Unitary Control in Quantum Ensembles: Maximizing Signal Intensity in Coherent Spectroscopy

Author:

Glaser S. J.12345,Schulte-Herbrüggen T.12345,Sieveking M.12345,Schedletzky O.12345,Nielsen N. C.12345,Sørensen O. W.12345,Griesinger C.12345

Affiliation:

1. S. J. Glaser, O. Schedletzky, C. Griesinger, Institut für Organische Chemie, J. W. Goethe-Universität, Marie-Curie-Strasse 11, D-60439 Frankfurt, Germany.

2. T. Schulte-Herbrüggen, Laboratorium für Physikalische Chemie, ETH Zentrum, CH-8092 Zürich, Switzerland.

3. M. Sieveking, Institut für Angewandte Mathematik, J. W. Goethe-Universität, Robert-Mayer-Strasse 6-10, D-60439 Frankfurt, Germany.

4. N. C. Nielsen, Instrument Center for Solid-State NMR Spectroscopy, Department of Chemistry, University of Aarhus, Langelandsgade 140, DK-8000 Aarhus C, Denmark.

5. O. W. Sørensen, Department of Chemistry, Carlsberg Laboratory, Gamle Carlsberg Vej 10, DK-2500 Valby, Denmark.

Abstract

Experiments in coherent magnetic resonance, microwave, and optical spectroscopy control quantum-mechanical ensembles by guiding them from initial states toward target states by unitary transformation. Often, the coherences detected as signals are represented by a non-Hermitian operator. Hence, spectroscopic experiments, such as those used in nuclear magnetic resonance, correspond to unitary transformations between operators that in general are not Hermitian. A gradient-based systematic procedure for optimizing these transformations is described that finds the largest projection of a transformed initial operator onto the target operator and, thus, the maximum spectroscopic signal. This method can also be used in applied mathematics and control theory.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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