arXiv subjects

Matthias Hengsberger

Publications and source records attributed to Matthias Hengsberger.

8 recordsLinked to original sources

arXiv2025

Detection of Image Potential States above the vacuum level in GeTe

The ferroelectric semiconductor α-GeTe(111) has attracted significant attention in the last decade due to its unique properties, with extensive studies focusing on its occupied electronic bandstructure. In contrast, its unoccupied states - particularly those near the conduction band minimum - remain largely unexplored. In an effort to characterize those states, we surprisingly observe three image potential states (IPS) in α-GeTe(111) extending up to 0.8 eV above the vacuum level. Using time and angle-resolved photoemission spectroscopy, we resolve the full parabolic dispersions of the first three IPS and determine their binding energies. Our analysis, combined with Bloch spectral function calculations, reveals that the unexpected persistence of IPS above the vacuum level originates from strong dipole transitions and the presence of large electron reservoirs in GeTe.

cond-mat.str-el↗

arXiv2021

Importance of surface oxygen vacancies for ultrafast hot carrier relaxation and transport in Cu$_2$O

Cu$_2$O has appealing properties as an electrode for photo-electrochemical water splitting, yet its practical performance is severely limited by inefficient charge extraction at the interface. Using hybrid DFT calculations, we investigate carrier capture processes by oxygen vacancies (V$_\mathrm{O}$) in the experimentally observed ($\sqrt{3} \times \sqrt{3}$)R30$^{\circ}$ reconstruction of the dominant (111) surface. Our results show that these V$_\mathrm{O}$ are doubly ionized and that associated defects states strongly suppress electron transport. In particular, the excited electronic state of a singly charged V$_\mathrm{O}$ plays a crucial role in the non-radiative electron capture process with a capture coefficient of about 10$^{-9}$~cm$^3$/s and a lifetime of 0.04~ps, explaining the experimentally observed ultrafast carrier relaxation. These results highlight that engineering the surface V$_\mathrm{O}$ chemistry will be a crucial step in optimizing Cu$_2$O for photoelectrode applications.

cond-mat.mtrl-sci↗

arXiv2018

Algorithms and image formation in orbital tomography

Orbital tomography has recently been established as a technique to reconstruct molecular orbitals directly from photoemission data using iterative phase retrieval algorithms. In this work, we present a detailed description of steps for processing of the photoemission data followed by an improved iterative phase retrieval procedure and the interpretation of reconstructed two-dimensional orbital distributions. We address the issue of background subtraction by suggesting a signal restoration routine based on the maximization of mutual information algorithm and solve the problem of finding the geometrical center in the reconstruction by using a tight-centered object support in a two-step phase retrieval procedure. The proposed image processing and improved phase retrieval procedures are used to reconstruct the highest occupied molecular orbital of pentacene on Ag(110), using photoemission data only. The results of the reconstruction agree well with the density functional theory simulation, modified to comply with the experimental conditions. By comparison with photoelectron holography, we show that the reconstructed two-dimensional orbital distribution can be interpreted as a superposition of the in-focus orbital distribution evaluated at the z = 0 plane and out-of-focus distributions evaluated at other z = const planes. Three-dimensional molecular orbital distributions could thus be reconstructed directly from two-dimensional photoemission data, provided the axial resolution of the imaging system is high enough.

physics.chem-ph↗

arXiv2016

Application of iterative phase-retrieval algorithms to ARPES orbital tomography

Electronic wave functions of planar molecules can be reconstructed via inverse Fourier transform of angle-resolved photoelectron spectroscopy (ARPES) data, provided the phase of the electron wave in the detector plane is known. Since the recorded intensity is proportional to the absolute square of the Fourier transform of the initial state wave function, information about the phase distribution is lost in the measurement. It was shown that the phase can be retrieved in some cases by iterative algorithms using a priori information about the object such as its size and symmetry. We suggest a more generalized and robust approach for the reconstruction of molecular orbitals based on state-of-the-art phase-retrieval algorithms currently used in coherent diffraction imaging. We draw an analogy between the phase problem in molecular orbital imaging by ARPES and of that in optical coherent diffraction imaging by performing an optical analogue experiment on micrometer-sized structures. We successfully reconstruct amplitude and phase of both the micrometer-sized objects and a molecular orbital from the optical and photoelectron far-field intensity distributions, respectively, without any prior information about the shape of the objects.

cond-mat.other↗

arXiv2014

Temporal and spectral disentanglement of laser-driven electron tunneling emission from a solid

By measuring energy spectra of the electron emission from a sharp tungsten tip induced by few-cycle laser pulses, the laser-field dependence of the emission mechanism was investigated. In strong laser fields, we confirm the appearance of laser-driven tunneling emission and find that it can be disentangled from the concomitant photo-excited electron emission, both temporally and spectrally, by the opening of a peculiar emission channel. This channel involves prompt laser-driven tunneling emission and subsequent laser-driven electron re-scattering off the surface, delayed by the electrons traveling far inside the metal before scattering. The quantitative understanding of these processes gives insights on attosecond tunneling emission from solids and should prove useful in designing new types of pulsed electron sources.

cond-mat.mes-hall↗

arXiv2011

Mechanism of Laser-induced Field Emission

We have measured electron energy distribution curves (EDCs) of the laser-induced field emission from a tungsten tip. Field emission from photo-excited nonequilibrium electron distributions were clearly observed, while no enhanced field emission due to optical electric fields appeared up to values of 1.3 V/nm. Thus, we experimentally confirm the emission mechanism. Simulated transient EDCs show that electron dynamics plays a significant role in the laser-induced field emission. The results should be useful to find optimal parameters for defining the temporal and spectral characteristics of electron pulses for many applications based on pulsed field emission.

cond-mat.mes-hall↗

arXiv2010

Laser-induced Field Emission from Tungsten Tip: Optical Control of Emission Sites and Emission Process

Field-emission patterns from a clean tungsten tip apex induced by femtosecond laser pulses have been investigated. Strongly asymmetric field-emission intensity distributions are observed depending on three parameters: (1) the polarization of the light, (2) the azimuthal and (3) the polar orientation of the tip apex relative to the laser incidence direction. In effect, we have realized an ultrafast pulsed field-emission source with site selectivity of a few tens of nanometers. Simulations of local fields on the tip apex and of electron emission patterns based on photo-excited nonequilibrium electron distributions explain our observations quantitatively. Electron emission processes are found to depend on laser power and tip voltage. At relatively low laser power and high tip voltage, field-emission after two-photon photo-excitation is the dominant process. At relatively low laser power and low tip voltage, photoemission processes are dominant. As the laser power increases, photoemission from the tip shank becomes noticeable.

cond-mat.mes-hall↗

arXiv2009

Optical Control of Field-Emission Sites by Femtosecond Laser Pulses

We have investigated field emission patterns from a clean tungsten tip apex induced by femtosecond laser pulses. Strongly asymmetric modulations of the field emission intensity distributions are observed depending on the polarization of the light and the laser incidence direction relative to the azimuthal orientation of tip apex. In effect, we have realized an ultrafast pulsed field-emission source with site selectivity on the 10 nm scale. Simulations of local fields on the tip apex and of electron emission patterns based on photo-excited nonequilibrium electron distributions explain our observations quantitatively.

cond-mat.mes-hall↗