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Journal of Modern Optics

Optical control of molecular switches

Ioannis Thanopulos, Petr Král, M. Shapiro, Emmanuel Paspalakis

Published Dec 17, 2008• 15 citations
Publisher

Abstract

We review recent applications of quantum control on molecular switches by optical means. We discuss diverse examples, as detection and automatic switching between nucleotide base-pairs and their undesired mutants, controlled operation of multi-configurational molecular devices for quantum information storage, and switching between the two enantiomeric forms of a chiral molecule. The variety of examples discussed demonstrates the wide range of applicability and the power of optical quantum control techniques in the fast emerging field of molecular devices.

DOI
10.1080/09500340802326815

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We review recent applications of quantum control on molecular switches by optical means. We discuss diverse examples, as detection and automatic switching between nucleotide base-pairs and their undesired mutants, controlled operation of multi-configurational molecular devices for quantum information storage, and switching between the two enantiomeric forms of a chiral molecule. The variety of examples discussed demonstrates the wide range of applicability and the power of optical quantum control techniques in the fast emerging field of molecular devices.
We review the principles and some recent advances in the theory of coherent control of molecular processes and discuss some of its experimental realizations. Amongst the topics discussed are: bichromatic and pump-dump control; the interference between N-photons and M-photon processes; the optical conversion of a mixture of left- and right-handed chiral molecules into an ensemble containing molecules of the handedness of choice; control of collisional processes; control over chaotic dynamics; effects of decoherence; the solution of the non-degenerate quantum control problem; and control over spontaneous emission and other decay processes.
Controlling the internal quantum states of chiral molecules for a selected enantiomer has a wide range of fundamental applications. Using tailored microwave fields, a chosen rotational state can be enriched for a selected enantiomer, even starting from a racemic mixture. This enables rapid switching between samples of different enantiomers in a given state, holding great promise, for instance, for measuring parity violation in chiral molecules. Achieving full enantiomer-specific state transfer is a key requirement for this and many other applications. Although theoretically feasible, achieving the required experimental conditions seemed unrealistic. Here, we realize near-ideal conditions, overcoming both the limitations of thermal population and spatial degeneracy in rotational states. Our results show that 96% state-specific enantiomeric purity can be obtained from a racemic mixture, in an approach that is universally applicable to all chiral molecules of C1 symmetry.
In a molecular system of energy donors and acceptors, resonance energy transfer is the primary mechanism by means of which electronic energy is redistributed between molecules, following the excitation of a donor. Given a suitable geometric configuration it is possible to completely inhibit this energy transfer in such a way that it can only be activated by application of an off-resonant laser beam: this is the principle of optically controlled resonance energy transfer, the basis for an all-optical switch. This paper begins with an investigation of optically controlled energy transfer between a single donor and acceptor molecule, identifying the symmetry and structural constraints and analyzing in detail the dependence on molecular energy level positioning. Spatially correlated donor and acceptor arrays with linear, square, and hexagonally structured arrangements are then assessed as potential configurations for all-optical switching. Built on quantum electrodynamical principles the concept of transfer fidelity, a parameter quantifying the efficiency of energy transportation, is introduced and defined. Results are explored by employing numerical simulations and graphical analysis. Finally, a discussion focuses on the advantages of such energy transfer based processes over all-optical switching of other proposed forms.
Laser control of molecular rotation is an area of active research. A number of recent studies has aimed at expanding the reach of rotational control to extreme, previously inaccessible rotational states, as well as controlling the directionality of molecular rotation. Dense ensembles of molecules undergoing ultrafast uni-directional rotation, known as molecular superrotors, are anticipated to exhibit unique properties, from spatially anisotropic diffusion and vortex formation to the creation of powerful acoustic waves and tuneable THz radiation. Here we describe our recent progress in controlling molecular rotation in the regime of high rotational excitation. We review two experimental techniques of producing uni-directional rotational wave packets with a "chiral train" of femtosecond pulses and an "optical centrifuge". Three complementary detection methods, enabling the direct observation, characterization and control of the superrotor states, are outlined: the one based on coherent Raman scattering, and two other methods employing both resonant and non-resonant multi-photon ionization. The capabilities of the described excitation and detection techniques are demonstrated with a few examples. The paper is concluded with an outlook for future developments.
We propose a scheme for molecule-based information processing by combining well-studied spectroscopic techniques and recent results from chemical dynamics. Specifically it is discussed how optical transitions in single molecules can be used to rapidly perform classical (Boolean) logical operations. In the proposed way, a restricted number of states in a single molecule can act as a logical gate equivalent to at least two switches. It is argued that the four-level scheme can also be used to produce gain, because it allows an inversion, and not only a switching ability. The proposed scheme is quantum mechanical in that it takes advantage of the discrete nature of the energy levels but, we here discuss the temporal evolution, with the use of the populations only. On a longer time range we suggest that the same scheme could be extended to perform quantum logic, and a tentative suggestion, based on an available experiment, is discussed. We believe that the pumping can provide a partial proof of principle, although this and similar experiments were not interpreted thus far in our terms.