08 Fakultät Mathematik und Physik

Permanent URI for this collectionhttps://elib.uni-stuttgart.de/handle/11682/9

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    The role of dimensionality and geometry in quench-induced nonequilibrium forces
    (2021) Nejad, Mehrana Raeisian; Khalilian, Hamidreza; Rohwer, Christian M.; Moghaddam, Ali Ghorbanzadeh
    We present an analytical formalism, supported by numerical simulations, for studying forces that act on curved walls following temperature quenches of the surrounding ideal Brownian fluid. We show that, for curved surfaces, the post-quench forces initially evolve rapidly to an extremal value, whereafter they approach their steady state value algebraically in time. In contrast to the previously-studied case of flat boundaries (lines or planes), the algebraic decay for curved geometries depends on the dimension of the system. Specifically, steady-state values of the force are approached in time as t-d/2 in d-dimensional spherical (curved) geometries. For systems consisting of concentric circles or spheres, the exponent does not change for the force on the outer circle or sphere. However, the force exerted on the inner circles or sphere experiences an overshoot and, as a result, does not evolve to the steady state in a simple algebraic manner. The extremal value of the force also depends on the dimension of the system, and originates from curved boundaries and the fact that particles inside a sphere or circle are locally more confined, and diffuse less freely than particles outside the circle or sphere.
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    Electrolyte solutions at heterogeneously charged surfaces
    (2020) Mußotter, Maximilian; Dietrich, Siegfried (Prof. Dr.)
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    Ionic liquids in conducting nanoslits : how important is the range of the screened electrostatic interactions?
    (2022) Groda, Yaroslav; Dudka, Maxym; Oshanin, Gleb; Kornyshev, Alexei A.; Kondrat, Svyatoslav
    Analytical models for capacitive energy storage in nanopores attract growing interest as they can provide in-depth analytical insights into charging mechanisms. So far, such approaches have been limited to models with nearest-neighbor interactions. This assumption is seemingly justified due to a strong screening of inter-ionic interactions in narrow conducting pores. However, how important is the extent of these interactions? Does it affect the energy storage and phase behavior of confined ionic liquids? Herein, we address these questions using a two-dimensional lattice model with next-nearest and further neighbor interactions developed to describe ionic liquids in conducting slit confinements. With simulations and analytical calculations, we find that next-nearest interactions enhance capacitance and stored energy densities and may considerably affect the phase behavior. In particular, in some range of voltages, we reveal the emergence of large-scale mesophases that have not been reported before but may play an important role in energy storage.
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    Entropy by neighbor distance as a new measure for characterizing spatiotemporal orders in microscopic collective systems
    (2023) Fu, Yulei; Wu, Zongyuan; Zhan, Sirui; Yang, Jiacheng; Gardi, Gaurav; Kishore, Vimal; Malgaretti, Paolo; Wang, Wendong
    Collective systems self-organize to form globally ordered spatiotemporal patterns. Finding appropriate measures to characterize the order in these patterns will contribute to our understanding of the principles of self-organization in all collective systems. Here we examine a new measure based on the entropy of the neighbor distance distributions in the characterization of collective patterns. We study three types of systems: a simulated self-propelled boid system, two active colloidal systems, and one centimeter-scale robotic swarm system. In all these systems, the new measure proves sensitive in revealing active phase transitions and in distinguishing steady states. We envision that the entropy by neighbor distance could be useful for characterizing biological swarms such as bird flocks and for designing robotic swarms.
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    Magnetic domains and domain wall pinning in atomically thin CrBr3 revealed by nanoscale imaging
    (2021) Sun, Qi-Chao; Song, Tiancheng; Anderson, Eric; Brunner, Andreas; Förster, Johannes; Shalomayeva, Tetyana; Taniguchi, Takashi; Watanabe, Kenji; Gräfe, Joachim; Stöhr, Rainer; Xu, Xiaodong; Wrachtrup, Jörg
    The emergence of atomically thin van der Waals magnets provides a new platform for the studies of two-dimensional magnetism and its applications. However, the widely used measurement methods in recent studies cannot provide quantitative information of the magnetization nor achieve nanoscale spatial resolution. These capabilities are essential to explore the rich properties of magnetic domains and spin textures. Here, we employ cryogenic scanning magnetometry using a single-electron spin of a nitrogen-vacancy center in a diamond probe to unambiguously prove the existence of magnetic domains and study their dynamics in atomically thin CrBr3. By controlling the magnetic domain evolution as a function of magnetic field, we find that the pinning effect is a dominant coercivity mechanism and determine the magnetization of a CrBr3 bilayer to be about 26 Bohr magnetons per square nanometer. The high spatial resolution of this technique enables imaging of magnetic domains and allows to locate the sites of defects that pin the domain walls and nucleate the reverse domains. Our work highlights scanning nitrogen-vacancy center magnetometry as a quantitative probe to explore nanoscale features in two-dimensional magnets.
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    Magnetic microrobot collectives as a model system for self-organisation
    (2023) Gardi, Gaurav; Holm, Christian (Prof. Dr.)
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    Axisymmetric spheroidal squirmers and self-diffusiophoretic particles
    (2020) Pöhnl, Ruben; Popescu, Mihail Nicolae; Uspal, William E.
    We study, by means of an exact analytical solution, the motion of a spheroidal, axisymmetric squirmer in an unbounded fluid, as well as the low Reynolds number hydrodynamic flow associated to it. In contrast to the case of a spherical squirmer - for which, e.g. the velocity of the squirmer and the magnitude of the stresslet associated with the flow induced by the squirmer are respectively determined by the amplitudes of the first two slip (‘squirming’) modes - for the spheroidal squirmer each squirming mode either contributes to the velocity, or contributes to the stresslet. The results are straightforwardly extended to the self-phoresis of axisymmetric, spheroidal, chemically active particles in the case when the phoretic slip approximation holds.
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    How to speed up ion transport in nanopores
    (2020) Breitsprecher, Konrad; Janssen, Mathijs; Srimuk, Pattarachai; Mehdi, B. Layla; Presser, Volker; Holm, Christian; Kondrat, Svyatoslav
    Electrolyte-filled subnanometre pores exhibit exciting physics and play an increasingly important role in science and technology. In supercapacitors, for instance, ultranarrow pores provide excellent capacitive characteristics. However, ions experience difficulties in entering and leaving such pores, which slows down charging and discharging processes. In an earlier work we showed for a simple model that a slow voltage sweep charges ultranarrow pores quicker than an abrupt voltage step. A slowly applied voltage avoids ionic clogging and co-ion trapping - a problem known to occur when the applied potential is varied too quickly - causing sluggish dynamics. Herein, we verify this finding experimentally. Guided by theoretical considerations, we also develop a non-linear voltage sweep and demonstrate, with molecular dynamics simulations, that it can charge a nanopore even faster than the corresponding optimized linear sweep. For discharging we find, with simulations and in experiments, that if we reverse the applied potential and then sweep it to zero, the pores lose their charge much quicker than they do for a short-circuited discharge over their internal resistance. Our findings open up opportunities to greatly accelerate charging and discharging of subnanometre pores without compromising the capacitive characteristics, improving their importance for energy storage, capacitive deionization, and electrochemical heat harvesting.