Andreas Buchleitner

Continuously parametrized quantum simulation of molecular electron transfer reactions

Frank Schlawin [1,2], Manuel Gessner [3,2], Andreas Buchleitner [2,4,5,6], Tobias Schaetz, Spiros S Skourtis

Abstract

A comprehensive description of molecular electron transfer reactions is essential for our understanding of fundamental phenomena in bio-energetics and molecular electronics. Experimental studies of molecular systems in condensed-phase environments, however, face difficulties to independently control the parameters that govern the transfer mechanism with high precision. We show that trapped-ion experiments instead allow to reproduce and continuously connect vastly different regimes of molecular charge transfer through precise tuning of, e.g., phonon temperature, electron-phonon interactions, and electronic couplings. Such a setting allows not only to reproduce widely-used transport models, such as Marcus theory. It also provides access to transfer regimes that are unattainable for molecular experiments, while controlling and measuring the relevant observables on the level of individual quanta. Our numerical simulations predict an unconventional quantum transfer regime, featuring a transition from quantum adiabatic- to resonance-assisted transfer as a function of the donor-acceptor energy gap, that can be reached by increasing the electronic coupling at low temperatures. Trapped ion-based quantum simulations thus promise to enhance our microscopic understanding of molecular electron transfer processes, and may help to reveal efficient design principles for synthetic devices.

Local probe of single phonon dynamics in warm ion crystals

Ahmed Abdelrahman, Omid Khosravani, Manuel Gessner, Heinz-Peter Breuer, Andreas Buchleitner, Dylan J. Gorman, Ryo Masuda, Thaned Pruttivarasin, Michael Ramm, Philipp Schindler, Hartmut Häffner

Abstract

The detailed characterization of non-trivial coherence properties of composite quantum systems of increasing size is an indispensable prerequisite for scalable quantum computation, as well as for understanding of nonequilibrium many-body physics. Here we show how autocorrelation functions in an interacting system of phonons as well as the quantum discord between distinct degrees of freedoms can be extracted from a small controllable part of the system. As a benchmark, we show this in chains of up to 42 trapped ions, by tracing a single phonon excitation through interferometric measurements of only a single ion in the chain. We observe the spreading and partial refocusing of the excitation in the chain, even on a background of thermal excitations. We further show how this local observable reflects the dynamical evolution of quantum discord between the electronic state and the vibrational degrees of freedom of the probe ion.

Probing Polariton Dynamics in Trapped Ions with Phase-Coherent Two-Dimensional Spectroscopy

Manuel Gessner [1], Frank Schlawin [1], Andreas Buchleitner [1,2]

Abstract

We devise a phase-coherent three-pulse protocol to probe the polariton dynamics in a trapped-ion quantum simulation. In contrast to conventional nonlinear signals, the presented scheme does not change the number of excitations in the system, allowing for the investigation of the dynamics within an $N$-excitation manifold. In the particular case of a filling factor one ($N$ excitations in an $N$-ion chain), the proposed interaction induces coherent transitions between a delocalized phonon superfluid and a localized atomic insulator phase. Numerical simulations of a two-ion chain demonstrate that the resulting two-dimensional spectra allow for the unambiguous identification of the distinct phases, and the two-dimensional lineshapes efficiently characterize the relevant decoherence mechanism.

Nonlinear Spectroscopy of Trapped Ions

Frank Schlawin [1,2], Manuel Gessner [1,3], Shaul Mukamel [2], Andreas Buchleitner [1]

Abstract

Nonlinear spectroscopy employs a series of laser pulses to interrogate dynamics in large interacting many-body systems, and has become a highly successful method for experiments in chemical physics. Current quantum optical experiments approach system sizes and levels of complexity which require the development of efficient techniques to assess spectral and dynamical features with scalable experimental overhead. However, established methods from optical spectroscopy of macroscopic ensembles cannot be applied straightforwardly to few-atom systems. Based on the ideas proposed in [M. Gessner et al. New J. Phys. 16 092001 (2014)], we develop a diagrammatic approach to construct nonlinear measurement protocols for controlled quantum systems and discuss experimental implementations with trapped ion technology in detail. These methods in combination with distinct features of ultra-cold matter systems allow us to monitor and analyze excitation dynamics in both the electronic and vibrational degrees of freedom. They are independent of system size, and can therefore reliably probe systems where, e.g., quantum state tomography becomes prohibitively expensive. We propose signals that can probe steady state currents, detect the influence of anharmonicities on phonon transport, and identify signatures of chaotic dynamics near a quantum phase transition in an Ising-type spin chain.

Observing a Quantum Phase Transition by Measuring a Single Spin

Manuel Gessner [1], Michael Ramm [2], Hartmut Haeffner, Andreas Buchleitner [1], Heinz-Peter Breuer [1]

Abstract

We show that the ground-state quantum correlations of an Ising model can be detected by monitoring the time evolution of a single spin alone, and that the critical point of a quantum phase transition is detected through a maximum of a suitably defined observable. A proposed implementation with trapped ions realizes an experimental probe of quantum phase transitions which is based on quantum correlations and scalable for large system sizes.