arXiv subjects

Pavel V. Kolesnichenko

Publications and source records attributed to Pavel V. Kolesnichenko.

6 recordsLinked to original sources

arXiv2024

Sub-100-fs formation of dark excitons in monolayer WS2

Two-dimensional semiconducting transition metal dichalcogenides (TMDs) are promising for optoelectronic applications due to their strongly bound excitons. While bright excitons have been thoroughly scrutinized, dark excitons are much less investigated as they are not observable with far-field spectroscopy. However, with their non-zero momenta, dark excitons are significant for applications requiring long-range transport or coupling to external fields. We access such dark excitons in WS2 monolayer using transient photoemission electron microscopy with sub-diffraction limited spatial resolution (75 nm) and exceptionally high temporal resolution (13 fs). Image time series of TMD flakes are recorded at several different fluences. We directly observe the ultrafast formation of dark K-Q excitons in monolayer WS2 occurring within 14-50 fs and follow their subsequent picosecond decay. We distinguish exciton dynamics between the interior and edges of the monolayer TMD and conclude that the long-term evolution of dark excitations is defect-mediated while intervalley scattering is not affected.

cond-mat.mes-hall↗

arXiv2024

Dark excitons and hot electrons modulate exciton-photon strong coupling in metal-organic optical microcavities

Polaritons, formed as a result of strong hybridization of matter with light, are promising for important applications including organic solar cells, optical logic gates, and qubits. Owing to large binding energies of Frenkel excitons (matter), strong matter-light coupling phenomena are possible at room temperature, high exciton densities, and even with low-quality-factor microcavities. In such cases, due to polaritons' high degree of delocalization, simultaneous effects from dark excitons and hot electrons may affect performance of potential devices. Their understanding, therefore, is of paramount importance, but their disentanglement in optical spectroscopy, however, thus far remained unattainable. Here, we overcome this challenge by careful and systematic analysis of transient polaritonic spectra, supported by analytical models. In doing so, we conclude that dark excitons affect the strength of exciton-photon coupling and manifest themselves as Fano-like polaritonic gain-loss spectra. Free electrons add additional loss component to and imprint a two-temperature dynamics on the polaritonic response. The developed general methodology can be applied to a variety of other microcavity structures. Our findings are significant for distinguishing polaritons and other excitations in studies of polariton-electron and plasmon-electron coupling phenomena as well as photonic control over photophysical and photochemical processes.

physics.app-ph↗

arXiv2024

Experimental Evidence of Direct Exchange Interaction Mediating Intramolecular Singlet Fission in Weakly-Coupled Dimers

The electronic interaction between an optically active singlet state ($S_1S_0$) and a dark state of singlet multiplicity, known as correlated triplet pair ($^1[TT]$), plays a crucial role in the effective transformation from $S_1S_0$ to $^1[TT]$ during intramolecular singlet fission (iSF). This process is understood through mechanisms such as direct exchange coupling and incoherent processes that involve super-exchange coupling through charge-transfer states. However, most insights into these mechanisms are derived from theoretical studies due to the difficulties in obtaining experimental evidence. In this study, we investigate the excited-state interactions between $S_1S_0$ and $^1[TT]$ in spiro-conjugated iSF sensitizers by employing transient two-dimensional electronic spectroscopy. This approach allows us to focus on the early stages of the conversion from $S_1S_0$ to $^1[TT]$. Upon optical excitation, a superposition of $S_1S_0$ and $^1[TT]$ is created, which gradually transitions to favor $^1[TT]$ within the characteristic time frames of iSF. The observed high-order signals indicate circular repopulation dynamic that effectively reinitiates the iSF process from higher energy electronic states. Our findings, supported by semi-quantum-mechanical simulations of the experimental data, suggest the presence of a direct iSF mechanism in the dimers, facilitated by weak non-adiabatic coupling between $S_1S_0$ and $^1[TT]$. This experiment provides new insights into the equilibrium between the two electronic states, a phenomenon previously understood primarily through theoretical models.

physics.chem-ph↗

arXiv2021

Neural-network-powered pulse reconstruction from one-dimensional interferometric cross-correlation traces

Any ultrafast optical spectroscopy experiment is usually accompanied by the necessary routine of ultrashort-pulse characterisation. The majority of pulse characterisation approaches solve either a one-dimensional (e.g. via interferometry) or a two-dimensional (e.g. via frequency-resolved measurements) problem. Solution of the two-dimensional pulse-retrieval problem is generally more consistent due to problem's over-determined nature. In contrast, the one-dimensional pulse-retrieval problem is impossible to solve unambiguously as ultimately imposed by the fundamental theorem of algebra. In cases where additional constraints are involved, the one-dimensional problem may be possible to solve, however, existing iterative algorithms lack generality, and often stagnate for complicated pulse shapes. Here we use a deep neural network to unambiguously solve a constrained one-dimensional pulse-retrieval problem and show the potential of fast, reliable, and complete pulse characterisation using interferometric cross-correlation time traces (determined by the pulses with partial spectral overlap).

physics.optics↗

arXiv2020

Multidimensional Analysis of Excitonic Spectra of Monolayers of Tungsten Disulphide: Towards Computer Aided Identification of Structural and Environmental Perturbations of 2D Materials

Despite 2D materials holding great promise for a broad range of applications, the proliferation of devices and their fulfillment of real-life demands are still far from being realized. Experimentally obtainable samples commonly experience a wide range of perturbations (ripples and wrinkles, point and line defects, grain boundaries, strain field, doping, water intercalation, oxidation, edge reconstructions) significantly deviating the properties from idealistic models. These perturbations, in general, can be entangled or occur in groups with each group forming a complex perturbation making the interpretations of observable physical properties and the disentanglement of simultaneously acting effects a highly non-trivial task even for an experienced researcher. Here we generalise statistical correlation analysis of excitonic spectra of monolayer WS2, acquired by hyperspectral absorption and photoluminescence imaging, to a multidimensional case, and examine multidimensional correlations via unsupervised machine learning algorithms. Using principle component analysis we are able to identify 4 dominant components that are correlated with tensile strain, disorder induced by adsorption or intercalation of environmental molecules, multi-layer regions and charge doping, respectively. This approach has the potential to determine the local environment of WS2 monolayers or other 2D materials from simple optical measurements, and paves the way towards advanced, machine-aided, characterisation of monolayer matter.

cond-mat.mes-hall↗

arXiv2019

Disentangling the effects of doping, strain and defects in monolayer WS2 by optical spectroscopy

Monolayers of transition metal dichalcogenides (TMdC) are promising candidates for realization of a new generation of optoelectronic devices. The optical properties of these two-dimensional materials, however, vary from flake to flake, or even across individual flakes, and change over time, all of which makes control of the optoelectronic properties challenging. There are many different perturbations that can alter the optical properties, including charge doping, defects, strain, oxidation, and water intercalation. Identifying which perturbations are present is usually not straightforward and requires multiple measurements using multiple experimental modalities, which presents barriers when attempting to optimise preparation of these materials. Here, we apply highresolution photoluminescence and differential reflectance hyperspectral imaging in situ to CVD-grown WS2 monolayers. By combining these two optical measurements and using a statistical correlation analysis we are able to disentangle three contributions modulating optoelectronic properties of these materials: electron doping, strain and defects. In separating these contributions, we also observe that the B-exciton energy is less sensitive to variations in doping density than A-excitons.

cond-mat.mtrl-sci↗