arXiv subjects

Daniel Wigger

Publications and source records attributed to Daniel Wigger.

At least 19 recordsLinked to original sources

arXiv2026

Coherent dynamics of individual excitons in a quantum dot embedded in a nanopost

We measured coherent ultrafast dynamics of exciton complexes in a single strongly-confined InAs quantum dot embedded in a GaAs nanopost. Such a photonic structure combines a wave guiding with a cavity effect and assures an enhanced light-matter coupling. Coherence properties of an exciton-biexciton system hosted by a quantum dot are assessed with four-wave mixing microscopy. Our results show that this broad-band photonic structure is an excellent asset to probe coherent couplings in a small set of solid state quantum systems and to investigate the coherence dynamics within the level structure of their excited states.

cond-mat.mes-hall↗

arXiv2026

Phonon polariton confinement in isotopically pure MOVPE-grown BN triangles

Phonon polaritons, quasiparticles formed by the resonant hybridization of light and lattice vibrations, exhibit unique properties like the possibility of hyperbolic dispersions. In this context, exfoliated hexagonal boron nitride (hBN) has emerged as a promising material for phonon polariton-based research. However, to advance toward practical applications, it is essential to demonstrate efficient phonon-polariton propagation and confinement in large-area epitaxial BN. To address this topic, we use metalorganic vapor phase epitaxy (MOVPE)-grown BN and investigate the phonon polariton properties using scattering-type scanning near-field optical microscopy (s-SNOM) and nanoscale Fourier transform infrared spectroscopy (nano-FTIR). We report remarkably long phonon polariton propagation lengths, indicating the high crystalline quality of the BN layer. By using epitaxially grown isotopically pure triangular islands, we further demonstrate efficient phonon-polariton confinement with mode patterns tunable by the incident light wavelength. Our results pave the way for implementing all-epitaxial, microscale, high-quality polariton resonators for nanophotonics and quantum optics.

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arXiv2026

Phonon-induced Markovian and non-Markovian effects on absorption spectra of moir\'e excitons in twisted transition metal dichalcogenide bilayers

The properties of moir\'e excitons in twisted bilayers of transition metal dichalcogenides (TMDCs) vary significantly with the twist angle, ranging from quasi localized excitons with flat dispersions for small twist angles to delocalized excitons for larger ones. This twist angle dependence directly impacts the exciton-phonon coupling, which plays a significant role for the optical properties of these materials. In this work we theoretically investigate the twist angle dependent influence of phonons on absorption spectra of intralayer moir\'e excitons in a twisted TMDC hetero-bilayer. For the lowest-lying intralayer moir\'e exciton we find that the exciton-phonon coupling interpolates between two physically distinct regimes when tuning the twist angle. At small twist angles non-Markovian polarization dynamics and phonon sidebands dominate the properties of absorption spectra for localized excitons. For larger twist angles Markovian processes become more important leading to additional line broadening. Furthermore, the absorption spectra here show a characteristic asymmetric peak similar to monolayer TMDCs. When taking into account multiple bright moir\'e exciton bands we find that intraband scattering due to optical phonons has a significant impact on absorption spectra, effectively suppressing absorption peaks of higher lying bands when their bandwidth surpasses the optical phonon energy.

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arXiv2025

Topical review on acousto-optical Floquet engineering of single-photon emitters

The combination of solid state single-photon emitters and mechanical excitations on a common platform is a promising approach for the development of hybrid quantum technologies. In this topical review we discuss state-of-the-art platforms for emitter-based acousto-optics and their feasibility for acousto-optical Floquet engineering. To this aim we investigate theoretically the resonance fluorescence (RF) spectrum of an acoustically modulated single-photon emitter under arbitrarily strong optical driving. In the spectrum, the combination of Mollow triplet physics and phonon sidebands results in a complex structure of crossings, anti-crossings, and line suppressions. We apply Floquet theory to develop an analytical expression for the RF spectrum. Complemented with perturbative and non-perturbative techniques, this allows us to fully understand the underlying acousto-optical double dressing physics of the hybrid quantum system, explaining the observed spectral features. We use these insights to perform an experimental feasibility study of existing emitter-based acousto-optical platforms and come to the conclusion that surface and bulk acoustic waves interfaced with quantum dots as an established Mollow triplet platform represent particularly promising infrastructures for acousto-optical Floquet engineering.

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arXiv2025

Fundamentals of heterodyne wave mixing spectroscopy: a tutorial

This tutorial provides a joint theoretical and experimental overview of heterodyne wave mixing spectroscopy, focusing mainly on four-wave mixing (FWM). This powerful and versatile time-resolved nonlinear optical spectroscopy technique enables the investigation of individual localized single photon emitters, as well as microscopy of extended samples, e.g., two-dimensional transition metal dichalcogenides. Starting with the fundamental theory of optically driven two-level systems, we motivate the utility of wave mixing spectroscopy via a discussion on homogeneous and inhomogeneous linewidths which can be independently measured using FWM. We then provide a detailed overview of the heterodyne wave mixing setup operated by one of the authors (JK) at Institut N\'eel in Grenoble, supported by theoretical modeling of the signal detection process. Throughout the paper we elaborate on important benefits of heterodyne wave mixing spectroscopy, e.g., background-free detection, measurement of the full signal field including amplitude and phase, and investigation of coupling mechanisms in few-level systems. Within the context of the latter point we discuss the significance of two-dimensional (2D) FWM spectra. This tutorial is dedicated to students, young researchers, as well as experts in the field of nonlinear spectroscopy in general and FWM in particular. It explains the fundamental concepts and building blocks required to operate a heterodyne wave mixing experiment both from the experimental and theoretical side. This joint approach is helpful for theoreticians who want to accurately and quantitatively model wave mixing signals, as well as for experimentalists who aim to interpret their recorded data.

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arXiv2025

Nanoscale resolved mapping of the dipole emission of hBN color centers with a scattering-type scanning near-field optical microscope

Color centers in hexagonal boron nitride (hBN) are promising candidates as quantum light sources for future technologies. In this work, we utilize a scattering-type near-field optical microscope (s-SNOM) to study the photoluminescence (PL) emission characteristics of such quantum emitters in metalorganic vapor phase epitaxy grown hBN. On the one hand, we demonstrate direct near-field optical excitation and emission through interaction with the nanofocus of the tip resulting in a sub-diffraction limited tip-enhanced PL hotspot. On the other hand, we show that indirect excitation and emission via scattering from the tip significantly increases the recorded PL intensity. This demonstrates that the tip-assisted PL (TAPL) process efficiently guides the generated light to the detector. We apply the TAPL method to map the in-plane dipole orientations of the hBN color centers on the nanoscale. This work promotes the widely available s-SNOM approach to applications in the quantum domain including characterization and optical control.

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arXiv2024

Theory of phonon sidebands in the absorption spectra of moir\'e exciton-polaritons

Excitons in twisted bilayers of transition metal dichalcogenides have strongly modified dispersion relations due to the formation of periodic moir\'e potentials. The strong coupling to a light field in an optical cavity leads to the appearance of moir\'e polaritons. In this paper, we derive a theoretical model for the linear absorption spectrum of the coupled moir\'e polariton-phonon system based on the time-convolutionless (TCL) approach. Results obtained by numerically solving the TCL equation are compared to those obtained in the Markovian limit and from a perturbative treatment of non-Markovian corrections. A key quantity for the interpretation of the findings is the generalized phonon spectral density. We discuss the phonon impact on the spectrum for realistic moir\'e exciton dispersions by varying twist angle and temperature. Key features introduced by the coupling to phonons are broadenings and energy shifts of the upper and lower polariton peak and the appearance of phonon sidebands between them. We analyze these features with respect to the role of Markovian and non-Markovian effects and find that they strongly depend on the twist angle. We can distinguish between the regimes of large, small, and intermediate twist angles. In the latter phonon effects are particularly pronounced due to dominating phonon transitions into regions which are characterized by van Hove singularities in the density of states.

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arXiv2024

High Harmonic Spectroscopy Probes Lattice Dynamics

The probing of coherent lattice vibrations in solids has been conventionally carried out using time-resolved transient spectroscopy where only the relative oscillation amplitude can be obtained. Using time-resolved X-ray techniques, absolute electron-phonon coupling strength could be extracted. However, the complexity of such an experiment renders it impossible to be carried out in conventional laboratories. Here we demonstrate that the electron-phonon, anharmonic phonon-phonon coupling, and their relaxation dynamics can be probed in real-time using high-harmonic spectroscopy. Our technique is background-free and has extreme sensitivity directly in the energy domain. In combination with the optical deformation potential calculated from density functional perturbation theory and the absolute energy modulation depth, our measurement reveals the maximum displacement of neighboring oxygen atoms in {\alpha}-quartz crystal to tens of picometers in real space. By employing a straightforward and robust time-windowed Gabor analysis for the phonon-modulated high-harmonic spectrum, we successfully observe channel-resolved four-phonon scattering processes in such highly nonlinear interactions. Our work opens a new realm for accurate measurement of coherent phonons and their scattering dynamics, which allows for potential benchmarking ab-initio calculations in solids

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arXiv2024

Determining Strain Components in a Diamond Waveguide from Zero-Field ODMR Spectra of NV$^{-}$ Center Ensembles

The negatively charged nitrogen-vacancy (NV$^{-}$) center in diamond has shown great potential in nanoscale sensing and quantum information processing due to its rich spin physics. An efficient coupling with light, providing strong luminescence, is crucial for realizing these applications. Laser-written waveguides in diamond promote NV$^{-}$ creation and improve their coupling to light but, at the same time, induce strain in the crystal. The induced strain contributes to light guiding but also affects the energy levels of NV$^{-}$ centers. We probe NV$^{-}$ spin states experimentally with the commonly used continuous-wave zero-field optically detected magnetic resonance (ODMR). In our waveguides, the ODMR spectra are shifted, split, and consistently asymmetric, which we attribute to the impact of local strain. To understand these features, we model ensemble ODMR signals in the presence of strain. By fitting the model results to the experimentally collected ODMR data, we determine the strain tensor components at different positions, thus determining the strain profile across the waveguide. This shows that zero-field ODMR spectroscopy can be used as a strain imaging tool. The resulting strain within the waveguide is dominated by a compressive axial component transverse to the waveguide structure, with a smaller contribution from vertical and shear strain components.

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arXiv2023

Quantum dots as optimized chiral emitters for photonic integrated circuits

Chiral coupling, which allows directional interactions between quantum dots (QDs) and photonic crystal waveguide modes, holds promise for enhancing the functionality of quantum photonic integrated circuits. Elliptical polarizations of QD transitions offer a considerable enhancement in directionality. However, in epitaxial QD fabrication, the lack of precise control over lateral QD positions still poses a challenge in achieving efficient chiral interfaces. Here, we present a theoretical analysis in which we propose to optimize the polarization of a QD emitter against the spatially averaged directionality and demonstrate that the resulting emitter offers a considerable technological advantage in terms of the size and location of high-directionality areas of the waveguide as well as their overlap with the regions of large Purcell enhancement, thereby improving the scalability of the device. Moreover, using $\mathbf{\mathit{k}}\cdot\mathbf{\mathit{p}}$ modeling, we demonstrate that the optimal elliptical polarization can be achieved for neutral exciton transitions in a realistic QD structure. Our results present a viable path for efficient chiral coupling in QD-based photonic integrated circuits, to a large extent overcoming the challenges and limitations of the present manufacturing technology.

quant-ph↗

arXiv2023

How to read out the phonon number statistics via resonance fluorescence spectroscopy of a single-photon emitter

In today's development of quantum technologies a hybrid integration of phononic excitations becomes increasingly attractive. As natural quasi-particle excitations in solid state systems, phonons couple to virtually any other excitation and therefore constitute a useful interaction channel between different building blocks in hybrid quantum systems. This work explores how the efficient light-scattering properties of a single-photon emitter and the appearance of characteristic sidebands in resonance fluorescence spectra, when interfaced with an arbitrary phonon quantum state, can be utilized for acousto-optical transduction. Within reasonable approximations, an analytical description for the optical spectra in the low excitation limit is developed which can be used to read the number statistics of the initial phonon state from a given spectrum. It is shown that the readout is faulty in situations where relevant resonant transitions are forbidden due to vanishing Franck-Condon factors, especially when considering spectra with a noisy background. Two possible solutions to this problem are presented: (A) changing the detuning of the laser relative to the single-photon emitter which modifies the relevant resonant transitions, or (B) increasing dissipation of the single-photon emitter to promote off-resonant transitions.

quant-ph↗

arXiv2023

Controlled Coherent Coupling in a Quantum Dot Molecule Revealed by Ultrafast Four-Wave Mixing Spectroscopy

Semiconductor quantum dot molecules are considered as promising candidates for quantum technological applications due to their wide tunability of optical properties and coverage of different energy scales associated with charge and spin physics. While previous works have studied the tunnel-coupling of the different excitonic charge complexes shared by the two quantum dots by conventional optical spectroscopy, we here report on the first demonstration of a coherently controlled inter-dot tunnel-coupling focusing on the quantum coherence of the optically active trion transitions. We employ ultrafast four-wave mixing spectroscopy to resonantly generate a quantum coherence in one trion complex, transfer it to and probe it in another trion configuration. With the help of theoretical modelling on different levels of complexity we give an instructive explanation of the underlying coupling mechanism and dynamical processes.

cond-mat.mes-hall↗

arXiv2023

Controlled coherent-coupling and dynamics of exciton complexes in a MoSe$_2$ monolayer

Quantifying and controlling the coherent dynamics and couplings of optically active excitations in solids is of paramount importance in fundamental research in condensed matter optics and for their prospective optoelectronic applications in quantum technologies. Here, we perform ultrafast coherent nonlinear spectroscopy of a charge-tunable MoSe$_2$ monolayer. The experiments show that the homogeneous and inhomogeneous line width and the population decay of exciton complexes hosted by this material can be directly tuned by an applied gate bias, which governs the Fermi level and therefore the free carrier density. By performing two-dimensional spectroscopy, we also show that the same bias-tuning approach permits us to control the coherent coupling strength between charged and neutral exciton complexes.

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arXiv2022

Resonant and phonon-assisted ultrafast coherent control of a single hBN color center

Single-photon emitters in solid-state systems are important building blocks for scalable quantum technologies. Recently, quantum light emitters have been discovered in the wide-gap van der Waals insulator hBN. These color centers have attracted considerable attention due to their quantum performance at elevated temperatures and wide range of transition energies. Here, we demonstrate coherent state manipulation of a single hBN color center with ultrafast laser pulses and investigate in our joint experiment-theory study the coupling between the electronic system and phonons. We demonstrate that coherent control can not only be performed resonantly on the optical transition giving access to the decoherence but also phonon-assisted, which reveals the internal phonon quantum dynamics. In the case of optical phonons we measure their decoherence, stemming in part from their anharmonic decay. Dephasing induced by the creation of acoustic phonons manifests as a rapid decrease of the coherent control signal when traveling phonon wave packets are emitted. Furthermore, we demonstrate that the quantum superposition between a phonon-assisted process and the resonant excitation causes ultrafast oscillations of the coherent control signal. Our results pave the way for ultrafast phonon quantum state control on the nanoscale and open up a new promising perspective for hybrid quantum technologies.

cond-mat.mes-hall↗

arXiv2022

Photon scattering from a quantum acoustically modulated two-level system

We calculate the resonance fluorescence signal of a two-level system coupled to a quantized phonon mode. By treating the phonons in the independent boson model and not performing any approximations in their description, we also have access to the state evolution of the phonons. We confirm the validity of our model by simulating the limit of an initial quasi-classical coherent phonon state, which can be compared to experimentally confirmed results in the semiclassical limit. In addition we predict photon scattering spectra in the limit of purely quantum mechanical phonon states by approaching the phononic vacuum. Our method further allows us to simulate the impact of the light scattering process on the phonon state by calculating Wigner functions. We show that the phonon mode is brought into characteristic quantum states by the optical excitation process.

cond-mat.mes-hall↗

arXiv2022

Coherent dynamics of a single Mn-doped quantum dot revealed by four-wave mixing spectroscopy

For future quantum technologies the combination of a long quantum state lifetime and an efficient interface with external optical excitation are required. In solids, the former is for example achieved by individual spins, while the latter is found in semiconducting artificial atoms combined with modern photonic structures. One possible combination of the two aspects is reached by doping a single quantum dot, providing a strong excitonic dipole, with a magnetic ion, that incorporates a characteristic spin texture. Here, we perform four-wave mixing spectroscopy to study the system's quantum coherence properties. We characterize the optical properties of the undoped CdTe quantum dot and find a strong photon echo formation which demonstrates a significant inhomogeneous spectral broadening. Incorporating the Mn$^{2+}$ ion introduces its spin-5/2 texture to the optical spectra via the exchange interaction, manifesting as six individual spectral lines in the coherent response. The random flips of the Mn-spin result in a special type of spectral wandering between the six transition energies, which is fundamentally different from the quasi-continuous spectral wandering that results in the Gaussian inhomogeneous broadening. Here, the discrete spin-ensemble manifests in additional dephasing and oscillation dynamics.

cond-mat.mes-hall↗

arXiv2021

Destructive photon echo formation in six-wave mixing signals of a MoSe$_2$ monolayer

Monolayers of transition metal dichalcogenides display a strong excitonic optical response. Additionally encapsulating the monolayer with hexagonal boron nitride allows to reach the limit of a purely homogeneously broadened exciton system. On such a MoSe$_{2}$-based system we perform ultrafast six-wave mixing spectroscopy and find a novel destructive photon echo effect. This process manifests as a characteristic depression of the nonlinear signal dynamics when scanning the delay between the applied laser pulses. By theoretically describing the process within a local field model we reach an excellent agreement with the experiment. We develop an effective Bloch vector representation and thereby demonstrate that the destructive photon echo stems from a destructive interference of successive repetitions of the heterodyning experiment.

cond-mat.mes-hall↗

arXiv2021

Resonance fluorescence spectral dynamics of an acoustically modulated quantum dot

Quantum technologies that rely on photonic qubits require a precise controllability of their properties. For this purpose hybrid approaches are particularly attractive because they offer a large flexibility to address different aspects of the photonic degrees of freedom. When combining photonics with other quantum platforms like phonons, quantum transducers have to be realized that convert between the mechanical and optical domain. Here, we realize this interface between phonons in the form of surface acoustic waves (SAWs) and single photons, mediated by a single semiconductor quantum dot exciton. In this combined theoretical and experimental study, we show that the different sidebands exhibit characteristic blinking dynamics that can be controlled by detuning the laser from the exciton transition. By developing analytical approximations we gain a better understanding of the involved internal dynamics. Our specific SAW approach allows us to reach the ideal frequency range of around 1 GHz that enables simultaneous temporal and spectral phonon sideband resolution close to the combined fundamental time-bandwidth limit.

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