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arXiv:2601.07549

Exciton coherence propagation measured with non-local four-wave mixing micro-spectroscopy

Mateusz Raczyński, Amadeusz Dydniański, Karolina Ewa Połczyńska, Gabriela Szwed, Adam Szczerba, Jin-Woo Jung, Gilles Nogues, W. Langbein, P. Kossacki, W. Pacuski, Jacek Kasprzak

Published Jan 12, 2026• 0 citations
arXivHTMLPDF

Abstract

Coherence transfer is a multi-disciplinary topic of interest, including chemistry, biology and physics. In quantum technologies, achieving non-local coherent coupling between solid-state qubits is of the utmost importance. Here, we demonstrate that excitons - i.e. electron-hole pairs bound by the Coulomb force within a quantum well - can act as a medium for mesoscopic optical coherence transfer in semiconductors. To this end, we use a femtosecond laser pulse to resonantly generate excitons within the light cone. These excitons can then either recombine radiatively or scatter out of the light cone, gaining an in-plane momentum in the process. In samples without disorder, such as the CdTe quantum wells used here, the resulting fast excitons can diffuse over mesoscopic distances before recombining radiatively. Using coherent nonlinear micro-spectroscopy, we carry out exciton time-of-flight measurements. Specifically, we monitor the spatio-temporal propagation of launched exciton wave packets, selectively observing their coherence or density on a scale of up to 10$\,μ$m. Our proof-of-principle experiment demonstrates that free excitons inherit a phase modulation from the optical pulsed excitation and can generate coherent links within excitonic circuits, offerring a higher level of miniaturisation and compactness than photonic or polaritonic architectures.

DOI
10.48550/arxiv.2601.07549

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Coherence transfer is a multi-disciplinary topic of interest, including chemistry, biology and physics. In quantum technologies, achieving non-local coherent coupling between solid-state qubits is of the utmost importance. Here, we demonstrate that excitons - i.e. electron-hole pairs bound by the Coulomb force within a quantum well - can act as a medium for mesoscopic optical coherence transfer in semiconductors. To this end, we use a femtosecond laser pulse to resonantly generate excitons within the light cone. These excitons can then either recombine radiatively or scatter out of the light cone, gaining an in-plane momentum in the process. In samples without disorder, such as the CdTe quantum wells used here, the resulting fast excitons can diffuse over mesoscopic distances before recombining radiatively. Using coherent nonlinear micro-spectroscopy, we carry out exciton time-of-flight measurements. Specifically, we monitor the spatio-temporal propagation of launched exciton wave packets, selectively observing their coherence or density on a scale of up to 10 μ\,μμm. Our proof-of-principle experiment demonstrates that free excitons inherit a phase modulation from the optical pulsed excitation and can generate coherent links within excitonic circuits, offerring a higher level of miniaturisation and compactness than photonic or polaritonic architectures.
Coherence transfer is a multi-disciplinary topic of interest, including chemistry, biology, and physics. In quantum technologies, achieving non-local coherent coupling between solid-state qubits is of the utmost importance. Here, we demonstrate that excitons—i.e., electron–hole pairs bound by the Coulomb force within a quantum well—can act as a medium for mesoscopic optical coherence transfer in semiconductors. To this end, we use a femtosecond laser pulse to resonantly generate excitons within the light cone. These excitons can then either recombine radiatively or scatter out of the light cone, gaining an in-plane momentum in the process. In samples without disorder, such as the CdTe quantum wells used here, the resulting fast excitons can diffuse over mesoscopic distances before recombining radiatively. Using coherent nonlinear micro-spectroscopy, we carry out exciton time-of-flight measurements. Specifically, we monitor the spatio-temporal propagation of launched exciton wave packets, selectively observing their coherence or density on a scale of up to 10 µm. Our proof-of-principle experiment demonstrates that free excitons inherit a phase modulation from the optical pulsed excitation and can generate coherent links within excitonic circuits, offering a higher level of miniaturisation and compactness than photonic or polaritonic architectures.
Summary form only given. The coherence decay of optically excited electronic systems provides one of the most powerful tools to investigate interaction processes of excited states. In semiconductors, the optical coherence phenomena are usually investigated by nonlinear techniques such as four wave mixing (FWM), photon echo, or reflectivity experiments. Exciton-phonon, exciton-exciton, or exciton-free carriers scattering processes have been explored in recent years with these techniques. As demonstrated recently, a direct measurement of the optical dephasing time can be obtained through the temporal coherent control of electronic excitations. In these experiments, the emission following the excitation by an ultrashort optical pulse sequence, is detected in a non-specular direction (secondary emission). This provides an alternative approach to FWM techniques, which allows us to analyse the scattering processes either with phonons or due to mutual collisions. Using the coherent control technique monitored through the secondary emission (SE), we report on the coherent dynamics of excitons in bare quantum wells (QW) and compare it to that of exciton-polaritons in microcavity (MC) embedded quantum wells.
Summary form only given. The optical properties of semiconductor quantum wells (QW) and, in particular, the coherent dynamics of excitons following resonant excitation with ultrafast laser pulses have attracted much attention in recent years. It is generally accepted that there is a transfer of coherence between the optical field and the QW that disappears in a characteristic time T/sub 2/ (picoseconds for GaAs) after the laser is turned off. However, the questions as to how the coherence is actually induced and that of the nature of the coherent state of the solid are poorly understood. In this work we address these points by re-examining the longstanding problem of the (classical vs. quantum) nature of the ubiquitous beats associated with the light-hole (LX) heavy-hole (HX) excitons, which are observed in transient optical experiments on QW. To this end, we consider the coherent behavior of excitons using the simplest albeit non-trivial model where they are treated as non-interacting bosons. Our results bear directly on studies for which nonlinear effects are not important and are not aimed directly at explaining the fourwave-mixing (FWM) experiments that dominate the field. Nevertheless, since nonlinear effects are, typically, weak compared with harmonic contributions, the free boson picture provides in all cases the correct lowest order wavefunction of the photoexcited solid.
The excitonic coherence in semiconductor quantum wells is measured by time-resolved speckle analysis and four-wave mixing. It is found that in the case of single GaAs quantum wells, the results of both methods are in agreement, and can be understood in the framework of an inhomogeneously broadened distribution of localized excitons which are subject to phonon-scattering and radiative recombination. The speckle analysis gives the additional distinction between recombination and pure dephasing processes. In multiple quantum wells, the radiative coupling between the quantum wells leads to a pronounced change of the observed dynamics. In the secondary emission, a strong coherent component with an oscillating time-structure is observed for small scattering angles. This is attributed to the beating of the radiative eigenstates of the stacked structure.
A detailed understanding of the population and coherence dynamics in optically driven individual emitters in solids and their signatures in ultrafast nonlinear-optical signals is of prime importance for their applications in future quantum and optical technologies. In a combined experimental and theoretical study on exciton complexes in single semiconductor quantum dots we reveal a detailed picture of the dynamics employing three-beam polarization-resolved four-wave mixing (FWM) micro-spectroscopy. The oscillatory dynamics of the FWM signals in the exciton-biexciton system is governed by the fine-structure splitting and the biexciton binding energy in an excellent quantitative agreement between measurement and analytical description. The analysis of the excitation conditions exhibits a dependence of the dynamics on the specific choice of polarization configuration, pulse areas and temporal ordering of driving fields. The interplay between the transitions in the four-level exciton system leads to rich evolution of coherence and population. Using two-dimensional FWM spectroscopy we elucidate the exciton-biexciton coupling and identify neutral and charged exciton complexes in a single quantum dot. Our investigations thus clearly reveal that FWM spectroscopy is a powerful tool to characterize spectral and dynamical properties of single quantum structures.
An overview on photon echo spectroscopy under resonant excitation of the exciton complexes in semiconductor nanostructures is presented. The use of four-wave-mixing technique with the pulsed excitation and heterodyne detection allowed us to measure the coherent response of the system with the picosecond time resolution. It is shown that, for resonant selective pulsed excitation of the localized exciton complexes, the coherent signal is represented by the photon echoes due to the inhomogeneous broadening of the optical transitions. In case of resonant excitation of the trions or donor-bound excitons, the Zeeman splitting of the resident electron ground state levels under the applied transverse magnetic field results in quantum beats of photon echo amplitude at the Larmor precession frequency. Application of magnetic field makes it possible to transfer coherently the optical excitation into the spin ensemble of the resident electrons and to observe a long-lived photon echo signal. The described technique can be used as a high-resolution spectroscopy of the energy splittings in the ground state of the system. Next, we consider the Rabi oscillations and their damping under excitation with intensive optical pulses for the excitons complexes with a different degree of localization. It is shown that damping of the echo signal with increase of the excitation pulse intensity is strongly manifested for excitons, while on trions and donor-bound excitons this effect is substantially weaker.