Zhuang Li

Novel nonenzymatic hydrogen peroxide sensor based on iron oxide-silver hybrid submicrospheres.

Fe(3)O(4)-Ag hybrid submicrosphere was synthesized and developed as hydrogen peroxide sensor in this study. The hybrid sphere was fabricated via a two-step route, and proved by characterizations such as TEM, SEM, EDX, and XPS. Recent studies of hydrogen peroxide sensor based on silver nanoparticles inspired us to study the electrocatalytic property of the as-prepared submicrosphere. Though the Ag amount is quite little in the hybrid spheres, the electrochemical sensor constructed by the hybrid spheres exhibited fast, stable and well-defined electrocatalytic activity towards H(2)O(2) reduction, which should be the contribution of the combination of Fe(3)O(4) and Ag. The detection limit of H(2)O(2) was also found to be 1.2microM, which was lower than some enzyme-based biosensors.

Carbon nanotube/raspberry hollow Pd nanosphere hybrids for methanol, ethanol, and formic acid electro-oxidation in alkaline media

In this paper, raspberry hollow Pd nanospheres (HPNs)-decorated carbon nanotube (CNT) was developed for electro-oxidation of methanol, ethanol, and formic acid in alkaline media. The electrocatalyst was fabricated simply by attaching HPNs onto the surface of CNT which had been functionalized by polymer wrapping. The as-prepared HPN-CNTs (CHPNs) were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The increasing interest and intensive research on fuel cell inspire us to investigate the electrocatalytic properties of the prepared nanostructures. Besides that, previous reports about alkaline other than acidic media could supply a more active environment guide us to examine the electrocatalytic properties in alkaline electrolyte. It is found that this novel hybrid electrocatalyst exhibits excellent electrocatalytic properties and can be further applied in fuel cells, catalysts, and sensors.

Facile synthesis of urchin-like gold submicrostructures for nonenzymatic glucose sensing

Urchin-like gold submicrostructures (UGS) were successfully synthesized by a seed-mediated method which is quite facile and does not need any template or surfactant agent. The effect of the added silver seeds on the morphology and size of final products were investigated, and a possible growth mechanism of crystals was proposed. Electrochemical characterization indicated that these UGS have better catalytic activity for the glucose oxidation compared with flower-like gold submicrostructures (FGS), which could be ascribed to its higher surface to volume ratio. An electrochemical nonenzymatic glucose sensor was fabricated simply by casting the UGS and Nafion solution onto glass carbon electrode. This sensor displays a wide linear range from 0.2 to 13.2mM with a high sensitivity of 16.8 μA mM(-1)cm(-2), and a detection limit of 10 μM. The unique properties of this sensor, such as fast response and well stability reveal the potential application of the UGS based materials in nonenzymatic detection of glucose.

Interaction between DNA and microcystin-LR studied by spectra analysis and atomic force microscopy.

Microcystin-LR (MC-LR) is one of the hepatotoxins produced by cyanobacteria in the eutrophicated fresh water. In this work, the minor groove binding mode of MC-LR to plasmid DNA was explored by using UV and fluorescence spectra, and the binding characteristics of MC-LR for plasmid DNA were calculated via the fluorescence quenching of ethidium bromide (EB) and mole ratio method. Furthermore, atomic force microscopy (AFM) was used to observe DNA morphology change in the presence of MC-LR. With the increasing concentration of MC-LR, circle DNA strands twined gradually to rod condensates. The possible reason for the condensation might be the masking of the electrostatic repulsion between DNA double strands by MC-LR. The present study might provide useful information for the pathopoiesis mechanism of MC-LR. More, because the condensation of DNA could affect the progresses of gene expression and protein transcription, it may implicate another trend to explore the nosogenesis of MC-LR.

Seed-Mediated Synthesis of Au Nanocages and Their Electrocatalytic Activity towards Glucose Oxidation

We report a modified seed-mediated approach for the synthesis of uniform Au nanocages (AuNCs). HAuCl(4) was reduced in an aqueous mixture of hexamethylenetetramine (HMT), poly(N-vinyl-2-pyrrolidone) (PVP), and AgNO(3). The nanocages were (54.6+/-13.3) nm in outer-edge length and about 12 nm in wall thickness. The structure of the AuNCs was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). Morphological changes associated with the seed-mediated growth of Au nanoparticles (AuNPs) in the absence of HMT or PVP were examined. The results demonstrate that both PVP and HMT play important roles in the formation of the nanocage structure. The function of AgNO(3) was also studied. A possible formation mechanism for the AuNCs was investigated by monitoring TEM images of the Au nanostructures formed at various reaction times. The electrocatalytic activity of the AuNCs towards the oxidation of glucose was explored, and a nonenzymatic glucose sensor with high sensitivity and good stability was further fabricated. To the best of our knowledge, this is the first report of the preparation of AuNCs by a seed-mediated strategy and of the application of AuNCs in the electrocatalytic oxidation of glucose. Our results should facilitate the creation of novel nanomaterials with various morphologies and the exploration of their applications in nanotechnological, optical, catalytic, and materials science fields.

Self-assembly of cinnamic acid-capped gold nanoparticles

In this work, a new capping agent, cinnamic acid (CA) was used to synthesize Au nanoparticles (NPs) under ambient conditions. The size of the NPs can be controlled by adjusting the concentration of reductant (in our experiment sodium borohydride was used) or CA. The CA-stabilized Auxa0NPs can self-assemble into nanowire-like or pearl-necklace-like nanostructures by adjusting the molar ratio of CA to HAuCl4 or by tuning the pH value of the Au colloidal solution. The process of Auxa0NPs self-assembly was investigated by UV–vis spectroscopy and transmission electron microscopy. The results reveal that the induced dipole–dipole interaction is the driving force of Au NP linear assemblies.

The structural transition of DNA-Tris(1,10-phenanthroline) cobalt(III) complexes in ethanol-water solution

The interaction of DNA with Tris(1,10-phenanthroline) cobalt(III) was studied by means of atomic force microscopy. Changes in the morphologies of DNA complex in the presence of ethanol may well indicate the crucial role of electrostatic force in causing DNA condensation. With the increase of the concentration of ethanol, electrostatic interaction is enhanced corresponding to a lower dielectric constant. Counterions condense along the sugar phosphate backbone of DNA when epsilon is lowered and the phosphate charge density can thus be neutralized to the level of DNA condensation. Electroanalytical measurement of DNA condensed with Co(phen)(3)(3+) in ethanol solution indicated that intercalating reaction remains existing. According to both the microscopic and spectroscopic results, it can be found that no secondary structure transition occurs upon DNA condensing. B-A conformation transition takes place at more than 60% ethanol solution.

Study of methanol adsorption on mica, graphite and ITO glass by using tapping mode atomic force microscopy

Tapping mode atomic force microscopy (AFM) was applied to study the adsorption behavior of methanol on mica, highly oriented pyrolytic graphite (HOPG) and indium-tin oxide (ITO) coated glass substrates. On mica and HOPG substrates surfaces, the thin films of methanol with bilayer and multilayer were observed, respectively. The formation of irregular islands of methanol was also found on HOPG surface. On ITO surface only aggregates and clusters of methanol molecules were formed. The influence of sample preparation on the adsorption was discussed.

Surface-Relevant Regulable DNA Toroids Induced by Dopamine

Dopamine (2-(3,4-dihydroxyphenyl)ethylamine) is known as a natural chemical neurotransmitter and is also a cytotoxic and genotoxic molecule for cell apoptosis. In this work, the interaction of DNA with dopamine was investigated. Though the electrostatic interaction of DNA and dopamine was weak in aqueous solution, dopamine condensed circular pBR322 DNA into toroids on the mica surface cooperatively with ethanol. The formed DNA toroids came from the shrinking of DNA that was driven by ethanol-enhanced DNA-dopamine electrostatic interaction. The size of the DNA toroids could be modulated by varying the concentration of dopamine. This study offers useful information about the DNA condensation induced by monovalent cations and the sample preparation for AFM measurement and application. On the other hand, this work provides the potential strategies to prepare morphology and size controllable DNA condensates, which have valuable applications in gene transfection and nanotechnology.

Formation of gold nanoparticle decorated lysozyme microtubes.

Gold nanoparticle decorated lysozyme microtubes, with the diameters of 1-2 μm and lengths on the order of millimeters, were spontaneously formed via a simple aging process of the lysozyme-gold nanoparticle aqueous solution under ambient conditions for 1 week. These novel microtubes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX), as well as Fourier-transform infrared (FTIR) spectroscopy. It was confirmed that the microtubes were made up of the protein lysozyme. In addition, formation of the microtubes was accompanied by a decrease in lysozyme concentration in the sample solution, which also indicated that these microtubes originated from lysozyme. The formation of microtubes was attributed to the formation of hydrogen bonding networks between the lysozyme molecules. Partially unfolded lysozyme molecules on gold nanoparticles probably seed the formation of the lysozyme microtubes. These novel protein microtubes not only provide some useful insights for protein study but may also have the potential to be used in the biomedical field.