BURSTEIN–MOSS SHIFT IN CdS NANOCRYSTALLITES SYNTHESIZED VIA AQUEOUS PRECIPITATION

We report here the UV-VIS study of CdS nanoparticles synthesized via Chemical precipitation in aqueous medium, the UV-VIS of CdS in aqueous medium shows an excitonic peak at 230 nm, while that of CdS quantum dots in solid form shows an absorption maximum at 480 nm. This bleaching of band gap may be attributed to Moss–Burstein shift in the absorbance edge.

Structural, optical and electrical properties of the novel semiconductor alloy ZnOxTe(1-x)

ABSTRACTEpitaxial films of undoped ZnOxTe(1-x) have been prepared on double-side polished c-axis oriented sapphire substrates with pulsed laser deposition. The method of epitaxial growth is expected to have the same domain matching epitaxial relationship with sapphire as does pure ZnO, where six lattice planes of ZnOxTe(1-x) match with seven lattice planes of sapphire [1,2]. High quality, single crystal, epitaxial alloys with around 4% Te have been grown that demonstrate excellent optical properties and a pronounced, sharp excitonic peak, in optical transmission. The incorporation of Te makes the compound more covalent, and less ionic than pure ZnO. Transmission electron microscopy (TEM) demonstrates single-crystal growth with a sharp interface. The low-resolution X-ray diffraction (XRD) pattern of ZnOxTe(1-x) films is almost indistinguishable from those of pure ZnO, except a usually diminished intensity of the (0004) peak. The incorporation of Te in ZnO was verified by a shift in excitonic peak position in absorption, and through a shift in cathodoluminescence (CL) peak. X-ray photoelectron spectroscopy (XPS) data verifies incorporation of telluride chemical state of tellurium atoms. Rutherford backscattering/channeling (RBS/C) confirmed crystal quality for the pure ZnO films. Hot-point probe measurements indicate as-grown, undoped films to be somewhat higher in resistivity than pure ZnO with inconclusive carrier type, as compared to the naturally n-type ZnO. This may be a consequence of the more covalent bonding between Zn and Te and suggests a possible strategy for p-type doping.