Jung-Pil Lee

Multipositional Silica-Coated Silver Nanoparticles for High-Performance Polymer Solar Cells

We demonstrate high-performance polymer solar cells using the plasmonic effect of multipositional silica-coated silver nanoparticles. The location of the nanoparticles is critical for increasing light absorption and scattering via enhanced electric field distribution. The device incorporating nanoparticles between the hole transport layer and the active layer achieves a power conversion efficiency of 8.92% with an external quantum efficiency of 81.5%. These device efficiencies are the highest values reported to date for plasmonic polymer solar cells using metal nanoparticles.

Helical Silicon/Silicon Oxide Core–Shell Anodes Grown onto the Surface of Bulk Silicon

We demonstrate a simple route for preparing Si/SiO(x) urchin-like structures in which Si/SiO(x) core-shell nanocoils protruded out from the surface of bulk Si, via high-temperature annealing of Pt-decorated Si powders. The carbon-coated urchin-like anodes with micro- and nanostructured composite exhibit a significantly improved electrochemical performance with a high specific capacity of 1600 mAh/g and a superior cycling performance of 70 cycles at a rate of 0.2 C due to the nanocoil conformation and SiO(x) buffer layer. More importantly, the composite results in a significantly enhanced the volumetric capacity with ∼3780 mAh/cc, compared to bulk Si (∼2720 mAh/cc) after fully lithiation to 0 V.

Etched Graphite with Internally Grown Si Nanowires from Pores as an Anode for High Density Li-Ion Batteries

A novel architecture consisting of Si nanowires internally grown from porous graphite is synthesized by etching of graphite with a lamellar structure via a VLS (vapor-liquid-solid) process. This strategy gives the high electrode density of 1.5 g/cm(3), which is comparable with practical anode of the Li-ion battery. Our product demonstrates a high volumetric capacity density of 1363 mAh/cm(3) with 91% Coulombic efficiency and high rate capability of 568 mAh/cm(3) even at a 5C rate. This good electrochemical performance allows porous graphite to offer free space to accommodate the volume change of Si nanowires during cycling and the electron transport to efficiently be improved between active materials.

Extremely Superhydrophobic Surfaces with Micro- and Nanostructures Fabricated by Copper Catalytic Etching

We demonstrate a simple method for the fabrication of rough silicon surfaces with micro- and nanostructures, which exhibited superhydrophobic behaviors. Hierarchically rough silicon surfaces were prepared by copper (Cu)-assisted chemical etching process where Cu nanoparticles having particle size of 10-30 nm were deposited on silicon surface, depending on the period of time of electroless Cu plating. Surface roughness was controlled by both the size of Cu nanoparticles and etching conditions. As-synthesized rough silicon surfaces showed water contact angles ranging from 93° to 149°. Moreover, the hierarchically rough silicon surfaces were chemically modified by spin-coating of a thin layer of Teflon precursor with low surface energy. And thus it exhibited nonsticky and enhanced hydrophobic properties with extremely high contact angle of nearly 180°.

Mass production of uniform-sized nanoporous silicon nanowire anodes viablock copolymer lithography

We present a simple, mass production of nonporous and nanoporous silicon nanowire anodes by combining block copolymer masks and metal catalytic etching. Carbon coated nanoporous silicon nanowire anodes exhibit a highly stable cycling performance with a reversible charge capacity of 1500 mA h g−1.

Hyaluronic acid and silver sulfadiazine-impregnated polyurethane foams for wound dressing application

Five different kinds of PU foam wound dressings were prepared to investigate their wound healing capability. They include (i) PU+silver sulfadiazine (AgSD), (ii) PU+alginate (Al), (iii) PU+Al+AgSD, (iv) PU+hyaluronic acid (HA), and (v) PU+HA+AgSD. Physical properties and in vitro behaviors of AgSD release and fibroblast adhesion on those dressings were evaluated. From the drug release and fibroblast adhesion studies, it was observed that PU foam impregnated with both HA and AgSD shows good drug release behavior and low adhesion of the cells. Furthermore, the HA and AgSD-containing PU foam showed excellent wound healing effect without any inflammation or yellow cluster. The wound size decreased around 77% after 1 week application of that foam dressing onto a rat skin defect.

Preparation of Ag-Embedded Polystyrene Nanospheres and Nanocapsules by Miniemulsion Polymerization

An isopropyl myristate (IPM) biocompatible oil and an IPM solution of dodecanethiol-capped Ag nanoparticles (NPs, 4.5 nm) were used as hydrophobes to suppress the Ostwald ripening of monomer/hydrophobe miniemulsified droplets in a surfactant-stabilized water phase. The formation of non-IPM-encapsulated nanospheres (48 nm) and IPM-encapsulated nanocapsules (90 nm) were precisely controlled by using a water-soluble and an oil-soluble initiator, respectively, in the presence of a pure IPM as a hydrophobe in miniemulsion polymerization. Well-defined PS nanospheres, on which surfaces were coated with Ag NPs (Ag/PS nanospheres, 65 nm), and nanocapsules encapsulating both NPs and IPM liquid phase (Ag-IPM/PS nanocapsules, 115 nm) were made by replacing the hydrophobe from pure IPM with Ag/IPM solution. These nanostructures were characterized by transmission and scanning electron microscopes.

Well-Organized CdS/C60 in Block Copolymer Micellar Cores

CdS nanoparticles of 4.5 nm diameter were synthesized in poly(2-vinylpyridine) micellar cores which were obtained by solvating a polystyrene-block-poly(2-vinylpyridine) block copolymer in polystyrene-selective toluene. Then, a C(60) -toluene solution was dispersed into the CdS micelle solution with stirring. This led to the well-defined organization of two different nanoparticles; specifically: a CdS NP decorated by several/dozens of C(60) molecules, because C(60) molecules were strongly coordinated with pyridine molecules in the micellar cores by charge-transfer complexation C 60δ--P2VP(δ+) . A harmoniously organized CdS/C(60) micellar structure was clearly verified by transmission electron microscopy. Fluorescent quenching of CdS nanoparticles, which was strongly affected by neighboring C(60) molecules, was observed.

The fabrication of nanopatterns with Au nanoparticles-embedded micelles via nanoimprint lithography

We fabricated nanopatterns with Au nanoparticles-embedded micelles (Au-micelles) by self-assembly of block copolymers via nanoimprint lithography. The micelle structure prepared by self-assembled block copolymers was used as a template for the synthesis of Au nanoparticles (Au NPs). Au NPs were synthesized in situ inside the micelles of polystyrene-block-poly(2-vinylpyridine) (PS- b-P2VP). Au-micelles were arranged on the trenches of the polymer template, which was imprinted by nanoimprint lithography. The fabrication of line-type and dot-type nanopatterns was carried out by the combined method. In addition, multilayer nanopatterns of the Au-micelles were also proposed.

Preparation of silica nanospheres and porous polymer membranes with controlled morphologies via nanophase separation

We successfully synthesized two different structures, silica nanospheres and porous polymer membranes, via nanophase separation, based on a sol–gel process. Silica sol, which was in situ polymerized from tetraorthosilicate, was used as a precursor. Subsequently, it was mixed with a polymer that was used as a matrix component. It was observed that nanophase separation occurred after the mixing of polymer with silica sol and subsequent evaporation of solvents, resulting in organizing various structures, from random network silica structures to silica spheres. In particular, silica nanospheres were produced by manipulating the mixing ratio of polymer to silica sol. The size of silica beads was gradually changed from micro- to nanoscale, depending on the polymer content. At the same time, porous polymer membranes were generated by removing the silica component with hydrofluoric acid. Furthermore, porous carbon membranes were produced using carbon source polymer through the carbonization process.