Eun Chul Cho

Metal−Polymer Hybrid Colloidal Particles with an Eccentric Structure†

We have synthesized metal-polymer hybrid colloidal particles characterized by an eccentric structure by precipitation polymerization in the presence of metal colloids. The key to the formation of an eccentric core-shell structure was to introduce metal colloids a few minutes after (rather than before) starting the polymerization. The hybrid particles were uniform in size, and each one of them contained only one metal nanoparticle at its surface after the experimental procedures had been optimized. This method could be extended to a number of different metal colloids stabilized by small molecules, and the yield was found to be more or less independent of the size of the metal nanoparticles. In addition, the position of the metal nanoparticle in the hybrid particle could be controlled by changing the concentration of cross-linker, and the overall size of the hybrid particles could be altered by solvent treatment. Because of the simplicity of this procedure, it should be possible to use it for the large-scale production of colloidal particles having a hybrid, complex structure.

Contact angles of oils on solid substrates in aqueous media: correlation with AFM data on protein adhesion.

This study presents a method to measure the contact angles of oils on a substrate in water. Diiodomethane and perfluorodecalin were used as model oils. Self-assembled monolayers (SAMs) were prepared by adjusting the mole ratio of CH 3- and OH-terminated alkanethiols. The contact angles of the two oils in water increased with increasing hydrophilicity of the SAMs, and the results are contrasted with the contact angles of oils on these surfaces in air. In addition, perfluorodecalin showed higher contact angles than diiodomethane on the same surface. On the poly(N-isopropylacrylamide) (PNiPAAM) monolayer surface, the contact angles of the two oils in water decreased sharply at the transition temperature of PNiPAAM (approximately 30 degrees C), but the surface retained fairly high hydrophilicity even after the transition. The above results are correlated with atomic force microscopy (AFM) measurements of the adhesion force between protein-immobilized AFM tips (human fibrinogen and bovine serum albumin) and these monolayers.

A Simple Evaporation Method for Large-Scale Production of Liquid Crystalline Lipid Nanoparticles with Various Internal Structures.

We present a simple and industrially accessible method of producing liquid crystalline lipid nanoparticles with various internal structures based on phytantriol, Pluronic F127, and vitamin E acetate. Bilayer vesicles were produced when an ethanolic solution dissolving the lipid components was mixed with deionized water. After the evaporation of ethanol from the aqueous mixture, vesicles were transformed into lipid-filled liquid crystalline nanoparticles with well-defined internal structures such as hexagonal lattices (mostly inverted cubic Pn3m), lined or coiled pattern (inverted hexagonal H2), and disordered structure (inverse microemulsion, L2), depending on the compositions. Further studies suggested that their internal structures were also affected by temperature. The internal structures were characterized from cryo-TEM and small-angle X-ray scattering results. Microcalorimetry studies were performed to investigate the degree of molecular ordering/crystallinity of lipid components within the nanostructures. From the comparative studies, we demonstrated the present method could produce the lipid nanoparticles with similar characteristics to those made from a conventional method. More importantly, the production only requires simple tools for mixing and ethanol evaporation and it is possible to produce 10 kg or so per batch of aqueous lipid nanoparticles dispersions, enabling the large-scale production of the liquid crystalline nanoparticles for various biomedical applications.

Solution-Processed Plasmonic–Dielectric Sunlight-Collecting Nanofilms for Solar Thermoelectric Application

It is important but remains a challenge to develop solution-processed plasmonic solar thermoelectricity films on various substrates, without strictly considering hierarchical plasmonic-dielectric-metal structures, to harvest a wide range of visible to near-infrared sunlight. We simply fabricate plasmonic silica metastructure sunlight-collecting nanofilms on highly reflective Cu and Si surfaces by introducing spin coating (with an Ag and silica colloidal mixture, a spin coater, and a heating plate) and low-temperature annealing (in an oven at 200 °C for 1 h) processes. The approximately 250 nm thick metastructure consists of a top 60 nm thick silica layer as an antireflective film and a bottom 190 nm thick Ag nanoparticle-silica hybrid film as a sunlight harvester. The metastructure film reduces the reflectivity of Cu (>90%) and Si (25-35%) to less than 5% at visible to near-infrared frequencies. The metastructure film on the Cu sheet has an absorptance of 0.95 and a thermal emittance of 0.06, ideal for high-performance sunlight absorbers. The solar thermoelectric powers of the film-coated Cu and Si are 15.4 and 4.7 times those of the uncoated Cu and Si substrates, respectively. The metastructure film on Cu exhibited a similar or slightly higher performance than that of a top-class vapor-deposited commercialized absorber film on Cu, demonstrating the robustness of the present method.