulated Raman adiabatic passage scheme is proposed to realize complete control of the population transfer branching ratio between two degenerate target states. The control is achieved via a three-node null eigenstate that can be correlated with an arbitrary superposition of the target states. Our results suggest that complete suppression of the yield of one of two degenerate product states, and therefore absolute selectivity in photochemistry, is achievable and predictable, even without studying the properties of the unwanted product state beforehand.
A five-level four-pulse phase-sensitive extended stimulated Raman adiabatic passage scheme is proposed to realize complete control of the population transfer branching ratio between two degenerate target states. The control is achieved via a three-node null eigenstate that can be correlated with an arbitrary superposition of the target states. Our results suggest that complete suppression of the yield of one of two degenerate product states, and therefore absolute selectivity in photochemistry, is achievable and predictable, even without studying the properties of the unwanted product state beforehand.
We study the dynamics of chirped adiabatic passage (CHIRAP) with temporally delayed pulses to selectively and fully transfer population in atoms and molecules. We show that the transfer of population via stimulated Raman adiabatic passage (STIRAP) and stimulated two-photon adiabatic absorption with temporally delayed laser pulses is not adversely affected by applying a chirp to the pulses, provided the intensity of the laser is sufficiently large to allow adiabatic passage. We then proceed to consider systems in which a near degeneracy of terminal state levels results in nonselective population of the terminal levels using nonchirped STIRAP or two-photon absorption stimulated passage, because the dynamics within the nearly degenerate pair of levels is not adiabatic. However, the CHIRAP process selectively populates only one of the terminal levels.