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Accueil > Équipes scientifiques > Dynamiques et Interactions : Rayonnement, Atomes, Molécules (DIRAM) > Cohérence et contrôle de la dynamique quantique > Offres de stages, thèses et post-docs > Quantum control of molecular processes : Towards quantum technologies in Chemistry (Theory)

Stage Niveau M2

Quantum control of molecular processes : Towards quantum technologies in Chemistry (Theory)

M2

par Martrenchard-Barra Séverine - 15 décembre 2021 (modifié le 16 décembre 2021)

Possibility to be followed by a PhD

Nota Bene : this thesis is particularly suitable for a student passionate about the in-depth understanding of quantum phenomena and their concrete applications.

Introduction

Our ability to manipulate quantum effects in customized systems and materials is now paving the way for a second quantum revolution, which takes quantum theory to its technological consequences. It should lead to devices with far superior performance and capabilities : for instance quantum computers that exploit the superposition principle of quantum mechanics and thus quantum coherence. In this context, a systematic use of quantum effects in molecular systems could have an enormous future potential since molecules are the building blocks of every-day life [1]. There is indeed growing evidence that a significant number of chemical reactions are impacted by strong quantum-mechanical effects involving both the electrons and the nuclei [2,3]. The advent of femtochemistry allows scientists to follow in real time the motion of nuclei in molecular processes. Tremendous progress has also been achieved experimentally with the possibility to produce even shorter laser pulses, at the attosecond (10-18 s) time scale. It thus becomes possible to follow and guide the motion of electrons and, in particular, to image the transfer of one electron from one molecular orbital to another. Attosecond pulses generate electronic wavepackets that could induce, in a second step, a specific motion of the nuclei leading to the field of “ attochemistry” where it will be possible to control all the most elementary aspects of a chemical act at a quantum mechanical level.

All the simulations will be performed with the Heidelberg Multi-Configuration Time-Dependent Hartree (MCTDH) package [4-7]. MCTDH can be seen as an algorithm to solve the time-dependent Schrödinger equation (i.e. to propagate wave packets) for multidimensional dynamical systems consisting of distinguishable particles. The MCTDH package is probably the most general software for time-dependent quantum simulations. The supervisors are contributors of the package and have a long-standing and continuous collaboration with the group of Heidelberg.

(i) Quantum control with lasers of non-adiabatic processes

The first goal of the internship will be the study and the control of the quantum mechanical behavior of molecular systems, with special emphasis put on the processes where both electrons and nuclei are strongly coupled through a so-called “conical intersection”. In particular, in collaboration with experimentalists (Lou Barreau and Lionel Poisson, ISMO), we will consider the case of the photo- dissociation of NO2 around 400 nm (Figure 1) for which many important experimental results are available [8] but unexplained.


Figure 1 After excitation of UV light, NO2 dissociates through a conical intersection (Ref. [8]).

Photons in the ultraviolet-visible region can promote molecules to highly excited electronic states. If no photodissociation occurs, an excited molecule can release its excess energy and return to the electronic ground state through spontaneous light emission : fluorescence from a singlet state or phosphorescence from a triplet state if the ground state is a singlet. However, in many cases, light emission is quenched by a much faster radiationless process that is due to the presence of non- adiabatic couplings between electronic states. In polyatomic molecules, non-Born-Oppenheimer processes occur mainly around topographical features known as conical intersections. A conical intersection induces strong couplings between electrons and nuclei. It acts as a funnel through which a new chemical reaction can occur and enables rapid conversion of the excess electronic energy into nuclear motion. Since conical intersections lead to very fast and efficient transfers, it is suspected that they have been selected by evolution in important biological processes such as vision and photosynthesis : understanding the corresponding quantum effects could lead to much more efficient solar cells for photovoltaic systems. The goal of the internship will be to understand for the first time in detail the quantum behavior around 400 nm for which new experiments will be performed by Lionel Poisson and Lou Barreau, members of the same team at ISMO. The goal of the student will be to analyze the existing and planned experiments and to devise strategies of control of the process by exploiting quantum interferences.

Very recently, new potential energy surfaces by our colleague Richard Dawes (Missouri, USA) have been produced that allow one to reproduce with an excellent agreement the photoabsorption spectrum of NO2 between 300 and 600 nm. We will use these potential energy surfaces for the simulations.


(ii) Coherent excitation of molecules on surfaces for quantum computing

Another aspect of the work will be the creation of quantum superposition of vibrational states for quantum computing. The possibilities offered through quantum computation have been well known for many years now [9,10]. A quantum computer is a computation device that makes direct use of quantum-mechanical phenomena, mainly the fact that the system can be in a coherent superposition of different eigenstates due to the superposition principle. In quantum computers, the unit of information is a “qubit” that is a coherent superposition of two quantum sates denoted 0 and 1. The main challenges in quantum computing is controlling quantum decoherence since the latter destroys the properties that are exploited in quantum computing. In addition to the superposition principle, quantum computers could exploit other quantum properties such as entanglement (for quantum teleportation, i.e., to transmit quantum information from one location to another) or wave function collapse (for cryptography [11]). In the context of molecular quantum dynamics, it has been proposed that vibrational states of molecules could be used for quantum computation processes [12]. Vibrationally excited molecules in the gas phase could be possible candidates to encode qubits since decoherence could be controlled more easily [12]. As aforementioned, the key issue in molecular quantum dynamics is the creation of a coherent superposition of quantum states and its conservation over time since quantum decoherence can occur very fast upon interaction with the environment.


Figure 2 Co on a Copper cell : a laser pulse will create a coherent superposition of states, the interaction with the surface leads to decoherence.

Recently, potential and dipole moment surfaces for CO on a surface of Copper have been developed by our colleagues R. Marquardt (Strasbourg) and J.-C. Tremblay (Metz) : see Figure 2. The student will use them and include explicitly the quantum decoherence in the simulations by means of a “Lindblad operator”. The goal of the internship will be to devise laser pulses to create efficiently a quantum superposition of vibrational states of the molecule of CO, special emphasis will be placed on the description of the molecule “dressed by the photons” (adiabatic Floquet theory) in order to choose the parameters of the exciting pulse and on the observation of the process of decoherence in order to minimize it.

Collaborations :

Experimentalists :

-  L. Barreau and L. Poisson, ISMO, Paris-Saclay.

Theoreticians :

-  H.-D. Meyer and O. Vendrell, group of theoretical chemistry, University of Heidelberg, Germany.
-  Richard Dawes, theoretical and computational chemistry, in Missouri university of science and technology, USA.
-  Roberto Marquardt, Laboratory of Quantum Chemistry, University of Strasbourg.
-  Jean-Christophe Tremblay, Laboratory of theoretical physics and chemistry, University of Lorraine.
-  Osman Atabek, ISMO, Paris-Saclay.

Contact :

Fabien Gatti, directeur de recherche au CNRS. Email : fabien.gatti@universite-paris-saclay.fr, Institut des Sciences Moléculaires d’Orsay,
Bâtiment 520, Université Paris-Saclay, 3ème étage, bureau 3.28. Tel : 01 6915 8283.
References :

[1] F. Gatti, Nature, « News and Views », 557 (2018) 641.

[2] “Applications of Quantum Dynamics to Chemistry”, F. Gatti, B. Lasorne, H.-D. Meyer and A. Nauts, Springer (2017) Heidelberg.

[3] “Molecular Quantum Dynamics”, Editor : F. Gatti, Springer (2014) Heidelberg.

[4] H.-D. Meyer, U. Manthe, and L.S. Cederbaum, Chem .Phys. Lett. 165 (1990) 73.

[5] U. Manthe, H.-D. Meyer, and L.S. Cederbaum, J. Chem. Phys. 97 (1992) 3199.

[6] M. H. Beck, A. Jäckle, G. A. Worth and H.-D. Meyer, Physics Reports 324 (2000) 1.

[7] H.-D. Meyer, F. Gatti, and G. A. Worth, Multidimensional Quantum Dynamics : MCTDH Theory and Applications 2009 Wiley-VCH.

[8] H. J. Wörmer et al., Science, 334 (2011) 208.

[9] R. P. Feynman, “Simulating physics with computers”, Int. J. Theo. Phys. 467 (1982) 258.

[10] D. Deutsch (1985) “Quantum theory, the church-Turing principle and the universal quantum computer”, Proc. Nat. Acad. Sci. USA, 400:97

[11] S. Barz , E. Kashefi , A. Broadbent, J.-F. Fitzsimons, A. Zeilinger, P. Walther (2012) “Demonstration of blind quantum computing”, Science, 335:303.

[12] C. M. Tesch, R. de Vivie-Riedle R (2002) “Quantum computation with vibrationally excited molecules”, Phys. Rev. Lett., 89:57901 261.

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master2 : theory quantum technologies chemistry - 205.3 kio