Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2009.08598 · Physical review. B./Physical review. B

Direct and ultrafast probing of quantum many-body interactions through coherent two-dimensional spectroscopy: From weak- to strong-interaction regimes

Nguyen Thanh Phuc, Trung Quang Pham

Published Sep 3, 2021• 9 citations
arXivHTMLPDF

Abstract

Interactions between particles in quantum many-body systems play a crucial role in determining the electric, magnetic, optical, and thermal properties of the system. The recent progress in the laser-pulse technique has enabled the manipulations and measurements of physical properties on ultrafast timescales. Here we propose a method for the direct and ultrafast probing of quantum many-body interaction through coherent two-dimensional (2D) spectroscopy. Using a two-band fermionic Hubbard model for the minimum two-site lattice system, we find that the 2D spectrum of a noninteracting system contains only diagonal peaks; the interparticle interaction manifests itself in the emergence of off-diagonal peaks in the 2D spectrum before all the peaks coalesce into a single diagonal peak as the system approaches the strongly interacting limit. The evolution of the 2D spectrum as a function of the time delay between the second and third laser pulses can provide important information on the ultrafast time variation of the interaction.

DOI
10.1103/physrevb.104.115105

Related papers

Probing many particle correlations in semiconductor quantum wells using double-quantum-coherence signal

Lijun Yang, Shaul Mukamel

Multidimensional analysis of coherent signals is commonly used in nuclear magnetic resonance to study correlations among spins. These techniques were recently extended to the femtosecond regime and applied to chemical, biological and semiconductor systems. In this work, we apply a two-dimensional correlation spectroscopy technique which employs double-quantum-coherence to investigate many-body effects in a semiconductor quantum well. The signal is detected along the direction k(1)+ k(2)- k(3), where k(1), k(2) and k(3) are the pulse wave vectors in chronological order. We show that this signal is particularly sensitive to many-body correlations which are missed by time-dependent Hartree-Fock approximation. The correlation energy of two-exciton can be probed with a very high resolution arising from a two-dimensional correlation spectrum, where two-exciton couplings spread the cross peaks along both axes of the 2D spectrum to create a characteristic highly resolved pattern. This level of detail is not available from conventional one-dimensional four-wave mixing or other two-dimensional correlation spectroscopy signals such as the photo echo (-k(1)+ k(2)+ k(3)).

Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE•Feb 11, 2010•1 citation

Ultrafast spectroscopy of single quantum dots

Wolpert, Christian

In this thesis, the coherent interaction of single semiconductor quantum dots and ultrafast optical pulses is studied. Under certain conditions, localized exciton transitions in quantum dots can be seen as semi-isolated two-level systems. While this description is sufficient for the explanation of some observations in coherent experiments, it is sometimes necessary to explicitly consider coupling of the discreet quantum states confined to the dot with the environment. We start out from simple, classical examples of coherent spectroscopy and then turn towards experiments where the interaction with the vicinity of the dot becomes an important factor. First, a novel method for transient differential reflectivity spectroscopy of single quantum systems is introduced. It is a pure far-field optical technique which does not require any sophisticated sample preparation steps which makes it applicable to a broad range of structures. Pump pulses excite the sample structure and probe pulses read out the pump-induced changes in the system after a variable delay time. In the case of a single dipole, the signal is given in the form of the spectral inteferogram between the backscattered wave from the particle and the probe light which is reflected at the sample surface. This form of homodyne detection amplifies the weak scattered wave from the particle and thus makes this kind of spectroscopy for single quantum dots feasible. In the remainder of this thesis our spectroscopic method is applied to either characterize the coherent properties of single quantum dots, to prepare and read-out a desired quantum state or to deliberately manipulate them. Coherence times and oscillator strengths are determined for localized exciton transitions. Arbitrary population states can be written by driving coherent population oscillations using resonant pulses, while entangled superpositions of two exciton states in a single dot are investigated by quantum beats on transient differential spectra. We finally exploit the interaction between the dot and a nearby absorbing layer to switch the dot's absorption spectrum on ultrafast timescales via light-induced transient electric fields.

•Jan 1, 2012•0 citations

Coherent spectroscopy of collective excitations in superfluid helium far from equilibrium

Gabriel Voith, Alexander A. Milner, Michael J. Desrochers +2 more

Ultrafast dynamics of collective excitations in superfluids remains largely unexplored beyond the roton region of the Landau excitation spectrum, despite the importance of such dynamics for understanding nonequilibrium processes in these systems. Here, we employ ultrafast coherent control with sequences of femtosecond pulses to perform spectroscopy of multiple quasiparticles in superfluid helium far from equilibrium. By measuring the time-resolved optical birefringence, we track the nonequilibrium dynamics of quasiparticle pairs associated with rotons, maxons and the Pitaevskii plateau region. The spectral lineshape of the roton peak is explained by an ab initio theoretical analysis of the roton-roton interaction. We also reveal strong energy shifts and short lifetimes of both maxon and Pitaevskii-plateau pairs, as well as an influence of the quasiparticle effective mass on the phase of their coherent response to laser pulses. These results demonstrate the ability to extract previously inaccessible information about collective excitations in a strongly interacting quantum fluid by probing its nonequilibrium dynamics on picosecond and sub-picosecond timescales.

cond-mat.otherCross-listedarXiv:2605.17835•May 19, 2026•0 citations

Sub-cycle multidimensional spectroscopy of strongly correlated materials

V. N. Valmispild, Evgeny Gorelov, Martin Eckstein +5 more

Abstract Strongly correlated solids are complex and fascinating quantum systems, where new electronic states continue to emerge, especially when interaction with light triggers interplay between them. In this interplay, a sub-laser-cycle electronic response is particularly attractive as a tool for the ultrafast manipulation of matter at the petahertz scale. Here we introduce a new type of nonlinear multidimensional spectroscopy, which allows us to unravel charge and energy flows in strongly correlated systems interacting with few-cycle infrared pulses and the complex interplay between different correlated states evolving on the sub-femtosecond timescale. We demonstrate that the sub-cycle spectroscopy of a single-particle electronic response is extremely sensitive to correlated many-body dynamics and provides direct access to many-body response functions. For the two-dimensional Hubbard model under the influence of ultrashort, intense electric-field transients, we resolve the sub-femtosecond pathways of charge and energy flows between localized and delocalized many-body states and the creation of a highly correlated state surviving after the end of the laser pulse. Our findings open the way towards a regime of imaging and manipulating strongly correlated materials at optical rates, beyond the multicycle approach employed in Floquet engineering, with the sub-cycle response being a key tool for accessing many-body phenomena.

Nature Photonics•Jan 24, 2024•31 citations

A coherent nonlinear optical signal induced by electron correlations

Shaul Mukamel, Rafał Oszwałdowski, Lijun Yang

The correlated behavior of electrons determines the structure and optical properties of molecules, semiconductors, and other systems. Valuable information on these correlations is provided by measuring the response to femtosecond laser pulses, which probe the very short time period during which the excited particles remain correlated. The interpretation of four-wave-mixing techniques, commonly used to study the energy levels and dynamics of many-electron systems, is complicated by many competing effects and overlapping resonances. Here we propose a coherent optical technique, specifically designed to provide a background-free probe for electronic correlations in many-electron systems. The proposed signal pulse is generated only when the electrons are correlated, which gives rise to an extraordinary sensitivity. The peak pattern in two-dimensional plots, obtained by displaying the signal versus two frequencies conjugated to two pulse delays, provides a direct visualization and specific signatures of the many-electron wave functions.

arXiv:0711.1848•The Journal of Chemical Physics•Dec 13, 2007•45 citations

Thermalization Dynamics in the Two-Dimensional Hubbard Model with Neural-Network Quantum States

Alessandro Sinibaldi, Luciano Loris Viteritti, Riccardo Rende +2 more

Thermalization in strongly correlated fermionic systems remains a central open problem in quantum many-body physics. In this work, we investigate the real-time dynamics and the approach to thermalization in the two-dimensional Hubbard model, a paradigmatic framework for correlated electrons, relevant to high-temperature superconductivity and ultracold quantum simulation. Focusing on the half-filled square lattice, we monitor the time evolution of the double occupancy following a quench in the on-site interaction $U$, and assess whether its long-time value is captured by a canonical thermal ensemble. We employ time-dependent variational Monte Carlo methods combined with transformer-based Neural-Network Quantum States to accurately describe the nonequilibrium dynamics of fermions, especially for the behavior at long times, thereby accessing regimes that were previously inaccessible to numerical simulations. Our results reveal two dynamical behaviors: for weak to intermediate interactions, the double occupancy rapidly approaches the thermal prediction, consistent with ergodic evolution; beyond a critical interaction $U_{C}$, the dynamics remains distinct from the thermal expectation on the timescales investigated, revealing signatures of a prethermal plateau delaying fast relaxation. These results establish numerical simulation as a powerful tool to probe nonequilibrium quantum phenomena in correlated fermionic matter.

cond-mat.str-elCross-listedarXiv:2606.05293•Jun 5, 2026•0 citations
Interactions between particles in quantum many-body systems play a crucial role in determining the electric, magnetic, optical, and thermal properties of the system. The recent progress in the laser-pulse technique has enabled the manipulations and measurements of physical properties on ultrafast timescales. Here we propose a method for the direct and ultrafast probing of quantum many-body interaction through coherent two-dimensional (2D) spectroscopy. Using a two-band fermionic Hubbard model for the minimum two-site lattice system, we find that the 2D spectrum of a noninteracting system contains only diagonal peaks; the interparticle interaction manifests itself in the emergence of off-diagonal peaks in the 2D spectrum before all the peaks coalesce into a single diagonal peak as the system approaches the strongly interacting limit. The evolution of the 2D spectrum as a function of the time delay between the second and third laser pulses can provide important information on the ultrafast time variation of the interaction.
Multidimensional analysis of coherent signals is commonly used in nuclear magnetic resonance to study correlations among spins. These techniques were recently extended to the femtosecond regime and applied to chemical, biological and semiconductor systems. In this work, we apply a two-dimensional correlation spectroscopy technique which employs double-quantum-coherence to investigate many-body effects in a semiconductor quantum well. The signal is detected along the direction k(1)+ k(2)- k(3), where k(1), k(2) and k(3) are the pulse wave vectors in chronological order. We show that this signal is particularly sensitive to many-body correlations which are missed by time-dependent Hartree-Fock approximation. The correlation energy of two-exciton can be probed with a very high resolution arising from a two-dimensional correlation spectrum, where two-exciton couplings spread the cross peaks along both axes of the 2D spectrum to create a characteristic highly resolved pattern. This level of detail is not available from conventional one-dimensional four-wave mixing or other two-dimensional correlation spectroscopy signals such as the photo echo (-k(1)+ k(2)+ k(3)).
In this thesis, the coherent interaction of single semiconductor quantum dots and ultrafast optical pulses is studied. Under certain conditions, localized exciton transitions in quantum dots can be seen as semi-isolated two-level systems. While this description is sufficient for the explanation of some observations in coherent experiments, it is sometimes necessary to explicitly consider coupling of the discreet quantum states confined to the dot with the environment. We start out from simple, classical examples of coherent spectroscopy and then turn towards experiments where the interaction with the vicinity of the dot becomes an important factor. First, a novel method for transient differential reflectivity spectroscopy of single quantum systems is introduced. It is a pure far-field optical technique which does not require any sophisticated sample preparation steps which makes it applicable to a broad range of structures. Pump pulses excite the sample structure and probe pulses read out the pump-induced changes in the system after a variable delay time. In the case of a single dipole, the signal is given in the form of the spectral inteferogram between the backscattered wave from the particle and the probe light which is reflected at the sample surface. This form of homodyne detection amplifies the weak scattered wave from the particle and thus makes this kind of spectroscopy for single quantum dots feasible. In the remainder of this thesis our spectroscopic method is applied to either characterize the coherent properties of single quantum dots, to prepare and read-out a desired quantum state or to deliberately manipulate them. Coherence times and oscillator strengths are determined for localized exciton transitions. Arbitrary population states can be written by driving coherent population oscillations using resonant pulses, while entangled superpositions of two exciton states in a single dot are investigated by quantum beats on transient differential spectra. We finally exploit the interaction between the dot and a nearby absorbing layer to switch the dot's absorption spectrum on ultrafast timescales via light-induced transient electric fields.
Ultrafast dynamics of collective excitations in superfluids remains largely unexplored beyond the roton region of the Landau excitation spectrum, despite the importance of such dynamics for understanding nonequilibrium processes in these systems. Here, we employ ultrafast coherent control with sequences of femtosecond pulses to perform spectroscopy of multiple quasiparticles in superfluid helium far from equilibrium. By measuring the time-resolved optical birefringence, we track the nonequilibrium dynamics of quasiparticle pairs associated with rotons, maxons and the Pitaevskii plateau region. The spectral lineshape of the roton peak is explained by an ab initio theoretical analysis of the roton-roton interaction. We also reveal strong energy shifts and short lifetimes of both maxon and Pitaevskii-plateau pairs, as well as an influence of the quasiparticle effective mass on the phase of their coherent response to laser pulses. These results demonstrate the ability to extract previously inaccessible information about collective excitations in a strongly interacting quantum fluid by probing its nonequilibrium dynamics on picosecond and sub-picosecond timescales.
Abstract Strongly correlated solids are complex and fascinating quantum systems, where new electronic states continue to emerge, especially when interaction with light triggers interplay between them. In this interplay, a sub-laser-cycle electronic response is particularly attractive as a tool for the ultrafast manipulation of matter at the petahertz scale. Here we introduce a new type of nonlinear multidimensional spectroscopy, which allows us to unravel charge and energy flows in strongly correlated systems interacting with few-cycle infrared pulses and the complex interplay between different correlated states evolving on the sub-femtosecond timescale. We demonstrate that the sub-cycle spectroscopy of a single-particle electronic response is extremely sensitive to correlated many-body dynamics and provides direct access to many-body response functions. For the two-dimensional Hubbard model under the influence of ultrashort, intense electric-field transients, we resolve the sub-femtosecond pathways of charge and energy flows between localized and delocalized many-body states and the creation of a highly correlated state surviving after the end of the laser pulse. Our findings open the way towards a regime of imaging and manipulating strongly correlated materials at optical rates, beyond the multicycle approach employed in Floquet engineering, with the sub-cycle response being a key tool for accessing many-body phenomena.
The correlated behavior of electrons determines the structure and optical properties of molecules, semiconductors, and other systems. Valuable information on these correlations is provided by measuring the response to femtosecond laser pulses, which probe the very short time period during which the excited particles remain correlated. The interpretation of four-wave-mixing techniques, commonly used to study the energy levels and dynamics of many-electron systems, is complicated by many competing effects and overlapping resonances. Here we propose a coherent optical technique, specifically designed to provide a background-free probe for electronic correlations in many-electron systems. The proposed signal pulse is generated only when the electrons are correlated, which gives rise to an extraordinary sensitivity. The peak pattern in two-dimensional plots, obtained by displaying the signal versus two frequencies conjugated to two pulse delays, provides a direct visualization and specific signatures of the many-electron wave functions.
Thermalization in strongly correlated fermionic systems remains a central open problem in quantum many-body physics. In this work, we investigate the real-time dynamics and the approach to thermalization in the two-dimensional Hubbard model, a paradigmatic framework for correlated electrons, relevant to high-temperature superconductivity and ultracold quantum simulation. Focusing on the half-filled square lattice, we monitor the time evolution of the double occupancy following a quench in the on-site interaction UUU, and assess whether its long-time value is captured by a canonical thermal ensemble. We employ time-dependent variational Monte Carlo methods combined with transformer-based Neural-Network Quantum States to accurately describe the nonequilibrium dynamics of fermions, especially for the behavior at long times, thereby accessing regimes that were previously inaccessible to numerical simulations. Our results reveal two dynamical behaviors: for weak to intermediate interactions, the double occupancy rapidly approaches the thermal prediction, consistent with ergodic evolution; beyond a critical interaction UCU_{C}UC​, the dynamics remains distinct from the thermal expectation on the timescales investigated, revealing signatures of a prethermal plateau delaying fast relaxation. These results establish numerical simulation as a powerful tool to probe nonequilibrium quantum phenomena in correlated fermionic matter.