Role of Au(NPs) in the enhanced response of Au(NPs)-decorated MWCNT electrochemical biosensor.

BACKGROUND: The combination of Au-metallic-NPs and CNTs are a new class of hybrid nanomaterials for the development of electrochemical biosensor. Concentration of Au(nanoparticles [NPs]) in the electrochemical biosensor is crucial for the efficient charge transfer between the Au-NPs-MWCNTs modified electrode and electrolytic solution. METHODS: In this work, the charge transfer kinetics in the glassy carbon electrode (GCE) modified with Au(NPs)-multiwalled carbon nanotube (MWCNT) nanohybrid with varied concentrations of Au(NPs) in the range 40-100 nM was studied using electrochemical impedance spectroscopy (EIS). Field emission scanning electron microscopy and transmission electron microscopy confirmed the attachment of Au(NPs) on the surface of MWCNTs. RESULTS: The cyclic voltammetry and EIS results showed that the charge transfer mechanism was diffusion controlled and the rate of charge transfer was dependent on the concentration of Au(NPs) in the nanohybrid. The formation of spherical diffusion zone, which was dependent on the concentration of Au(NPs) in nanohybrids, was attributed to result in 3 times the increase in the charge transfer rate ks, 5 times increase in mass transfer, and 5% (9%) increase in Ipa (Ipc) observed in cyclic voltammetry in 80 nM Au(NP) nanohybrid-modified GCE from MWCNT-modified GCE. The work was extended to probe the effect of charge transfer rates at various concentrations of Au(NPs) in the nanohybrid-modified electrodes in the presence of Escherichia coli. The cyclic voltammetry results clearly showed the best results for 80 nM Au(NPs) in nanohybrid electrode. CONCLUSION: The present study suggested that the formation of spherical diffusion zone in nanohybrid-modified electrodes is critical for the enhanced electrochemical biosensing applications.

Significance of postgrowth processing of ZnO nanostructures on antibacterial activity against gram-positive and gram-negative bacteria.

In this work, we highlighted the effect of surface modifications of one-dimensional (1D) ZnO nanostructures (NSs) grown by the vapor-solid mechanism on their antibacterial activity. Two sets of ZnO NSs were modified separately - one set was modified by annealing in an Ar environment, and the second set was modified in O2 plasma. Annealing in Ar below 800°C resulted in a compressed lattice, which was due to removal of Zn interstitials and increased O vacancies. Annealing above 1,000°C caused the formation of a new prominent phase, Zn2SiO4. Plasma oxidation of the ZnO NSs caused an expansion in the lattice due to the removal of O vacancies and incorporation of excess O. Photoluminescence (PL) spectroscopy was employed for the quantification of defects associated with Zn and O in the as-grown and processed ZnO NS. Two distinct bands were observed, one in the ultraviolet (UV) region, due to interband transitions, and other in the visible region, due to defects associated with Zn and O. PL confirmed the surface modification of ZnO NS, as substantial decrease in intensities of visible band was observed. Antibacterial activity of the modified ZnO NSs demonstrated that the surface modifications by Ar annealing limited the antibacterial characteristics of ZnO NS against Staphylococcus aureus. However, ZnO NSs annealed at 1,000°C or higher showed a remarkable antibacterial activity against Escherichia coli. O2 plasma-treated NS showed appreciable antibacterial activity against both E. coli and S. aureus. The minimum inhibition concentration was determined to be 0.5 mg/mL and 1 mg/mL for Ar-annealed and plasma-oxidized ZnO NS, respectively. It was thus proved that the O content at the surface of the ZnO NS was crucial to tune the antibacterial activity against both selected gram-negative (E. coli) and gram-positive (S. aureus) bacterial species.

Electrochemical immunosensor for prostate-specific antigens using a label-free second antibody based on silica nanoparticles and polymer brush.

In this paper, we propose a sensitive electrochemical immunosensor synthesized using a surface-initiated atom transfer radical polymerization process for the detection of prostate-specific antigen (PSA). Electrochemical immunosensors based on polymer brush [oligo(ethylene glycol)methacrylate-co-glycidyl methacrylate] (OEGMA-co-GMA) were grown on plane Au and nanostructured (NS) Au electrodes, characterized and compared for their sensitivity to detect PSA. Due to a large capacity for antibody loading and high resistance to nonspecific antibody adsorption of POEGMA-co-GMA brush, the Au-NS immunosensor exhibited detection in a wide dynamic range of five orders of magnitude with an improved lower limit of detection of 2pgml(-1), which was better than the synthesized immunosensor with the polymer brush grown on plane Au electrode. The Au-NS electrode showed improved detection sensitivity of 4.9µAng(-1)ml for PSA detection, which was almost 2 times better than the plane Au electrode. Finally, the use of silica nanoparticles (Si-NPs) conjugated with polyclonal antibody enhanced the response of the immunosensor. The proposed electrochemical immunosensor would be an exciting addition in medical diagnostics for the early detection of cancer biomarkers, e.g., PSA due to improved limit of detection (LOD); eventually helpful in circumventing cancer metastasis.

Anomalous optical and magnetic behavior of multi-phase Mn doped Zn(2)SiO(4) nanowires: a new class of dilute magnetic semiconductors.

We present the synthesis of Mn doped Zn(2)SiO(4) dense nanowire bundles using the VLS mode of growth with unusual optical and magnetic properties. The synthesized Zn(2)SiO(4) nanowires were identified with two phases, α-Zn(2)SiO(4) as the major phase and ß-Zn(2)SiO(4) as the minor phase. XPS studies confirmed that Zn(2)SiO(4) nanowires were Zn rich and Mn doped. Temperature dependent photoluminescence (PL) measurements showed three distinct emission bands: green, yellow and red due to Mn doping in the α-phase, ß-phase and the substitution of Si with Mn in the α-phase, respectively. The PL analysis showed that these emission bands followed anomalous Berthelot-type behavior. The carrier escape energies were 70 ± 3 meV, 49 ± 2 meV and 65 ± 4 meV for the 530, 570 and 660 nm bands, respectively, while the radiation rates (Er =) were 1.0 ± 0.4 meV, 3.10 ± 1.10 meV and 1.4 ± 0.4 meV corresponding to the three respective bands. Mn doping of Zn(2)SiO(4) nanowires induced ferromagnetism, which was observed above room temperature, with a Curie temperature well above 380 K. The observation of magnetic behavior in this class of semiconductors has potential applications in high temperature spintronics and magneto-optical devices.

Optical analysis of hafnium oxide-aluminum multilayer structures for transparent heat mirrors.

We report on HfO2/Al/HfO2 multilayer thin films for heat mirror applications prepared on corning glass substrates by electron beam evaporation. Films fabricated at a substrate temperature of 100 °C show nano-polycrystals of HfO2 embedded in a disordered lattice according to X-ray diffraction results. Atomic force microscopy revealed that HfO2/Al/HfO2 layers possess smooth surface that is appropriate for optical heat mirror applications. Study of optical properties by UV-Visible spectrophotometer demonstrated that transmittance of HfO2/Al/HfO2 device was decreasing from UV to VIS and then slightly increasing in the NIR regions, with an opposite trend followed by reflectance. Optical constants i.e. refractive index, extinction coefficient, band gap energy, Urbach energy has also been calculated. The optical band gap and Urbach energy are found to be 4.34 eV and 3.164 eV, respectively. The collective oscillation energy loss for heat mirrors applications are also observed.

Removal of micrometer size morphological defects and enhancement of ultraviolet emission by thermal treatment of Ga-doped ZnO nanostructures.

Mixed morphologies of Ga-doped Zinc Oxide (ZnO) nanostructures are synthesized by vapor transport method. Systematic scanning electron microscope (SEM) studies of different morphologies, after periodic heat treatments, gives direct evidence of sublimation. SEM micrographs give direct evidence that morphological defects of nanostructures can be removed by annealing. Ultra Violet (UV) and visible emission depends strongly on the annealing temperatures and luminescent efficiency of UV emission is enhanced significantly with each subsequent heat treatment. X-Ray diffraction (XRD) results suggest that crystal quality improved by annealing and phase separation may occur at high temperatures.