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A series of cadmium telluride (CdTe) nanocrystals were synthesized by a modified organometallic synthesis method at various reaction temperatures ranging from 130 to 250°C. In this method, octadecylamine (ODA) was introduced as an additional coordinating component to the mixture of trioctylphosphine oxide (TOPO) and trioctylphosphine (TOP). CdO was used as a precursor. The prepared CdTe nanocrystals were studied by the absorption and emission spectra as well as the powder X-ray diffraction (XRD) patterns. The result shows that besides the traditional continuous-growth mode observed frequently at relatively high reaction temperature, a discontinuous-growth mode was confirmed at the initial growth stage of CdTe nanocrystals, arising from the change of the absorption spectra of CdTe nanocrystals with the reaction time at relatively low reaction temperature. The structures of CdTe nanocrystals, e.g., the cubic zinc blende structure at 160°C and the hexagonal wurtzite structure at 250°C, were characterized by XRD.
Colloidal CdSe nanocrystals (NCs) were etched after Se/TBP and Zinc stearate/ODE were injected into the mixture of as-prepared CdSe NCs and Copper (II) acetate in ODE solvent. Spectroscopic and structural investigations demonstrate the etching process. Along with the etching time, both the absorption and photoluminescence (PL) spectra of etched NCs showed blue-shift while the transmission electron microscopy (TEM) images indicated that the size of the NCs became from 5.6nm to 2.6nm. X-ray diffraction (XRD) patterns suggested that no other clusters or core/shell NCs were formed in the etching process and inductively coupled plasma (ICP) data demonstrated that only selenium and cadmium comprised the etched NCs. Electronic paramagnetic resonance (EPR) spectra indicated the deoxidization of Cu2+ ions and suggested the etching mechanism through cation exchange process.
A novel procedure to fabricate nanoarchitectures of crystalline titania hollow shells was developed by using assembled latex particles as templates. Latex particles were assembled on the surface of solid substrates and covered with ultrathin titania films by the surface sol–gel process. When the titania-covered latex particle was subjected to oxygen plasma treatment, hollow titania spheres were formed at the original site of particle deposition. Following calcination of the amorphous, titania hollow shells induced their crystallization to titania nanocrystals (anatase).
Monodispersed DAST nanocrystals have almost been successfully fabricated by means of the inverse reprecipitation method. By employing AC electric field, high electric field of above ca. 1.0 kVcm-1 could be applied to polar DAST nanocrystals dispersed in decahydronaphthalene, so as to avoid electrophoresis of nanocrystals under DC electric field. The response of DAST nanocrystal dispersion to applied AC electric field was analyzed phenomenologically by fitting Langevin function, which provided a large permanent dipole moment of DAST nanocrystal. In addition, we have succeeded in in situ observation of AC electric-field-induced orientational motion of DAST crystals by using an optical microscope. The present DAST nanocrystal dispersion system will be expected as an optical device like display monitor.