Visible fluorescence induced by the metal semiconductor transition in composites of carbon nanotubes with noble metal nanoparticles

We show that single-walled carbon nanotube (SWNT) bundles emit visible fluorescence in the presence of noble metal nanoparticles and nanorods in the solid state. Conductivity measurements with metallic nanotubes, isolated from pristine SWNTs, show that they become semiconducting in the presence of the metal nanoparticles. Nanoparticle binding increases the defects in the nanotube structures which is evident in the Raman spectra. The metal-semiconductor transition removes the nonradiative decay channels of the excited states enabling visible fluorescence. Nanotube structures are imaged using this emission with resolution below the classical limits

Anisotropic nanomaterials: structure, growth, assembly, and functions

Comprehensive knowledge over the shape of nanomaterials is a critical factor in designing devices with desired functions. Due to this reason, systematic efforts have been made to synthesize materials of diverse shape in the nanoscale regime. Anisotropic nanomaterials are a class of materials in which their properties are direction-dependent and more than one structural parameter is needed to describe them. Their unique and fine-tuned physical and chemical properties make them ideal candidates for devising new applications. In addition, the assembly of ordered one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) arrays of anisotropic nanoparticles brings novel properties into the resulting system, which would be entirely different from the properties of individual nanoparticles. This review presents an overview of current research in the area of anisotropic nanomaterials in general and noble metal nanoparticles in particular. We begin with an introduction to the advancements in this area followed by general aspects of the growth of anisotropic nanoparticles. Then we describe several important synthetic protocols for making anisotropic nanomaterials, followed by a summary of their assemblies, and conclude with major applications

Reversible assembly and disassembly of gold nanorods induced by EDTA and its application in SERS tuning

A facile and reversible method for assembling and disassembling gold nanorods (GNRs) using a common chelating agent, ethylenediaminetetraacetic acid (EDTA), is reported. Assembly was induced by the electrostatic interaction between the cetyltrimethylammonium bromide (CTAB) bilayer present on GNRs and EDTA. At lower concentrations of EDTA, end-to-end assembled chains were formed. At higher concentrations of EDTA, these chains come together to form sheet-like structures. The complex of CTAB and EDTA, being labile, disassembles in the presence of stronger chelating agents. Upon addition of metal ions having higher formation constants, EDTA detaches from the GNRs and forms stronger complexes with metal ions, resulting in disassembly. Characteristic changes were observed in the UV/vis spectra. Addition of EDTA resulted in a red shift of longitudinal surface plasmon (LSP) resonance at lower concentrations, indicating an end-to-end assembly. At higher concentrations, the characteristic of side-by-side assembly was seen in the UV/vis spectra. TEM analysis proved the existence of end-to-end chains at lower concentrations of EDTA and side-by-side assembled sheet-like structures at higher concentrations. The addition of metal ions induced disassembly. Even 2 ppb of metal ion was detected using the spectral changes. Disassembly was studied in detail, taking Pb(II) as the model system. Upon addition of Pb(II), TSP showed a blue shift and decreased in intensity while the LSP showed a red shift and increased in intensity. A new peak at a higher wavelength region emerged, pointing to the existence of both side-by-side and end-to-end assembly in the system. TEM analysis showed that the disassembly involves the formation of bundled chains which may be the reason for the observed spectral changes. Surface-enhanced Raman scattering (SERS) activity of the system could be tuned by controlling the concentration of EDTA and the metal ion, Pb(II)

Tubular nanostructures of Cr<SUB>2</SUB>Te<SUB>4</SUB>O<SUB>11</SUB> and Mn<SUB>2</SUB>TeO<SUB>6</SUB> through room temperature chemical transformations of tellurium nanowires

Tubular ternary nanostructures of tellurium were made through chemical transformations of tellurium nanowires (Te NWs). These transformations occur through reactions with CrO3 and KMnO4, two of the strongest oxidizing agents. In the case of CrO3, the 1D structure of the NWs remained intact and the morphology changed to hollow wires of Cr2Te4O11, but reaction with KMnO4 resulted in the loss of 1D structure, forming a carbon onion-like object composed of Mn2TeO6. As the reaction proceeded, the crystallinity of the NWs decreased, and the final products were amorphous. The reaction products were characterized using different spectroscopic and microscopic techniques. Time-dependent transmission electron microscopic (TEM) analysis of both of the reaction products showed that first a shell is formed around the NWs. Further reaction results in the formation of hollow structures. During the reaction with CrO3, TEM in the intermediate stages showed that the periphery of the material was amorphous, whereas the inside, where unreacted parts of Te NWs remained, was crystalline with a clear lattice structure. X-ray photoelectron spectroscopy (XPS) as well as Raman spectroscopy showed a redox reaction in both cases. Studies suggest that both redox reactions and nanoscale Kirkendall effect might be involved in the formation mechanism