Huang-Kai Lin

(110)-exposed gold nanocoral electrode as low onset potential selective glucose sensor.

A straightforward electrochemical deposition process was developed to grow gold nanostructures, including nanocoral, nanothorn, branched belt, and nanoparticle, on carbon electrodes by reducing HAuCl4 under constant potentials in mixtures containing CTAC and/or NaNO3. Among the nanostructures, the quasi-one-dimensional nanocoral electrode showed the highest surface area. Because of this, it provided excellent electrochemical performances in cyclic voltammetric (CV) studies for kinetic-controlled enzyme-free glucose oxidation reactions. In amperometric studies carried out at 0.200 V in PBS (pH 7.40, 0.100 M), the nanocoral electrode showed the highest anodic current response. It also offered the greatest sensitivity, 22.6 μAmM(-1)cm(-2), an extended linear range, 5.00×10(-2) mM to 3.00×10(1) mM, and a low detection limit, 1.00×10(1) μm among the electrodes investigated in this study. In addition, the glucose oxidation by the nanocoral electrode started at -0.280 V, more negative than the one of using a commercial Au electrode as the working electrode. This is attributed to the presence of exposed Au (110) surfaces on the electrode. The feature was applied to oxidize glucose selectively in the presence of ascorbic acid (AA) and uric acid (UA), common interferences found in physiological analytes. With an applied voltage at -0.100 V, the AA oxidation (started at -0.080 V) can be avoided while the glucose oxidation still provides a significant response.

Growth of Carbon Nanocoils from K and Ag Cooperative Bicatalyst Assisted Thermal Decomposition of Acetylene

Growth of amorphous carbon nanocoil (CNC) from acetylene on Si substrates was achieved by using nanosized Ag and K as the catalysts. The deposition of CNC was carried out inside a hot-wall reactor at 723 K using H2 as the carrier gas. Based on the observed results, we propose a cooperative bimetal catalyst enhanced vapor-liquid-solid (VLS) growth mechanism to rationalize the CNC growth. In the reaction, the liquid phase metallic K dehydrogenated acetylene into the solid-state carbon, while the Ag nanoparticle assisted the extension of carbon one-dimensionally (1-D) via a tip-growth mechanism. Due to the adhesive force between the K liquid and the carbon, the 1-D solid curled along the C-K interface into the nanocoil shape. Some CNC samples were further heat-treated at 1423 K and showed very good field emission properties. They emitted electrons (10 microA/cm2) at a turn-on field Eto of 2.51 V/microm, while Jmax reached 17.71 mA/cm2 at 5.64 V/microm. The field enhancement factor beta was calculated to be 2124, comparable to other carbon nanotube (CNT) and CNC based emitters. The CNC was also characterized by using the electrochemical behavior of K3[Fe(CN)6] via cyclic voltammetry (CV). The electrochemical surface area of a CNC electrode (geometric surface area 0.078 cm2) was calculated to be 0.143 cm2. These properties suggest that the CNC electrodes may have potential applications in field emission and electrochemical devices.

Growth of High-Aspect-Ratio Gold Nanowires on Silicon by Surfactant-Assisted Galvanic Reductions

A simple galvanic reduction for direct growth of Au nanowires on silicon wafers is developed. The nanowires were prepared by reacting HAuCl4aq with Sns in the presence of CTACaq (cetyltrimethylammonium chloride) and NaNO3aq, which were important to the product morphology development. The nanowire diameter was 50-100 nm, and the length was more than 20 microm.

Growth of pagoda-topped tetragonal copper nanopillar arrays.

Growth of arrays of pagoda-topped tetragonal Cu nanopillar (length 1- 6 mum; width 150 +/- 25 nm) with {100} side faces on Au/glass is achieved by a simple electrochemical reduction of CuCl(2)(aq) by Al(s) in aqueous dodecyltrimethylammonium chloride. Field-emission measurement shows that the Cu nanopillars can emit electrons (10 muA cm(-2)) at a turn-on field of 12.4 V mum(-1) with a calculated field enhancement factor of 713.

Conversion of potassium titanate nanowires into titanium oxynitride nanotubes.

Tunnel-structured potassium titanate with a K(3)Ti(8)O(17) phase was synthesized by direct oxidation of titanium powder mixed with KF(aq) in water vapor at 923 K. The reaction conditions were adjusted so that uniform single crystalline potassium titanate nanowires with [010] growth direction (length: 5-30 μm, diameter: 80-100 nm) were obtained. Nitridation of the nanowires by NH(3)(g) at 973-1073 K converted the titanate nanowires into rock-salt structured cubic phase single crystalline titanium oxynitride TiN(x)O(y) nanotubes (x = 0.88, y = 0.12, length = 1-10 μm, diameter = 150-250 nm, wall thickness = 30 - 50 nm) and nanorods (x = 0.5, y = 0.5, length = 1-5 μm, diameter = 100-200 nm) with rough surfaces and [200] growth direction. The overall conversion of the titanate nanowires into the nanotubes and the nanorods can be rationalized by Ostwald ripening mechanism. We fabricated an electrode by adhering TiN(x)O(y) nanotubes (0.2 mg) on a screen-printed carbon electrode (geometric area: 0.2 cm(2)). Electrochemical impedance spectroscopy demonstrated its charge transfer resistance to be 20Ω. The electrochemical surface area of the nanotubes on the electrode was characterized by cyclic voltammetry to be 0.32 cm(2). This property suggests that the TiN(x)O(y) nanostructures can be employed as potential electrode materials for electrochemical applications.