Dipole Force Research Articles

Active fractal networks with stochastic force monopoles and force dipoles: Application to subdiffusion of chromosomal loci.

Motivated by the well-known fractal packing of chromatin, we study the Rouse-type dynamics of elastic fractal networks with embedded, stochastically driven, active force monopoles and force dipoles that are temporally correlated. We compute, analytically-using a general theoretical framework-and via Langevin dynamics simulations, the mean square displacement (MSD) of a network bead. Following a short-time superdiffusive behavior, force monopoles yield anomalous subdiffusion with an exponent identical to that of the thermal system. In contrast, force dipoles do not induce subdiffusion, and the early superdiffusive MSD crosses over to a relatively small, system-size-independent saturation value. In addition, we find that force dipoles may lead to "crawling" rotational motion of the whole network, reminiscent of that found for triangular micro-swimmers and consistent with general theories of the rotation of deformable bodies. Moreover, force dipoles lead to network collapse beyond a critical force strength, which persists with increasing system size, signifying a true first-order dynamical phase transition. We apply our results to the motion of chromosomal loci in bacteria and yeast cells' chromatin, where anomalous sub-diffusion, MSD∼tν with ν≃0.4, was found in both normal and cells depleted of adenosine triphosphate (ATP), albeit with different apparent diffusion coefficients. We show that the combination of thermal, monopolar, and dipolar forces in chromatin is typically dominated by the active monopolar and thermal forces, explaining the observed normal cells vs the ATP-depleted cells behavior.

Immersed boundary method for dynamic simulation of polarizable colloids of arbitrary shape in explicit ion electrolytes.

We develop a computational method for modeling electrostatic interactions of arbitrarily shaped, polarizable objects on colloidal length scales, including colloids/nanoparticles, polymers, and surfactants, dispersed in explicit ion electrolytes and nonionic solvents. Our method computes the nonuniform polarization charge distribution induced in a colloidal particle by both externally applied electric fields and local electric fields arising from other charged objects in the dispersion. This leads to expressions for electrostatic energies, forces, and torques that enable efficient molecular dynamics and Brownian dynamics simulations of colloidal dispersions in electrolytes, which can be harnessed to accurately predict structural and transport properties. We describe an implementation in which colloidal particles are modeled as rigid composites of small spherical beads that tessellate the surface of the particle. The electrostatics calculations are accelerated using a spectrally accurate particle-mesh-Ewald technique implemented on a graphics processing unit and regularized such that the electrostatic calculations are well-defined even for overlapping bodies. We illustrate the effectiveness of this approach with a comprehensive set of calculations: the induced dipole moments and forces for individual, paired, and lattice configurations of spherical colloids in an electric field; the induced dipole moment and torque for anisotropic particles subjected to an electric field; the equilibrium ion distribution in the double layer surrounding charged colloids; the dynamics of charged colloids; and the behavior of ions in the double layer of a polarizable colloid under the influence of an electric field.

Effects of the chirp rate on single-shot coherent Rayleigh-Brillouin scattering

Single-shot coherent Rayleigh-Brillouin scattering (CRBS) is modeled using direct simulation Monte Carlo (DSMC). In CRBS, an optical lattice generated by the interference of two pump lasers traps the neutral particles via the dipole force. The gradient of refractive index due to the trapped particles of the gaseous media leads to coherent scattering of a probe beam, resulting in the CRBS signal. Additionally, using a chirped laser beam, CRBS signals can be obtained in a single laser shot, shortening the measurement time of the gas flow (on the order of 100 ns). The DSMC results of single-shot CRBS assuming Maxwellian velocity distribution functions (VDFs) show good agreement with experimental data, including argon, carbon dioxide, and xenon, for different gas pressures. One of the key observations obtained from the present simulations is that the CRBS signals become asymmetric when using a fast chirp rate due to finite time for collisionless trapping and collisional thermalization. Published by the American Physical Society 2024

Continuous Focusing of Particles by AC-Electroosmosis and Induced Dipole Interactions.

Continuous particle focusing by using microfluidics is an effective method for separating particles, cells, or droplets for analytical purposes. Previously, it was shown that an alternating current across rectangular microchannels with slightly deformed side walls results in vortex flow patterns caused by alternating current electroosmosis (AC-EOF) and could lead to particle focusing. In this work, we explore this mechanism by experimentally studying the particle focusing behavior for various fluid flow velocities through a microchannel. Since it is unlikely that the particles are kept in their focused position solely by convection, a theoretical force balance between the hydrodynamic and the induced dipole force was determined. In our experiments, it was found that there is no substantial effect of the pressure-driven fluid velocity on the particle focusing velocity within the studied range. From the theoretical force balance calculations, it was determined that while the addition of the induced dipole force can still not completely describe the experimentally observed particle focusing, the induced dipole can be strong enough to overcome the hydrodynamic force. Finally, it is hypothesized that under specific circumstances, including a repulsive electrostatic force between a particle and electrode wall can complete the theoretical particle focusing force balance. Alternative phenomena that could also play a role in particle focusing are proposed.

Resolving Coffee Waste and Water Pollution-A Study on KOH-Activated Coffee Grounds for Organophosphorus Xenobiotics Remediation.

This study investigates using KOH-activated coffee grounds (KACGs) as an effective adsorbent for removing organophosphorus xenobiotics malathion and chlorpyrifos from water. Malathion and chlorpyrifos, widely used as pesticides, pose significant health risks due to their neurotoxic effects and environmental persistence. Spent coffee grounds, abundant biowaste from coffee production, are chemically activated with KOH to enhance their adsorptive capacity without thermal treatment. This offers a sustainable solution for biowaste management and water remediation. Adsorption kinetics indicating rapid initial adsorption with high affinity were observed, particularly for chlorpyrifos. Isotherm studies confirmed favorable adsorption conditions, with higher maximum adsorption capacities for chlorpyrifos compared to malathion (15.0 ± 0.1 mg g-1 for malathion and 22.3 ± 0.1 mg g-1 for chlorpyrifos), highlighting its potential in mitigating water pollution. Thermodynamic analysis suggested the adsorption process was spontaneous but with the opposite behavior for the investigated pesticides. Malathion interacts with KACGs via dipole-dipole and dispersion forces, while chlorpyrifos through π-π stacking with aromatic groups. The reduction in neurotoxic risks associated with pesticide exposure is also shown, indicating that no more toxic products were formed during the remediation. This research contributes to sustainable development goals by repurposing biowaste and addressing water pollution challenges through innovative adsorbent materials.

Strengthening mechanism of large-diameter magnetic particles on ferrofluid nanoparticle chaining

The magnetization of nano ferrofluid is lower than that of micrometer magnetorheological fluid, which limits its application in seals, dampers, and various other fields. To enhance the ferrofluid performance, this paper incorporates large-diameter magnetic particles into the ferrofluid to strengthen chaining among nanoparticles. A matrix discrete element method model is constructed to investigate the strengthening mechanism of large-diameter magnetic particles on ferrofluid nanoparticle chaining. Additionally, the chain formation process involving both large and small particles and the influence of large particle volume fractions on chain length, particle number, and yield strength are studied based on the simulation. The results show that small particles and large particles together constitute different complex structures, such as the columnar structure and column-net structure under the strong magnetic dipole force of the large particles, leading to the high chain structure strength. In addition, the chain formation speed, average chain length, average particle number, yield strength, and additional viscosity are influenced by the volume fractions and particle sizes of large particles. The method will enhance the ferrofluid sealing performance and expand the ferrofluid application areas.

Individual and collective manipulation of multifunctional bimodal droplets in three dimensions.

Spatiotemporally controllable droplet manipulation is vital across numerous applications, particularly in miniature droplet robots known for their exceptional deformability. Despite notable advancements, current droplet control methods are predominantly limited to two-dimensional (2D) deformation and motion of an individual droplet, with minimal exploration of 3D manipulation and collective droplet behaviors. Here, we introduce a bimodal actuation strategy, merging magnetic and optical fields, for remote and programmable 3D guidance of individual ferrofluidic droplets and droplet collectives. The magnetic field induces a magnetic dipole force, prompting the formation of droplet collectives. Simultaneously, the optical field triggers isothermal changes in interfacial tension through Marangoni flows, enhancing buoyancy and facilitating 3D movements of individual and collective droplets. Moreover, these droplets can function autonomously as soft robots, capable of transporting objects. Alternatively, when combined with a hydrogel shell, they assemble into jellyfish-like robots, driven by sunlight. These findings present an efficient strategy for droplet manipulation, broadening the capabilities of droplet-based robotics.

Effects of surface wettability and density change during solidification of paraffin phase change materials

Phase change materials (PCMs) are widely used for thermal energy storage and other applications. During the solidification of a PCM, a volume change occurs due to thermal expansion and structural change of the molecules. A concave shape may be created during the solidification shrinkage. This paper investigates the shrinkage profile formed during the solidification of paraffin wax and its relationship with the surface wettability (contact angle), considering the effect of density changes. The contact angle of a paraffin droplet on a surface indicates the extent of adhesion between the solid surface and paraffin. The experimental study examines a mixture of wax with nanoparticles, wax with surfactants, different coatings on the container surface, and different solidification temperatures. Enhanced adhesion and increased shrinkage height are observed due to the non-polar interaction between coated surfaces and paraffin, facilitated by induced dipole-induced dipole forces. The addition of 3% octadecylamine enhances adhesion between paraffin and the container, as driven by dipole–dipole forces between the hydroxyl group on epoxy resin-container surfaces and the hydrophilic amine group of octadecylamine. The shrinkage height increases with a decrease in the contact angle of paraffin on the surface. The shrinkage profile also changes with the solidification temperature. The highest shrinkage profile is achieved for the highest solidification temperature.

Fluorophilic Sigma(σ)‐Lock Self‐Healable Copolymers

AbstractAlthough F‐Containing molecules and macromolecules are often used in molecular biology to increase the binding with Lewis acidic groups by introducing favorable C−F dipoles, there is virtually no experimental evidence and limited understanding of the nature of these interactions, especially their role in synthetic polymeric materials. These studies elucidate the molecular origin of inter‐ and intra‐Chain interactions responsible for self‐healing of F‐Containing copolymers composed of pentafluorostyrene and n‐butyl acrylate units (p(PFS/nBA). Guided by dynamic surface oscillating force (SOF) and spectroscopic measurements supported by molecular dynamics (MD) simulations, these studies show that the reformation of σ‐σ orbitals in −C−F of PFS and CH3CH2− of nBA units enables the recovery of entropic energy via fluorophilic‐σ‐lock van der Waals forces when PFS/nBA molar ratios are ~50/50. The strength of these interactions determined experimentally for self‐healable PFS/nBA compositions is in the order ~0.3 kcal/mol which primarily comes from fluorophilic‐σ‐lock (~70 %) contributions. These interactions are significantly diminished for non‐self‐healable counterparts. Strongly polarized −C−F σ orbitals create lateral dipolar forces enhancing the affinity towards −C−H orbitals, facilitating energetically favorable interactions. Entropic recovery driven by non‐Covalent bonding offers a valuable tool in designing materials with unique functionalities, particularly self‐healable batteries and energy storage devices.

Fluorophilic Sigma(σ)-Lock Self-Healable Copolymers.

Although F-Containing molecules and macromolecules are often used in molecular biology to increase the binding with Lewis acidic groups by introducing favorable C-F dipoles, there is virtually no experimental evidence and limited understanding of the nature of these interactions, especially their role in synthetic polymeric materials. These studies elucidate the molecular origin of inter- and intra-Chain interactions responsible for self-healing of F-Containing copolymers composed of pentafluorostyrene and n-butyl acrylate units (p(PFS/nBA). Guided by dynamic surface oscillating force (SOF) and spectroscopic measurements supported by molecular dynamics (MD) simulations, these studies show that the reformation of σ-σ orbitals in -C-F of PFS and CH3CH2- of nBA units enables the recovery of entropic energy via fluorophilic-σ-lock van der Waals forces when PFS/nBA molar ratios are ~50/50. The strength of these interactions determined experimentally for self-healable PFS/nBA compositions is in the order ~0.3 kcal/mol which primarily comes from fluorophilic-σ-lock (~70 %) contributions. These interactions are significantly diminished for non-self-healable counterparts. Strongly polarized -C-F σ orbitals create lateral dipolar forces enhancing the affinity towards -C-H orbitals, facilitating energetically favorable interactions. Entropic recovery driven by non-Covalent bonding offers a valuable tool in designing materials with unique functionalities, particularly self-healable batteries and energy storage devices.

In Situ‐Tunable Spin–Spin Interactions in a Penning Trap with In‐Bore Optomechanics

AbstractExperimental implementations of quantum simulation must balance control‐field‐induced decoherence with the controllability of the quantum system. The ratio of coherent interaction strength to decoherence induced by stimulated emission in atomic systems is typically determined by hardware constraints, limiting the flexibility needed to explore different operating regimes. Here, an optomechanical system is presented for in situ tuning of the coherent spin‐motion and spin‐spin interaction strength in 2D ion crystals in a Penning trap. Enabled by precision closed‐loop piezo‐actuated positioners integrated into the confined space of a superconducting magnet's bore, the system allows tuning of the angle‐of‐incidence of Raman laser beams up to , governing the ratio of coherent to incoherent light‐matter interaction for fixed optical power. System characterization involves measurements of the induced mean‐field spin precession under the application of an optical dipole force in ion crystals cooled below the Doppler limit through electromagnetically induced transparency cooling. These experiments show approximately a variation in the coherent to incoherent interaction ratio with changing , consistent with theoretical predictions. The system stability is characterized over 6000 s, resulting in a drift rate of h–1. These technical developments will be crucial in future quantum simulations and sensing applications.

Optical dipolar chiral sorting forces and their manifestation in evanescent waves and nanofibers

Optical dipolar chiral sorting forces and their manifestation in evanescent waves and nanofibers

What Is the "Hydrogen Bond"? A QFT-QED Perspective.

In this paper we would like to highlight the problems of conceiving the "Hydrogen Bond" (HB) as a real short-range, directional, electrostatic, attractive interaction and to reframe its nature through the non-approximated view of condensed matter offered by a Quantum Electro-Dynamic (QED) perspective. We focus our attention on water, as the paramount case to show the effectiveness of this 40-year-old theoretical background, which represents water as a two-fluid system (where one of the two phases is coherent). The HB turns out to be the result of the electromagnetic field gradient in the coherent phase of water, whose vacuum level is lower than in the non-coherent (gas-like) fraction. In this way, the HB can be properly considered, i.e., no longer as a "dipolar force" between molecules, but as the phenomenological effect of their collective thermodynamic tendency to occupy a lower ground state, compatible with temperature and pressure. This perspective allows to explain many "anomalous" behaviours of water and to understand why the calculated energy associated with the HB should change when considering two molecules (water-dimer), or the liquid state, or the different types of ice. The appearance of a condensed, liquid, phase at room temperature is indeed the consequence of the boson condensation as described in the context of spontaneous symmetry breaking (SSB). For a more realistic and authentic description of water, condensed matter and living systems, the transition from a still semi-classical Quantum Mechanical (QM) view in the first quantization to a Quantum Field Theory (QFT) view embedded in the second quantization is advocated.

Surface-phonon-polariton-enhanced photoinduced dipole force for nanoscale infrared imaging.

The photoinduced dipole force (PiDF) is an attractive force arising from the Coulombic interaction between the light-induced dipoles on the illuminated tip and the sample. It shows extreme sample-tip distance and refractive index dependence, which is promising for nanoscale infrared (IR) imaging of ultrathin samples. However, the existence of PiDF in the mid-IR region has not been experimentally demonstrated due to the coexistence of photoinduced thermal force (PiTF), typically one to two orders of magnitude higher than PiDF. In this study, we demonstrate that, with the assistance of surface phonon polaritons, the PiDF of c-quartz can be enhanced to surpass its PiTF, enabling a clear observation of PiDF spectra reflecting the properties of the real part of permittivity. Leveraging the detection of the PiDF of phonon polaritonic substrate, we propose a strategy to enhance the sensitivity and contrast of photoinduced force responses in transmission images, facilitating the precise differentiation of the heterogeneous distribution of ultrathin samples.

Cilia-Like Observer for Tumor Recurrence in Active Soft Matter

Cilia-like sensitivity observer, at an adaptive treatment of a tumor recurrence in active soft matter, is built. Therefore, the activity of soft matter is shown as active colloidal chains with a cilia-like and flagella-like motility; the tumor recurrence, in active soft matter, is considered as run-away/quantum aging of soft matter; the adaptive treatment energy is defined as electromagnetic field energy, stabilizing or destabilizing life, and as energy of a force dipole. Information recovery at an adaptive treatment is fulfilled via two cilia-like quantum extremal islands. Information recovery is obtained for a mean maximum-tolerated dose of the adaptive treatment and cilia-like tumor growth in active soft matter. There are introduced four strategies for an adaptive treatment for run-away/quantum aging active soft matter with a mean maximum-tolerated dose at stabilized tumor/tumor diffusion. It is graphically determined, for each of these four strategies, the mean sensitivity of the adaptive treatment for three tumor types in 27 patients, according to a maximum-tolerated treatment dose and cilia-like tumor growth in active soft matter.

Many-body interactions between contracting living cells.

The organization of live cells into tissues and their subsequent biological function involves inter-cell mechanical interactions, which are mediated by their elastic environment. To model this interaction, we consider cells as spherical active force dipoles surrounded by an unbounded elastic matrix. Even though we assume that this elastic medium responds linearly, each cell's regulation of its mechanical activity leads to nonlinearities in the emergent interactions between cells. We study the many-body nature of these interactions by considering several geometries that include three or more cells. We show that for different regulatory behaviors of the cells' activity, the total elastic energy stored in the medium differs from the superposition of all two-body interactions between pairs of cells within the system. Specifically, we find that the many-body interaction energy between cells that regulate their position is smaller than the sum of interactions between all pairs of cells in the system, while for cells that do not regulate their position, the many-body interaction is larger than the superposition prediction. Thus, such higher-order interactions should be considered when studying the mechanics of multiple cells in proximity.

Structured light and ultracold atoms in a driven optical cavity

We consider a far-red-detuned optical cavity, driven by a pump, which contains an ultracold atomic medium. Using coupled partial differential equations which describe the evolution of the atomic and optical fields, we demonstrate that our model leads to novel self-structuring, led by the optical field through the dipole force, within the ultracold atomic medium. Introducing OAM to the optical pump, we demonstrate that these structures may be made to rotate, forming atomic fields analogous to persistent phase currents.

Hydrodynamically induced aggregation of two dimensional oriented active particles.

We investigate a system of co-oriented active particles interacting only via hydrodynamic and steric interactions in a two-dimensional fluid. We offer a new method of calculating the flow created by any active particle in such a fluid, focusing on the dynamics of flow fields with a high-order spatial decay, which we analyze using a geometric Hamiltonian. We show that when the particles are oriented and the flow has a single, odd power decay, such systems lead to stable, fractal-like aggregation, with the only exception being the force dipole. We discuss how our results can easily be generalized to more complicated force distributions and to other effective two-dimensional systems.

A Magnetic Pincher for the Dynamic Measurement of the Actin Cortex Thickness in Live Cells.

The actin cortex is an essential element of the cytoskeleton allowing cells to control and modify their shape. It is involved in cell division and migration. However, probing precisely the physical properties of the actin cortex has proved to be challenging: it is a thin and dynamic material, and its location in the cell-directly under the plasma membrane-makes it difficult to study with standard light microscopy and cell mechanics techniques. In this chapter, we present a novel protocol to probe dynamically the thickness of the cortex and its fluctuations using superparamagnetic microbeads in a uniform magnetic field. A bead ingested by the cell and another outside the cell attract each other due to dipolar forces. By tracking their position with nanometer precision, one can measure the thickness of the cortex pinched between two beads and monitor its evolution in time. We first present the set of elements necessary to realize this protocol: a magnetic field generator adapted to a specific imaging setup and the aforementioned superparamagnetic microbeads. Then we detail the different steps of a protocol that can be used on diverse cell types, adherent or not.

Magnetic-actuated hydrogel microrobots with multimodal motion and collective behavior.

Magnetic-actuated miniature robots have sparked growing interest owing to their promising potential in biomedical applications, such as noninvasive diagnosis, cargo delivery, and microsurgery. Innovations are required to combine biodegradable materials with flexible mobility to promote the translation of magnetic robots towards in vivo application. This study proposes a biodegradable magnetic hydrogel robot (MHR) with multimodal locomotion and collective behavior through magnetic-assisted fabrication. The MHRs with aligned magnetic chains inside their structures have more significant maximum motion speeds under rotating magnetic fields than the robots without magnetic alignment. By reconfiguring the external magnetic fields, three types of stable motion modes (tumbling, spinning, and wobbling modes) of the individual MHRs can be triggered, while flexible conversion can be achieved between each motion mode. The motion mechanism of each motion mode under diverse rotating magnetic fields has been analyzed. The collective behavior of the MHRs, which is triggered by the magnetic dipole force, can enhance the motion performance and pass through sophisticated terrains. Furthermore, the experimental results demonstrate that the assembled MHRs can execute complicated tasks such as targeted cargo delivery. The proposed MHRs with multimodal locomotion and assembled behavior show effective motion efficiency, flexible maneuverability, and remarkable targeting ability, providing a new choice for magnetic robots in biomedical applications.