arXiv subjects

Ingo Barke

Publications and source records attributed to Ingo Barke.

10 recordsLinked to original sources

arXiv2026

Photoemission intermittency via stochastic gating in rubrene nanowires coupled to plasmonic silver nanoparticles

In this work, we report a new nanoscale phenomenon observed as photoemission intermittency (On-Off electron emission), manifested as stochastic bursts in electron yield at quasi-one-dimensional organic wires and silver nanoparticles interface. Energy-resolved measurements reveal that the emitted electrons carry out hybrid information, containing photoelectron yield enhancement associated with the nanoparticles and kinetic energies determined by the organic semiconductor. The intermittency results in a dynamic shift of the electron spectra correlating with the photoelectron yield. We attribute the observed behaviour to the photo-hole accumulation and stochastic gating of charge due to electron-hole separation at the nano interface. These findings introduces the photoemission intermittency as a nanoscale phenomenon indicating a new dynamic regime of charge assisted emission at organic-plasmonic interfaces. Keywords: rubrene, nanoparticle, PEEM, exciton, charge

cond-mat.mtrl-sci↗

arXiv2026

Dual-wavelength control of charge accumulation in rubrene microcrystals with anisotropic conductivity

Previously, a novel type of rubrene microcrystals was reported, forming two distinct sectors -- diamond- and triangular-shaped -- that exhibit pronounced contrasts in photoluminescence (PL) spectra and exciton dynamics. In the present work, their internal electronic structure is investigated using time-of-flight photoemission electron spectroscopy (TOF-PES), revealing that the two sector's different charging characteristics arising from anisotropic conductivities. Upon photoemission via a one-photon photoemission (1PPE) process excited by 6.2 eV (200 nm) photons, the diamond-shaped sectors accumulate significant charge, whereas the triangular sectors remain essentially uncharged. The charge accumulation in the diamond sectors can be neutralized by additional sub-threshold illumination, which generates charge carriers through internal photoeffect. The dynamics and energetics of the observed band shifting is described quantitatively by a model combining surface capacitance and drift-diffusion. These crystalline systems enable the creation of built-in charge landscapes that can be manipulated both spatially and temporally.

cond-mat.mtrl-sci↗

arXiv2025

Plasmon-assisted photoelectron emission in a model cluster using time-dependent density functional theory and the time-dependent surface-flux method

We investigate plasmon-assisted photoelectron emission using a one-dimensional time-dependent density-functional theory (TDDFT) model. Photoelectron spectra are computed with the time-dependent surface-flux (t-SURFF) method. In addition to the expected above-threshold ionization (ATI) comb, we observe peaks that arise from long-lived plasmon oscillations and the associated electron emission occurring after the laser pulse. We further analyze the positions of these peaks and their scaling behavior with the laser intensity.

quant-ph↗

arXiv2025

Zone-sectored organic crystals with spatially resolved exciton dynamics

Among the organic semiconductors, rubrene stands out in terms of hole mobility, luminescence yield and exciton migration distance. A novel type of rubrene microcrystal is prepared in the orthorhombic phase, exhibiting zone-sectored tabular domains with distinct photoluminescence (PL) characteristics. These sectors exhibit distinct PL spectra and time-evolution, arising from differences in the in-plane orientation of the orthorhombic unit cell relative to the crystal surface. A combination of polarised optical microscopy, fluorescence lifetime imaging microscopy (FLIM), and atomic force microscopy (AFM) is used to characterise the samples in terms of crystal orientation, fluorescence lifetime, and photoluminescence spectra. Spatially resolved PL spectroscopy reveals that the redshifted 650 nm emission band has polarisation along the transition dipole moment and is associated with high photon absorption due to the alignment of excitation polarisation and transition dipole moment and selectively localized within specific sectors of the crystal. The detected photon originates from direct emission of a geminate coherent triplet pair, or from its fusion. This band exhibits pure mono-exponential dynamics with 3.7 ns lifetime. The triplet fusion behaviour in the succeeding time regimes can be treated in the framework of power law scaling and random walk. The emission kinetics are modelled using rate equations describing geminate and non-geminate exciton fusion processes, enabling a quantitative interpretation of the spatially resolved PL kinetics. These findings introduce a material-based strategy, opening novel routes for photonic applications and light harvesting.

physics.optics↗

arXiv2025

Imaging domain boundaries of rubrene thin crystallites by photoemission electron microscopy

The progress of designing organic semiconductors is extensively dependent on the quality of prepared organic molecular assemblies, since the charge transport mechanism is strongly efficient in highly ordered crystals compared to amorphous domains. Here we present a comprehensive photoemission electron microscopy (PEEM) and time-of-flight (TOF) spectroscopic study of rubrene ($\mathrm{C}_{48}\mathrm{H}_{24}$) thin crystals focusing on recently developed orthorhombic crystalline morphologies applied in organic electronic devices. Using femtosecond pulsed lasers with photon energies between 3-6 eV, we explore the interplay between photoemission processes, crystal morphology, and defect states. In a 2-photon photoemission process (2PPE), the PEEM images reveal dominant emission localized at domain boundaries, indicating strong contributions from trap states. In contrast, in 1PPE nm excitation uniform emission across the crystal surface is observed, highlighting a fundamental difference in photoemission mechanisms. Furthermore, in the intermediate photon energy range, we identify a nonlinear, non-integer photon order, where mostly the triclinic morphology contributes to the emission, distinguishing it from the orthorhombic phase. These findings provide a new framework for assessing the quality and internal structure of organic semiconductor thin films via wavelength-dependent photoemission imaging and spectroscopy.

cond-mat.mtrl-sci↗

arXiv2024

Morphology and structural properties of thin rubrene crystallites grown on graphite

Crystallization of rubrene, progressing from an amorphous phase to a triclinic meta-stable and ultimately to the orthorhombic stable phase, offers broad applications not only in organic electronic devices but also for in-depth studies of optical and electronic properties, including exciton distribution and dynamics. We investigate the crystallization of rubrene on highly oriented pyrolytic graphite (HOPG), aiming at the growth of the preferred rubrene orthorhombic phase, which has been reported to have one of the highest charge mobilities in organic semiconductors. This is achieved through controlled heating and enhanced partial pressure. Through precise control of the initial deposition on the substrate, we investigate the growth habit of rubrene crystals by high-rate heat treatment beyond the second crystallization temperature. Furthermore, this work addresses thermal stability and photodegradation across various morphologies.

cond-mat.mtrl-sci↗

arXiv2023

Melting, bubble-like expansion and explosion of superheated plasmonic nanoparticles

We report on time-resolved coherent diffraction imaging of gas-phase silver nanoparticles, strongly heated via their plasmon resonance. The x-ray diffraction images reveal a broad range of phenomena for different excitation strengths, from simple melting over strong cavitation to explosive disintegration. Molecular dynamics simulations fully reproduce this behavior and show that the heating induces rather similar trajectories through the phase diagram in all cases, with the very different outcomes being due only to whether and where the stability limit of the metastable superheated liquid is crossed.

physics.atm-clus↗

arXiv2022

Three-Dimensional Coherent Diffractive Imaging of Isolated Faceted Nanostructures

The structure and dynamics of isolated nanosamples in free flight can be directly visualized via single-shot coherent diffractive imaging using the intense and short pulses of X-ray free-electron lasers. Wide-angle scattering images even encode three-dimensional morphological information of the samples, but the retrieval of this information remains a challenge. Up to now, effective three-dimensional morphology reconstructions from single shots were only achieved via fitting with highly constrained models, requiring a priori knowledge about possible geometrical shapes. Here we present a much more generic imaging approach. Relying on a model that allows for any sample morphology described by a convex polyhedron, we reconstruct wide-angle diffraction patterns from individual silver nanoparticles. In addition to known structural motives with high symmetries, we retrieve imperfect shapes and agglomerates which were not accessible previously. Our results open new routes towards true 3D structure determination of single nanoparticles and, ultimately, 3D movies of ultrafast nanoscale dynamics.

physics.atm-clus↗

arXiv2022

The Scatman: an approximate method for fast wide-angle scattering simulations

Single-shot Coherent Diffraction Imaging (CDI) is a powerful approach to characterize the structure and dynamics of isolated nanoscale objects such as single viruses, aerosols, nanocrystals or droplets. Using X-ray wavelengths, the diffraction images in CDI experiments usually cover only small scattering angles of few degrees. These small-angle patterns represent the magnitude of the Fourier transform of the two-dimensional projection of the sample's electron density, which can be reconstructed efficiently but lacks any depth information. In cases where the diffracted signal can be measured up to scattering angles exceeding 10 degrees, i.e. in the wide-angle regime, three-dimensional morphological information of the target is contained in a single-shot diffraction pattern. However, the extraction of the 3D structural information is no longer straightforward and defines the key challenge in wide-angle CDI. So far, the most convenient approach relies on iterative forward fitting of the scattering pattern using scattering simulations. Here we present the Scatman, an approximate and fast numerical tool for the simulation and iterative fitting of wide-angle scattering images of isolated samples. Furthermore, we publish and describe in detail our Open Source software implementation of the Scatman algorithm, PyScatman. The Scatman approach yields quantitative results for weakly scattering samples. PyScatman is capable of computing wide-angle scattering patterns in few milliseconds even on consumer-level computing hardware. The high computational efficiency of PyScatman enables effective data analysis based on model fitting, thus representing an important step towards a systematic application of 3D Coherent Diffraction Imaging from single wide-angle diffraction patterns in various scientific communities.

physics.comp-ph↗

arXiv2009

Structure and energetics of Si(111)-(5x2)-Au

We propose a new structural model for the Si(111)-(5x2)-Au reconstruction. The model incorporates a new experimental value of 0.6 monolayer for the coverage of gold atoms, equivalent to six gold atoms per 5x2 cell. Five main theoretical results, obtained from first-principles total-energy calculations, support the model. (1) In the presence of silicon adatoms the periodicity of the gold rows spontaneously doubles, in agreement with experiment. (2) The dependence of the surface energy on the adatom coverage indicates that a uniformly covered phase is unstable and will phase-separate into empty and covered regions, as observed experimentally. (3) Theoretical scanning tunneling microscopy images are in excellent agreement with experiment. (4) The calculated band structure is consistent with angle-resolved photoemission spectra; analysis of their correspondence allows the straightforward assignment of observed surface states to specific atoms. (5) The calculated activation barrier for diffusion of silicon adatoms along the row direction is in excellent agreement with the experimentally measured barrier.

cond-mat.mtrl-sci↗