Soft polymeric Janus nanoparticles (JNPs), made from polystyrene-b-poly(butadiene)-b-poly(methylmethacrylate), PS-PB-PMMA, triblock terpolymers, assemble into a monolayer at the water–oil interface to reduce interfacial tension. The extent to which the polymer chains can deform influences the packing density of the JNPs at the interface. The longer the polymer chains are relative to the core, the softer are the JNPs, resulting in a JNPs assembly with a lower initial lateral packing density. The interfacial activity of JNPs can be further tuned by complexation of the PMMA chains with lithium ions that are introduced into the water phase. This work provides a fundamental understanding of soft JNPs packing at the water–oil interface and provides a strategy to tailor the areal density of soft JNPs at liquid–liquid interface, enabling the design of smart responsive structured-liquid systems. 相似文献
Blowing bubbles : Hydrogen evolution by proton reduction with [(C5Me5)2Fe] occurs at a soft interface between water and 1,2‐dichloroethane (DCE). The reaction proceeds by proton transfer assisted by [(C5Me5)2Fe] across the water–DCE interface with subsequent proton reduction in DCE. The interface essentially acts as a proton pump, allowing hydrogen evolution by directly using the aqueous proton.
Colloidal microcapsules (MCs) are highly modular, inherently multiscale constructs of capsules stabilized by nano‐/microparticle shells, with applications in many areas of materials and biological sciences, such as drug delivery, encapsulation, and microreactors. Until recently, fabrication of colloidal MCs focused on the use of submicron‐sized particles because the smaller nanoparticles (NPs) are inherently unstable at the interface owing to thermal disorder. However, stable microcapsules can now be obtained by tuning the interactions between the nanometer‐sized building blocks at the liquid–liquid interface. This Review highlights recent developments in the fabrication of colloidal MCs using NPs. 相似文献
The electrochemical deposition of Cu nanoparticles with an average diameter of approximately 25–35 nm has been reported at liquid–liquid interfaces by using the organic‐phase electron‐donor decamethylferrocene (DMFc). The electrodeposited Cu nanoparticles display excellent catalytic activity for the hydrogen evolution reaction (HER); this is the first reported catalytic effect of Cu nanoparticles at liquid–liquid interfaces. 相似文献
Metal nanoparticles are readily formed, with a reasonable degree of size and shape control, using solution‐based reduction methods under ambient conditions. Despite the large number of reports in this field, much of our knowledge of nanoparticle growth is largely empirical, with the relationship between particle form and growth conditions, for example, still not well understood. Many nanoparticle preparation routes actually depend on not one, but two, solution phases, i.e. the syntheses involve reaction or transfer at the liquid–liquid (organic–water) interface. This interface can be polarised electrochemically, an approach that offers promise as a route to better understanding, and ultimately control, of nanoparticle growth. 相似文献
Biomembrane models built at the interface between two immiscible electrolytes (ITIES) are useful systems to study phenomena of biological relevance by means of their electrochemical processes. The unique properties of ITIES allow one either to control or measure the potential difference across the biomimetic membranes. Herein we focus on phospholipid monolayers adsorbed at liquid–liquid interfaces, and besides discussing recent developments on the subject, we describe electrochemical techniques that can be used to get insight on the interfacial processes and electrostatic properties of phospholipid membranes at the ITIES. In particular, we examine the electrochemical and physicochemical properties of (modified) phospholipid monolayers and their interaction with other biologically relevant compounds. The use of liquid–liquid electrochemistry as a powerful tool to characterize drug properties is outlined. Although this review is not a survey of all the work in the field, it provides a comprehensive referencing to current research.相似文献
Nanoparticles are the focus of much attention due to their astonishing properties and numerous possibilities for applications in nanotechnology. For realising versatile functions, assembly of nanoparticles in regular patterns on surfaces and at interfaces is required. Assembling nanoparticles generates new nanostructures, which have unforeseen collective, intrinsic physical properties. These properties can be exploited for multipurpose applications in nanoelectronics, spintronics, sensors, etc. This review surveys different techniques, currently employed and being developed, for assembling nanoparticles in to ordered nanostructures. In this endeavour, the principles and methods involved in the development of assemblies are discussed. Subsequently, different possibilities of nanoparticle‐based nanostructures, obtained in multi‐dimensions, are presented. 相似文献
Janus particles endowed with controlled anisotropies represent promising building blocks and assembly materials because of their asymmetric functionalities. Herein, we show that using the seeded monomer swelling and polymerization technique allows us to obtain bi‐compartmentalized Janus microparticles that are generated depending on the phase miscibility of the poly (alkyl acrylate) chains against the polystyrene seed, thus minimizing the interfacial free energy. When tetradecyl acrylate is used, complete compartmentalization into two distinct bulbs can be achieved, while tuning the relative dimension ratio of compartmented bulb against the whole particle. Finally, we have demonstrated that selectively patching the silica nanoparticles onto one of the bulb surfaces gives amphiphilicity to the particles that can assemble at the oil–water interface with a designated level of adhesion, thus leading to development of a highly stable Pickering emulsion system. 相似文献
At the water–trihexyl(tetradecyl)phosphonium tris(pentafluoroethyl)trifluorophosphate ([P14,6,6,6][FAP]) ionic liquid interface, the unusual electrochemical transfer behavior of protons (H+) and deuterium ions (D+) was identified. Alkali metal cations (such as Li+, Na+, K+) did not undergo this transfer. H+/D+ transfers were assisted by the hydrophobic counter anion of the ionic liquid, [FAP]?, resulting in the formation of a mixed capacitive layer from the filling of the latent voids within the anisotropic ionic liquid structure. This phenomenon could impact areas such as proton‐coupled electron transfers, fuel cells, and hydrogen storage where ionic liquids are used as aprotic solvents. 相似文献
A new electrochemical framework for tracking individual soft particles in solution and monitoring their fusion with polarized liquid–liquid interfaces is reported. The physicochemical principle lies in the interfacial transfer of an ionic probe confined in the particles dispersed in solution and that is released upon their collision and fusion with the fluid interface. As a proof‐of‐concept, spike‐like transients of a stochastic nature are reported in the current–time response of 1,2‐dichloroethane(DCE)|water(W) submilli‐interfaces after injection of DCE‐in‐W emulsions. The sign and potential dependence of the spikes reflect the charge and lipophilicity of the ionic load of the droplets. A comparison with dynamic light scattering measurements indicates that each spike is associated with the collision of a single sub‐picoliter droplet. This opens a new framework for the study of single fusion events at the micro‐ and nanoscale and of ion transport across biomimetic soft interfaces. 相似文献
Thermal wetting can simply, selectively and reversibly join patchy particles into clusters (2D and 3D) and also colloidal crystals over the narrow temperature range of 1–2 °C. This is demonstrated with Janus particles (gold half‐coated silica spheres) immersed in a binary mixture of water/2,6‐lutidine, such that the relative strength of gold–gold bonding through hydrophobic interaction and silica–silica bonding through the wetting‐induced attraction is reversibly switched according to temperature. 相似文献
Bubbling up : Dissolution of CO2 bubbles in a suspension of colloidal particles chemically induces the assembly of particles on the surface of shrunken bubbles, and thus yields rapid continuous formation of a colloidal armor. This approach maintains the high colloidal stability of particles in bulk, has increased productivity, and allows the formation of bubbles with precisely controlled dimensions.