Photon-induced formation of CdS nanocrystals in selected areas of polymer matrices

We demonstrate light-induced formation of semiconductor quantum dots in TOPAS (R) polymer matrix with very high control of their size and their spatial localization. Irradiation with UV laser pulses of polymer films embedding Cd thiolate precursors results in the formation of cadmium sulfide nanocrystals well confined in the irradiation area, through a macroscopically nondestructive procedure for the host matrix. With increasing number of laser pulses, we accomplish the formation of nanoparticles with gradually increasing dimensions, resulting in the dynamic change of the spectra emitted by the formed nanocomposite areas. The findings are supported by x-ray diffraction and transmission electron microscopy measurements. (C) 2007 American Institute of Physic

Strain gauge properties of Pd+-ion-implanted polymer:

Pd+ ions (90 keV) were implanted at normal incidence and at room temperature in different highly insulating (>200 GΩ) thermoplastic polymers (poly(methyl methacrylate), polypropylene, polyethylene terephthalate glycol-modified, and polycarbonate). At high fluence and optimized process parameters, the ion implantation gives rise to the formation of a nanocomposite thin surface layer constituted by Pd nanoclusters and carbonaceous material (nanographite/amorphous carbon). The morphological, microstructural, and microanalytical properties of the nanocomposite layers were investigated by He-ion microscopy, glancing incidence X-ray diffraction, and Raman scattering, respectively. The electrical properties were characterized by resistance, van der Pauw, and Hall measurements. We performed accurate simultaneous deformation/bending experiments and electrical resistance measurements. We show that the electrical resistance varies linearly with the mechanical deformation (beam deflection) applied. The experimental results are interpreted by "hopping conductivity" model considering the nanostructure configuration of the nanocomposite layers. A gauge factor in the range between 4 and 8, depending on the ion-implanted polymer, was obtained for prototype strain gauge devices

Synthesis and Microstructural Investigations of Organometallic Pd(II) Thiol-Gold Nanoparticles Hybrids

In this work the synthesis and characterization of gold nanoparticles functionalized by a novel thiol-organometallic complex containing Pd(II) centers is presented. Pd(II) thiol,trans, trans-[dithiolate-dibis(tributylphosphine)dipalladium(II)-4,4′-diethynylbiphenyl] was synthesized and linked to Au nanoparticles by the chemical reduction of a metal salt precursor. The new hybrid made of organometallic Pd(II) thiol-gold nanoparticles, shows through a single S bridge a direct link between Pd(II) and Au nanoparticles. The size-control of the Au nanoparticles (diameter range 2–10 nm) was achieved by choosing the suitable AuCl4−/thiol molar ratio. The size, strain, shape, and crystalline structure of these functionalized nanoparticles were determined by a full-pattern X-ray powder diffraction analysis, high-resolution TEM, and X-ray photoelectron spectroscopy. Photoluminescence spectroscopy measurements of the hybrid system show emission peaks at 418 and 440 nm. The hybrid was exposed to gaseous NOxwith the aim to evaluate the suitability for applications in sensor devices; XPS measurements permitted to ascertain and investigate the hybrid –gas interaction

Multi-photon in situ synthesis and patterning of polymer-embedded nanocrystals

The in situ synthesis and patterning of CdS nanocrystals in a polymer matrix is performed via multi-photon absorption. Quantum-sized CdS nanocrystals are obtained by irradiating a cadmium thiolate precursor dispersed in a transparent polymer matrix with a focused near infrared femtosecond laser beam. High resolution transmission electron microscopy evidences the formation of nanocrystals with wurtzite crystalline phase. Fluorescent, nanocomposite patterns with sub-micron spatial resolution are fabricated by scanning the laser beam on the polymer-precursor composite. Moreover, the emission energy of the CdS nanocrystals can be tuned in the range 2.5-2.7 eV, by changing the laser fluences in the range 0.10-0.45 J cm -2. This method enables therefore the synthesis of luminescent, CdS-based composites to be used within patterned nanophotonic and light-emitting devices

Mono- and bi-functional arenethiols as surfactants for gold nanoparticles: synthesis and characterization

Stable gold nanoparticles stabilized by different mono and bi-functional arenethiols, namely, benzylthiol and 1,4-benzenedimethanethiol, have been prepared by using a modified Brust's two-phase synthesis. The size, shape, and crystalline structure of the gold nanoparticles have been determined by high-resolution electron microscopy and full-pattern X-ray powder diffraction analyses. Nanocrystals diameters have been tuned in the range 2 ÷ 9 nm by a proper variation of Au/S molar ratio. The chemical composition of gold nanoparticles and their interaction with thiols have been investigated by X-ray photoelectron spectroscopy. In particular, the formation of networks has been observed with interconnected gold nanoparticles containing 1,4-benzenedimethanethiol as ligand

Atomic pair distribution function (PDF) study of iron oxide nanoparticles in aqueous suspension

Size is the key regulating the crystalline structure of iron oxide nanoparticles. The effect of the crystal size on the microstructure of these nanoparticles was investigated in an aqueous dilute suspension by energy dispersive X-ray diffraction (EDXD) and in an aqueous concentrated suspension by X-ray powder diffraction (XRD), at 293 K. Nanoparticle structure was also investigated by HRTEM. Structural results were interpreted in terms of theoretical models built using structural parameters obtained by the Rietveld method on XRD. The ability of the pair distribution function (PDF) to measure medium-range correlation lengths and size in nanoscale crystalline materials was also investigated and discussed. The sensitivity of the PDF technique allowed modelling of sample polydispersity

Ligand mediated synthesis of AgInSe2 nanoparticles with tetragonal/orthorhombic crystal phases

Nanosized AgInSe2 particles (d similar to 7-25 nm) were synthesized using colloidal chemistry method at 270 degrees C. As solvents/surface ligands 1-octadecene, trioctylphosphine, and oleylamine were used. It was shown that choice of ligand has crucial impact not only on final crystal phase of nanoparticles, but also at mechanism of crystal growth. X-ray diffraction and TEM/HRTEM techniques were used to identify obtained crystal phases and to measure average size and shape of nanoparticles. UV/Vis data were used to estimate band-gap energies of obtained samples. It was shown that presented routes can provide synthesis of nanoparticles with desired crystal phase (tetragonal and/or orthorhombic), with band-gap energies in the range from 1.25 to 1.53 eV

Structural and Optical Characterization of Flower-Like Rutile Nanostructures Doped with Fe3+

Flower-like agglomerates with sizes of 200-400 nm of pure and Fe3+-doped TiO2 with rutile crystalline structure were synthesized by the coprecipitation method. The morphology of the agglomerates was determined by electron microscopy (TEM and HRTEM). TiO2 agglomerates consist of nanorods with clearly visible crystalline faces, parallel to the axis of elongation whose direction was along the [101] direction of pure TiO2 and the [111] direction of doped TiO2. Furthermore, nanorods consist of chains of spherical particles, most likely interconnected through the so-called oriented attachment or grain-rotation-induced grain coalescence (GRIGC) process. UV/Vis reflection measurements revealed that the absorption of pure TiO2 was significantly shifted from UV toward the visible spectral region upon the incorporation of Fe3+ into the TiO2 host