Papers by Author: Young Hwan Kim

Abstract: In the past decades, porous materials have attracted great scientific and industrial interest due to their appealing structures and potential applications in separation, purification, catalysis, devices, and so forth. The developing community of ordered mesoporous materials has carried on this exploration of the mesoscopical territory, which promises their unique capacities related to large molecules and their transportation in confined space. Thus rational control and adjustment of pores have been continually focused during the synthesis of ordered mesoporous materials with diverse intrinsic properties. In this work, vitamin C encapsulated mesoporous silica was successfully synthesized with tetraethylorthosilicate (TEOS). TEOS was subjected to sol-gel process in the presence of cetyltrimethylammonium bromide (CTAB). The composition and size of mesoporous silica was controlled by fitting the molar ratio of starting materials. The mesoporous silica can be applied to the field of the cosmetics and bio-medicine as drug delivery.

Abstract: A room temperature route for doping silica particles with Cu nanoparticles to achieve hybrid structures is introduced. First, silica nanoparticles were synthesized according to the well-known Stöber method by hydrolysis and condensation of TEOS in a mixture of ethanol with water, using ammonia as catalyst to initiate the reaction. These SiO2 nanoaprticles were dried at 100 oC. We measured the size of these nanoparticles with transmission electron microscopy (TEM). Second, Cu-SiO2 nanoparticles were synthesized by reaction with CuCl2 and SiO2 nanoparticles in presence of catalyst at room temperature for 12 hrs. Results show silica nanoparticles of about 70 nm size with regularly deposited Cu nanoparticles. Cu-SiO2 nanoparticles were investigated with TEM images, energy dispersive X-ray analysis (EDX) spectrum and so on.

Abstract: Core/shell structured TiO2/ZnO was synthesized in a basic aqueous solution through a simple hydrolyzing method. The powder X-ray diffraction (XRD) and transmission electron microscopy of the initial TiO2/ZnO powder showed diffraction peaks corresponding to the ZnO and TiO2 phase. The structure and thickness of ZnO shell (about 2.5 nm) coated TiO2 surface as thin layers or nanoclusters, depends upon the reactant concentration and the reaction time. The characteristics of the optical absorption were described by UV-visible absorption spectroscopy.

Abstract: The magnetic α-Fe nanoparticles were carried out using two-preparation methods that include solution phase metal salt reduction and organometallic precursor decomposition. Under the different reaction conditions such as precursor and reaction time, the magnetic properties of α-Fe nanoparticles were studied. The size of nanoparticle was confirmed by transmission electron microscope (TEM) images. The magnetic properties were characterized with saturation magnetization(Ms) from hysteresis loop by vibrating sample magnetometer (VSM). The crystallinity and structure of α-Fe nanoparticles was investigated by X-ray diffraction (XRD).

Abstract: We report the core/shell type as the interesting one of the various techniques to prepare exchange-coupled permanent magnet. In this study, the exchange-coupled Nd2Fe14B/α-Fe was prepared by high energy ball mill process and chemical reduction. Nd15Fe77B8 powder prepared by high energy ball mill process was coated with α-Fe nanoparticle by chemical reduction. α-Fe nanoparticle on the ball milled Nd15Fe77B8 was synthesized by chemical reduction with borohydride as a reducing agent in aqueous solution. After annealing, Nd2Fe14B/α-Fe forming core/shell shape has exchange-coupling effect and was identified by using XRD, FE-SEM, VSM, TMA and EDX.

Abstract: Co nanoparticles were synthesized via a solventless thermal decomposition of Co2+-oleate2. The crystalline structure is strongly affected by the thermal treatment of the Co nanoparticles. Further, the annealing also results in the decomposition of surfactant around Co particles. The size of nanoparticles was confirmed by transmission electron microscopy (TEM). The crystal structure of nanoparticles was characterized by X-ray diffraction pattern (XRD). The magnetic properties were characterized by vibrating sample magnetometer (VSM).