Characteristics of Oil-in-Oil Emulsions under AC Electric Fields.

Emulsions have been applied in a number of industries such as pharmaceutics, cosmetics, and food, which are also of great scientific interest. Although aqueous emulsions are commonly used in our daily life, oil-in-oil (o/o) emulsions also play an irreplaceable role in view of their unique physics and complementary applications. In this paper, we investigate typical behaviors of organic droplets surrounded by organic medium (o/o emulsions) with different functional groups controlled by the AC electric field. Droplet behaviors can be catalogued into five types: namely, "no effect", "movement", "deformation", "interface rupture", and "disorder". We identify the key dimensionless number Wee·Ca, combined with the channel geometry, for characterizing the typical behaviors in silicon oil/1,6-hexanediol diacrylate and mineral oil/1,6-hexanediol diacrylate emulsions. Unlike aqueous emulsion, the Maxwell-Wagner relaxation inhibits the electric effect and leads to an effective frequency, ranging from 0.5 to 3 kHz. The increasing viscosity of the droplet facilitates the escalation by promoting the shearing effect under the same flow conditions. Ethylene glycol droplets primarily show the efficient coalescence even at a low Wee·Ca, which is attributed to the attraction of free charges induced by the increasing conductivity. In 1,6-hexanediol diacrylate/silicon oil emulsion, the droplet tends to form a liquid film that expands into the entire channel due to the affinity of the droplet to the channel wall. A variety of elongated columns are observed to oscillate between the electrodes at high voltages. These findings can contribute to understanding the electrohydrodynamic physics in o/o emulsion and controlling droplet behaviors in a fast response, programmable, and high-throughput way. We expect that this droplet manipulation technology can be widely adopted in a broad range of chemical synthesis and biological and material science.

AC-electric-field-controlled multi-component droplet coalescence at microscale.

Droplet coalescence with fast response, high controllability and monodispersity has been widely investigated in industrial production and bioengineering. Especially for droplets with multiple components, programmable manipulation of such droplets is crucial for practical applications. However, precise control of the dynamics can be challenging, owing to the complex boundaries and the interfacial and fluidic properties. AC electric fields, with their fast response and high flexibility, have attracted our interest. We design and fabricate an improved flow-focusing microchannel configuration together with a non-contact type of electrode featuring asymmetric geometries, based on which we conduct systematic investigations of the AC-electric-field-controlled coalescence of multi-component droplets at the microscale. Parameters such as flow rates, component ratio, surface tension, electric permittivity and conductivity were given our attention. The results show that droplet coalescence in different flow parameters can be achieved in milliseconds by adjusting the electrical conditions, which shows high controllability. Specifically, both the coalescence region and reaction time can be adjusted by a combination of applied voltage and frequency, and unique merging phenomena have appeared. One is contact coalescence with the approach of paired droplets, while the other is squeezing coalescence, which occurs in the start position and promotes the merging process. The fluid properties, such as the electric permittivity, conductivity and surface tension, present a significant influence on merging behavior. The increasing relative dielectric constant leads to a dramatic reduction of the start merging voltage from the original 250 V to 30 V. The range of effective voltage for coalescence decreases with the addition of surfactant, offering a stricter and yet higher selectivity on electrical conditions, about 1500 V. The conductivity presents a negative correlation with the start merging voltage due to the reduction of the dielectric stress, from 400 V to 1500 V. Finally, we achieve the precise fabrication process of the Janus droplet via implementation of the proposed method, where the components of the droplets and the coalescence conditions are well controlled. Our results can serve as a potent methodology to decipher the physics of multi-component droplet electro-coalescence and contribute to applications in chemical synthesis, bioassay and material synthesis.

Investigation of Shear-Driven and Pressure-Driven Liquid Crystal Flow at Microscale: A Quantitative Approach for the Flow Measurement.

The liquid crystal-based method is a new technology developed for flow visualizations and measurements at microscale with great potentials. It is the priority to study the flow characteristics before implementation of such a technology. A numerical analysis has been applied to solve the simplified dimensionless two-dimensional Leslie-Ericksen liquid crystal dynamic equation. This allows us to analyze the coupling effect of the LC's director orientation and flow field. We will be discussing two classic shear flow cases at microscale, namely Couette and Poiseuille flow. In both cases, the plate drag speed in the state of Couette flow are varied as well as the pressure gradients in Poiseuille flow state are changed to study their effects on the flow field distributions. In Poiseuille flow, with the increase of applied pressure gradient, the influence of backflow significantly affects the flow field. Results show that the proposed method has great advantages on measurement near the wall boundaries which could complement to the current adopted flow measurement technique. The mathematical model proposed in this article could be of great potentials in the development of the quantitatively flow measurement technology.

Particle free optical imaging of flow field by liquid crystal polarization.

This paper proposes and demonstrates a particle free method for flow field visualizations by analyzing liquid crystal polarizations. The proposed concept is implemented by imaging of liquid crystal flow under microfluidic environment using a crossed polarization microscopy configuration. Fringe patterns give good representation of flow characterizations for different nozzle/diffuser microchannel designs. The obtained results demonstrate that the flow field under various conditions can be evaluated. Visualizations of the flow fields are carried out by the liquid crystal polarization induced fringe patterns in nozzle/diffuser microchannels. We achieve good match between the flow field obtained by LC polarization and the simulated one. It is envisaged that the proposed methodology can make a potential impact in flow field visualization studies and related analysis.

Self-trapped exciton emission from carbon dots investigated by polarization anisotropy of photoluminescence and photoexcitation.

Carbon dots have attracted tremendous attention because of their intrinsic advantages that open up opportunities to replace traditional fluorescent materials in various application fields. However, until now, the emission mechanism from carbon dots has been controversial, substantially hindering the extensive exploitation of these materials. Here, we explore systematically the essential emission behavior of carbon dots by using polarization anisotropy spectroscopy, electric-field modulation spectroscopy, and time-resolved photoluminescence measurements. We probe the momentum evolution dynamics and evaluate the decay process of the photoexcited hot carriers, which manifest characteristics that are distinct from band edge emission. We provide clear evidence that carbon dot emission originates from radiative recombination of self-trapped excitons, where the mobilization of the carriers is largely impeded due to the existence of a strong local potential field and thus the relaxation of the hot carriers is strongly suppressed. Based on the self-trapped exciton model, all the optical properties of carbon dots inferred from both steady-state and time-resolved optical spectroscopy can be interpreted consistently. Our investigation provides an alternative insight into the emission mechanisms of carbon dots, which may improve our understanding of these novel materials.

Fast Dynamic Visualizations in Microfluidics Enabled by Fluorescent Carbon Nanodots.

Microfluidic systems have become a superior platform for explorations of fascinating fluidic physics at microscale as well as applications in biomedical devices, chemical reactions, drug delivery, etc. Exploitations of this platform are built upon the fundamental techniques of flow visualizations. However, the currently employed fluorescent materials for microfluidic visualization are far from satisfaction, which severely hinders their widespread applications. Here fluorescent carbon nanodots are documented as a game-changer, applicable in versatile fluidic environment for the visualization in microfluidics with unprecedented advantages. One of the fastest fluorescent imaging speeds up to 2500 frames per second under a normal contionous wave (CW) laser line is achieved by adopting carbon nanodots in microfluidics. Besides better visualizations of the fluid or interface, fluorescent carbon nanodots-based microparticles enable quantitative studies of high speed dynamics in fluids at microscale with a more than 90% lower cost, which is inaccessible by traditionally adopted fluorescent dye based seeding particles. The findings hold profound influences to microfluidic investigations and may even lead to revolutionary changes to the relevant industries.

Experimental and theoretical investigations of non-Newtonian electro-osmotic driven flow in rectangular microchannels.

With the development of microfluidics, electro-osmotic (EO) driven flow has gained intense research interest as a result of its unique flow profile and the corresponding benefits in its application in the transportation of sensitive samples. Sensitive samples, such as DNA, are incapable of enduring strong flow shear induced by conventional hydrodynamic driven methods. EO driven flow is thus a niche area. However, even though there are a few research studies focusing on bio-fluidic samples related to EO driven flow, the majority of them are merely theoretical modeling without solid evidence from experiments due to the inherent complex rheological behavior of the bio-fluids. Challenges occur when the EO driven mechanism meets with complex rheology; vital questions such as can the zeta potential still be assumed to be constant when dealing with fluids with complex rheology? and "Does the shear thinning effect enhance electro-osmotic driven flow?" need to be answered. We conducted experiments using current monitoring and microscopy fluorescence methods, and developed a theoretical model by coupling a generalized Smoluchowski approach with the power-law constitutive model. We calculated the zeta potential and compared the experimental results with modeling to answer the questions. The results show a reduction of zeta potential in the presence of PEO aqueous solutions. A constant zeta potential is also indicated by varying the PEO concentration and the electric field strength.The shear thinning effect is also addressed via experimental data and theoretical calculations. The results show a promising enhancement of the EO driven velocity due to the shear thinning effect.