arXiv subjects

Ran Niu

Publications and source records attributed to Ran Niu.

14 recordsLinked to original sources

arXiv2026

Automated decision-making by chemical echolocation in active droplets

Motile microorganisms, like bacteria and algae, unify abilities like self-propulsion, autonomous navigation, and decision-making on the micron scale. While recent breakthroughs have led to the creation of synthetic microswimmers and nanoagents that can also self-propel, they still lack the functionality and sophistication of their biological counterparts. This study pioneers a mechanism enabling synthetic agents to autonomously navigate and make decisions, allowing them to solve mazes and transport cargo through complex environments without requiring external cues or guidance. The mechanism exploits chemo-hydrodynamic signals, produced by agents like active droplets or colloids, to remotely sense and respond to their environment - similar to echolocation. Our research paves the way for endowing autonomous, motile synthetic agents with functionalities that have been so far exclusive to biological organisms.

cond-mat.soft↗

arXiv2023

Self-solidifying active droplets showing memory-induced chirality

Most synthetic microswimmers do not reach the autonomy of their biological counterparts in terms of energy supply and diversity of motion. Here we report the first all-aqueous droplet swimmer powered by self-generated polyelectrolyte gradients, which shows memory-induced chirality while self-solidifying. An aqueous solution of surface tension-lowering polyelectrolytes self-solidifies on the surface of acidic water, during which polyelectrolytes are gradually emitted into the surrounding water and induce linear self-propulsion via spontaneous symmetry breaking. The low diffusion coefficient of the polyelectrolytes leads to long-lived chemical trails which cause memory effects that drive a transition from linear to chiral motion without requiring any imposed symmetry breaking. The droplet swimmer is capable of highly efficient removal (up to 85%) of uranium from aqueous solutions within 90 min, benefiting from self-propulsion and flow-induced mixing. Our results provide a route to fueling self-propelled agents which can autonomously perform chiral motion and collect toxins.

cond-mat.soft↗

arXiv2023

Writing in Water

Writing is an ancient communication technique dating back at least 30,000 years. While even sophisticated contemporary writing techniques hinge on solid surfaces for engraving or the deposition of ink, writing within a liquid medium requires a fundamentally different approach. We here demonstrate writing of lines, letters, and complex patterns in water by assembling lines of colloidal particles. Unlike established techniques for underwater writing on solid substrates, these lines are fully reconfigurable and do not require any fixation onto the substrate. Exploiting gravity, we roll an ion-exchange bead (pen) across a layer of sedimented colloidal particles (ink). The pen evokes a hydrodynamic flow collecting ink-particles into a durable, high-contrast line along its trajectory. Deliberate substrate-tilting sequences facilitate pen-steering and thus to draw and write. We complement our experiments with a minimal model that quantitatively predicts the observed parameter dependence for writing in fluids and highlights the generic character of writing by line-assembly. Overall, our approach opens a versatile route for writing, drawing, and patterning fluids - even at the micro-scale.

cond-mat.soft↗

arXiv2018

Unraveling Modular Microswimmers: From Self-Assembly to Ion-Exchange Driven Motors

Active systems contain self-propelled particles and can spontaneously self-organize into patterns making them attractive candidates for the self-assembly of smart soft materials. One key limitation of our present understanding of these materials hinges on the complexity of the microscopic mechanisms driving its components forward. Here, by combining experiments, analytical theory and simulations we explore such a mechanism for a class of active system, modular microswimmers, which self-assemble from colloids and ion-exchange resins on charged substrates. Our results unveil the self-assembly processes and the working mechanism of the ion-exchange driven motors underlying modular microswimmers, which have so far been illusive, even qualitatively. We apply these motors to show that modular microswimmers can circumvent corners in complex environments and move uphill. Our work closes a central knowledge gap in modular microswimmers and provides a facile route to extract mechanical energy from ion-exchange processes.

cond-mat.soft↗

arXiv2018

Colloidal electro-phoresis in the presence of symmetric and asymmetric electro-osmotic flow

We characterize the electro-phoretic motion of charged sphere suspensions in the presence of substantial electro-osmotic flow using a recently introduced small angle super-heterodyne dynamic light scattering instrument (ISASH-LDV). Operation in integral mode gives access to the particle velocity distribution over the complete cell cross-section. Obtained Doppler spectra are evaluated for electro-phoretic mobility, wall electro-osmotic mobility and particle diffusion coefficient. Simultaneous measurements of differing electro-osmotic mobilities leading to asymmetric solvent flow are demonstrated in a custom made electro-kinetic cell fitting standard microscopy slides as exchangeable sidewalls. Scope and range of our approach are discussed demonstrating the possibility of an internal calibration standard and using the simultaneously measured electro-kinetic mobilities in the interpretation of microfluidic pumping experiment involving an inhomogeneous electric field and a complex solvent flow pattern.

cond-mat.soft↗

arXiv2018

Modular approach to microswimming

The field of active matter in general and microswimming in particular has experienced a rapid and ongoing expansion over the last decade. A particular interesting aspect is provided by artificial autonomous microswimmers constructed from individual active and inactive functional components into self-propelling complexes. Such modular microswimmers may exhibit directed motion not seen for each individual component. In this review, we focus on the establishment and recent developments in the modular approach to microswimming. We introduce the bound and dynamic prototypes, show mechanisms and types of modular swimming and discuss approaches to control the direction and speed of modular microswimmers. We conclude by highlighting some challenges faced by researchers as well as promising directions for future research in the realm of modular swimming.

cond-mat.soft↗

arXiv2018

Seedless assembly of colloidal crystals by inverted micro-fluidic pumping

We propose a simple seedless approach to assemble millimeter sized monolayer single colloidal crystals with desired orientations at predetermined locations on an unstructured charged substrate. This approach utilizes the millimeter-ranged fluid flow on the bottom glass substrate induced by an ion exchange resin (IEX) fixed on top of the closed sample cell. This fluid flow increases with decreasing height of the sample cell and increasing radius R of the IEX. For a single inverted pump, millimeter sized monolayer single crystals of hexagonal close packing can be obtained. For two closely spaced (D ~ 4R) pumps, the formed crystals have a predefined orientation along the line connecting the two IEX. By patterning IEX into different structures, colloidal crystals of different complex patterns form. The present method paves a convenient way for fabricating high quality monolayer colloidal crystals for a variety of applications.

cond-mat.soft↗

arXiv2017

Formation of a transient amorphous solid in low density aqueous charged sphere suspensions

Colloidal glasses form from hard spheres, nearly hard spheres, ellipsoids and platelets or their attractive variants have been studied in detail. Complementing and checking theoretical approaches and simulations, the many different types of model systems have significantly advanced our understanding of the glass transition in general. Despite their early prediction, however, no experimental charged sphere glasses have been found at low density, where the competing process of crystallization prevails. We here report the formation of a transient amorphous solid formed from charged polymer spheres suspended in thoroughly deionized water at volume fractions of 0.0002-0.01. From optical experiments, we observe the presence of short-range order and an enhanced shear rigidity as compared to the stable polycrystalline solid of body centred cubic structure. On a density dependent time scale of hours to days, the amorphous solid transforms into this stable structure. We further present preliminary dynamic light scattering data showing the evolution of a second slow relaxation process possibly pointing to a dynamic heterogeneity known from other colloidal glasses and gels.We compare our findings to the predicted phase behaviour of charged sphere suspensions and discuss possible mechanisms for the formation of this peculiar type of colloidal glass.

cond-mat.soft↗

arXiv2017

Large scale Micro-Photometry for high resolution pH-characterization during electro-osmotic pumping and modular micro-swimming

Micro-fluidic pumps as well as artificial micro-swimmers are conveniently realized exploiting phoretic solvent flows based on local gradients of temperature, electrolyte concentration or pH. We here present a facile micro-photometric method for monitoring pH gradients and demonstrate its performance and scope on different experimental situations including an electro-osmotic pump and modular micro-swimmers assembled from ion exchange resin beads and polystyrene colloids. In combination with the present microscope and DSLR camera our method offers a 2 μm spatial resolution at video frame rate over a field of view of 3920x2602 μm^2. Under optimal conditions we achieve a pH-resolution of 0.05 with about equal contributions from statistical and systematical uncertainties. Our quantitative micro-photometric characterization of pH gradients which develop in time and reach out several mm is anticipated to provide valuable input for reliable modeling and simulations of a large variety of complex flow situations involving pH-gradients including artificial micro-swimmers, microfluidic pumping or even electro-convection.

cond-mat.soft↗

arXiv2017

Assembly and speed control in ion exchange based modular phoretic micro-swimmers

We report an experimental study on ion-exchange based modular micro-swimmers in low-salt water. Cationic ion-exchange particles and passive cargo particles assemble into self-propelling complexes, showing self-propulsion at speeds of several microns per second over extended distances and times. We quantify the assembly and speed of the complexes for different combinations of ion exchange particles and cargo particles, substrate types, salt types and concentrations, and cell geometries. Irrespective of experimental boundary conditions, we observe a regular development of the assembly shape with increasing number of cargo. Moreover, the swimming speed increases stepwise upon increasing the number of cargo and then saturates at a maximum speed, indicating an active role of cargo in modular swimming. We propose a geometric model of self-assembly to describe the experimental observations in a qualitative way. Our study also provides some constraints for future theoretical modelling and simulation.

cond-mat.soft↗

arXiv2017

Self-assembly of colloidal molecules due to self-generated flow

The emergence of structure through aggregation is a fascinating topic and of both fundamental and practical interest. Here we demonstrate that self-generated solvent flow can be used to generate long-range attractions on the colloidal scale, with sub-pico Newton forces extending into the millimeter-range. We observe a rich dynamic behavior with the formation and fusion of small clusters resembling molecules, the dynamics of which is governed by an effective conservative energy that decays as $1/r$. Breaking the flow symmetry, these clusters can be made active.

cond-mat.soft↗

arXiv2017

Microfluidic Pumping by Micromolar Salt Concentrations

An ion-exchange-resin-based microfluidic pump is introduced that utilizes trace amounts of ions to generate fluid flows. We show experimentally that our pump operates in almost deionized water for periods exceeding 24h and induces fluid flows of um/s over hundreds of um. This flow displays a far-field, power-law decay which is characteristic of two-dimensional (2D) flow when the system is strongly confined and of three-dimensional (3D) flow when it is not. Using theory and numerical calculations we demonstrate that our observations are consistent with electroosmotic pumping driven by umol/L ion concentrations in the sample cell that serve as 'fuel' to the pump. Our study thus reveals that trace amounts of charge carriers can produce surprisingly strong fluid flows; an insight that should benefit the design of a new class of microfluidic pumps that operate at very low fuel concentrations.

cond-mat.soft↗

arXiv2016

Controlled assembly of single colloidal crystals using electro-osmotic micro-pumps

We assemble charged colloidal spheres at deliberately chosen locations on a charged unstructured glass substrate utilizing ion exchange based electro-osmotic micro-pumps. Using microscopy, a simple scaling theory and Brownian Dynamics simulations, we systematically explore the control parameters of crystal assembly and the mechanisms through which they depend on the experimental boundary conditions. We demonstrate that crystal quality depends crucially on the assembly distance of the colloids. This is understood as resulting from the competition between inward transport by the electro-osmotic pump flow and the electro-phoretic outward motion of the colloids. Optimized conditions include substrates of low and colloids of large electro-kinetic mobility. Then a sorting of colloids by size is observed in binary mixtures with larger particles assembling closer to the ion exchanger beads. Moreover, mono-sized colloids form defect free single domain crystals which grow outside a colloid-free void with facetted inner crystal boundaries centred on the ion exchange particle. This works remarkably well, even with irregularly formed ion exchange resin splinters.

cond-mat.soft↗

arXiv2016

To make a glass - avoid the crystal

Colloidal model systems allow for a flexible tuning of particle sizes, particle spacings and mutual interactions at constant temperature. Colloidal suspensions typically crystallize as soon as the interactions get sufficiently strong and long-ranged. Several strategies have been successfully applied to avoid crystallization and instead produce colloidal glasses. Most of these amorphous solids are formed at high particle concentrations. This paper shortly reviews experimental attempts to produce amorphous colloidal solids using strategies based on topological, thermodynamic and kinetic considerations. We complement this overview by introducing a (transient) amorphous solid forming in a thoroughly deionized aqueous suspension of highly charged spheres at low salt concentration and very low volume fractions.

cond-mat.soft↗