Searcharxiv⌕ Search

arXiv subjects

Martin Weinelt

Publications and source records attributed to Martin Weinelt.

12 recordsLinked to original sources
arXiv2025

Ultrafast non-equilibrium magnon generation and collapse of spin-orbit hybridization gaps in iron

We distinguish between longitudinal and transverse spin excitations in the ultrafast response of iron by probing exchange splitting {\Delta}Eex and magnetic linear dichroism (MLD) in time- and angleresolved photoemission. Comparing spin-split partner bands at the Fermi level shows that {\Delta}Eex remains constant upon optical excitation. In contrast, the different MLD response of spin-orbitsplit valence bands reveals non-equilibrium, transverse spin dynamics. Magnon generation in Fe is ultrafast, electronic band specific, and drives the collapse of spin-orbit hybridization gaps.

cond-mat.other↗
arXiv2025

Momentum transfer in the ponderomotive potential of near-infrared laser pulses leads to sizable energy shifts and electron-wavepacket squeezing in time-resolved ARPES

We observe momentum transfer in the ponderomotive potential of near-infrared (NIR) laser pulses in time- and angle-resolved photoemission spectroscopy (tr-ARPES) experiments with ultrashort extreme ultraviolet probe pulses. Acceleration of photoelectrons in the transient grating provided by an intense laser pulse reflected at a surface leads to delay-dependent oscillations of electric kinetic energies. Photon and electron momenta determine the oscillation frequency. We experimentally observe and theoretically simulate electron yield modulations driven by a novel electron-energy bunching effect. Measurement results are simulated and fitted with high accuracy. Complete reversion of the ponderomotive momentum transfer allows for retrieval of the undisturbed initial state and the transient band structure for overlapping pump and probe pulses.

cond-mat.mes-hall↗
arXiv2025

Non-Equilibrium Multiplet Excitations probed by the $M_{5,4}$ Branching Ratio in $3d \rightarrow 4f$ X-ray Absorption Spectroscopy

We show that ultrafast electronic $4f$ multiplet transitions in terbium metal are manifested by changes in the relative spectral weight of the $M_5$ and $M_4$ X-ray absorption resonances. Our experimental results are supported by a simulation of excited multiplet spectra with atomistic calculations; they prove that the so-called third rule of Thole and van der Laan, which relates the branching ratio of the spin-orbit split resonances to the total angular momentum $J$ of the excited ion, is also valid in non-equilibrium. The presented detection scheme allows to detect $J$-changing excitation, \textit{i.e}, alterations of spin and orbital states, even in samples without net magnetization. This makes branching-ratio spectroscopy a powerful tool for the quantitative investigation of ultrafast changes in angular momentum $J$.

cond-mat.mtrl-sci↗
arXiv2025

Magnon-mediated terahertz spin transport in metallic Gd|Pt stacks

We study femtosecond spin transport in a Gd|Pt stack induced by a laser pulse. Remarkably, the dynamics of the spin current from Gd to Pt suggests that its dominant driving force is the ultrafast spin Seebeck effect. As the contribution of a transient spin voltage in the metal Gd is minor, Gd acts akin a magnetic insulator here. This view is supported by time- and spin-resolved photoemission, which indicates that a buildup of spin voltage is suppressed by exchange scattering, leading to similar amplitudes and relaxation rates of hot majority- and minority-spin electron populations.

cond-mat.mes-hall↗
arXiv2025

Femtosecond charge and spin dynamics in CoPt alloys

The use of advanced X-ray sources plays a key role in the study of dynamic processes in magnetically ordered materials. The progress in X-ray free electron lasers enables the direct and simultaneous observation of the femtosecond evolution of electron and spin systems through transient X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD), respectively. Such experiments allow us to resolve the response seen in the population of the spin-split valence states upon optical excitation. Here, we utilize circularly polarized ultrashort soft X-ray pulses from the new helical afterburner undulator at the free-electron laser FLASH in Hamburg to study the femtosecond dynamics of a laser-excited CoPt alloy at the Co $L_{3}$ absorption edge. Despite employing a weaker electronic excitation level we find a comparable demagnetization for the Co $3d$-states in CoPt compared to previous measurements on CoPd. This is attributed to distinctly different orbital hybridization and spin-orbit coupling between $3d$ and $4d$ vs. $3d$ and $5d$ elements in the corresponding alloys and multilayers.

cond-mat.mtrl-sci↗
arXiv2024

Local work-function manipulation by external optical stimulation

Strongly differing static dipole moments of the trans and cis isomers of photochromic azobenzene allow for optical switching the work function of azobenzene-functionalized self-assembled monolayers (SAMs). We apply these properties in a fundamental experiment to manipulate the area size of the switched SAM. Azobenzene molecules were excited by ultraviolet laser illumination and the transient isomerization profile of the SAM was spatially resolved recording photoemission electron microscopy (PEEM) images. Thereby we demonstrate the spatial tuning of the SAM work-function and discuss the role of the laser spot-profile in generating sharp edges or gradual changes of the work function.

cond-mat.mes-hall↗
arXiv2021

The role of spin-lattice coupling for ultrafast magnetization changes in rare earth metals

By comparing femtosecond laser-pulse-induced spin dynamics in the surface state of the rare earth metals Gd and Tb we show that the spin polarization of the valence states in both materials decays with significantly different time constants of 15\,ps and 400\,fs, respectively. The distinct spin polarization dynamics in Gd and Tb are opposed by similar exchange splitting dynamics in the two materials. The different time scales observed in our experiment can be attributed to weak and strong $4f$ spin to lattice coupling in Gd and Tb suggesting an intimate coupling of spin polarization and 4f magnetic moment. While in Gd the lattice mainly acts as a heat sink, it contributes significantly to ultrafast demagnetization of Tb. This helps explain why all optical switching is observed in FeGd -- but rarely in FeTb-based compounds.

cond-mat.mes-hall↗
arXiv2021

Strong Momentum-Dependent Electron-Magnon Renormalization of a Surface Resonance on Iron

The coupling of fermionic quasiparticles to magnons is essential for a wide range of processes, from ultrafast magnetization dynamics in ferromagnets to Cooper pairing in superconductors. Although magnon energies are generally much larger than phonon energies, up to now their electronic band renormalization effect in ferromagnetic metals suggests a significantly weaker quasiparticle interaction. Here, using spin- and angle-resolved photoemission, we show an extraordinarily strong renormalization leading to replica-band formation of an iron surface resonance at ~200 meV. Its strong magnetic linear dichroism unveils the magnetic nature and momentum dependence of the energy renormalization. By determining the frequency- and momentum-dependent self-energy due to generic electron-boson interaction to compute the resultant electron spectral function, we show that the surface-state replica formation is consistent with strong coupling to an optical spin wave in a Fe thin film.

cond-mat.mes-hall↗
arXiv2016

Optical properties of azobenzene-functionalized self-assembled monolayers: Intermolecular coupling and many-body interactions

In a joint theoretical and experimental work the optical properties of azobenzene-functionalized self-assembled monolayers (SAMs) are studied at different molecular packing densities. Our results, based on density-functional and many-body perturbation theory, as well as on differential reflectance (DR) spectroscopy, shed light on the microscopic mechanisms ruling photo-absorption in these systems. While the optical excitations are intrinsically excitonic in nature, regardless of the molecular concentration, in densely-packed SAMs intermolecular coupling and local-field effects are responsible for a sizable weakening of the exciton binding strength. Through a detailed analysis of the character of the electron-hole pairs, we show that distinct excitations involved in the photo-isomerization at low molecular concentrations are dramatically broadened by intermolecular interactions. Spectral shifts in the calculated DR spectra are in good agreement with the experimental results. Our findings represent an important step forward to rationalize the excited-state properties of these complex materials.

cond-mat.mtrl-sci↗
arXiv2011

Hot electron driven enhancement of spin-lattice coupling in 4f ferromagnets observed by femtosecond x-ray magnetic circular dichroism

Femtosecond x-ray magnetic circular dichroism was used to study the time-dependent magnetic moment of 4 fs electrons in the ferromagnets Gd and Tb, which are known for their different spin-lattice coupling. We observe a two-step demagnetization with an ultrafast demagnetization time of 750 fs identical for both systems and slower times which differ sizeably with 40 ps for Gd and 8 ps for Tb. We conclude that spin-lattice coupling in the electronically excited state is enhanced up to orders of magnitude compared to equilibrium.

cond-mat.mtrl-sci↗
arXiv2010

Azobenzene versus 3,3',5,5'-tetra-tert-butyl-azobenzene (TBA) at Au(111): Characterizing the role of spacer groups

We present large-scale density-functional theory (DFT) calculations and temperature programmed desorption measurements to characterize the structural, energetic and vibrational properties of the functionalized molecular switch 3,3',5,5'-tetra-tert-butyl-azobenzene (TBA) adsorbed at Au(111). Particular emphasis is placed on exploring the accuracy of the semi-empirical dispersion correction approach to semi-local DFT (DFT-D) in accounting for the substantial van der Waals component in the surface chemical bond. In line with previous findings for benzene and pure azobenzene at coinage metal surfaces, DFT-D significantly overbinds the molecule, but seems to yield an accurate adsorption geometry as far as can be judged from the experimental data. Comparing the trans adsorption geometry of TBA and azobenzene at Au(111) reveals a remarkable insensitivity of the structural and vibrational properties of the -N=N- moiety. This questions the established view of the role of the bulky tert-butyl-spacer groups for the switching of TBA in terms of a mere geometric decoupling of the photochemically active diazo-bridge from the gold substrate.

cond-mat.mtrl-sci↗