arXiv subjects

Jiajia Zhou

Publications and source records attributed to Jiajia Zhou.

At least 37 records · Page 2Linked to original sources

arXiv2020

Wide-field Decodable Orthogonal Fingerprints of Single Nanoparticles Unlock Multiplexed Digital Assays

The control in optical uniformity of single nanoparticles and tuning their diversity in orthogonal dimensions, dot to dot, holds the key to unlock nanoscience and applications. Here we report that the time-domain emissive profile from single upconversion nanoparticle, including the rising, decay and peak moment of the excited state population (T2 profile), can be arbitrarily tuned by upconversion schemes, including interfacial energy migration, concentration dependency, energy transfer, and isolation of surface quenchers. This allows us to significantly increase the coding capacity at the nanoscale. We further implement both time-resolved wide-field imaging and deep-learning techniques to decode these fingerprints, showing high accuracies at high throughput. These high-dimensional optical fingerprints provide a new horizon for applications spanning from sub-diffraction-limit data storage, security inks, to high-throughput single-molecule digital assays and super-resolution imaging.

physics.app-ph↗

arXiv2020

Topological nanophotonics for photoluminescence control

Rare-earth doped nanocrystals are emerging light sources used for many applications in nanotechnology enabled by human ability to control their various optical properties with chemistry and material science. However, one important optical problem -- polarisation of photoluminescence -- remains largely out of control by chemistry methods. Control over photoluminescence polarisation can be gained via coupling of emitters to resonant nanostructures such as optical antennas and metasurfaces. However, the resulting polarization is typically sensitive to position disorder of emitters, which is difficult to mitigate. Recently, new classes of disorder-immune optical systems have been explored within the framework of topological photonics. Here we explore disorder-robust topological arrays of Mie-resonant nanoparticles for polarisation control of photoluminescence of nanocrystals. We demonstrate polarized emission from rare-earth-doped nanocrystals governed by photonic topological edge states supported by zigzag arrays of dielectric resonators. We verify the topological origin of polarised photoluminescence by comparing emission from nanoparticles coupled to topologically trivial and nontrivial arrays of nanoresonators.

physics.optics↗

arXiv2020

Theoretical analysis for flattening of a rising bubble in a Hele-Shaw cell

We calculate the shape and the velocity of a bubble rising in an infinitely large and closed Hele-Shaw cell using Park and Homsy's boundary condition which accounts for the change of the three dimensional structure in the perimeter zone. We first formulate the problem in the form of a variational problem, and discuss the shape change assuming that the bubble takes elliptic shape. We calculate the shape and the velocity of the bubble as a function of the bubble size, gap distance and the inclination angle of the cell. We show that the bubble is flattened as it rises. This result is in agreement with experiments for large Hele-Shaw cells.

physics.flu-dyn↗

arXiv2020

Modelling Elastically-Mediated Liquid-Liquid Phase Separation

We propose a continuum theory of the liquid-liquid phase separation in an elastic network where phase-separated microscopic droplets rich in one fluid component can form as an interplay of fluids mixing, droplet nucleation, network deformation, thermodynamic fluctuation, \emph{etc}. We find that the size of the phase separated droplets decreases with the shear modulus of the elastic network in the form of $\sim[\mathrm{modulus}]^{-1/3}$ and the number density of the droplet increases almost linearly with the shear modulus $\sim[\mathrm{modulus}]$, which are verified by the experimental observations. Phase diagrams in the space of (fluid constitution, mixture interaction, network modulus) are provided, which can help to understand similar phase separations in biological cells and also to guide fabrications of synthetic cells with desired phase properties.

cond-mat.soft↗

arXiv2020

Dynamics of a viscoelastic liquid filament connected to two mobile droplets

A filament of liquid is usually unstable and breaks up into small droplets, while a filament of polymer solution is known to be quite stable against such instability, and they form a stable configuration of filament connecting two spherical droplets. If the droplets are fixed in space, the liquid flows from the filament region to the droplet region to reduce the surface energy and the filament gets thinner. If the whole liquid is placed in another viscous fluid, the droplets approach each other, and the filament can get thicker. Here we study the dynamics of such system. We derive time evolution equations for the radius and the length of the filament taking into account the fluid flux from filament to droplets and the motion of the droplets. We will show that (a) if the centers of the droplets are fixed, the filament thins following the classical prediction of Entov and Hinch, and that (b) if the droplets are mobile (subject to the Stokes drag in the viscous medium), the thinning of the filament is suppressed, and under certain conditions, the filament thickens. This theory explains the phenomena observed by Yang and Xu [Phys. Fluids 20, 043101 (2008)] in four-roller mill device.

cond-mat.soft↗

arXiv2019

Application of Onsager Machlup integral in solving dynamic equations in non-equilibrium systems

In 1931, Onsager proposed a variational principle which has become the base of many kinetic equations for non-equilibrium systems. We have been showing that this principle is useful in obtaining approximate solutions for the kinetic equations, but our previous method has a weakness that it can be justified, strictly speaking, only for small incremental time. Here we propose an improved method which does not have this drawback. The new method utilizes the integral proposed by Onsager and Machlup in 1953, and can tell us which of the approximate solutions is the best solution without knowing the exact solution. The new method has an advantage that it allows us to determine the steady state in non-equilibrium system by a variational calculus. We demonstrate this using three examples, (a) simple diffusion problem, (b) capillary problem in a tube with corners, and (c) free boundary problem in liquid coating, for which the kinetic equations are written in second or fourth order partial differential equations.

cond-mat.soft↗

arXiv2019

Thermal enhanced NIR-NIR anti-Stokes emission in rare earth doped nanocrystals

Nanoparticles with anti-Stokes emissions enable many sensing applications, but their efficiencies are considerably low. The key to enable the process of anti-Stokes emissions is to create phonons and assist the excited photons to be pumped from a lower energy state onto a higher one. Increasing the temperature will generate more phonons, but it unavoidably quenches the luminescence. Here by quantifying the number of phonons being generated from the host crystal and at the surface of Yb3+/Nd3+ co-doped nanoparticles, we systematically investigated mechanisms towards the large enhancements of the phonon-assisted anti-Stokes emissions from 980 nm to 750 nm and 803 nm. Moreover, we provided direct evidence that moisture release from the nanoparticle surface at high temperature was not a main reason. We further demonstrated that the brightness of 10 nm nanoparticles were enhanced by more than two orders of magnitude, standing in stark contrast to the thermal quenching effect.

physics.optics↗

arXiv2019

Dynamics of Taylor Rising

We study the dynamics of liquid climbing in a narrow and tilting corner, inspired by recent work on liquid transportation on the peristome surface of Nepenthes alata. Considering the balance of gravity, interfacial tension and viscous force, we derive a partial differential equation for the meniscus profile, and numerically study the behavior of the solution for various tilting angle $β$. We show that the liquid height $h(t)$ at time $t$ satisfy the same scaling law found for vertical corner, i.e., $h(t) \propto t^{1/3}$ for large $t$, but the coefficient depends on the tilting angle $β$. The coefficient can be calculated approximately by Onsager principle, and the result agrees well with that obtained by numerical calculation. Our model can be applied for a weakly curved corner and may provide guidance to the design of biomimetic surfaces for liquid transportation.

cond-mat.soft↗

arXiv2019

Elastic Property of Membranes Self-assembled from Diblock and Triblock Copolymers

The elastic property of membranes self-assembled from AB diblock and ABA triblock copolymers, as coarse-grained model of lipids and the bolalipids, are studied using the self-consistent field theory (SCFT). Specifically, solutions of the SCFT equations, corresponding to membranes in different geometries (planar, cylindrical, spherical, and pore) have been obtained for a model system composed of amphiphilic AB diblock copolymers and ABA triblock copolymers dissolved in A homopolymers. The free energy of the membranes with different geometries is then used to extract the bending modulus, Gaussian modulus, and line tension of the membranes. The results reveal that the bending modulus of the triblock membrane is greater than that of the diblock membrane. Furthermore, the Gaussian modulus and line tension of the triblock membrane indicate that the triblock membranes have higher pore formation energy than that of the diblock membranes. The equilibrium bridging and looping fractions of the triblock copolymers are also obtained. Implications of the theoretical results on the elastic properties of biologically equivalent lipid bilayers and the bolalipid membranes are discussed.

cond-mat.soft↗

arXiv2018

Directional freezing of binary colloidal suspensions: A model for size fractionation of graphene oxide

The performance of graphene oxide(GO)-based materials strongly depends on the lateral size and size distribution of GO nanosheets. Various methods are employed to prepare GO nanosheets with a narrow size distribution. One of the promising method was proposed recently by directionally freezing of a GO aqueous dispersion at a controlled growth rate of the freezing front. We develop a theoretic model of binary colloids suspension, incorporating both the moving freezing boundary and the preferential adsorption of colloidal particles to the ice phase. We numerically solve the coupled diffusion equations and present state diagrams of size fractionation. Selective trapping of colloids according to their size can be achieved by a suitable choice of the experimental parameters, such as the adsorption rates and the freezing speed.

cond-mat.soft↗

arXiv2018

Capillary imbibition in a square tube

When a square tube is brought in contact with bulk liquid, the liquid wets the corners of the tube, and creates finger-like wetted region. The wetting of the liquid then takes place with the growth of two parts, the bulk part where the cross section is entirely filled with the liquid and the finger part where the cross section of the tube is partially filled. In the previous works, the growth of these two parts has been discussed separately. Here we conduct the analysis by explicitly accounting for the coupling of the two parts. We propose coupled equations for the liquid imbibition in both parts and show that (a) the length of each part, $h_0$ and $h_1$, both increases in time $t$ following the Lucas-Washburn's law, $h_0 \sim t^{1/2}$ and $h_1 \sim t^{1/2}$, but that (b) the coefficients are different from those obtained in the previous analysis which ignored the coupling.

cond-mat.soft↗

arXiv2018

Dynamics of Viscoelastic Filaments Based on Onsager Principle

When a polymer solution is uniaxially stretched and held fixed at both ends, the solution quickly separates into droplets connected by strings and takes the beads-on-string structure. The string then becomes thinner by capillary forces. Here we develop a theoretical framework on viscoelastic fluids based on Onsager principle, and apply it to the dynamics of viscoelastic filaments. We show that the beads-on-string structure is a thermodynamic quasi-equilibrium state, and derive an equation for the coexistence condition in the pseudo-equilibrium state. Using the condition, we solve the evolution equation analytically and show that the string radius and the tensile stress vary exponentially as predicted by the classical theory of Entov and Hinch [J. Non-Newtonian Fluid Mech. 72, 31 (1997)], but the prefactor for the tensile stress is different from their theory and agrees with the numerical solutions of Clasen et al. [J. Fluid Mech. 556, 283 (2006)].

cond-mat.soft↗

arXiv2018

Capillary filling in closed-end nanotubes

Capillary filling in small length scale is an important process in nanotechnology and microfabrication. When one end of the tube or channel is sealed, it is important to consider the escape of the trapped gas. We develop a dynamic model on capillary filling in closed-end tubes, based on the diffusion-convection equation and Henry's law of gas dissolution. We systematically investigate the filling dynamics for various sets of parameters, and compare the results with a previous model which assumes a linear density profile of dissolved gas and neglect the convective term.

cond-mat.soft↗

arXiv2017

Structure Formation in Soft Matter Solutions Induced by Solvent Evaporation

Solvent evaporation in soft matter solutions (solutions of colloidal particles, polymers and their mixtures) is an important process in material making and in printing and coating industries. The solvent evaporation process determines the structure of the materials, and strongly affects their performance. Solvent evaporation involves many physico-chemical processes: flow, diffusion, crystallization, gelation, glass transition, etc., and is quite complex. In this article, we report recent progresses in this important process, with a special focus on theoretical and simulation studies.

cond-mat.soft↗

arXiv2017

Cross-interaction drives stratification in drying film of binary colloidal mixtures

When a liquid film of colloidal solution consisting of particles of different sizes is dried on a substrate, the colloids often stratify, where smaller colloids are laid upon larger colloids. This phenomenon is counter intuitive because larger colloids which have smaller diffusion constant are expected to remain near the surface during the drying process, leaving the layer of larger colloids on top of smaller colloids. Here we show that the phenomenon is caused by the interaction between the colloids, and can be explained by the diffusion model which accounts for the interaction between the colloids. By studying the evolution equation both numerically and analytically, we derive the condition at which the stratified structures are obtained.

cond-mat.soft↗

arXiv2016

Protein corona composition of PEGylated nanoparticles correlates strongly with amino acid composition of protein surface

Extensive molecular dynamics simulations reveal that the interactions between proteins and poly(ethylene glycol)(PEG) can be described in terms of the surface composition of the proteins. PEG molecules accumulate around non-polar residues while avoiding polar ones. A solvent-accessible-surface-area model of protein adsorption on PEGylated nanoparticles accurately fits a large set of data on the composition of the protein corona recently obtained by label-free proteomic mass spectrometry.

physics.bio-ph↗

arXiv2016

Complex Formation between Polyelectrolytes and Oppositely Charged Oligoelectrolytes

We study the complex formation between one long polyanion chain and many short oligocation chains by computer simulations. We employ a coarse-grained bead-spring model for the polyelectrolyte chains, and model explicitly the small salt ions. We systematically vary the concentration and the length of the oligocation, and examine how the oligocations affects the chain conformation, the static structure factor, the radial and axial distribution of various charged species, and the number of bound ions in the complex. At low oligocation concentration, the polyanion has an extended structure. Upon increasing the oligocation concentration, the polyanion chain collapses and forms a compact globule, but the complex still carries a net negative charge. Once the total charge of the oligocations is equal to that of the polyanion, the collapse stops and is replaced by a slow expansion. In this regime, the net charge on the complexes is positive or neutral, depending on the microion concentration in solution. The expansion can be explained by the reduction of the oligocation bridging. We find that the behavior and the structure of the complex are largely independent of the length of oligocations, and very similar to that observed when replacing the oligocations by multivalent salt cations, and conclude that the main driving force keeping the complex together is the release of monovalent counterions and coions. We speculate on the implications of this finding for the problem of controlled oligolyte release and oligolyte substitution.

cond-mat.soft↗

arXiv2015

Computer simulations of single particles in external electric fields

Applying electric fields is an attractive way to control and manipulate single particles or molecules, e.g., in lab-on-a-chip devices. However, the response of nanosize objects in electrolyte solution to external fields is far from trivial. It is the result of a variety of dynamical processes taking place in the ion cloud surrounding charged particles and in the bulk electrolyte, and it is governed by an intricate interplay of electrostatic and hydrodynamic interactions. Already systems composed of one single particle in electrolyte solution exhibit a complex dynamical behaviour. In this review, we discuss recent coarse-grained simulations that have been performed to obtain a molecular-level understanding of the dynamic and dielectric response of single particles and single macromolecules to external electric fields. We address both the response of charged particles to constant fields (DC fields), which can be characterized by an electrophoretic mobility, and the dielectric response of both uncharged and charged particles to alternating fields (AC fields), which is described by a complex polarizability. Furthermore, we give a brief survey of simulation algorithms and highlight some recent developments.

cond-mat.soft↗