arXiv subjects

Hannes Böckmann

Publications and source records attributed to Hannes Böckmann.

3 recordsLinked to original sources

arXiv2026

Surface-Sensitive Mapping of Anisotropic Phonon Cascades in T$_{d}$-WTe$_{2}$

Understanding how energy flows from photoexcited carriers into the lattice is essential for describing nonequilibrium phenomena in low-symmetry quantum materials. Here, we use ultrafast low-energy electron diffraction and diffuse scattering to probe momentum-resolved phonon dynamics at the surface of T$_d$-WTe$_2$, a strongly anisotropic semimetal. Following optical excitation, the Debye--Waller suppression of Bragg peaks exhibits a biexponential increase of the mean-squared atomic displacement, indicating sequential lattice relaxation. Analysis of the diffuse background reveals a preferential intensity build-up parallel to the tungsten-chain axis in the material, attributed to anisotropic electron--phonon coupling during electronic cooling which precedes anharmonic phonon--phonon scattering and subsequent thermalization across the surface Brillouin zone. The results identify a hierarchical relaxation pathway in which energy is first deposited into selected finite-momentum phonons before spreading through the broader lattice bath. Our work highlights the importance of momentum-resolved diffuse scattering for disentangling electron--phonon and phonon--phonon relaxation in anisotropic topological semimetals.

cond-mat.mtrl-sci↗

arXiv2024

Valley-controlled photoswitching of metal-insulator nanotextures

Spatial heterogeneity and phase competition are hallmarks of strongly-correlated materials, promising tunable functionality on the nanoscale. Light-induced switching of a correlated insulator to a metallic state is well established. However, optical excitation generally lacks the specificity to select sub-wavelength domains and control final textures. Here, we employ valley-selective photodoping to drive the domain-specific quench of a textured Peierls insulator. Polarized excitation leverages the anisotropy of quasi-one-dimensional states at the correlated gap to initiate an insulator-to-metal transition with minimal electronic heating. We find that averting dissipation facilitates domain-specific carrier confinement, control over nanotextured phases, and a prolonged lifetime of the metastable metallic state. Complementing existing manipulation schemes, valley-selective photoexcitation will enable the activation of electronic phase separation beyond thermodynamic limitations, facilitating optically-controlled hidden states, engineered heterostructures, and polarization-sensitive percolation networks.

cond-mat.str-el↗

arXiv2022

Mode-selective ballistic pathway to a metastable electronic phase

Exploiting vibrational excitation for the dynamic control of material properties is an attractive goal with wide-ranging technological potential. Most metal-to-insulator transitions are mediated by few structural modes and are thus ideal candidates for the selective driving towards a desired electronic phase. Such targeted navigation within a generally multi-dimensional potential energy landscape requires microscopic insight into the non equilibrium pathway. However, the exact role of coherent inertial motion across the transition state has remained elusive. Here, we demonstrate mode-selective control over the metal-to-insulator phase transition of atomic indium wires on the Si(111) surface, monitored by ultrafast low-energy electron diffraction. We use tailored pulse sequences to individually enhance or suppress key phonon modes and thereby steer the collective atomic motion within the potential energy surface underlying the structural transformation. Ab initio molecular dynamics simulations demonstrate the ballistic character of the structural transition along the deformation vectors of the Peierls amplitude modes. Our work illustrates that coherent excitation of collective modes via exciton-phonon interactions evades entropic barriers and enables the dynamic control of materials functionality.

cond-mat.mes-hall↗