Potential-modulation spectroscopy at solid/liquid and liquid/liquid interfaces.

Potential-modulation spectroelectrochemical methods at solid/liquid and liquid/liquid interfaces are reviewed. After a brief summary of the basic features and advantages of the methods, practical applications of potential-modulation spectroscopy are demonstrated using our recent studies of solid/liquid and liquid/liquid interfaces, including reflection measurements for a redox protein on a modified gold electrode and fluorescence measurements for various dyes at a polarized water/1,2-dichloroethane interface. For both interfaces, the use of linearly polarized incident light enabled an estimation of the molecular orientation. The use of a potential-modulated transmission-absorption measurement for an optically transparent electrode with immobilized metal nanoparticles is also described. The ability of potential-modulated fluorescence spectroscopy to clearly elucidate the charge transfer and adsorption mechanisms at liquid/liquid interfaces is highlighted.     

Modifying the liquid/liquid interface: pores, particles and deposition

The modification of the liquid/liquid interface with solid phases is discussed in this article. Modified interfaces can be formed with molecular assemblies, but here attention is focussed on solid materials such as mesoscopic particles, or microporous and mesoporous membranes. Charge transfer across the modified liquid/liquid interface is considered in particular. The most obvious consequence of the introduction of such modifying components is their effect on the transport to, and the transfer of material across, the liquid/liquid interface, as measured voltammetrically for example. One particularly interesting reaction is interfacial metal deposition, which can also be studied under electrochemical control: the initial formation of metal nuclei at the interface transforms it from the bare, pristine state to a modified state with very different reactivity. Deposition at interfaces between liquids is compared and contrasted with the cases of metal deposition in bulk solution and conventional heterogeneous deposition on conducting solid surfaces. Comparison is also made with work on the assembly of pre-formed micron and nanometre scale solids at the liquid/liquid interface.     

Tensions at liquid interfaces: a general filter for the separation of micro-/nanoparticles

In this letter, we put forward a new strategy for the separation of micro-/nanoparticles with different sizes and densities by using the tensions at liquid interfaces. The interactions between particles and a liquid-liquid interface have been analyzed. Furthermore, we applied our strategy to the separation of two size-distributed Cu2O particles by using the water and n-pentanol interface, which demonstrates the feasibility of the proposed separation method.     

Probing non-polarizable liquid/liquid interfaces using scanning ion conductance microscopy

The study of microscopic structure of a liquid/liquid interface is of fundamental importance due to its close relation to the thermodynamics and kinetics of interfacial charge transfer reactions.In this article,the microscopic structure of a non-polarizable water/nitrobenzene(W/NB) interface was evaluated by scanning ion conductance microscope(SICM).Using SICM with a nanometer-sized quartz pipette filled with an electrolyte solution as the probe,the thickness of this type of W/NB interface could be measured at sub-nanometer scale,based on the continuous change of ionic current from one phase to another one.The effects for thicknesses of the non-polarizable W/NB interfaces with different electrolyte concentrations,the Galvani potentials at the interface and the applied potentials on the probe were measured and systematically analyzed.Both experimental setups,that is an organic phase up and an aqueous down,and a reverse version,were employed to acquire the approach curves.These data were compared with those of an ideal polarizable interface under the similar experimental conditions,and several characteristics of non-polarizable interfaces were found.The thickness of a non-polarizable interface increases with the decrease of electrolyte concentration and the increase of applied potential,which is similar to the situation of a polarizable liquid/liquid interface.We also find that the Galvani potential across a non-polarizable interface can also influence the interfacial thickness,this phenomenon is difficult to observe when using polarizable interface.Most importantly,by the comparison of two kinds of liquid/liquid interfaces,we experimentally proved that much more excess ions are gathered in the space charge layer of non-polarizable interfaces than in that of polarizable interfaces.These results are consistent with the predictions of molecular dynamic simulations and X-ray reflectivity measurements.     

Electrochemical recognition of synthetic heparin mimetic at liquid/liquid microinterfaces

Electrochemically controlled molecular recognition of a synthetic heparin mimetic, Arixtra, at nitrobenzene/water microinterfaces was investigated to obtain a greater understanding of interfacial recognition and sensing of heparin and its analogues with biomedical importance. In contrast to unfractionated heparin, this synthetic pentasaccharide that mimics the unique Antithrombin III binding domain of heparin possesses well-defined structure and ionic charge to enable quantitative interpretation of cyclic voltammetric/chronoamperometric responses based on the interfacial recognition at micropipet electrodes. Arixtra is electrochemically extracted from the water phase into the bulk nitrobenzene phase containing highly lipophilic ionophores, methyltridodecylammonium or dimethyldioctadecylammonium. Numerical analysis of the kinetically controlled cyclic voltammograms demonstrates for the first time that formal potentials and standard rate constants of polyion transfer at liquid/liquid interfaces are ionophore dependent. Moreover, octadecylammonium and octadecylguanidinium are introduced as new, simple ionophores to model recognition sites of heparin-binding proteins at liquid/liquid interfaces. In comparison to octadecyltrimethylammonium, the best ionophore for heparin recognition at liquid/liquid interfaces reported so far, these new ionophores dramatically facilitate Arixtra adsorption at the interfaces. With a saline solution at physiological pH, an Arixtra molecule is selectively and cooperatively bound to 5 molecules of the guanidinium ionophore, suggesting hydrogen-bond-directed interactions of each guanidinium with a few of 10 negatively charged sulfo or carboxyl groups of Arixtra at the interfaces.     

Impact experiments at the Interface between Two Immiscible Electrolyte Solutions (ITIES)

Within the field of single-entity electrochemistry through so-called impact experiments, the use of soft interfaces can be a valuable and advantageous complement to conventional solid microelectrodes, as recently demonstrated for both hard and soft micro- and nanoparticles. Additionally, this approach can offer a new platform for fundamental studies of key aspects of electronic and ionic transfers across liquid–liquid interfaces, with applications in relevant biological, technological and industrial systems. Experimental results with Interfaces between Two Immiscible Electrolyte Solutions (ITIES) are reviewed and discussed under the light of theoretical treatments are here revisited or developed.     

Dynamic behaviors of molecular assemblies at liquid/liquid interfaces studied by time-resolved quasi-elastic laser scattering spectroscopy.

The dynamic behaviors of molecular assemblies at two immiscible liquid interfaces are intriguing topics in many fields of science and technology. However, it is generally difficult to investigate the dynamic behaviors of such molecular assemblies because of the buried nature of liquid/liquid interfaces. In the present paper, our recent investigations on dynamic behaviors of various molecular self-assemblies at liquid/liquid interfaces are reviewed. We monitored dynamic behaviors of the molecular assemblies by time-resolved quasi-elastic laser scattering (TR-QELS) and fluorescent spectroscopy. The former method allows us to monitor the change in interfacial tension with millisecond time-resolution. As molecular assemblies, bis(2-ethylhexyl)sulfosuccinate (AOT) microemulsion, phospholipid biomembrane models, and liposome-DNA complexes have all been studied, since they are relevant in material sciences and biological technologies. At liquid/liquid interfaces, these molecular assemblies showed characteristic behaviors. We review the finding of rebound response of the interfacial tension at the liquid/liquid interface induced by the adsorption of the AOT microemulsion. We monitored the hydrolysis reaction of phospholipid biomembrane models formed at oil/water interfaces, observing the different types of behavior of liposome-DNA complexes at biomembrane models with different kinds of phospholipids.     

Formation of mesoscopic silver particles at micro- and nano-liquid/liquid interfaces

Silver particles have been deposited at externally polarised 1,2-dichloroethane (DCE)/water interfaces supported at the tip of micro- and nanopipettes. The electrochemical process involved the reduction of silver ion in the aqueous phase by an organic-phase electron donor (butylferrocene). The silver nucleation and growth process was investigated using potential step chronoamperometry, and the resulting current–time transients were analysed to extract nucleus numbers. At larger pipettes, with diameters of several micrometers, multi-particle nucleation was observed and optical microscopy provided direct evidence for metal electrodeposition at the liquid/liquid interface. For pipettes with radii of 0.5 μm or smaller, the current–time behaviour was consistent with single particle generation. Under some conditions, detachment of the particle from the liquid/liquid interface was inferred from the current–time characteristics, and it is suggested that controlled-detachment from micropipettes could provide a method for the deposition of small metal structures on surfaces.     

Electromagnetic liquid pistons for capillarity-based pumping

The small scales associated with lab-on-a-chip technologies lend themselves well to capillarity-dominated phenomena. We demonstrate a new capillarity-dominated system where two adjoining ferrofluid droplets can behave as an electronically-controlled oscillator or switch by an appropriate balance of magnetic, capillary, and inertial forces. Their oscillatory motion can be exploited to displace a surrounding liquid (akin to an axial piston pump), forming electromagnetic "liquid pistons." Such ferrofluid pistons can pump a precise volume of liquid via finely tunable amplitudes (cf. pump stroke) or resonant frequencies (cf. pump speed) with no solid moving parts for long-term operation without wear in a small device. Furthermore, the rapid propagation of electromagnetic fields and the favorable scaling of capillary forces with size permit micron sized devices with very fast operating speeds (～kHz). The pumping dynamics and performance of these liquid pistons is explored, with experimental measurements showing good agreement with a spherical cap model. While these liquid pistons may find numerous applications in micro- and mesoscale fluidic devices (e.g., remotely activated drug delivery), here we demonstrate the use of these liquid pistons in capillarity-dominated systems for chip-level, fast-acting adaptive liquid lenses with nearly perfect spherical interfaces.     

The boundary element method: the simulation of voltammetry at immiscible liquid/liquid interfaces

The boundary element method is presented as an efficient and powerful method for the analysis of time-dependent electrochemical processes occurring at immiscible liquid/liquid interfaces. This paper outlines the theory and numerical details required for the development and application of two-dimensional transient diffusion models for the simulation of cyclic voltammetry behaviour at a range externally polarised immiscible liquid/liquid interfaces of differing topography. The benefits of the BEM approach are discussed, including the reduction in dimensionality brought about by the formulation procedure and complete elimination of the need for domain discretisation with the time-domain convolution approach. The versatility and efficiency of the numerical procedures are examined with respect to a number of liquid/liquid interface geometries and a series of working curves established to quantify the influence of interface topography on the observed voltammetric behaviour.     

Small solid particles and liquid lenses at fluid/fluid interfaces

The behaviour of small solid particles and liquid droplets at fluid interfaces is of wide interest, in part because of the roles they play in the stability of foams and emulsions. Here we focus on solid particles at liquid interfaces, both singly and in highly structured monolayers. We briefly mention small oil lenses on water in connection with the determination of line tension, τ. Particles are surface-active in the sense that they often adhere quite strongly to liquid surfaces, although of course they are not usually amphiphilic. The three-phase contact line around a particle at an interface is associated with an excess free energy resulting in a tendency of the line to contract (positive τ, which is a 1D analogue of surface tension) or to expand (negative τ). Positive line tension acts so as to push the contact angle of a particle with the fluid interface further away from 90°, i.e. to force the particle towards the more “wetting” of the two bulk phases. It also leads to activation barriers to entry and departure of particles from an interface. The behaviour of particle monolayers at octane/water interfaces is also discussed . It is found that, for monodisperse spherical polystyrene particles containing ionisable sulphate groups at the surface, highly ordered monolayers are formed. This appears to result from very long range electrostatic repulsion mediated through the oil phase. Surface pressure–surface area isotherms are discussed for particle monolayers and it is shown, using light microscopy, that at monolayer “collapse” particles are not expelled from the monolayers but rather the monolayer folds, remaining intact. This has an important bearing on methods, involving the use of the Langmuir trough, for the experimental determination of contact angles and line tensions in particulate systems. Received: 18 July 1999/Accepted: 30 August 1999     

Molecular simulation of protein adsorption and conformation at gas-liquid,liquid–liquid and solid–liquid interfaces

The adsorption of proteins at surfaces and interfaces is important in a wide range of industries. Understanding and controlling the conformation of adsorbed proteins at surfaces is critical to stability and function in many technological applications including foods and biomedical testing kits or sensors. Studying adsorbed protein conformation is difficult experimentally and so over the past few decades researchers have turned to computer simulation methods to give information at the atomic level on this important area. In this review we summarize some of the significant simulation work over the past four years at both fluid (liquid–liquid and gas–liquid interfaces) and solid–liquid interfaces. Of particular significance is the work on surfactant proteins such as fungal hydrophobins, ranspumin-2 from the túngara frog and the bacteria protein BslA. These have evolved unique structures impart very high surface-active properties to the molecules. A highlight is the elucidation of the clam-shell unhinging mechanism of ranspumin-2 adsorption to the gas–liquid interface that is responsible for its adsorption to and stabilization of the air bubbles in túngara frog foam nests.     

Excited-state dynamics of organic dyes at liquid/liquid interfaces

Liquid/liquid interfaces play a crucial role in numerous areas of science. However, direct spectroscopic access to this thin (～1 nm) region is not possible with conventional optical methods. After a brief review of the most used techniques to perform interfacial optical spectroscopy, we will focus on time-resolved surface second harmonic generation, which allows the measurement of the excited-state dynamics of probe molecules at interfaces. By comparing these dynamics with those measured in bulk solutions, precious information on the properties of the interfacial region can be obtained. To illustrate this, several studies performed in our group will be presented.     

Experimental characterization of adsorbed macromolecule layers at solid/liquid interfaces

A survey will be given on the experimental methods to characterize the structure of adsorbed polymer layers at solid/liquid interfaces. Characterization parameters accessible by experimental methods are: adsorption isotherm mostly determined from the difference in the solution concentration; fraction of adhered segments, obtained from IR-, NMR- ESR-spectrometry and from microcalorimetry; layer thicknesses of different type from ellipsometry, diffusion, sedimentation, viscosimetry, electrophoresis, force-distance measurements between contacting layers and from segment density profiles obtained by SANS; adsorption enthalpies from microcalorimetry and from displacer-technique. Own experimental data of the adsorption of olystyrene, poly(ethylene oxide)s (PHD), poly(N-vinyl-2-pyrrolidone), poly-(butyl methacrylate)s, poly(vinyl alcohol)s as well as copolymers from ethylene oxide and propylene oxide on interfaces of colloidal silica- and latexparticles and partially on flat chromium-, platinum-and gold surfaces from organic and aqueous solutions and characteristic results from the literature will be compared and discussed in order to get insight into the conformation of the adsorbed macromolecules.     

Exploring catalytic solid/liquid interfaces by in situ attenuated total reflection infrared spectroscopy

In situ attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopy has gained considerable attention as a powerful tool for exploring processes occurring at solid/liquid and solid/liquid/gas interfaces as encountered in heterogeneous catalysis and electrochemistry. Understanding of the molecular interactions occurring at the surface of a catalyst is not only of fundamental interest but constitutes the basis for a rational design of heterogeneous catalytic systems. Infrared spectroscopy has the exceptional advantage to provide information about structure and environment of molecules. In the last decade, in situ ATR-FT-IR has been developed rapidly and successfully applied for unraveling processes occurring at solid/liquid interfaces. Additionally, the kinetics of complex reactions can be followed by quantifying the concentration of products and reactants simultaneously in a non-destructive way. In this tutorial review we discuss some key aspects which have to be taken into account for successful application of in situ ATR-FT-IR to examine solid/liquid catalytic interfaces, including different experimental aspects concerned with the internal reflection element, catalyst deposition, cell design, and advanced experimental methods and spectrum analysis. Some of these aspects are illustrated using recent examples from our research. Finally, the potential and some limitations of ATR will be elucidated.     

Mesoscopic structure and properties of liquid crystalline mesophase pitch and its transformation into carbon fiber

The history and present state of the art in the chemistry of mesophase pitch, which is an important precursor for carbon fiber and other high-performance industrial carbons, are reviewed relative to their structural properties. The structural concepts in both microscopic and macroscopic views are summarized in terms of the sp(2) carbon hexagonal plane as a basic unit common to graphitic materials, its planar stacking in clusters, and cluster assembly into microdomains and domains, the latter of which reflect the isochromatic unit of optical anisotropy. Such a series of structural units is described in a semiquantitative manner corresponding to the same units of graphitic materials, although the size and stacking height of the hexagonal planes (graphitic sheets) are very different. Mesophase pitch is a liquid crystal material whose basic structural concepts are maintained in the temperature range of 250 to 350 degrees C. The melt flow and thermal properties are related to its micro- and mesoscopic structure. The structure of mesophase-pitch-based carbon fiber of high tensile strength, modulus, and thermal conductivity has been formed through spinning, and has inherited the same structural concepts of mesophase pitch. Stabilization settles the structure in successive heat treatments up to 3000 degrees C. Carbonization and graphitization enable growth of the hexagonal planes and their stacking into units of graphite. Such growth is governed and controlled by the alignment of micro- and mesoscopic structures in the mesophase pitch, which define the derived carbon materials as nanostructural materials. Their properties are controlled by the nanoscopic units that are expected to behave as nanomaterials when appropriately isolated or handled.     

Hydrogen-bond-assisted excited-state deactivation at liquid/water interfaces

The excited-state dynamics of eosin B (EB) at dodecane/water and decanol/water interfaces has been investigated with polarization-dependent and time-resolved surface second harmonic generation. The results of the polarization-dependent measurements vary substantially with (1) the EB concentration, (2) the age of the sample, and (3) the nature of the organic phase. All of these effects are ascribed to the formation of EB aggregates at the interface. Aggregation also manifests itself in the time-resolved measurements as a substantial shortening of the excited-state lifetime of EB. However, independently of the dye concentration used, the excited-state lifetime of EB at both dodecane/water and decanol/water interfaces is much longer than in bulk water, where the excited-state population undergoes hydrogen-bond-assisted non-radiative deactivation in a few picoseconds. These results indicate that hydrogen bonding between EB and water molecules at liquid/water interfaces is either much less efficient than in bulk water or does not enhance non-radiative deactivation. This strong increase of the excited-state lifetime of EB at liquid/water interfaces opens promising avenues of applying this molecule as a fluorescent interfacial probe.     

Lactone cleavage reaction kinetics of rhodamine dye at liquid/liquid interfaces studied by micro-two-phase sheath flow/two-photon excitation fluorescence microscopy

Two-photon excitation fluorescence microscopy was combined with the two-phase microflow system in order to measure the fast interfacial reaction rate at liquid/liquid interfaces. The lactone cleavage kinetics of octadecylrhodamine B (C(18)RB) at the toluene/water and heptane/water interfaces was studied by this new method. The organic solution containing the nonfluorescent lactone of C(18)RB was made to flow as an inner flow with an aqueous outer sheath flow. The diameter of the inner flow was <20 microm. A focused fundamental beam of a Ti:sapphire pulse laser of 780 nm was irradiated to the interface, and emitted fluorescence from the fluorescent product was detected by a charge-coupled device (CCD) camera or a streakscope. The increase in the concentration of the fluorescent form of C(18)RB was measured along the interface of the inner flow of the toluene/water and heptane/water systems for 80 micros just after the contact of two phases. The analysis made by the time-dependent Langmuir adsorption model with the aid of the digital simulation method gave the cleavage reaction rate constants of the lactone form of C(18)RB at the liquid/liquid interfaces.     

Multiphase flow in microfluidic systems --control and applications of droplets and interfaces

Micro- and nanotechnology can provide us with many tools for the production, study and detection of colloidal and interfacial systems. In multiphase flow in micro- and nanochannels several immiscible fluids will be separated from each other by flexible fluidic interfaces. The multiphase coexistence and the small-volume confinement provide many attractive characteristics. Multiphase flow in microfluidic systems shows a complicated behavior but has many practical uses compared to a single-phase flow. In this paper, we discuss the methods of controlling multiphase flow to generate either micro- or nano-droplets (or bubbles) or stable stratified interfaces between fluidic phases. Furthermore, applications of the droplets and interfaces in microchannels are summarized.