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Physical Review A

Multilevel adiabatic population transfer

BERNARD SHORE, Klaas Bergmann, J. Oreg, Salman Rosenwaks

Published Dec 1, 1991• 167 citations
Publisher

Abstract

We present a theoretical description of a scheme in which coordinated laser pulses transfer population efficiently from any initially populated state (e.g., the ground state) to a multiply excited state of an atom or molecule without producing appreciable population in intermediate states. Our analytic results for multilevel excitation transfer provide a simple yet instructive extension to the counterintuitive pulse sequence studied previously for a three-state system.

DOI
10.1103/physreva.44.7442

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We present a theoretical description of a scheme in which coordinated laser pulses transfer population efficiently from any initially populated state (e.g., the ground state) to a multiply excited state of an atom or molecule without producing appreciable population in intermediate states. Our analytic results for multilevel excitation transfer provide a simple yet instructive extension to the counterintuitive pulse sequence studied previously for a three-state system.
We present explicit analytic expressions for adiabatic dressed states which, in suitable limits, produce complete population transfer between initial and final states of a four-state excitation chain without ever placing appreciable population into intermediate states. The population-transfer scheme is a generalization of the three-state stimulated Raman adiabatic passage that makes use of counterintuitive pulse sequences. We demonstrate analytically and numerically that the four-state system differs in a very significant qualitative way from previously studied N-state systems with odd N. In particular, we find that the presence of modest detuning from single-photon resonance is critical to the success of population transfer.
We present detailed experimental and theoretical results on population transfer with frequency-swept picosecond laser pulses. Here, we demonstrate that intense frequency-swept pulses, when applied in the adiabatic limit, lead to both more efficient and more selective excitation than do unmodulated laser pulses. The experimental work is performed on quasi-two-level systems (pentacene/p-terphenyl crystal and Na vapor), quasi-three-level systems (Na vapor), and on more complex multilevel systems (I2 vapor). We discuss the different characteristics of adiabatic population transfer in both few-level, and multilevel cases, and, in particular, present computer calculations to explore the effects of molecular rotations in multilevel adiabatic population transfer.
Enhanced population transfer from the lowest to the highest level in the three-state ladder 5s\ensuremath{\rightarrow}5p\ensuremath{\rightarrow}5d of the rubidium atom by frequency-swept ultrashort laser pulses is observed if the frequency sweep first makes the pulse resonant with the 5s\ensuremath{\rightarrow}5p transition, and later with the 5p\ensuremath{\rightarrow}5d transition. With this ``intuitive'' scheme it is possible to achive complete population inversion via the intermediate level by two successive adiabatic passages. Complete inversion is also obtained by a ``counterintuitive'' direction of the frequency sweep, in which case population of the intermediate level during the pulse is strongly reduced.
Highly efficient and selective population transfer in NO molecules in the electronic ground state (X2{\mathit{X}}^{2}X2${\mathrm{\ensuremath{\Pi}}}_{1/2}$) from the vibrational level v''=0 to the level v''=6 is demonstrated. It shows, for the first time with pulsed lasers, that a rather generally applicable scheme for complete control over the level population in atoms and molecules is now available. The efficiency relies on a counterintuitive interaction sequence of two lasers with the molecule in a process of stimulated Raman scattering involving adiabatic passage.
This paper analyzes the extension of the three-state process of stimulated Raman adiabatic passage to chainwise-connected multistate systems. A necessary condition for such a process is the existence of an adiabatic-transfer state, which connects adiabatically the initial state of the chain to its final state. Various counterintuitive pulse sequences are examined, in all of which the pulse that drives the last transition of the chain precedes the pulse driving the first transition, while the pulses driving the intermediate transitions may have different timings. The paper demonstrates some important qualitative differences and similarities between the systems with odd and even number of states. In the on-resonance case, an adiabatic-transfer state always exists for an odd number of states while it never exists for an even number of states. In the off-resonance case, however, the two types of systems behave in a very similar manner and the condition for existence of an adiabatic-transfer state is essentially the same. This condition, which imposes certain limitations on the laser parameters, is derived in a simple and compact form. It is also shown analytically that, besides by large detunings, the populations of the intermediate states (which are generally nonzero during the transfer) can be damped by large intermediate couplings. It is concluded that for an odd number of states, the optimal case is the on-resonance one, with equal and large intermediate couplings. For an even number of states, the optimal (off-resonance) case is when the intermediate couplings and the detunings have similar values. Various numerical examples of success and failure of multistate population transfer confirm the analytic conclusions.