arXiv subjects

Thorsten Gölz

Publications and source records attributed to Thorsten Gölz.

4 recordsLinked to original sources

arXiv2026

Phonon-polaritonic skyrmions: Transition from bubble- to Néel-type

Optical skyrmions are members of the emerging topological branch of solid-state physics and photonics, allowing for control over topological light textures through light-matter interactions. However, in nanophotonics their practical application has been severely limited by high inherent losses in plasmonic materials, resulting in the lack of tunability between different topological properties. Here, we utilize the strong dispersion of silicon carbide thin films to realize highly confined surface phonon-polariton skyrmion lattices, which we image via near-field microscopy. We experimentally demonstrate topological tuning between bubble- and Néel-type skyrmions, a unique advantage that polar dielectrics offer over most existing approaches. Changing the excitation wavelength by only 10% switches the skyrmion type, revealed by examination of the skyrmion number density contrast. Analysis of domain wall size and steepness in analogy to magnetic materials also confirms this transition. Our results are a starting point to investigate other topological features in phononic systems such as merons, skyrmion bags, and other complex structured light fields. Furthermore, strong light-matter hybridization and nonlinear effects owing to anharmonicity of the phonons may be observed in the future, possibly leading towards the discovery of polaritonic skyrmion-skyrmion interactions and hence applications in topology-based information processing.

physics.optics↗

arXiv2024

Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water

Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions and with minimal interference is crucial for advancing nanomedicine, photopharmacology, drug delivery, nanotheranostics and synthetic biology. Yet, analytical methods struggle to combine precise chemical imaging and measurements without perturbative labeling. This challenge is exemplified for azobenzene-based photoswitchable lipids, which are intriguing reagents for controlling nanocarrier properties on fast timescales, enabling, e.g., precise light-induced drug release processes. Here, we leverage the chemical recognition and high spatio-temporal resolution of scattering-type scanning near-field optical microscopy (s-SNOM) to demonstrate non-destructive, label-free mid-infrared (MIR) imaging and spectroscopy of photoswitchable liposomes below the diffraction limit and the tracking of their dynamics down to 50 ms resolution. The vesicles are adsorbed on an ultrathin 10-nm SiN membrane, which separates the sample space from the tip space for stable and hour-long observations. By implementing a transient nanoscopy approach, we accurately resolve, for the first time, photoinduced changes in both the shape and the MIR spectral signature of individual vesicles and reveal abrupt change dynamics of the underlying photoisomerization process. Our findings highlight the methods potential for future studies on the complex dynamics of unlabeled nanoscale soft matter, as well as, in a broader context, for host-guest systems, energy materials or drugs.

physics.optics↗

arXiv2024

Revealing mode formation in quasi-bound states in the continuum metasurfaces via near-field optical microscopy

Photonic metasurfaces offer exceptional control over light at the nanoscale, facilitating applications spanning from biosensing, and nonlinear optics to photocatalysis. Many metasurfaces, especially resonant ones, rely on periodicity for the collective mode to form, which makes them subject to the influences of finite size effects, defects, and edge effects, all of which have considerable negative impact at the application level. These aspects are especially important for quasi-bound state in the continuum (BIC) metasurfaces, for which the collective mode is highly sensitive to perturbations due to high quality factors and strong near-field enhancement. Here, we quantitatively investigate the mode formation in quasi-BIC metasurfaces on the individual resonator level using scattering scanning near-field optical microscopy (s-SNOM) in combination with a new image processing technique. We find that the quasi-BIC mode is formed at a minimum size of 10 x 10-unit cells much smaller than expected from far-field measurements. Furthermore, we show that the coupling direction of the resonators, defects and edge states have pronounced influence on the quasi-BIC mode. This study serves as a link between the far-field and near-field responses of metasurfaces, offering crucial insights for optimizing spatial footprint and active area, holding promise for augmenting applications such as catalysis and biospectroscopy.

physics.optics↗

arXiv2024

Nanoscale mechanical manipulation of ultrathin SiN membranes enabling infrared near-field microscopy of liquid-immersed samples

Scattering scanning near-field optical microscopy (s-SNOM) is a powerful technique for mid-infrared spectroscopy at nanometer length scales. By investigating objects in aqueous environments through ultrathin membranes, s-SNOM has recently been extended towards label-free nanoscopy of the dynamics of living cells and nanoparticles, assessing both the optical and the mechanical interactions between the tip, the membrane and the liquid suspension underneath. Here, we report that the tapping AFM tip induces a reversible nanometric deformation of the membrane manifested as either an indentation or protrusion. This mechanism depends on the driving force of the tapping cantilever, which we exploit to minimize topographical deformations of the membrane to improve optical measurements. Furthermore, we show that the tapping phase, or phase delay between driving signal and tip oscillation, is a highly sensitive observable for quantifying the mechanics of adhering objects, exhibiting highest contrast for low tapping amplitudes where the membrane remains nearly flat. We correlate mechanical responses with simultaneously recorded spectroscopy data to reveal the thickness of nanometric water pockets between membrane and adhering objects. Besides a general applicability of depth profiling, our technique holds great promise for studying mechano-active biopolymers and living cells, biomaterials that exhibit complex behaviors when under a mechanical load.

physics.optics↗