arXiv subjects

Rudolf Weeber

Publications and source records attributed to Rudolf Weeber.

13 recordsLinked to original sources

arXiv2026

LPC3D: An Enhanced Parallel Software for Large-Scale Simulation of Adsorption in Porous Carbons and Supercapacitors

Simulations of electrochemical double layer capacitors based on porous carbon electrodes, energy storage systems which accumulate and release energy through reversible ion adsorption at electrode/electrolyte interfaces, are often performed at the microscopic scale, using molecular dynamics. Such simulations provide crucial information to understand the adsorption of ions and the effect of confinement on some electrochemical properties. However, their computational cost limits the size of the systems studied to a few nanometers and a few pores while experimental materials are highly heterogeneous with a distribution of particle and pore sizes. LPC3D is a software designed for mesoscopic simulations of porous carbon particles and carbon-based supercapacitors which allow for the inclusion of such heterogeneity. The code calculates quantities of adsorbed ions, diffusion coefficients and NMR spectra of ions / molecules adsorbed in porous carbon matrices. In this work, we report on a new implementation of LPC3D, written in Python using the PyStencils module which can generate optimized C++ and CUDA code. This implementation is parallel, can be run on CPU and GPU, and allows one to simulate systems going from a single carbon particle to a supercapacitor with hundreds of micrometers in length. Here, we apply the new implementation of LPC3D to the simulation of supercapacitors with porous carbon electrodes represented as monoliths or carbon films to investigate the influence of the microstructure on the resulting adsorption and spectroscopic properties.

cond-mat.mtrl-sci↗

arXiv2021

Lees-Edwards boundary conditions for translation invariant shear flow: implementation and transport properties

Molecular dynamics (MD) simulations represent a powerful investigation tool in the field of soft matter. By using shear flows, one can probe the bulk rheology of complex fluids, also beyond the linear response regime, in a way that imitates laboratory experiments. One solution to impose a shear flow in particle-based simulations is the Lees-Edwards technique which ensures that particles experience shear by imposing rules for motion and interactions across the boundary in the direction of the shear plane. Despite their presentation in 1972, a readily available public implementation of Lees-Edwards boundary conditions has been missing from MD simulation codes. In this article, we present our implementation of the Lees-Edwards technique and discuss the relevant technical choices. We used ESPResSo, the extensible simulation package for research on soft matter, for molecular dynamics simulations which can be used as a reference for other implementers. We illustrate our implementation using bulk dissipative particle dynamics fluids, compare different viscosity measurement techniques, and observe the anomalous diffusion in our samples during continuous and oscillatory shear, in good comparison to theoretical estimates.

cond-mat.soft↗

arXiv2020

Frequency-dependent magnetic susceptibility of magnetic nanoparticles in a polymer solution: a simulation study

Magnetic composite materials i.e. elastomers, polymer gels, or polymer solutions with embedded magnetic nanoparticles are useful for many technical and bio-medical applications. However, the microscopic details of the coupling mechanisms between the magnetic properties of the particles and the mechanical properties of the (visco)elastic polymer matrix remain unresolved. Here we study the response of a single-domain spherical magnetic nanoparticle that is suspended in a polymer solution to alternating magnetic fields. As interactions we consider only excluded volume interactions with the polymers and hydrodynamic interactions mediated through the solvent. The AC susceptibility spectra are calculated using a linear response Green-Kubo approach, and the influences of changing polymer concentration and polymer length are investigated. Our data is compared to recent measurements of the AC susceptibility for a typical magnetic composite system [Roeben et al., Colloid and Polymer Science, 2014, 2013--2023], and demonstrates the importance of hydrodynamic coupling in such systems.

cond-mat.soft↗

arXiv2020

An Environment for Sustainable Research Software in Germany and Beyond: Current State, Open Challenges, and Call for Action

Research software has become a central asset in academic research. It optimizes existing and enables new research methods, implements and embeds research knowledge, and constitutes an essential research product in itself. Research software must be sustainable in order to understand, replicate, reproduce, and build upon existing research or conduct new research effectively. In other words, software must be available, discoverable, usable, and adaptable to new needs, both now and in the future. Research software therefore requires an environment that supports sustainability. Hence, a change is needed in the way research software development and maintenance are currently motivated, incentivized, funded, structurally and infrastructurally supported, and legally treated. Failing to do so will threaten the quality and validity of research. In this paper, we identify challenges for research software sustainability in Germany and beyond, in terms of motivation, selection, research software engineering personnel, funding, infrastructure, and legal aspects. Besides researchers, we specifically address political and academic decision-makers to increase awareness of the importance and needs of sustainable research software practices. In particular, we recommend strategies and measures to create an environment for sustainable research software, with the ultimate goal to ensure that software-driven research is valid, reproducible and sustainable, and that software is recognized as a first class citizen in research. This paper is the outcome of two workshops run in Germany in 2019, at deRSE19 - the first International Conference of Research Software Engineers in Germany - and a dedicated DFG-supported follow-up workshop in Berlin.

cs.GL↗

arXiv2018

ESPResSo 4.0 -- An Extensible Software Package for Simulating Soft Matter Systems

ESPResSo 4.0 is an extensible simulation package for research on soft matter. This versatile molecular dynamics program was originally developed for coarse-grained simulations of charged systems Limbach et al., Comput. Phys. Commun. 174, 704 (2006). The scope of the software has since broadened considerably: ESPResSo can now be used to simulate systems with length scales spanning from the molecular to the colloidal. Examples include, self-propelled particles in active matter, membranes in biological systems, and the aggregation of soot particles in process engineering. ESPResSo also includes solvers for hydrodynamic and electrokinetic problems, both on the continuum and on the explicit particle level. Since our last description of version 3.1 Arnold et al., Meshfree Methods for Partial Differential Equations VI, Lect. Notes Comput. Sci. Eng. 89, 1 (2013), the software has undergone considerable restructuring. The biggest change is the replacement of the Tcl scripting interface with a much more powerful Python interface. In addition, many new simulation methods have been implemented. In this article, we highlight the changes and improvements made to the interface and code, as well as the new simulation techniques that enable a user of ESPResSo 4.0 to simulate physics that is at the forefront of soft matter research.

cond-mat.soft↗

arXiv2018

Accelerating the calculation of dipolar interactions in particle based simulations with open boundary conditions by means of the P2NFFT method

Magnetic gels are soft elastic materials consisting of magnetic particles embedded in a polymer network. Their shape and elasticity can be controlled by an external magnetic field, which gives rise to both, engineering and biomedical applications. Computer simulations are a commonly used tool to study these materials. A well-known bottleneck of these simulations is the demanding calculation of dipolar interactions. Under periodic boundary conditions established algorithms are available for doing this, however, at the expense of restricting the way in which the gels can deform in an external magnetic field. Moreover, the magnetic properties depend on the sample shape, ruling out periodic boundary conditions entirely for some research questions. In this article we will employ the recently developed dipolar variant of the P$^2$NFFT method that is able to calculate dipolar interactions under open boundary conditions with an $N \log N$ scaling in the number of particles, rather than the expensive $N^2$ scaling of a direct summation of pair forces. The dipolar P$^2$NFFT method has been implemented within the ScaFaCoS library. The molecular dynamics software ESPResSo has been extended to make use of the library. After a short summary of the method, we will discuss its value for studying magnetic soft matter systems. A particular focus is put on developing a tuning strategy to reach the best performance of the method at a predefined accuracy, and lastly applying the method to a magnetic gel model. Here, adapting to the gel's change in shape during the course of a simulation is of particular interest.

cond-mat.soft↗

arXiv2017

Interplay between particle microstructure, network topology and sample shape in magnetic gels -- A molecular dynamics simulation study

Ferrogels, i.e., hydrogels loaded with magnetic nanoparticles, have the ability to deform in external magnetic fields. The precise shape of deformation and the alignment of the gel in the field, however, depend on the interplay of several factors. In this paper, we introduce a coarse-grained simulation model, which takes into account the configuration of magnetic particles in the gel, the sample shape, and aspects of the polymer network topology. We use this model to show that in gels with an isotropic microstructure, an external magnetic field reduces clustering, while this is not the case for uniaxial gels, in which the particle configuration is anisotropic due to the presence of a magnetic field during cross-linking. For ellipsoidal gels, we find that a uniaxial microstructure additionally can override the deformation and alignment expected as indicated the demagnetization energy. Finally, we examine to what degree gels with different network topologies maintain the particle microstructure ``frozen in`` during the cross-linking process.

cond-mat.soft↗

arXiv2015

Towards a scale-bridging description of ferrogels and magnetic elastomers

Ferrogels and magnetic elastomers differentiate themselves from other materials by their unique capability of reversibly changing shape and mechanical properties under the influence of an external magnetic field. A crucial issue in the study of these outstanding materials is the interaction between the mesoscopic magnetic particles and the polymer matrix in which they are embedded. Here we analyze interactions between two such particles connected by a polymer chain, a situation representative for particle-crosslinked magnetic gels. To make a first step towards a scale-bridging description of the materials, effective potentials for mesoscopic configurational changes are specified using microscopic input obtained from simulations. Furthermore, the impact of the presence of magnetic interactions on the probability distributions and thermodynamic quantities of the system is considered. The resulting mesoscopic model potentials can be used to economically model the system on the particle length scales. This first coarse-graining step is important to realize simplified but realistic scale-bridging models for these promising materials.

cond-mat.soft↗

arXiv2015

Ferrogels cross-linked by magnetic particles: Field-driven deformation and elasticity studied using computer simulations

Ferrogels, i.e. swollen polymer networks into which magnetic particles are immersed, can be considered as "smart materials" since their shape and elasticity can be controlled by an external magnetic field. Using molecular dynamics simulations on the coarse-grained level we study a ferrogel in which the magnetic particles act as the cross-linkers of the polymer network. In a homogeneous external magnetic field the direct coupling between the orientation of the magnetic moments and the polymers by means of covalent bonds gives rise to a deformation of the gel, independent of the interparticle dipole-dipole interaction. In this paper we report quantitative measurements of this deformation, the gel's elastic moduli and its magnetic response. Our results demonstrate that these properties depend significantly on the topology of the polymer network.

physics.chem-ph↗

arXiv2015

Buckling of paramagnetic chains in soft gels

We study the magneto-elastic coupling behavior of paramagnetic chains in soft polymer gels exposed to external magnetic fields. To this end, a laser scanning confocal microscope is used to observe the morphology of the paramagnetic chains together with the deformation field of the surrounding gel network. The paramagnetic chains in soft polymer gels show rich morphological shape changes under oblique magnetic fields, in particular a pronounced buckling deformation. The details of the resulting morphological shapes depend on the length of the chain, the strength of the external magnetic field, and the modulus of the gel. Based on the observation that the magnetic chains are strongly coupled to the surrounding polymer network, a simplified model is developed to describe their buckling behavior. A coarse-grained molecular dynamics simulation model featuring an increased matrix stiffness on the surfaces of the particles leads to morphologies in agreement with the experimentally observed buckling effects.

cond-mat.soft↗

arXiv2014

Modelling nano-particle agglomeration using local interactions

Nano-particle agglomeration plays an important role in processes such as spray drying and particle flame synthesis. These processes have in common that nano-particles collide at low concentrations and get irreversibly linked at the point of contact due to plastic deformation. In this paper, we investigate several models of irreversible connections, which require only local interactions between the colliding nano-particles and thus allow for scalable simulations. The models investigated here connect the particles upon collision by non-bonded strongly attractive interactions, bonded interactions or by binding agents placed at the point of contact. Models using spherically symmetric interactions form compact agglomerates and are therefore unsuitable to study agglomeration. In contrast, models that are either based on both central and angular potentials (type one) or on binding agents (type two) efficiently prevent restructuring of the agglomerates, and are therefore useful for modeling contacts formed by plastic deformation. Moreover, both types of models allow to control the rigidity and by that the degree of restructuring. The first type of model is computationally more efficient at low fractional dimensions of the aggregates, while the second gives easy access to local shear forces, which is important when breaking of agglomerates is to be considered. As example applications, we reproduce the well-known diffusion-limited agglomeration (DLA) and report results on soot aggregation.

cond-mat.soft↗

arXiv2012

Hydrodynamic interactions in active colloidal crystal microrheology

In dense colloids it is commonly assumed that hydrodynamic interactions do not play a role. However, a found theoretical quantification is often missing. We present computer simulations that are motivated by experiments where a large colloidal particle is dragged through a colloidal crystal. To qualify the influence of long-ranged hydrodynamics, we model the setup by conventional Langevin dynamics simulations and by an improved scheme with limited hydrodynamic interactions. This scheme significantly improves our results and allows to show that hydrodynamics strongly impacts on the development of defects, the crystal regeneration as well as on the jamming behavior.

cond-mat.soft↗

arXiv2007

Colloids dragged through a polymer solution: experiment, theory and simulation

We present micro-rheological measurments of the drag force on colloids pulled through a solution of lambda-DNA (used here as a monodisperse model polymer) with an optical tweezer. The experiments show a violation of the Stokes-Einstein relation based on the independently measured viscosity of the DNA solution: the drag force is larger than expected. We attribute this to the accumulation of DNA infront of the colloid and the reduced DNA density behind the colloid. This hypothesis is corroborated by a simple drift-diffusion model for the DNA molecules, which reproduces the experimental data surprisingly well, as well as by corresponding Brownian dynamics simulations.

cond-mat.soft↗