arXiv subjects

Peter Schall

Publications and source records attributed to Peter Schall.

At least 19 recordsLinked to original sources

arXiv2026

The Physics of Topological Defects in Glasses

Topological defects play a central role in the mechanical behavior of crystalline materials, yet their relevance to amorphous solids has only recently begun to emerge. Over the last few years, theoretical, computational, and experimental studies have revealed the presence of well-defined topological invariants in vibrational eigenmodes, non-affine displacement fields, and deformation-induced vector fields of glasses. These defects have been shown to correlate strongly with soft spots, localized plastic rearrangements, yielding, and shear-band formation, suggesting a new perspective on the microscopic origins of plasticity in disordered materials. In this review, we provide a comprehensive overview of recent developments in the rapidly growing field of topological defects in glasses. We discuss the underlying theoretical concepts, including Burgers vectors, non-affine plasticity, vibrational modes, and topological invariants, and review recent numerical and experimental advances. Finally, we assess the current achievements, limitations, and open questions, and discuss future directions toward a unified topological description of plasticity and mechanical failure in amorphous solids.

cond-mat.dis-nn↗

arXiv2026

Large-Area Deterministic Stamping of 2D Materials on Arbitrarily Patterned Surfaces

2D materials and their monolayers have attracted widespread interest by virtue of their unique electronic and optical properties. In addition to their remarkable physical characteristics, their atomically thin nature enables their integration in ultra-compact photonic and electronic devices, with potential for dynamic tunability via strain, charge carrier modulation or heterostructure engineering. While early research relied on micrometer-scale mechanically exfoliated flakes, recent advances, particularly gold-assisted exfoliation of transition metal dichalcogenides (TMDCs), have enabled the preparation of high-quality, large-area monolayers, opening new opportunities for scalable device integration. For the field of nanophotonics in particular, the ability to transfer large-area 2D materials onto both flat and patterned substrates is essential for the development of functional devices. However, existing transfer techniques are often limited in scalability, and compatibility with structured surfaces. Here, we present a versatile and reliable transfer method of large-area monolayers and hBN/monolayer heterostructures onto both flat and nanostructured substrates. Our approach, based on the physical properties of low-density polyethylene, preserves the intrinsic optical quality of the materials and is compatible with a variety of device architectures. We demonstrate its applicability by fabricating devices that modulate the photoluminescence of TMDC monolayers through the manipulation of the photonic environment, strain or electrical gating. We further demonstrate the fabrication of van der Waals heterostructures using the same method. By enabling clean transfer of a wide range of monolayers and heterostructures, this technique offers a practical pathway for the development of next-generation optoelectronic platforms with improved functionality, scalability, and tunability.

cond-mat.mes-hall↗

arXiv2025

Metasurface lasers programmed by optical pump patterns

Metasurface lasers offer unprecedented control over light emission, yet their spatial and modal characteristics are typically fixed post-fabrication. Here, we introduce a reconfigurable plasmonic metasurface laser platform in which the lasing area geometry, and thus the emission properties, are dynamically programmed via spatially structured optical pumping. Using hexagonal arrays of silver nanoparticles embedded in dye-doped waveguides, we demonstrate lasing at high-symmetry points of the Brillouin zone, including the K and M points. K-point lasing exhibits spontaneous symmetry breaking (SSB) in relative intensity between degenerate K and K' modes, with no bias induced by pump geometry, even for geometries that explicitly break symmetry. In contrast, M-point lasing allows deterministic control over emission channels via asymmetric pumping. We further show that spatially separated K-point lasers synchronize in phase and amplitude, undergoing SSB in lockstep. A theoretical density matrix approach cast into stochastic differential equations reproduces the observed real- and Fourier-space intensity distributions and SSB behavior. Our findings establish spatially programmable metasurface lasers as a versatile platform for exploring dynamic phenomena in photonic lattices, with potential applications in vortex beam shaping, optical logic, and true random number generation.

physics.optics↗

arXiv2025

Shear induced topological changes of local structure in dense colloidal suspensions

Understanding the structural origins of glass formation and mechanical response remains a central challenge in condensed matter physics. Recent studies have identified the local caging potential experienced by a particle due to its nearest neighbors as a robust structural metric that links microscopic structure to dynamics under thermal fluctuations and applied shear. However, its connection to locally favored structural motifs has remained unclear. Here, we analyze structural motifs in colloidal crystals and glasses and correlate them with the local caging potential. We find that icosahedral motifs in glasses are associated with deeper caging potentials than crystalline motifs such as face-centered cubic (FCC) and hexagonal close-packed (HCP) structures. Both crystalline and amorphous systems also contain large number of particles belonging to stable defective motifs, which are distortions of the regular motifs. Under shear, large clusters of defective motifs fragment into smaller ones, driving plastic deformation and the transition from a solid-like to a liquid-like state in amorphous suspensions. Particles that leave clusters of stable motifs are associated with shallower caging potentials and are more prone to plastic rearrangements, ultimately leading to motif disintegration during shear. Our results thus reveal that the loss of mechanical stability in amorphous suspensions is governed by the topological evolution of polytetrahedral motifs, uncovering a structural mechanism underlying plastic deformation and fluidization.

cond-mat.soft↗

arXiv2025

Quantum and Critical Casimir Effects: Bridging Fluctuation Physics and Nanotechnology

Fluctuation-induced forces, primarily represented by quantum and critical Casimir effects, play a pivotal role at the nanoscale. This review explores the theoretical and experimental landscapes of these forces, offering a comprehensive analysis of their similarities and distinctions. We emphasize the effects of material properties, geometry, and temperature in shaping these forces and their roles in various nanoscale systems, both colloidal and solid-state. We devote special attention to the Casimir torque, the influence of magnetism on the Casimir force, and the use of Casimir effects for the generation of optical resonators. Through this comparative study, we elucidate the underlying physics of these phenomena, fostering insights that advance applications in nanomechanics, optomechanics, and quantum technologies.

quant-ph↗

arXiv2024

Structural origin of relaxation in dense colloidal suspensions

Amorphous solids relax via slow molecular rearrangement induced by thermal fluctuations or applied stress. Although microscopic structural signatures predicting these structural relaxations have long been sought, a physically motivated structural measure relevant to diverse systems remains elusive. Here, we introduce a structural order parameter derived from the mean-field caging potential experienced by the particles due to their neighbors, which reliably predicts the occurrence of structural relaxations. The parameter, derived from density functional theory, is a measure of susceptibility to particle rearrangements that can effectively identify weak or defect-like regions in disordered systems. Using experiments on dense colloidal suspensions, we demonstrate a causal relationship between this order parameter and the structural relaxations of the amorphous solid. In quiescent suspensions, increasing the density leads to stronger correlations between the structure and dynamics. Under applied shear, the mean structural order parameter increases with increasing strain, signaling shear-induced softening, which is accompanied by the proliferation of plastic events. In both cases, the order parameter reliably identifies weak regions where the plastic rearrangements due to thermal fluctuation or applied shear preferentially occur. Our study paves the way to a structural understanding of the relaxation of a wide range of amorphous solids, from suspensions to metallic glasses.

cond-mat.soft↗

arXiv2024

Electric field enhances the electronic and diffusion properties of penta-graphene nanoribbons for application in lithium-ion batteries: a first-principles study

Enhancing the electronic and diffusion properties of lithium-ion batteries is crucial for improving the performance of the fast-growing energy storage devices. Recently, fast-charging capability of commercial-like lithium-ion anodes with the least modification of the current manufactoring technology is of great interest. Here we use first principles methods with density functional theory and the climbing image-nudged elastic band method to evaluate the impact of an external electric field on the stability, electronic and diffusion properties of penta-graphene nanoribbons upon lithium adsorption. We show that by adsorbing a lithium atom, these semiconductor nanoribbons become metal with a formation energy of - 0.22 (eV). The lithium-ion mobility of this material is comparable to that of a common carbon graphite layer. Under a relatively small vertical electric field, the structural stability of these lithium-ion systems is even more stable, and their diffusion coefficient is enhanced significantly of ~719 times higher than that of the material in the absence of an applied electric field and ~521 times higher than in the case of commercial graphitic carbon layers. Our results highlight the role of an external electric field as a novel switch to improve the efficiency of lithium-ion batteries with penta-graphene nanoribbon electrodes and open a new horizon for the use of more environmentally friendly pentagonal materials as anode materials in lithium-ion battery industry.

cond-mat.mtrl-sci↗

arXiv2023

Spontaneous symmetry breaking in plasmon lattice lasers

Spontaneous symmetry breaking (SSB) is key for our understanding of phase transitions and the spontaneous emergence of order. Photonics provide versatile systems to study SSB. In this work, we report that for a two-dimensional (2D) periodic nonlocal metasurface with gain, SSB occurs in the lasing transition, breaking parity symmetry. We study diffractive hexagonal plasmon nanoparticle lattices, where the K-points in momentum space provide two modes that are exactly degenerate in frequency and identically distributed in space. Using femtosecond pulses to energize the gain medium, we simultaneously capture single shot realspace and wavevector resolved Fourier images of laser emission. By combining Fourier- and real-space, we resolve the two order parameters for which symmetry breaking simultaneously occurs: spatial parity and U(1) (rotational) symmetry breaking, evident respectively as random relative mode amplitude and phase. Thereby, we quantify for the first time SSB in 2D periodic metasurfaces. These currently receive much interest as experimentally accessible implementations of seminal solid-state physics Hamiltonians and provide a large design space for exploring SSB in scenarios with different symmetries, mode degeneracies and topological properties. The methodology reported in this work is generally applicable to 2D plasmonic and dielectric metasurfaces and opens numerous opportunities for the study of SSB and emergence of spatial coherence in metaphotonics.

physics.optics↗

arXiv2023

Power-law intermittency in the gradient-induced self-propulsion of colloidal swimmers

Active colloidal microswimmers serve as archetypical active fluid systems, and as models for biological swimmers. Here, by studying in detail their velocity traces, we find robust power-law intermittency with system-dependent exponential cut off. We model the motion by an interplay of the field gradient-dependent active force and the locally fluctuating hydrodynamic drag, set by the wetting properties of the substrate. The model closely describes the velocity distributions of two disparate swimmer systems: AC field activated and catalytic swimmers. The generality is highlighted by the collapse of all data in a single master curve, suggesting the applicability to further systems, both synthetic and biological.

cond-mat.soft↗

arXiv2023

Self-oscillation and Synchronisation Transitions in Elasto-Active Structures

The interplay between activity and elasticity often found in active and living systems triggers a plethora of autonomous behaviors ranging from self-assembly and collective motion to actuation. Amongst these, spontaneous self-oscillations of mechanical structures is perhaps the simplest and most wide-spread type of non-equilibrium phenomenon. Yet, we lack experimental model systems to investigate the various dynamical phenomena that may appear. Here, we report self-oscillation and synchronization transitions in a centimeter-sized model system for one-dimensional elasto-active structures. By combining precision-desktop experiments of elastically coupled self-propelled particles with numerical simulations and analytical perturbative theory, we demonstrate that the dynamics of single chain follows a Hopf bifurcation. We show that this instability is controlled by a single non-dimensional elasto-active number that quantifies the interplay between activity and elasticity. Finally, we demonstrate that pairs of coupled elasto-active chains can undergo a synchronization transition: the oscillations phases of both chains lock when the coupling link is sufficiently stiff. Beyond the canonical case considered here, we anticipate our work to open avenues for the understanding and design of the self-organisation and response of active artificial and biological solids, e.g. in higher dimensions and for more intricate geometries.

cond-mat.soft↗

arXiv2023

Microscopic strain correlations in sheared amorphous solids

We investigate spatial correlations of strain fluctuations in sheared colloidal glasses and simulations of sheared amorphous solids. The correlations reveal a quadrupolar symmetry reminiscent of the strain field due to an Eshelby's inclusion. However, they display an algebraic decay $1/r^α$, where the exponent $α$ is close to $1$ in the steady state, unlike the Eshelby field, for which $α=3$ . The exponent takes values between $3$ to $1$ in the transient stages of deformation. We explain these observations using a simple model based on interacting Eshelby inclusions. As the system is sheared beyond the linear response to plastic flow, the density correlations of inclusions are enhanced and it emerges as key to understanding the elastoplastic response of the system to applied shear.

physics.app-ph↗

arXiv2021

Self-assembly of Colloidal Superballs Under Spherical Confinement of a Drying Droplet

Understanding the relationship between colloidal building block shape and self-assembled material structure is important for the development of novel materials by self-assembly. In this regard, colloidal superballs are unique building blocks because their shape can smoothly transition between spherical and cubic. Assembly of colloidal superballs under spherical confinement results in macroscopic clusters with ordered internal structure. By utilizing Small Angle X-Ray Scattering (SAXS), we probe the internal structure of colloidal superball dispersion droplets during confinement. We observe and identify four distinct drying regimes that arise during compression via evaporating droplets, and we track the development of the assembled macrostructure. As the superballs assemble, we found that they arrange into the predicted paracrystalline, rhombohedral C1-lattice that varies by the constituent superballs' shape. This provides insights in the behavior between confinement and particle shape that can be applied in the development of new functional materials.

cond-mat.soft↗

arXiv2021

Effects of structure and temperature on the nature of excitons in the Mo0.6W0.4S2 alloys

We have studied the nature of excitons in the transition metal dichalcogenide alloy Mo0.6W0.4 S2, compared to pure MoS2 and WS2 grown by atomic layer deposition (ALD). For this, optical absorption/transmission spectroscopy and time-dependent density functional theory (TDDFT) were used. Effects of temperature on the A and B exciton peak energies and linewidths in the optical transmission spectra were compared between the alloy and pure MoS2 and WS2. On increasing the temperature from 25 K to 293 K the energy of the A and B exciton peaks decreases, while their linewidth increases due to exciton-phonon interactions. The exciton-phonon interactions in the alloy are closer to those for MoS2 than WS2. This suggests that the exciton wave functions in the alloy have a larger amplitude on Mo atoms than on W atoms. The experimental absorption spectra could be reproduced by TDDFT calculations. Interestingly, for the alloy the Mo and W atoms had to be distributed over all layers. Conversely, we could not reproduce the experimental alloy spectrum by calculations on a structure with alternating layers, in which every other layer contains only Mo atoms and the layers in between also W atoms. For the latter atomic arrangement, the TDDFT calculations yielded an additional optical absorption peak that could be due to excitons with some charge transfer character. From these results we conclude that ALD yields an alloy in which Mo and W atoms are distributed uniformly among all layers.

cond-mat.mtrl-sci↗

arXiv2021

Shape and Interaction Decoupling for Colloidal Pre-Assembly

Creating materials with structure that is independently controllable at a range of scales requires breaking naturally occurring hierarchies. Breaking these hierarchies can be achieved via the decoupling of building block attributes from structure during assembly. Here, we demonstrate both geometric and interaction decoupling in pre-assembled colloidal structures of cube-like particles with rounded edges. Through computer simulations and experiments, we show that compressing a small number of such cubes in spherical confinement results in clusters with highly reproducible structures that can be used as mesoscale building blocks to form the next level of structural hierarchy. These clusters demonstrate geometric decoupling between particle shape and cluster structure; namely, for clusters of up to nine particles, the colloidal superballs pack consistently like spheres, despite the presence of shape anisotropy and facets in the cubic-like particles. We confirm that cluster structure is also decoupled from inter-particle interaction, showing that the same structures arise from the spherical confinement of both non-magnetic and magnetic colloidal cubes with strong dipolar interactions. To highlight the potential of these superball clusters for hierarchical assembly, we demonstrate, using computer simulations, that clusters of six to nine particles can self-assemble into high-order structures that differ from those of similarly shaped particles without pre-assembly. These results demonstrate decoupling for anisotropic building blocks that can be further exploited for hierarchical materials development.

cond-mat.soft↗

arXiv2021

Revealing polymerization kinetics with colloidal dipatch particles

Limited-valency colloidal particles can self-assemble into polymeric structures analogous to molecules. While their structural equilibrium properties have attracted wide attention, insight into their dynamics has proven challenging. Here, we investigate the polymerization dynamics of semiflexible polymers in two dimensions (2D) by direct observation of assembling divalent particles, bonded by critical Casimir forces. The reversible critical Casimir force creates living polymerization conditions with tunable chain dissociation, association and bending rigidity. We find that unlike dilute polymers that show exponential size distributions in excellent agreement with Flory theory, concentrated samples exhibit arrest of rotational and translational diffusion due to a continuous isotropic-to-nematic transition in 2D, slowing down the growth kinetics. These effects are circumvented by addition of higher-valency particles, cross-linking the polymers into networks. Our results connecting polymer flexibility, polymer interactions and the peculiar isotropic-nematic transition in 2D offer insight into polymerization processes of synthetic two-dimensional polymers, and biopolymers at membranes and interfaces.

cond-mat.soft↗

arXiv2021

Magnetic coupling in colloidal clusters for hierarchical self-assembly

Manipulating the way in which colloidal particles self-organise is a central challenge in the design of functional soft materials. Meeting this challenge requires the use of building blocks that interact with one another in a highly specific manner. Their fabrication, however, is limited by the complexity of the available synthesis procedures. Here, we demonstrate that, starting from experimentally available magnetic colloids, we can create a variety of complex building blocks suitable for hierarchical self-organisation using a simple scalable process. Using computer simulations, we compress spherical and cubic magnetic colloids in spherical confinement, and investigate their suitability to form small clusters with reproducible structural and magnetic properties. We find that, while the structure of these clusters is highly reproducible, their magnetic character depends on the particle shape. Only spherical particles have the rotational degrees of freedom to produce consistent magnetic configurations, whereas cubic particles frustrate the minimisation of the cluster energy, resulting in various magnetic configurations. To highlight their potential for self-assembly, we demonstrate that already clusters of three magnetic particles form highly nontrivial Archimedean lattices, namely staggered kagome, bounce and honeycomb, when viewing different aspects of the same monolayer structure. The work presented here offers a conceptually different way to design materials by utilizing pre-assembled magnetic building blocks that can readily self-organise into complex structures.

cond-mat.soft↗

arXiv2021

Nonequilibrium master kinetic equation modelling of colloidal gelation

We present a detailed study of the kinetic cluster growth process during gelation of weakly attractive colloidal particles by means of experiments on critical Casimir attractive colloidal systems, simulations and analytical theory. In the experiments and simulations, we follow the mean coordination number of the particles during the growth of clusters to identify an attractive-strength independent cluster evolution as a function of mean coordination number. We relate this cluster evolution to the kinetic attachment and detachment rates of particles and particle clusters. We find that single-particle detachment dominates in the relevant weak attractive-strength regime, while association rates are almost independent of the cluster size. Using the limit of single-particle dissociation and size-independent association rates, we solve the master kinetic equation of cluster growth analytically to predict power-law cluster mass distributions with exponents $-3/2$ and $-5/2$ before and after gelation, respectively, which are consistent with the experimental and simulation data. These results suggest that the observed critical Casimir-induced gelation is a second-order nonequilibrium phase transition (with broken detailed balance). Consistent with this scenario, the size of the largest cluster is observed to diverge with power-law exponent according to three-dimensional percolation upon approaching the critical mean coordination number.

cond-mat.soft↗

arXiv2020

Emergence of New Materials for Exploiting Highly Efficient Carrier Multiplication in Photovoltaics

In conventional solar cell semiconductor materials (predominantly Si) photons with energy higher than the band gap initially generate hot electrons and holes, which subsequently cool down to the band edge by phonon emission. Due to the latter process, the energy of the charge carriers in excess of the band gap is lost as heat and does not contribute to the conversion of solar to electrical power. If the excess energy is more than the band gap it can in principle be utilized through a process known as carrier multiplication (CM) in which a single absorbed photon generates two (or more) pairs of electrons and holes. Thus, through CM the photon energy above twice the band gap enhances the photocurrent of a solar cell. In this review, we discuss recent progress in CM research in terms of fundamental understanding, emergence of new materials for efficient CM, and CM based solar cell applications. Based on our current understanding, the CM threshold can get close to the minimal value of twice the band gap in materials where a photon induces an asymmetric electronic transition from a deeper valence band or to a higher conduction band. In addition, the material must have a low exciton binding energy and high charge carrier mobility, so that photoexcitation leads directly to the formation of free charges that can readily be extracted at external electrodes of a photovoltaic device. Percolative networks of coupled PbSe quantum dots, Sn/Pb based halide perovskites, and transition metal dichalcogenides such as MoTe2 fulfill these requirements to a large extent. These findings point towards promising prospects for further development of new materials for highly efficient photovoltaics.

physics.app-ph↗