arXiv subjects

Regine von Klitzing

Publications and source records attributed to Regine von Klitzing.

At least 19 recordsLinked to original sources

arXiv2026

Anomalously Large Screening Lengths in Highly Concentrated Electrolytes: A Matter of Experimental Conditions

Considerable debate exists about anomalous underscreening. Whilst surface force apparatus (SFA) measurements have confirmed anomalously large screening lengths ($λ$) in concentrated aqueous electrolytes, colloidal probe atomic force microscopy (CP-AFM) measurements have not. We demonstrate that by tuning experimental conditions, similarly large $λ$ can be achieved in concentrated aqueous LaCl$_3$ electrolytes with CP-AFM. Structural forces were also observed at high LaCl$_3$ concentrations, which we suggest stem from the formation of diffuse ion clusters, and that the remaining counter-ions yield the large deduced $λ$.

cond-mat.soft↗

arXiv2026

Excitonic fingerprints of magnetic configurations and switching in multilayer CrSBr

The coupling between electronic states and magnetism provides a route towards optical readout and control of magnetic information. In the magnetic semiconductor CrSBr, excitons are coupled to magnetic order, making their optical response sensitive to the underlying magnetization. Here, we show that the energy and oscillator strength of bulk and surface excitons provide distinct spectroscopic fingerprints of magnetic configurations and switching pathways. We distinguish domain-wall-mediated magnetization reversal, manifested by continuous spectral evolution as a domain wall traverses the optical spot, from abrupt, large-area magnetization reversal. Using the resulting excitonic fingerprints, we reconstruct successive magnetic configurations in 4- and 5-layer CrSBr during the transition from ferromagnetic to antiferromagnetic order. We further find that the sensitivity to magnetic order is strongly exciton-dependent: low-energy excitons resolve intermediate and surface-related configurations, whereas a higher-energy exciton predominantly exhibits a transfer of oscillator strength between ferromagnetic and antiferromagnetic resonances. These results establish excitonic spectroscopy as a sensitive probe of layer-dependent magnetic configurations and their switching pathways in layered magnetic semiconductors.

cond-mat.mtrl-sci↗

arXiv2026

Detecting Magnetic Phase Transitions in Ion-Irradiated CrSBr Through Resonant Raman Scattering

Controlling magnetic phases and accurately determining their transition temperatures are essential for the development of low-dimensional magnetic materials. Here, we demonstrate that He$^+$ ion irradiation provides a versatile route for engineering magnetic phases in layered CrSBr and establish temperature-dependent polarization-resolved Raman spectroscopy as a sensitive optical probe for identifying irradiation-induced magnetic phase transitions. We reveal that the magnetic response of the modified CrSBr is governed by both irradiation dose and crystal thickness. The temperature evolution of the Raman tensor elements resolves the antiferromagnetic transition in pristine CrSBr at T$_N \approx 132$ K as well as irradiation-induced magnetic transitions at T$_C \approx 105-110$ K and T$_D \approx 40$ K corresponding to ferromagnetic and defect-related magnetic phase transitions. Complementary magneto-optical measurements confirm the progressive suppression of antiferromagnetic order and the emergence of new defect-engineered magnetic phases, including pure ferromagnetic behavior at high irradiation doses. These findings establish irradiated CrSBr as a platform for controllable magnetic phase engineering while demonstrating polarization-resolved Raman spectroscopy as a rapid, non-destructive, and broadly applicable method for probing magnetic phase transitions in van der Waals magnets.

cond-mat.mtrl-sci↗

arXiv2026

A Multi-scale Investigation of Aqueous Foams Stabilised by PNIPAM Microgels

Aqueous foams possess multiple structural motifs across different length scales: macroscopic foam, bubbles, foam films and the air/water interface. In this study, macroscopic foams are generated by sparging gas through an aqueous dispersion of PNIPAM microgels which act as foam stabilisers due to their surface activity. The stiffness of the microgels and thus their interfacial activity are tuned by variation of the cross-linker density. The effect of the cross-linker density and the microgel concentration on the resulting foam formation properties (foamability) and the foam stability are investigated. A lower cross-linker density and a higher microgel concentration enhance the foamability, generate foams with smaller bubbles and higher liquid fractions, and increase the foam stability. These observations are correlated with the microgel behavior at the single air/water interface examined by pendant drop tensiometry and Langmuir compression experiments as well as the mobility in single free-standing foam films determined using a Thin Film Pressure Balance. Our findings highlight good agreement across all length scales: increased foamability correlates with a faster decrease in surface tension, and higher foam stability with a higher surface elastic modulus of a microgel-covered single air/water interface and decreasing mobility in foam films.

cond-mat.soft↗

arXiv2026

Exploring structure-property relationship on a nanoscale for tailoring films of amphiphilic polymer co-networks

Amphiphilic polymer co-networks (APCNs) provide a large toolbox for tuning coatings important for applications such as bio-interfaces. Therefore, we investigate the influence of network composition and environmental conditions on the structure and mechanical and adhesive properties of thin films composed of hydrophobic tetra-PCL and hydrophilic tetra-PEG stars of varying sizes. State-of-the-art atomic force microscopy (AFM) techniques, including phase imaging, fast quantitative static indentation and dynamic indentation, provide insights into the structure-property-relationship on various length scales. PEG-rich networks exhibit amorphous morphologies with spherical nanodomains and elastic moduli of a few MPa, while PCL-rich networks form semicrystalline cylindrical arrangements with moduli up to several hundred MPa in water. Temperature-dependent measurements in water revealed a strong hysteresis of elastic moduli while shifting the melting/crystallization transitions or preventing crystallization in PEG-rich networks. All networks displayed predominantly elastic behavior. Co-networks in non-selective solvent conditions are overall softer, less adhesive and structurally more homogeneous. These results establish a predictable correlation of network composition, physical and chemical environment, structure and properties, which makes them suitable for a rational design of amphiphilic systems for various applications.

cond-mat.soft↗

arXiv2025

In situ vs ex situ: Comparing the structure of PNIPAM microgels at the air/water and air/solid interfaces

For studying the structure of microgel particles at the air/water interface, specular and off-specular X-ray reflectivity (OSR/XRR) allows in situ measurements without any labelling techniques. Herein we investigate the vertical and lateral structure of poly(N-isopropylacrylamide) (PNIPAM) microgels (MGs) at the air/water interface and the effect of Langmuir-Blodgett (LB) transfer onto solid substrates. The initial ex situ atomic force microscopy (AFM) scans of LB-transferred MGs at the air/solid interface reveal strong lateral 2D hexagonal ordering across a broad range of lateral surface pressures at the air/water interface before LB-transfer. Notably, for the first time, these results were confirmed by OSR, demonstrating the existence of the long-range hexagonal ordering at low and intermediate surface pressures. For in situ conditions and upon uniaxial compression at the air/water interface, the MG lattice constant decreases non-monotonically. This indicates the formation of domains at low pressures that approach each other and only compress when the surface isotherm reaches a plateau. Comparing the results of in situ and ex situ measurements, our study demonstrates a clear transfer effect during the LB-deposition on the lateral ordering of the MGs: the distance between the particles decreased during LB-transfer, and at high pressures ($Π\,>\,17\,\mathrm{mNm^{-1}}$) a second distance occurs indicating small domains with hexagonal internal ordering. The novel surface characterisation approaches debuted here highlight the use of both XRR and OSR to probe the vertical and lateral structure of adsorbed MGs, offering in situ, non-invasive insights without the need for doping or transfer-induced artefacts.

cond-mat.soft↗

arXiv2025

Twist-tuned exchange and hysteresis in a bilayer van der Waals magnet

Moiré superlattices in twisted bilayers enable profound reconstructions of the electronic bandstructure, giving rise to correlated states with remarkable tunability. Extending this paradigm to van der Waals magnets, twisting creates spatially varying interlayer exchange interactions that stabilize emergent spin textures and the coexistence of ferromagnetic and antiferromagnetic domains. Here, we demonstrate the emergence of robust magnetic hysteresis in bilayer CrSBr upon twisting by an angle of ~ 3°. This is observed as the corresponding hysteretic evolution of the exciton energy, that directly correlates with the bilayer magnetic state, in magnetic field dependent photoluminescence measurements. A two-sublattice model captures this behavior, attributing it to the twist-induced reduction of interlayer exchange that stabilizes both parallel and antiparallel spin configurations across a broad field range. Comparison with experiment enables quantitative extraction of the effective exchange strength. Remarkably, the system exhibits coherent averaging across the moiré supercell, yielding an effective monodomain response characterized by switching into the antiferromagnetic state, rather than forming spin textures or fragmented domains. Spatially resolved measurements further uncover local variations in hysteresis loops, consistent with position-dependent modulation of the average exchange interaction. Our results establish twist engineering as a powerful route to programmable magnetic memories in two-dimensional magnets, harnessing the robustness of antiferromagnetic order.

cond-mat.mtrl-sci↗

arXiv2025

Interplay of vibrational, electronic, and magnetic states in CrSBr

The van der Waals antiferromagnet CrSBr exhibits coupling of vibrational, electronic, and magnetic degrees of freedom, giving rise to distinctive quasi-particle interactions. We investigate these interactions across a wide temperature range using polarization-resolved Raman spectroscopy at various excitation energies, complemented by optical absorption and photoluminescence excitation (PLE) spectroscopy. Under 1.96 eV excitation, we observe pronounced changes in the A$_g^1$, A$_g^2$, and A$_g^3$ Raman modes near the Néel temperature, coinciding with modifications in the oscillator strength of excitonic transitions and clear resonances in PLE. The distinct temperature evolution of Raman tensor elements and polarization anisotropy for Raman modes indicates that they couple to different excitonic and electronic states. The suppression of the excitonic state's oscillation strength above the Néel temperature could be related to the magnetic phase transition, thereby connecting these excitonic states and Raman modes to a specific spin alignment. These observations make CrSBr a versatile platform for probing quasi-particle interactions in low-dimensional magnets and provide insights for applications in quantum sensing and quantum communication.

cond-mat.mtrl-sci↗

arXiv2025

Jetting with gels: Soft microgel networks stabilize and extend nozzle-free water jets

The stability of high-speed liquid jets is crucial for applications ranging from precision printing to needle-free drug delivery, yet it is fundamentally limited by capillary-driven breakup. A common strategy to stabilize jets is to use surfactants to lower surface tension. However, in nozzle-free jetting driven by surface acoustic waves (SAWs), extreme deformation rates cause conventional surfactants to desorb, calling for alternative strategies to stabilize jets. In particular, we find that tuning the nanoscale softness of PNIPAM microgels provides a robust, biocompatible strategy to overcome this limitation. Soft, low-cross-linker-density microgels form elastic interfacial networks at the air-water interface that suppress surface tension recovery, delay Rayleigh-Plateau instabilities, and extend SAW-driven jet lengths by up to 44%. In contrast, stiffer microgels lose network cohesion under strain, leading to rapid jet breakup. To gain molecular-level insights, we perform dissipative particle dynamics simulations, which reveal that polymer bridges in soft microgels remain entangled during elongation, maintaining a reduced effective surface tension. Finally, a simple scaling analysis, balancing the SAW-driven kinetic energy imparted to the droplet against the surface energy required to form a jet, quantitatively predicts the observed length enhancement. This surfactant-free, biocompatible approach lays the foundation for long-lived jets, enabling precision needle-free drug delivery, high-speed printing, and other high-strain interfacial flow applications.

cond-mat.soft↗

arXiv2025

Magnetic Correlation Spectroscopy in CrSBr

CrSBr is an air-stable magnetic van der Waals semiconductor with strong magnetic anisotropy, where the interaction of excitons with the magnetic order enables the optical identification of different magnetic phases. Here, we study the magnetic anisotropy of multi-layer CrSBr inside a three-axis vector magnet and correlate magnetic order and optical transitions in emission and absorption. We identify layer by layer switching of the magnetization through drastic changes of the optical emission and absorption energy and strength as a function of the applied magnetic field. We correlate optical transitions in reflection spectra with photoluminescence (PL) emission using a transfer-matrix analysis and find that ferromagnetic and antiferromagnetic order between layers can coexist in the same crystal. In the multi-peak PL emission the intensity of energetically lower lying transitions reduces monotonously with increasing field strength whereas energetically higher lying transitions around the bright exciton $X_B$ brighten close to the saturation field. Using this contrasting behavior we can therefore correlate transitions with each other.

cond-mat.mtrl-sci↗

arXiv2024

Drying of Soft Colloidal Films

Thin films made of deformable micro- and nano-units, such as biological membranes, polymer interfaces, and particle-laden liquid surfaces, exhibit a complex behavior during drying, with consequences for various applications like wound healing, coating technologies, and additive manufacturing. Studying the drying dynamics and structural changes of soft colloidal films thus holds the potential to yield valuable insights to achieve improvements for applications. In this study, we employ interfacial monolayers of core-shell microgels with varying degrees of softness as model systems and investigate their drying behavior on differently modified solid substrates (hydrophobic vs. hydrophilic). By leveraging on video microscopy, particle tracking, and thin film interference, we shed light on the interplay between microgel adhesion to solid surfaces and the immersion capillary forces that arise in the thin liquid film. We discovered that a dried replica of the interfacial microstructure can be more accurately achieved on a hydrophobic substrate relative to a hydrophilic one, particularly when employing softer colloids as opposed to harder counterparts. These observations are qualitatively supported by experiments with a thin film pressure balance which allows mimicking and controlling the drying process and by computer simulations with coarse-grained models.

cond-mat.soft↗

arXiv2024

Ion-specific Stability of Gold Nanoparticle Suspensions

Gold nanoparticles (AuNPs) play an important role in fundamental research and development due to their versatile applications and biocompatibility. This study addresses the aging of three AuNP suspensions after the addition of various sodium salts along the well-known Hofmeister series (NaF, NaCl, NaBr, NaI, NaSCN) at different salt concentrations between 10 mM and 100 mM. The AuNP types differ in size (5 nm vs. 11 nm in diameter) and the capping type (physisorbed citrate vs. covalently bound mercaptopropionic acid (MPA)). We monitor the aggregation of the AuNPs and the suspension stability optically (absorption spectroscopy, photography) and by electron microscopy. The large range of salt concentrations results in a large variety of colloidal stability, e.g., from stable suspensions to fast destabilization followed by sedimentation. At intermediate and high salt concentration strong ion-specific effects emerge that are non-monotonous with respect to the Hofmeister series. In particular, the chaotropic salts, NaI and NaSCN, strongly alter the absorption spectra in very different ways. NaI fuses AuNPs together influencing the primary absorption, while NaSCN retains AuNP structure during aggregation much stronger than the remaining sodium halides, resulting in a secondary absorption peak. Although decreasing the size of AuNPs leads to more stable suspensions, the ion specific effects are even more pronounced due to the increase in total available surface. Even the covalently bound MPA capping is not able to stabilize AuNPs against particle fusion by NaI, although it delays the process. Despite the complex interplay between different effects of ions on the stability of colloidal dispersions, this study disentangles the different effects from electrostatic screening, via adsorption at the interface and bridging of AuNPs, to the competition between ions and the capping agent of the AuNPs.

cond-mat.soft↗

arXiv2023

An analytical study of capillary rise dynamics: Critical conditions and hidden oscillations

The rise of a liquid column inside a thin capillary against the action of gravity is a prototypical example of a dynamic wetting process and plays an important role for applications but also for fundamental research in the area of multiphase fluid dynamics. Since the pioneering work by Lucas and Washburn, many research articles have been published which aim at a simplified description of the capillary rise dynamics using complexity-reduced models formulated as ordinary differential equations. Despite the fact that these models are based on profound simplifications, they may still be able to describe the essential physical mechanisms and their interplay. In this study, we focus on the phenomenon of oscillations of the liquid column. The latter has been observed experimentally for liquids with sufficiently small viscosity leading to comparably small viscous dissipation. Back in 1999, Quere et al. formulated a condition for the appearance of rise height oscillations for an ODE model introduced by Bosanquet in 1923. This model has later been extended to include further dissipative mechanisms. In this work, we extend the mathematical analysis to a larger class of models including additional channels of dissipation. We show that Quere's critical condition is generalized to $Ω+ β< 2$, where $Ω$ was introduced earlier and $β$ is an additional non-dimensional parameter describing, e.g., contact line friction. A quantitative prediction of the oscillation dynamics is achieved from a linearization of the governing equations. We apply the theory to experimental data by Quere et al. and, in particular, reveal the oscillatory behavior of dynamics for the nearly critically damped case of ethanol.

physics.flu-dyn↗

arXiv2023

Frequency-dependent Ultrasonic Stimulation of PNIPAM Microgels in Water

As a novel stimulus, we used high-frequency ultrasonic waves to provide the required energy for breaking hydrogen bonds between Poly(N-isopropylacrylamide) (PNIPAM) and water molecules while the solution temperature maintains below the volume phase transition temperature (VPTT=$$32^\circ C$$). Ultrasonic waves propagate through the solution and their energy will be absorbed due to the liquid viscosity. The absorbed energy partially leads to the generation of a streaming flow and the rest will be spent to break the hydrogen bonds. Therefore, the microgels collapse and become insoluble in the water and agglomerate, resulting in turbidity. We used turbidity to quantify the ultrasound energy absorption and showed that the acousto-response of PNIPAM microgels is a temporal phenomenon that depends on the duration of the actuation. Increasing the solution concentration leads to a faster hydrogen bond breakage and turbidity evolution. Furthermore, the frequency of imposed waves is important and affects the stimulation kinetics of PNIPAM microgels. Increasing the frequency of actuation increases the speed of hydrogen bond breakage and thus turbidity evolution. This is due to the increase in ultrasound energy absorption by liquids at higher frequencies.

cond-mat.soft↗

arXiv2023

Conceptualizing flexible papers using cellulose model surfaces and polymer particles

Cellulose, as a naturally abundant and biocompatible material, is still gaining interest due to its high potential for functionalization. This makes cellulose a promising candidate for replacing plastics. Understanding how cellulose interacts with various additives is crucial for creating composite materials with diverse properties, as it is the case for plastics. In addition, the mechanical properties of the composite materials are assumed to be related to the mobility of the additives against the cellulose. Using a well-defined cellulose model surface (CMS), we aim to understand the adsorption and desorption of two polymeric particles (core-shell particles and microgels) to/from the cellulose surface. The nanomechanics of particles and CMS are quantified by indentation measurements with an atomic force microscope (AFM). AFM topography measurements quantified particle adsorption and desorption on the CMS, while peak force AFM measurements determined the force needed to move individual particles. Both particles and the CMS exhibited pH-dependent charge behavior, allowing a tunable interaction between them. Particle adsorption was irreversible and driven by electrostatic forces. In contrast, desorption and particle mobility forces are dominated by structural morphology. In addition, we found that an annealing procedure consisting of swelling/drying cycles significantly increased the adhesion strength of both particles. Using the data, we achieve a deeper understanding of the interaction of cellulose with polymeric particles, with the potential to advance the development of functional materials and contribute to various fields, including smart packaging, sensors, and biomedical applications.

cond-mat.soft↗

arXiv2023

Influence of Dopamine Methacrylamide on swelling behaviour and nanomechanical properties of PNIPAM microgels

The combination of the catechol-containing co-monomer dopamine methacrylamide (DMA) with stimuli-responsive microgels such as poly(N-isopropylacrylamide) (PNIPAM) bears a huge potential in research and for applications due to the versatile properties of catechols. This research gives first detailed insights into the influence of DMA on the swelling of PNIPAM microgels and the correlation with their nanomechanical properties. Dynamic light scattering (DLS) was used to analyse the swelling behaviour of microgels in bulk solution. The incorporation of DMA decreases the volume phase transition temperature (VPTT) and completion temperature (VPT CT) due to its higher hydrophobicity when compared to NIPAM, while sharpening the transition. The cross-linking ability of DMA decreases swelling ratios and mesh sizes of the microgels. Microgels adsorbed at the solid surface are characterised by atomic force microscopy (AFM): Scanning provides information about the microgel's shape on the surface and force spectroscopy measurements determines their nanomechanical properties ($E$ modulus). As the DMA content increases, microgels protrude more from the surface, correlating with an increase of $E$ modulus and a stiffening of the microgels - confirming the cross-linking ability of DMA. Force spectroscopy measurements below and above the VPTT display a stiffening of the microgels with the incorporation of DMA and upon heating across it's entire cross-section. The affine network factor $β$, derived from the Flory-Rehner theory describing the elasticity and swelling of the microgel network, is linearly correlated with the $E$ moduli of the microgels for both - pure PNIPAM and P(NIPAM-co-DMA) microgels. However, for large amounts of DMA, DMA appears to hinder the microgel shrinking, while still ensuring mechanical stiffness, possibly due to catechol interactions within the microgel network.

cond-mat.soft↗

arXiv2023

Impact of Ultrasound on the Motion of Compact Particles and Acousto-responsive Microgels

In this study, we investigate dynamic light scattering (DLS) from both randomly diffusing silica particles and acousto-responsive microgels in aqueous dispersions under ultrasonic vibration. Employing high-frequency ultrasound (US) with low amplitude ensures that the polymers remain intact without damage. We derive theoretical expressions for the homodyne autocorrelation function, incorporating the US term alongside the diffusion term. Subsequently, we successfully combine US with a conventional DLS system to experimentally characterize compact silica particles and microgels under the influence of US. Our model allows us to extract essential parameters, including particle size, frequency, and amplitude of particle vibration, based on the correlation function of the scattered light intensity. The studies involving non-responsive silica particles demonstrate that US does not disrupt size determination, establishing them as suitable reference systems. Microgels show the same swelling/shrinking behavior as that induced by temperature, but with significantly faster kinetics. The findings of this study have potential applications in various industrial and biomedical fields that benefit from the characterization of macromolecules subjected to US.

cond-mat.soft↗

arXiv2023

How does the preparation strategy influence the gold cap of thermophoretic Janus swimmers and their propulsion?

The motion of partly gold (Au)-coated Janus particles under laser irradiation is caused by self-thermophoresis. Despite numerous studies addressing this topic, the impact of the preparation method and the degree of coverage of the particle with Au on the resulting thermophoretic velocity has not yet been fully understood. A detailed understanding of the most important tuning parameters during the preparation process is crucial to design Janus particles that are optimized in Au coverage to receive a high thermophoretic velocity. In this study, we explore the influence of the fabrication process, which changes the Au cap size, on the resulting self-propulsion behavior of partly Au-coated polystyrene particles (Au-PS). Additionally, also the impact of an underlying adhesion chromium layer is investigated. In addition to the most commonly used qualitative SEM and EDX measurements, we propose a novel technique utilizing AFM studies to quantify the cap size. This non-invasive technique can be used to determine both the size and the maximum thickness of the Au cap. The Au cap size was systematically varied in a range between about 36 % and 74 % by different preparation strategies. Nevertheless, we showed that the differing Au cap size of the Janus particles in this range has no effect on the thermophoretic velocity. This surprising result is discussed in the paper.

cond-mat.soft↗