Wave packet Isotope Separation WIS - Wave Packet Isotope Separation

We have suggested a novel approach to laser isotope separation, which is based on short laser pulse excitation of quantum wave packets inside the individual molecules of an isotopic mixture. With the course of time, the excited wave packets of different isotopes start moving out of phase because of the isotope shift in the oscillation frequency. This can be used for a selective excitation of the (spatially separated) wave packets by a second laser pulse and extraction of the excited species. To prevent the quantum-mechanical spreading of the wave packets, we rely on the phenomenon of full and fractional revivals of the wave packets. The WIS method realizes a mechanical isotope separation machine at a single atom/molecule level. It combines the advantage of mechanical separation schemes (robustness and universality) with very the high single-stage enrichment typical of laser separation methods.

How to choose excitation parameters?

Wave packet Isotope Separation & Overlap

The principles of the WIS method were first demonstrated in collaboration with the group of A. Stolow at the Steasie Institute for Molecular Science (Ottawa) by an experiment on separation of a bromine isotopic mixture. The Stolow’s experiment presents, probably, the first successful application of quantum wave packets to a technologically important problem.

Recently, we have considerably advanced the approach by applying the powerful formalism of optimal control to the separation process. We identified a new separation mechanism that uses isotopically selective quantum interference between several wave packets excited in the same molecular potential by a specially designed train of pumping pulses.

Presently, we are studying a new class of separation schemes which are based on rotational wave packets. These schemes involve alignment of a molecular isotopic mixture followed by a long-time free evolution of the aligned rotational states. Small differences in the moment of inertia of the isotopes result in distinct transient angular distributions, which may be used for separation and enrichment. Rotational WIS has certain important advantages as it can be performed in the ground electronic state by non-resonant pulsed lasers. This approach becomes even more attractive because of the new method for enhanced molecular alignment developed by us in 2001-2003.

Rotational WIS based on Laser Molecular Alignment