Marcel Reutzel

Bio: Marcel Reutzel is an academic researcher from University of Göttingen. The author has contributed to research in topics: Physics & Excited state. The author has an hindex of 11, co-authored 25 publications receiving 308 citations. Previous affiliations of Marcel Reutzel include University of Marburg & University of Pittsburgh.

Coherent Two-Dimensional Multiphoton Photoelectron Spectroscopy of Metal Surfaces

Abstract: A new technique for studying interactions between light and metals provides insight into how some electrons are excited by incoming photons, overturning a more than 20-year-old accepted model.

Nonlinear Plasmonic Photoelectron Response of Ag(111).

Abstract: Photons can excite collective and single-particle excitations in metals; the collective plasmonic excitations are of keen interest in physics, chemistry, optics, and nanotechnology because they enhance coupling of electromagnetic energy and can drive nonlinear processes in electronic materials, particularly where their dielectric function ϵ(ω) approaches zero We investigate the nonlinear angle-resolved two-photon photoemission (2PP) spectroscopy of the Ag(111) surface through the ϵ(ω) near-zero region In addition to the Einsteinian single-particle photoemission, the 2PP spectra report unequivocal signatures of nonlocal dielectric, plasmonically enhanced, excitation processes

Time-resolved momentum microscopy with a 1 MHz high-harmonic extreme ultraviolet beamline.

Abstract: Recent progress in laser-based high-repetition rate extreme ultraviolet (EUV) light sources and multidimensional photoelectron spectroscopy enables the build-up of a new generation of time-resolved photoemission experiments. Here, we present a setup for time-resolved momentum microscopy driven by a 1 MHz fs EUV table-top light source optimized for the generation of 26.5 eV photons. The setup provides simultaneous access to the temporal evolution of the photoelectron’s kinetic energy and in-plane momentum. We discuss opportunities and limitations of our new experiment based on a series of static and time-resolved measurements on graphene.

Complex Surface Chemistry of an Otherwise Inert Solvent Molecule: Tetrahydrofuran on Si(001)

Abstract: The reaction of tetrahydrofuran (THF), an otherwise inert solvent molecule, on Si(001) was experimentally studied in ultrahigh vacuum. Using scanning tunneling microscopy (STM) and photoelectron spectroscopy at variable temperature, we could both isolate a datively bound intermediate state of THF on Si(001), as well as the final configuration that bridges two dimer rows of the Si(001) surface after ether cleavage. The

Chemoselective Reactivity of Bifunctional Cyclooctynes on Si(001)

Abstract: Controlled organic functionalization of silicon surfaces as an integral part of semiconductor technology offers new perspectives for a wide range of applications. The high reactivity of the silicon dangling bonds, however, presents a major hindrance for the first basic reaction step of such a functionalization, that is, the chemoselective attachment of bifunctional organic molecules on the pristine silicon surface. We overcome this problem by employing cyclooctyne as the major building block of our strategy. Functionalized cyclooctynes are shown to react on Si(001) selectively via the strained cyclooctyne triple bond while leaving the side groups intact. The achieved selectivity originates from the distinctly different adsorption dynamics of the separate functionalities: A direct adsorption pathway is demonstrated for cyclooctyne as opposed to the vast majority of other organic functional groups. The latter ones react on Si(001) via a metastable intermediate, which makes them effectively unreactive in com...

a Quantum-Mechanical Theory of the Contribution of Excitons to the Complex Dielectric Constant of Crystals.

Abstract: It is shown that the ordinary semiclassical theory of the absorption of light by exciton states is not completely satisfactory (in contrast to the case of absorption due to interband transitions). A more complete theory is developed. It is shown that excitons are approximate bosons, and, in interaction with the electromagnetic field, the exciton field plays the role of the classical polarization field. The eigenstates of the system of crystal and radiation field are mixtures of photons and excitons. The ordinary one-quantum optical lifetime of an excitation is infinite. Absorption occurs only when "three-body" processes are introduced. The theory includes "local field" effects, leading to the Lorentz local field correction when it is applicable. A Smakula equation for the oscillator strength in terms of the integrated absorption constant is derived.

Valley selective optical Stark effect in monolayer WS2

Abstract: Breaking space-time symmetries in two-dimensional crystals (2D) can dramatically influence their macroscopic electronic properties. Monolayer transition metal dichalcogenides (TMDs) are prime examples where the intrinsically broken crystal inversion symmetry permits the generation of valley-selective electron populations [1–4], even though the two valleys are energetically degenerate, locked by time-reversal symmetry. Lifting the valley degeneracy in these materials is of great interest because it would allow for valley-specific band engineering and offer additional control in valleytronic applications. While applying a magnetic field should in principle accomplish this task, experiments to date have observed no valley-selective energy level shifts in fields accessible in the laboratory. Here we show the first direct evidence of lifted valley degeneracy in the monolayer TMD WS2 [5]. By applying intense circularly polarized light, which breaks time-reversal symmetry, we demonstrate that the exciton level in each valley can be selectively tuned by as much as 18 meV via the optical Stark effect. These results offer a novel way to control valley degree of freedom and may provide a means to realize new valley-selective Floquet topological phases [6–8] in 2D TMDs.

Angle-Resolved Photoemission Studies of Quantum Materials

Abstract: Angle-resolved photoemission spectroscopy (ARPES) has emerged as a leading experimental probe for studying the complex phenomena in quantum materials, a subject of increasing importance The power of this technique stems from the directness and the richness of the momentum-resolved information it can provide, such as band dispersion, Fermi surface topology, and electron self-energy Over the past decade, the significantly improved energy and momentum resolution and carefully matched experiments have turned this technique into a sophisticated tool in characterizing the electronic structure of complex materials This revolution is mostly evident in the study of cuprate high-temperature superconductors More recently, this technique has played a critical role in advancing our understanding of the newly discovered iron-based superconductors and topological insulators In this paper we review some of the recent ARPES results and discuss the future perspective in this rapidly developing field

Strong-field nano-optics

Abstract: The present status and development of strong-field nano-optics, an emerging field of nonlinear optics, is discussed. A nonperturbative regime of light-matter interactions is reached when the amplitude of the external electromagnetic fields that are driving a material approach or exceed the field strengths that bind the electrons inside the medium. In this strong-field regime, light-matter interactions depend on the amplitude and phase of the field, rather than its intensity, as in more conventional perturbative nonlinear optics. Traditionally such strong-field interactions have been intensely investigated in atomic and molecular systems, and this has resulted in the generation of high-harmonic radiation and laid the foundations for contemporary attosecond science. Over the past decade, however, a new field of research has emerged, the study of strong-field interactions in solid-state nanostructures. By using nanostructures, specifically those made out of metals, external electromagnetic fields can be localized on length scales of just a few nanometers, resulting in signficantly enhanced field amplitudes that can exceed those of the external field by orders of magnitude in the vicinity of the nanostructures. This leads not only to dramatic enhancements of perturbative nonlinear optical effects but also to significantly increased photoelectron yields. It resulted in a wealth of new phenomena in laser-solid interactions that have been discovered in recent years. These include the observation of above-threshold photoemission from single nanostructures, effects of the carrier-envelope phase on the photoelectron emission yield from metallic nanostructures, and strong-field acceleration of electrons in optical near fields on subcycle timescales. The current state of the art of this field is reviewed, and several scientific applications that have already emerged from the fundamental discoveries are discussed. These include, among others, the coherent control of localized electromagnetic fields at the surface of solid-state nanostructures and of free-electron wave packets by such optical near fields, resulting in the creation of attosecond electron bunches, the coherent control of photocurrents on nanometer length and femtosecond timescales by the electric field of a laser pulse, and the development of new types of ultrafast electron microscopes with unprecedented spatial, temporal, and energy resolution. The review concludes by highlighting possible future developments, discussing emerging topics in photoemission and potential strong-field nanophotonic devices, and giving perspectives for coherent ultrafast microscopy techniques. More generally, it is shown that the synergy between ultrafast science, plasmonics, and strong-field physics holds promise for pioneering scientific discoveries in the upcoming years. (Less)