No description available.

Electroosmotic flow is a convenient mechanism for transporting polar fluid in a microfluidic device. The flow is generated through the application of an external electric field that acts on the free charges that exists in a thin Debye layer at the channel walls. The charge on the wall is due to the chemistry of the solid-fluid interface, and it can vary along the channel, e.g. due to modification of the wall. This investigation focuses on the simulation of the electroosmotic flow (EOF) profile in a cylindrical microchannel with step change in zeta potential. The modified Navier-Stoke equation governing the velocity field and a non-linear two-dimensional Poisson-Boltzmann equation governing the electrical double-layer (EDL) field distribution are solved numerically using finite control-volume method. Continuities of flow rate and electric current are enforced resulting in a non-uniform electrical field and pressure gradient distribution along the channel. The resulting parabolic velocity distribution at the junction of the step change in zeta potential, which is more typical of a pressure-driven velocity flow profile, is obtained. / Singapore-MIT Alliance (SMA)

abstract: Scarcity of potable water is one of the major problems faced in the world today. Majority of this problem can be solved if technology is developed to obtain potable water from brackish or saline water. The present desalination methods face challenges such as high costs in terms of energy consumption and infrastructure, physical size of the system, requirement of membrane and high pressure systems and hence have been facing various issues in implementation of the same. This research provides a new low pressure, low energy, portable method to desalinate water without the need for separation membranes, heat or chemical reactions. This method is energy efficient, cost effective, compact, environment friendly and suitable for portable desalination units. This technology, named as Polyphase Alternating current Bi-Ionic Propulsion System (PACBIPS) makes use of polyphase alternating current source to create a gradient in salt concentration. The gradient in salt concentration is achieved due to the creation of a traveling wave which attracts anions on its positive peak (crests) and cations on its negative peak (troughs) and travels along a central pipe thereby flushing the ions down. Another method of PACBIPS is based on Helmholtz capacitor which involves the formation of an electric double layer between the electrode and electrolyte consisting of equal and opposite ions which can be approximated as a capacitor. Charging and discharging this capacitor helps adsorb the ions onto a carbon electrode which has high surface area and electrical conductivity. This desalinates seawater and provides pure water. Mathematical modeling, analysis and implementation of the two methods have been presented in this work. The effects of zeta potential, electric field screening, electric mobility on desalination have been discussed. / Dissertation/Thesis / Masters Thesis Electrical Engineering 2014

Master of Science / Department of Chemistry / Jun Li / This study is focused on exploring the mechanisms of DNA dynamics at carbon electrode surfaces under a strong electric field for the development of novel DNA hybridization sensors. Oligonucleotides with FAM6 attached at the distal end are covalently tethered on the carbon electrode surface. The fluorescence emission from the FAM6 is strongly quenched in close proximity to the electrode surface. The modulation to the fluorescence intensity is correlated with the reversible reorientation of the negatively charged DNA molecules under the electric field within the electric double layer. The orientation dynamics are apparently determined by the interplay of the electropotential, salt concentration, and stiffness of the DNA molecules. We have observed that dsDNAs switch with fast dynamics (in < 0.05 second) followed by relaxation at a slower rate (in > 0.1 second) when the electric field is altered by stepping the electropotential to a more positive or negative value. The DNA reorientation exhibits strong dependence on the PBS buffer concentration and electric double layer thickness. A preliminary calculation based on dipole-surface energy transfer theory indicates that the critical distance between FAM6 and glassy carbon surface is 10.95 nm. In connection with the fluorescence study, the effect of DNA hybridization on electrochemical impedance spectroscopy (EIS) has also been investigated by two methods in an attempt to develop a fast electronic detection method. First, EIS at high AC amplitude (141 mV rms) with DNA-modified glassy carbon electrodes before and after target DNA hybridization have shown notable change at high frequencies, likely related to the DNA reorientation processes. Second, reversible EIS detection of DNA hybridization has been demonstrated with patterned regular carbon nanofiber arrays at normal AC amplitude (10 mV rms). The combination of these two methods will be explored in future studies. The effects of the electric field on surface-tethered molecular beacons (MBs) have also been studied with fluorescence spectroscopy. An increase in fluorescence at negative bias is observed accompanying the opening of the MB stem, which leads to larger separation between fluorophore and quencher. At positive bias, the rehybridization of the MB stem leads to a decrease in fluorescence intensity.

The development of energy storage devices has represented a significant technological challenge for the past few years. Electrochemical double-layer capacitors (EDLCs), also named as supercapacitors, are a likely competitor for alternative energy storage because of their low-cost, high power density, and high fast charge/discharge rate. The recent development of EDLCs requires them to be lightweight and flexible. There are many fabrication techniques used to manufacture flexible EDLCs, and these methods can include pre-treatment to ensure more efficient penetration of activated carbon (AC) patterns onto the substrate, or those that utilise masks for the definitions of patterns on substrates. However, these methods are inconvenient for building cost-effective devices. Therefore, it was necessary to find a suitable process to reduce the steps of manufacture and to be able to print multiple materials uniformly. This research work describes the first use of a 3D printing technology to produce flexible EDLCs for energy storage. In this research work, the four essential elements for the EDLCs substrate, current collector, activated electrode, and gel electrolyte were investigated. The AC powder was milled by ball milling to optimise the paste deposition and the electrochemical performance. A flexible composite EDLC was designed and manufactured by 3D printing. The electrochemical performance of the flexible composite EDLCs was then examined. Being highly flexible is one of the critical demands for the recent development of EDLCs. Therefore, highly flexible EDLCs were designed and manufactured by only one single extrusion process. The 3D highly flexible EDLC maintains significant electrochemical performance under a mechanical bending test. To meet the power and energy requirements, the EDLCs were connected and tested in series and parallel circuits. A supercapacitor based on printed AC material displays an area specific capacitance of 1.48 F/cm2 at the scan rate of 20 mV/s. The coulombic efficiency for the flexible EDLC was found to be 59.91%, and the cycling stability was achieved to be 56% after 500 cycles. These findings indicate that 3D printing technology may be increasingly used to develop more sophisticated flexible wearable electronic devices.

<p>This work considers the transport and attachment of nanoscale particles to surfaces and the associated phenomena that dictate particle-surface interactions. A consideration of the deposition of nano-scale particles on surfaces is a natural outgrowth of more than a century of research in the area of colloid science, and has taken on new pertinence in the context of understanding the fate and transport of engineered nanoparticles in aqueous environments. More specifically, the goal of this work is to better understand the effects of particle size, surface polymer coatings, and aggregation state on the kinetics of nanoparticle deposition. Theoretical tools such as those developed by Derjaguin-Landau-Verwey-Overbeek (DLVO) and Flory-Krigbaum , as well as the soft particle theory and surface element integration scaling methods are employed to address certain problems that were not considered with the existing theoretical frameworks for the conventional colloidal problems. Consequences of theoretical predictions are evaluated experimentally using column experiments or the quartz crystal microbalance techniques to monitor deposition kinetics. One of the key findings of this work is the observation that polymer coatings may stabilize nanoparticles against deposition or increase deposition, depending on whether the polymer coatings exist on both of the interacting surfaces and the interaction between the polymer and the collector surface. Both steric and bridging mechanisms are possible depending on whether contact between the polymer and collector surface can result in successful attachment. In addition, limitations in the use of conventional, equilibrium-based DLVO theory to describe the deposition of nano-scale particles at very low ionic strength are also identified and discussed. Moreover, it is demonstrated that the interaction between the aggregated nano-scale particles and environmental surfaces is controlled by the characteristic size of the primary particles rather than that of the aggregates. Thus despite an increase in hydrodynamic diameter, aggregation is predicted to reduce deposition only from the hydrodynamic aspects, but not from the colloidal interaction aspect. The affinity between aggregated nanoparticles and a surface may be increased at the initial stage of deposition while being unaffected by aggregation state during later stages of deposition. The results of this study lead to better understandings, at least on a qualitative level, of the factors that controlling the kinetics of deposition and, in a broader sense, the fate and transport of nanoscale particles in the aqueous environment.</p> / Dissertation

Energy storage devices are generally evaluated on two main requirements; power and energy. In supercapacitors these two performance criteria are altered by the capacitance, resistance and voltage. (For complete abstract open document)

This master thesis deals with supercapacitors based on electrical double layer and proper carbon electrodes for this type of supercapacitors. In theoretical part of work is described theory of supercapacitors, energy storage principles and their properties. In the next part are described carbon materials, their properties and electrochemical methods of measurements that we used. In the experimental part is described preparation of electrodes, results and conclusion.

No description available.

Environmental separation processes such as removal of heavy metals from aqueous solutions, electrosorption in groundwater remediation, and capacitive desalination, as well as energy storage in supercapacitors, are based on the electrical double layer (EDL) formation within nanoporous carbon materials. This research is focused on the nano-scale phenomena of EDL formation inside the confined space of nanopores. The electrosorption behavior of nanoporous carbon materials was characterized by measuring the double-layer capacitance using cyclic voltammetry. The presence of micropores results in the occurrence of EDL overlapping, corresponding to a considerable loss of the double-layer capacitance. Hence, pore size distribution plays an important role in determining the double-layer capacitance. EDL formation has significant influence on ion transport and sorption inside nanopores. The data obtained by simple diffusion and electrochemically-aided diffusion experiments demonstrated the size-exclusion effects on pore accessibility by ions. A larger ion-exclusion volume prevents larger ions from penetrating inside the pores. Batch equilibrium electrosorption experiments using nanoporous carbon materials showed that selective electrosorption, imposed by the difference in the size of hydrated ions, occurs in a competitive environment. Molecular modeling based on Monte Carlo methods was developed to simulate the EDL formation in a slit-type nanopore. Simulation results indicated that the competition in asymmetries of ion charge and size not only determines the screening of surface charge but also affects the electrolyte distribution within charged pores. In a mixture of electrolytes, the charge/size competitive effects can dominate pore accessibility. Multivalent counterions with large size have the energetic advantage of screening surface charge. On the other hand, small monovalent counterions present a ¡§size affinity¡¨ to access the pores. Therefore, electrosorption selectivity of counterions with different properties is a result of a counterbalance between minimization of potential energy and size-exclusion effects. Manipulation of electrosorption selectivity to separate ions could in principle be achieved via tuning the EDL formation inside the pores. The findings of the thesis have several significant implications for the development of advanced techniques for selective separation of ions in environmental systems and energy storage.