Electronic quantum coherence in glycine molecules probed with ultrashort x-ray pulses in real time

Author:

Schwickert David1ORCID,Ruberti Marco2ORCID,Kolorenč Přemysl3ORCID,Usenko Sergey14ORCID,Przystawik Andreas1ORCID,Baev Karolin14ORCID,Baev Ivan4ORCID,Braune Markus1ORCID,Bocklage Lars15ORCID,Czwalinna Marie Kristin1ORCID,Deinert Sascha1,Düsterer Stefan1ORCID,Hans Andreas6ORCID,Hartmann Gregor6,Haunhorst Christian78,Kuhlmann Marion1,Palutke Steffen1ORCID,Röhlsberger Ralf18910ORCID,Rönsch-Schulenburg Juliane1,Schmidt Philipp6ORCID,Toleikis Sven1,Viefhaus Jens11ORCID,Martins Michael4ORCID,Knie André6,Kip Detlef7ORCID,Averbukh Vitali2ORCID,Marangos Jon P.2ORCID,Laarmann Tim15ORCID

Affiliation:

1. Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607 Hamburg, Germany.

2. Department of Physics, Imperial College London, Prince Consort Road, London SW7 2AZ, UK.

3. Faculty of Mathematics and Physics, Charles University, V Holesovickach 2, 180 00 Praha 8, Czech Republic.

4. Department of Physics, University of Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.

5. The Hamburg Centre for Ultrafast Imaging CUI, Luruper Chaussee 149, 22761 Hamburg, Germany.

6. Institute of Physics, University of Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany.

7. Faculty of Electrical Engineering, Helmut Schmidt University, Holstenhofweg 85, 22043 Hamburg, Germany.

8. Helmholtz Institute Jena, Fröbelstieg 3, 07743 Jena, Germany.

9. Helmholtz Centre for Heavy Ion Research (GSI), Planckstr. 1, 64291 Darmstadt, Germany.

10. Friedrich-Schiller-Universität Jena, Max-Wien-Platz 1, 07743 Jena, Germany.

11. Helmholtz-Zentrum Berlin für Materialien und Energie, Albert-Einstein-Straße 15, 12489 Berlin, Germany.

Abstract

Here, we use x-rays to create and probe quantum coherence in the photoionized amino acid glycine. The outgoing photoelectron leaves behind the cation in a coherent superposition of quantum mechanical eigenstates. Delayed x-ray pulses track the induced coherence through resonant x-ray absorption that induces Auger decay and by photoelectron emission from sequential double photoionization. Sinusoidal temporal modulation of the detected signal at early times (0 to 25 fs) is observed in both measurements. Advanced ab initio many-electron simulations allow us to explain the first 25 fs of the detected coherent quantum evolution in terms of the electronic coherence. In the kinematically complete x-ray absorption measurement, we monitor its dynamics for a period of 175 fs and observe an evolving modulation that may implicate the coupling of electronic to vibronic coherence at longer time scales. Our experiment provides a direct support for the existence of long-lived electronic coherence in photoionized biomolecules.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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