arXiv subjects

Jacek Kasprzak

Publications and source records attributed to Jacek Kasprzak.

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

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

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.

physics.optics↗

arXiv2025

Hole to Electron Crossover in a (Cd,Mn)Te Quantum Well through Surface Metallization

In this work we look into how the contact material influences the local charge properties of a p-type CdTe-based quantum well. We study five metals deposited as 10 nm layers on the sample surface: Au, Ag, Cr, Ni and Ti. We use magneto-spectroscopy to discriminate their charge states through monitoring the Zeeman shifts at singlet-triplet transitions. Most tested metals retain the original p-type of the QW, while gold and nickel coverage flips the local doping to n-type. This is attributed to a robust bonding of these two metals to the semiconductor, efficiently passivating its surface and thus improving electron diffusion from the metal to the quantum well.

cond-mat.mes-hall↗

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 Néel 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.

cond-mat.mes-hall↗

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

Coherent imaging and dynamics of excitons in MoSe$_2$ monolayers epitaxially grown on hexagonal boron nitride

Using four-wave mixing microscopy, we measure the coherent response and ultrafast dynamics of excitons and trions in MoSe$_2$ monolayers grown by molecular beam epitaxy on thin films of hexagonal boron nitride. We assess inhomogeneous and homogeneous broadenings in the transition spectral lineshape. The impact of phonons on the homogeneous dephasing is inferred via the temperature dependence of the dephasing. Four-wave mixing mapping, combined with the atomic force microscopy, reveals spatial correlations between exciton oscillator strength, inhomogeneous broadening and the sample morphology. The quality of coherent optical response of the epitaxially grown transition metal dichalcogenides becomes now comparable with the samples produced by mechanical exfoliation, enabling coherent nonlinear spectroscopy of innovative materials, like magnetic layers or Janus semiconductors.

cond-mat.mtrl-sci↗

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.

cond-mat.mes-hall↗

arXiv2022

Quantum dot molecule devices with optical control of charge status and electronic control of coupling

Tunnel-coupled pairs of optically active quantum dots - quantum dot molecules (QDMs) - offer the possibility to combine excellent optical properties such as strong light-matter coupling with two-spin singlet-triplet ($S-T_0$) qubits having extended coherence times. The $S-T_0$ basis formed using two spins is inherently protected against electric and magnetic field noise. However, since a single gate voltage is typically used to stabilize the charge occupancy of the dots and control the inter-dot orbital couplings, operation of the $S-T_0$ qubits under optimal conditions remains challenging. Here, we present an electric field tunable QDM that can be optically charged with one (1h) or two holes (2h) on demand. We perform a four-phase optical and electric field control sequence that facilitates the sequential preparation of the 2h charge state and subsequently allows flexible control of the inter-dot coupling. Charges are loaded via optical pumping and electron tunnel ionization. We achieve one- and two-hole charging efficiencies of 93.5 $\pm$ 0.8 % and 80.5 $\pm$ 1.3 %, respectively. Combining efficient charge state preparation and precise setting of inter-dot coupling allows control of few-spin qubits, as would be required for on-demand generation of two-dimensional photonic cluster states or quantum transduction between microwaves and photons.

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

Local field effects in ultrafast light-matter interaction measured by pump-probe spectroscopy of monolayer MoSe$_{\boldsymbol 2}$

Using a novel approach to ultrafast resonant pump-probe spectroscopy we investigate the spectral shape and dynamics of absorption features related to the A exciton in an hBN/MoSe$_2$/hBN van der Waals heterostructure. While in a pure two-level system a pump-probe experiment measures the occupation or the polarization dynamics, depending on the time ordering of the pulse pair, in the transition metal dichalcogenide (TMD) system both quantities get thoroughly mixed by strong exciton-exciton interaction. We find that for short positive delays the spectral lines experience pronounced changes in their shape and energy and they relax to the original situation on a picosecond time scale. For negative delays distinctive spectral oscillations appear indicating the first-time observation of perturbed free induction decay for a TMD system. The comparison between co-circular and cross-circular excitation schemes further allows us to investigate the rapid inter-valley scattering. By considering a three-level system as a minimal model including the local field effect, excitation induced dephasing and scattering between the excited states we explain all phenomena observed in the experiment with excellent consistency. Our handy model can be even further reduced to two levels in the case of a co-circular excitation, for which we derive analytic expressions to describe the detected signals. This allows us to trace back the spectral shapes and shifts to the impact of local field effect and excitation induced dephasing thus fully reproducing the complex behavior of the observed effects.

cond-mat.mes-hall↗

arXiv2021

Influence of local fields on the dynamics of four-wave mixing signals from 2D semiconductor systems

In recent years the physics of two-dimensional semiconductors was revived by the discovery of the class of transition metal dichalcogenides. In these systems excitons dominate the optical response in the visible range and open many perspectives for nonlinear spectroscopy. To describe the coherence and polarization dynamics of excitons after ultrafast excitation in these systems, we employ the Bloch equation model of a two-level system extended by a local field describing the exciton-exciton interaction. We calculate four-wave mixing signals and analyze the dependence of the temporal and spectral signals as a function of the delay between the exciting pulses. Exact analytical results obtained for the case of ultrafast ($δ$-shaped) pulses are compared to numerical solutions obtained for finite pulse durations. If two pulses are used to generate the nonlinear signal, characteristic spectral line splittings are restricted to short delays. When considering a three-pulse excitation the line splittings, induced by the local field effect, persist for long delays. All of the found features are instructively explained within the Bloch vector picture and we show how the exciton occupation dynamics govern the different four-wave mixing signals.

cond-mat.mes-hall↗

arXiv2020

Four-wave mixing dynamics of a strongly coupled quantum-dot--microcavity system driven by up to 20 photons

The Jaynes-Cummings (JC) model represents one of the simplest ways in which single qubits can interact with single photon modes, leading to profound quantum phenomena like superpositions of light and matter states. One system, that can be described with the JC model, is a single quantum dot embedded in a micropillar cavity. In this joint experimental and theoretical study we investigate such a system using four-wave mixing (FWM) micro-spectroscopy. Special emphasis is laid on the dependence of the FWM signals on the number of photons injected into the microcavity. By comparing simulation and experiment, which are in excellent agreement with each other, we infer that up to ~20 photons take part in the observed FWM dynamics. Thus we verify the validity of the JC model for the system under consideration in this non-trivial regime. We find that the inevitable coupling between the quantum dot exciton and longitudinal acoustic phonons of the host lattice influences the real time FWM dynamics and has to be taken into account for a sufficient description of the quantum dot-microcavity system. Performing additional simulations in an idealized dissipation-less regime, we observe that the FWM signal exhibits quasi-periodic dynamics, analog to the collapse and revival phenomenon of the JC model. In these simulations we also see that the FWM spectrum has a triplet structure, if a large number of photons is injected into the cavity.

cond-mat.mes-hall↗

arXiv2020

Coherent dynamics and mapping of excitons in single-layer MoSe$_2$ and WSe$_2$ at the homogeneous limit

We perform coherent nonlinear spectroscopy of excitons in single-layers of MoSe$_2$ and WSe$_2$ encapsulated between thin films of hexagonal boron nitride. Employing four-wave mixing microscopy we identify virtually disorder free areas, generating exciton optical response at the homogeneous limit. Focussing on such areas, we measure exciton homogeneous broadening as a function of environmental factors, namely temperature and exciton density. Exploiting FWM imaging, we find that at such locations, nonlinear absorption of the exciton excited states and their coherent couplings can be observed. Using the WSe$_2$ heterostructure, we infer coherence and density dynamics of the exciton 2S state. Owing to its increased radiative lifetime, at low temperatures, the dephasing of the 2S state is longer than of the 1S transition. While scanning various heterostructures across tens of micrometers, we conclude that the disorder, principally induced by strain variations, remain to be present creating spatially varying inhomogeneous broadening.

cond-mat.mtrl-sci↗

arXiv2020

Dynamics of resonantly excited excitons in MoSe$_2$ and WS$_2$ single-layers monitored with four-wave mixing

We investigate dynamics of resonantly excited excitons in single-layers of MoSe$_2$ and WS$_2$ down to 4.5 K. To this end, we measure the delay dependence of the heterodyne four-wave mixing (FWM) amplitude induced by three, short laser pulses. This signal depends not only on the population of optically active excitons, which affects the absorption of the probe, but also on the population of optically inactive states, by interaction-induced energy shift, influencing the refractive index experienced by the probe. As such, it offers insight into density dynamics of excitons which do not directly couple to photons. Reproducing the coherent signal detected in amplitude and phase, the FWM delay dependence is modeled by a coherent superposition of several exponential decay components, with characteristic time constants from 0.1 picosecond up to 1 nanosecond. With increasing excitation intensity and/or temperature, we observe strong interference effects in the FWM field amplitude, resulting in progressively more complex and nonintuitive signal dynamics. We attribute this behaviour to increasingly populated exciton dark states, which change the FWM field phase by the relative effect on absorption and refractive index. We observe that exciton recombination occurs on a significantly longer timescale in WS$_2$ with respect to MoSe$_2$, which is attributed to the dark character of exciton ground state in the former and the bright in the latter.

cond-mat.mes-hall↗

arXiv2020

Acoustic Phonon Sideband Dynamics During Polaron Formation in a Single Quantum Dot

When an electron-hole pair is optically excited in a semiconductor quantum dot the host crystal lattice needs to adapt to the presence of the generated charge distribution. Therefore the coupled exciton-phonon system has to establish a new equilibrium, which is reached in the form of a quasiparticle called polaron. Especially, when the exciton is abruptly generated on a timescale faster than the typical lattice dynamics, the lattice displacement cannot follow adiabatically. Consequently, a rich dynamics on the picosecond timescale of the coupled system is expected. In this study we combine simulations and measurements of the ultrafast, coherent, nonlinear optical response, obtained by four-wave mixing spectroscopy, to resolve the formation of this polaron. By detecting and investigating the phonon sidebands in the four-wave mixing spectra for varying pulse delays and different temperatures we have access to the influence of phonon emission and absorption processes which finally result in the emission of an acoustic wave packet out from the quantum dot.

cond-mat.mes-hall↗

arXiv2018

Coherence and density dynamics of excitons in a single-layer MoS$_2$ reaching the homogeneous limit

We measure the coherent nonlinear response of excitons in a single-layer of molybdenum disulphide embedded in hexagonal boron nitride, forming a $h$-BN/MoS$_2$/$h$-BN heterostructure. Using four-wave mixing microscopy and imaging, we correlate the exciton homogeneous and inhomogeneous broadenings. We find that the exciton dynamics is governed by microscopic disorder on top of the ideal crystal properties. Analyzing the exciton ultra-fast density dynamics using amplitude and phase of the response, we investigate the relaxation pathways of the resonantly driven exciton population. The surface protection via encapsulation provides stable monolayer samples with low disorder, avoiding surface contaminations and the resulting exciton broadening and modifications of the dynamics. We identify areas localized to a few microns where the optical response is totally dominated by homogeneous broadening. Across the sample of tens of micrometers, weak inhomogeneous broadening and strain effects are observed, attributed to the remaining interaction with the $h$-BN and imperfections in the encapsulation process.

cond-mat.mes-hall↗

arXiv2018

Rabi oscillations of a quantum dot exciton coupled to acoustic phonons: coherence and population readout

While the advanced coherent control of qubits is now routinely carried out in low frequency (GHz) systems like single spins, it is far more challenging to achieve for two-level systems in the optical domain. This is because the latter evolve typically in the THz range, calling for tools of ultrafast, coherent, nonlinear optics. Using four-wave mixing micro-spectroscopy, we here measure the optically driven dynamics of a single exciton quantum state confined in a semiconductor quantum dot. In a combined experimental and theoretical approach, we reveal the intrinsic Rabi oscillation dynamics by monitoring both central exciton quantities, i.e., its occupation and the microscopic coherence, as resolved by the four-wave mixing technique. In the frequency domain this oscillation generates the Autler-Townes splitting of the light-exciton dressed states, directly seen in the four-wave mixing spectra. We further demonstrate that the coupling to acoustic phonons strongly influences the FWM dynamics on the picosecond timescale, because it leads to transitions between the dressed states.

cond-mat.mes-hall↗