Ordered Ag/Si nanowires array: wide-range surface-enhanced Raman spectroscopy for reproducible biomolecule detection.

Surface-enhanced Raman scattering (SERS) systems utilizing the interparticle nanogaps as hot spots have demonstrated ultrasensitive single-molecule detection with excellent selectivity yet the electric fields are too confined in the small nanogaps to enable reproducible biomolecule detections. Here, guided by finite-difference-time-domain simulation, we report hexagonal-packed silver-coated silicon nanowire (Ag/SiNW) arrays as a nanogap-free SERS system with wide-range electric fields and controlled interwire separation. Significantly, the system achieves a SERS detection of long double-strand DNA of 25-50 nm in length with a relative standard deviation (RSD) of 14% for measurements of above 4000 spots over an area of 200 × 200 µm(2). The high reproducibility in the SERS detection is attributed to (1) the large interwire spacing of 150 nm that allows access and excitation of large biomolecules; and (2) 600 nm wide-range electric field generated by propagating surface plasmons along the surface of continuous Ag coating on a SiNW. Moreover, a reproducible multiplex SERS measurement is also demonstrated with RSDs of 7-16% with an enhancement factor of ~10(6). The above results show that the ordered Ag/SiNW array system may serve as an excellent SERS platform for practical chemical and biological detection.

Near-infrared-emitting Cd(x)Hg(1-x)Se nanorods fabricated by ion exchange in an aqueous medium.

Whereas CdSe nanorods that are grown in organic solution have a hexagonal wurtzite structure, which is the limiting case for exchange, HgSe is more commonly encountered as a cubic zinc blende system. An exchange process was performed at room temperature and at atmospheric pressure in an aqueous environment after phase transfer of the original CdSe nanorods, which reinforced the tendency for the endpoint of HgSe to be cubic. Consequently, we observed that under ambient conditions, the exchange process terminated with an average composition of only Cd(0.9)Hg(0.1)Se. Following the changes during the process by optical spectroscopy and high angle annular dark field (HAADF) scanning transmission electron microscopy (STEM), we observed that the Hg(2+) ions diffused into the rods to a point limited by the formation of stacking faults due to the different lattice structures of the two limiting cases of zinc blende and wurtzite. HAADF-STEM and energy dispersive spectroscopy analyses also confirmed that the Hg substitution did not occur uniformly throughout the individual nanorods, as Hg-poor and Hg-rich regions coexist around the stacking faults. The formation of near-infrared-emitting alloyed Cd(x)Hg(1-x)Se nanorods in an aqueous medium highlights the subtle dependence of the ion-exchange process on the differences in the crystal structures of the two endpoint lattices.

Large-scale synthesis of Cu2SnS3 and Cu(1.8)S hierarchical microspheres as efficient counter electrode materials for quantum dot sensitized solar cells.

Exploration of new catalytic semiconductors with novel structures as counter electrode materials is a promising approach to improve performances of quantum dot sensitized solar cells (QDSSCs). In this work, nearly mono-disperse tetragonal Cu(2)SnS(3) (CTS) and rhombohedral Cu(1.8)S hierarchical microspheres with nanometer-to-micrometer dimensions have been synthesized respectively via a simple solvothermal approach. These microspheres are also demonstrated as efficient counter electrode materials in solar cells using ZnO/ZnSe/CdSe nanocables as photoanode and polysulfide (S(n)(2-)/S(2-)) solution as electrolyte. While copper sulfide is regarded as one of the most effective counter electrode materials in QDSSCs, we demonstrate the CTS microspheres to show higher electrocatalytic activity for the reduction of polysulfide electrolyte than the Cu(1.8)S microspheres. This contributes to obvious enhancement of photocurrent density (J(SC)) and fill factor (FF). Power conversion efficiency (PCE) is significantly enhanced from 0.25% for the cell using a pure FTO (SnO(2):F) glass as counter electrode, to 3.65 and 4.06% for the cells using counter electrodes of FTO glasses coated respectively with Cu(1.8)S and CTS microspheres.

Nanostructural transformation and formation of heterojunctions from Si nanowires.

Si nanowires coated with Ni showed interesting structural transformation behaviors as observed by in situ transmission electron microscopy. Owing to the presence of the native oxide on Si nanowire surfaces, the Ni thin shells initially segregated into nanosized droplets on the oxide surfaces. The native oxide shells protected the Si cores from reacting with Ni at temperatures below 1350 °C. Ni started the reaction with Si nanowires preferentially at the defects or bending regions of the nanowires. Because the reaction temperature was sufficiently high, the structural transformation was extremely fast and completed within 0.1 s. The resulting nanowires were single crystalline NiSi(2), the most desirable Ni silicide structure for potential applications. Nanowire junctions of NiSi(2)/Si and nanowire-nanotube junctions of NiSi(2)/SiC have been obtained upon further annealing.

High-quality ZnO nanowire arrays directly fabricated from photoresists.

We report a simple and effective method for fabricating and patterning high-quality ZnO nanowire arrays using carbonized photoresists to control the nucleation site, density, and growth direction of the nanowires. The ZnO nanowires fabricated using this method show excellent alignment, crystal quality, and optical properties that are independent of the substrates. The carbonized photoresists provide perfect nucleation sites for the growth of aligned ZnO nanowires and they also perfectly connect to the nanowires to form ideal electrodes that can be used in many applications of ZnO nanomaterials.