arXiv subjects

Matthias Hensen

Publications and source records attributed to Matthias Hensen.

6 recordsLinked to original sources

arXiv2026

Disentangling Single- and Biexciton Dynamics with Photoelectron-Detected Two-Dimensional Electronic Spectroscopy

Action-detected two-dimensional (2D) spectroscopy resolves the time-dependent nonlinear optical response of a quantum system by recording incoherently detected observables such as fluorescence, photoelectrons, or photocurrents which reflect the system's excited-state population. Processes such as exciton-exciton annihilation alter this population and obscure, for instance, energy transfer processes. This limits the information available from action-detected 2D spectra compared to their coherently detected counterparts. Here we investigate time gating and kinetic-energy filtering in photoelectron-detected 2D spectroscopy to disentangle various processes. We implement a numerical simulation protocol that allows us to calculate photoelectron-detected 2D spectra for various systems, demonstrating that time gating can extract the same information as coherently detected 2D spectroscopy, even when annihilation is present. Furthermore, we can directly infer annihilation dynamics. Kinetic-energy filtering additionally enables the isolation of specific excited-state dynamics. Our simulations demonstrate that time gating and kinetic-energy filtering are promising extensions for photoelectron-detected 2D spectroscopy.

physics.chem-ph↗

arXiv2025

Probing plexciton dynamics with higher-order spectroscopy

Coupling molecular transition dipole moments to surface-plasmon polaritons (SPPs) results in the formation of new optical quasiparticles, i.e., plexcitons. Mixing the specific properties of matter excitations and light modes has proven to be an efficient strategy to alter a variety of molecular processes ranging from chemical reactions to exciton transport. Here, we investigate energy transfer in a plexcitonic system of zinc phthalocyanine (ZnPc) molecules aggregated in the crystalline {\alpha}-phase and an SPP on a planar gold surface. By tuning the angle of incidence, we vary the degree of mixing between excitonic and SPP character of the excited state. We apply our recently developed higher-order pump-probe spectroscopy to separate the system's fifth-order signal describing the dynamics of two-particle interactions. The time it takes for two quasiparticles to meet and annihilate is a measure of their movement and thus the transport of excitation energy in the system. We find that the transport extracted from the fifth-order signal is surprisingly unaffected by the mixing ratio of exciton and SPP contributions of the plexciton. Using a rate equation model, we explain this behavior by fast transition from the plexcitonic states to many localized excitonic dark states that do not have an SPP contribution. Our results give an indication of how hybrid exciton-plasmon systems should be designed to exploit the delocalization of the involved plasmon modes for improved transport.

physics.chem-ph↗

arXiv2025

Plasmonic Su-Schrieffer-Heeger chains with strong coupling amplitudes

Plasmonic many-particle systems with precisely tuned resonances and coupling strengths can exhibit emergent collective properties governed by universal principles. In one-dimensional chains with alternating couplings, known as Su-Schrieffer-Heeger (SSH) systems, this includes the formation of topologically protected mid-gap modes whose intensities localize at the chain's ends. This subwavelength localization at optical frequencies is crucial for achieving strong coupling of mid-gap modes to two-level systems under ambient conditions, extending topological protection to hybrid light-matter states. Here, we have fabricated SSH chains from plasmonic nanoslit resonators with strong inter-resonator coupling. The alternating distance between the nanoslit resonators is controlled with sub-nanometer precision, enabling accurate prediction and experimental observation of topologically protected mid-gap modes via photoemission electron microscopy (PEEM). Our results open the path towards experimental realizations of two-dimensional photonic metasurfaces exhibiting higher-order topological modes that can be strongly coupled to single emitters and quantum materials at ambient conditions.

physics.optics↗

arXiv2022

Pure dephasing induced single-photon parametric down-conversion in an ultrastrong coupled plasmon-exciton system

In coupled quantum systems pure dephasing mechanisms acting on one constituent of the hybrid system break symmetry and enable optical transitions which are forbidden in the non-coupled system, i.e., the pure dephasing bath opens a cascaded dissipation pathway. Here we show that this mechanism enables single-photon induced parametric down-conversion in an ultrastrongly coupled plasmon-exciton system. Fast pure dephasing of the exciton is shown to support photon pair generation as the dominant energy relaxation pathway.

quant-ph↗

arXiv2021

Tunable Surface Phonon Polariton based THz Cavity

Designing and realizing switchable cavities at the infrared and THz frequencies is crucial for achieving novel integrated photonic circuits. Semiconductors like SiC support the propagation of surface phonon polaritons with the ability to tune carrier concentrations via doping. In this manuscript, we investigate the tunability of coupled surface-phonon-plasmon polariton waves inside an elliptical cavity build from a metal-semiconductor heterostructure. We theoretically study the impact of the extra n- and p-carrier doping on the resonant modes of the cavity and we show that for certain cavity modes a Purcell factor of 180 and an on/off switching behavior can be achieved via charge injection. The cavity mode tuning range spans approximately 13 times the resonance width.

physics.optics↗

arXiv2019

Coherent photon coincidence spectroscopy of single quantum systems

Non-equilibrium photon correlations of coherently excited single quantum systems can reveal their internal quantum dynamics and provide spectroscopic access. Here we propose and discuss the fundamentals of a coherent photon coincidence spectroscopy based on the application of laser pulses with variable delay and the detection of an time-averaged two-photon coincidence rate. For demonstration, two simple but important cases, i.e., an exciton - biexciton in a quantum dot and two coupled quantum emitters, are investigated based on quantum dynamics simulations demonstrating that this nonlinear spectroscopy reveals information specific to the particular single quantum system.

quant-ph↗