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This work describes the synthesis and magnetic–optical properties of Fe 3 O 4 nanowires decorated by CdTe quantum dots. The composite nanowires with a length of 1 μm and an average diameter of 23±3 nm were prepared in a high yield through the preferential growth of Fe 3 O 4 on CdTe quantum dots using ethylenediamine as template. Their growth mechanism was discussed based on the results of control experiments. Studies on the optical and magnetic properties of the composite nanowires reveal that they assume not only yellow-green emission feature but also room temperature ferromagnetism.

High-quality Cu3Se2 nanoplates were synthesized in a large scale through microwave-enhanced reaction between selenium and copper(I) oleate. The nanoplates are approximately round with thickness of 17 nm and the diameter in the range of 700∼1000 nm. The distinct shape of the nanoplates provides an ideal site for combining functional units, and as an example, carboxyl-terminated CdTe quantum dots were adsorbed onto Cu3Se2 nanoplates to form Cu3Se2−CdTe nanocluster by the chemical linkage of carboxyl to Cu. The fabricated nanoclusters exhibit an enhanced photovoltaic property (i.e., large photocurrent and short response time). Furthermore, this work provides a rational method to the design and fabrication of quantum dots decorated semiconductor nanocomposites.

In this manuscript we have demonstrated a template-free route to the preparation of hollow In 2 S 3 nanospheres by solvothermally treating solid In 2 S 3 spheres comprised of small particles at 180 °C for 24 h. This method is simple but highly efficient, which can transform the solid precursors into hollow nanostructures in an extremely high yield. Investigations into the intermediates reveal that the formation of hollow spheres is through the mergence of the smaller particles within the solid spheres by the relatively large ones in the ripening process (i.e., Ostwald ripening). The well crystalline hollow nanospheres have the diameters of 40–70 nm and an average wall thickness of 7 nm. Due to the closeness of the size of hollow nanospheres to the Bohr radius (33.8 nm) of the excition in In 2 S 3 , an obvious quantum size confinement and morphology-dependent property are observed. Hollow In 2 S 3 nanospheres show an intense absorption between 318 and 512 nm, which is blue-shifted to shorter wavelengths relative to that of bulk In 2 S 3 . Hollow In 2 S 3 nanospheres also exhibit a strong photoluminescence. The green band centered 518 nm is due to the band-band transitions and the orange emission centered at 624 nm originates from the indium interstitial defect. These hollow In 2 S 3 nanospheres could be used as a distinctive multicolored phosphor and material for producing photoelectrochemical devices.

The dielectric properties of Z-type hexaferrite Sr3Co2Fe24O41 (SCFO) have been investigated as a function of temperature from 153 to 503 K between 1 and 2 GHz. The dielectric responses of SCFO are found to be frequency dependent and thermally activated. The relaxation-type dielectric behavior is observed to be dominating in the low frequency region and resonance-type dielectric behavior is found to be dominating above 108 Hz. This frequency dependence of dielectric behavior is explained by the damped harmonic oscillator model with temperature dependent coefficients. The imaginary part of impedance (Z″) and modulus (M″) spectra show that there is a distribution of relaxation times. The scaling behaviors of Z″ and M″ spectra further suggest that the distribution of relaxation times is temperature independent at low frequencies. The dielectric loss spectra at different temperatures have not shown a scaling behavior above 108 Hz. A comparison between the Z″ and the M″ spectra indicates that the short-range charges motion dominates at low temperatures and the long-range charges motion dominates at high temperatures. The above results indicate that the dielectric dispersion mechanism in SCFO is temperature independent at low frequencies and temperature dependent at high frequencies due to the domination of resonance behavior.

This work describes the synthesis and magnetic–optical properties of Fe 3 O 4 nanowires decorated by CdTe quantum dots. The composite nanowires with a length of 1 μm and an average diameter of 23±3 nm were prepared in a high yield through the preferential growth of Fe 3 O 4 on CdTe quantum dots using ethylenediamine as template. Their growth mechanism was discussed based on the results of control experiments. Studies on the optical and magnetic properties of the composite nanowires reveal that they assume not only yellow-green emission feature but also room temperature ferromagnetism.