Wan-Joong Kim

Temperature-induced control of aspect ratio of gold nanorods

Aspect ratio of gold nanorods can be controlled by simply adjusting the reaction temperature in the seed-mediated synthesis of the nanorods. The gold nanorods were synthesized by the injection of gold nanoparticle seeds of around 4nm in diameter into a reaction mixture containing hydrogen tetrachloroaurate, hexadecyltrimethylammonium bromide, and ascorbic acid. Average aspect ratio of the resulting nanorod increases from 1 to about 40 with decreasing the reaction temperature from 315to276K, which can be attributed to the temperature-induced change in the shape of the micellar templates. For further understanding of the growth mechanism, silver nanoparticles were also used as seeds in the preparation of the gold nanorod.

Response to cardiac markers in human serum analyzed by guided-mode resonance biosensor.

Cardiac markers in human serum with concentrations less than 0.1 ng/mL were analyzed by use of a guided-mode resonance (GMR) biosensor. Cardiac troponin I (cTnI), creatine kinase MB (CK-MB), and myoglobin (MYO) were monitored in the serum of both patients and healthy controls. Dose-response curves ranging from 0.05 to 10 ng/mL for cTnI, from 0.1 to 10 ng/mL for CK-MB, and from 0.03 to 1.7 μg/mL for MYO were obtained. The limits of detection (LOD) for cTnI, CK-MB, and MYO were less than 0.05, 0.1, and 35 ng/mL, respectively. Analysis time was 30 min, which is short enough to meet clinical requirements. Antibody immobilization and the hydrophilic properties of the guided-mode resonance filter (GMRF) surface were investigated by X-ray photoelectron spectroscopy (XPS) and by monitoring the peak wavelength shift and water contact angle (CA). Both assays used to evaluate the surface density of the immobilized antibodies, a sandwich enzyme-linked immunosorbent assay (ELISA) and a sandwich immunogold assay, showed that the antibodies were successfully immobilized and sufficiently aligned to detect the low concentration of biomarkers. Our results show that the GMR biosensor will be very useful in developing low-cost portable biosensors that can screen for cardiac diseases.

Enhanced Protein Immobilization Efficiency on a TiO2 Surface Modified with a Hydroxyl Functional Group

An antibody immobilization was investigated using a self-assembled monolayer (SAM) over the highly refractive coatings with a SiO2, TiO2, or Si3N4 substrate. The immobilization was characterized by analyzing the hydrophilic properties of hydroxyl (OH) groups on surface coatings with contact angle (CA) measurements to enhance protein immobilization. The hydroxyl (OH) group was formed in greater amounts as the oxygen plasma exposure time was increased, which resulted in a large enhancement in antibody immobilization. It indicated that hydroxyl (OH) group formation is critical for developing a label-free optical transducer with a high sensitivity.

Enhancement in light emission efficiency of Si nanocrystal light-emitting diodes by a surface plasmon coupling

We report an enhancement in light emission efficiency form Si nanocrystal (NC) light-emitting diodes (LEDs) via surface plasmons (SPs) by employing Au nanoparticles (NPs). Photoluminescence intensity of Si NCs with Au NPs was enhanced by 2 factors of magnitude due to the strong coupling of Si NCs and SP resonance modes of Au NPs. The electrical characteristics of Si NC LED were significantly improved, which was attributed to an increase in an electron injection into the Si NCs due to the formation of inhomogeneous Schottky barrier at the SiC-indium tin oxide interface. Moreover, light output power from the Si NC LED was enhanced by 50% due to both SP coupling and improved electrical properties. The results presented here can provide a very promising way to significantly enhance the performance of Si NC LED.

Binding of aromatic isocyanides on gold nanoparticle surfaces investigated by surface-enhanced Raman scattering.

The adsorption structure and binding of phenyl isocyanide (PNC), 2,6-dimethyl phenyl isocyanide (DMPNC), and benzyl isocyanide (BZI) on gold nanoparticle surfaces have been studied by means of surface-enhanced Raman scattering (SERS). PNC, DMPNC, and BZI have been found to adsorb on gold assuming a standing geometry with respect to the surfaces. The presence of the v(CH) band in the SERS spectra denotes a vertical orientation of the phenyl ring of PNC, DMPNC, and BZI on Au. The lack of a substantial red shift and significant band broadening of the ring breathing modes implied that a direct ring π orbital interaction with metal substrates should be quite low. For PNC, the band ascribed to the C–NC stretching vibration was found to almost disappear after adsorption on Au. On the other hand, the C–NC band remained quite strong for DMPNC after adsorption. This result suggests a rather bent angle of C–N≡C: for the nitrogen atom of the NC binding group on the surfaces, whereas a linear angle of C–N≡C: should be more favorable on gold surfaces due to an intramolecular steric hindrance of its two methyl groups. SERS of BZI on gold nanopaticles also supports a bent angle of: C≡N–CH2 for its nitrogen atom, suggesting a preference of sp3 (or sp2) hybridization for the nitrogen atom.

Fabrication of anionic sulfate-functionalized nanoparticles as an immunosensor by protein immobilization.

Anionic sulfate (SO(4)(-))-functionalized polystyrene (PS) nanoparticles were prepared by the thermal decomposition of potassium persulfate (KPS) in the presence of sodium tetraborate via emulsion polymerization. The presence of a SO(4)(-) group at a solid/liquid interface of a particle surface was confirmed by a zeta potential value of -40.6 mV as well as the shifting of S 2p spectra toward a lower-binding-energy region around 162.7 eV (2p(3/2)) and 164.4 eV (2p(1/2)) in X-ray photoelectron spectroscopy (XPS) analysis. The electrostatic attraction between positively charged antibodies of human immunoglobulin G (hIgG) and cardiac troponin I (cTnI) and negatively charged particle surfaces was accomplished. The atomic force microscopy (AFM) measurement and bicinchoninic acid (BCA) assay results show binding structure between hIgG and antibodies of hIgG (anti-hIgG) with a gradual increase in particle diameter to 152.6 nm (bare), 170.2 nm (hIgG), and 178.9 nm (hIgG/anti-hIgG). Surface coverage densities of 331.4 ng/cm(2) (hIgG) and 320.3 ng/cm(2) (cTnI) and the binding capacity of hIgG to HyLite-750-labeled Fab-specific anti-hIgG (approximately 81.2%) indicate that the majority of hIgG was immobilized with a Y-shaped orientation. The sandwich immunoassay results provide the evidence that the immunological activity of cTnI on the PS nanoparticle surface was retained because the binding activity of the cTnI-PS nanoparticle/cTnI (antigen)/detection cTnI-antibody reaction showed a 5-fold higher activity than that of the cTnI-PS nanoparticle/human serum albumin (HSA)/detection cTnI antibody used as a negative control.

Effects of electron injection efficiency on performances of Si nanocrystal light‐emitting diodes

We have investigated the effects of electron injection efficiency on the electrical and optical performances of the nc‐Si LEDs. The current‐voltage curves of nc‐Si LED with 6‐periods of SiCN/SiC multiple electron injection layers was better than that of nc‐Si LED with single SiC electron injection layer. This can be attributed to the increase in an electron density of the 6‐periods of SiCN/SiC multiple electron layers compared to that of the single SiC electron injection layer because the electron density of SiCN layer is higher than SiC layer. Light output power of the LED with 6‐periods of SiCN/SiC multiple electron injection layers was improved by 50% compared to that of LED with single SiC electron injection layer. We show here that the use of the multiple electron injection structure could be used to realize a highly efficient nc‐Si LED.

Electromagnetic Contribution to Surface Enhanced Raman Scattering of Rhodamine 6G Molecules on Rice-Shaped Au Nanocrystals

The factor of electromagnetic contribution to SERS of Rh6G on rice-shaped Au nanocrystals was estimated to be around six-order higher than Raman scattering of Rh6G.