Facile synthesis of Cu2O nanorods in the presence of NaCl by successive ionic layer adsorption and reaction method and its characterizations.

Cuprous oxide (Cu2O) nanorods have been deposited on soda-lime glass substrates by the modified successive ionic layer adsorption and reaction technique by varying the concentration of NaCl electrolyte into the precursor complex solution. The structural, electrical and optical properties of synthesized Cu2O nanorod films have been studied by a variety of characterization tools. Structural analyses by X-ray diffraction confirmed the polycrystalline Cu2O phase with (111) preferential growth. Raman scattering spectroscopic measurements conducted at room temperature also showed characteristic peaks of the pure Cu2O phase. The surface resistivity of the Cu2O nanorod films decreased from 15 142 to 685 Ω.cm with the addition of NaCl from 0 to 4 mmol and then exhibited an opposite trend with further addition of NaCl. The optical bandgap of the synthesized Cu2O nanorod films was observed as 1.88-2.36 eV, while the temperature-dependent activation energies of the Cu2O films were measured as about 0.14-0.21 eV. Scanning electron microscope morphologies demonstrated Cu2O nanorods as well as closely packed spherical grains with the alteration of NaCl concentration. The Cu2O phase of nanorods was found stable up to 230°C corroborating the optical bandgap results of the same. The film fabricated in presence of 4 mmol of NaCl showed the lowest resistivity and activation energy as well as comparatively uniform nanorod morphology. Our studies demonstrate that the nominal presence of NaCl electrolytes in the precursor solutions has a significant impact on the physical properties of Cu2O nanorod films which could be beneficial in optoelectronic research.

Three-dimensional band structure and surface electron accumulation of rs-CdxZn1-xO studied by angle-resolved photoemission spectroscopy.

Three-dimensional band structure of rock-salt (rs) CdxZn1-xO (x = 1.0, 0.83, and 0.60) have been determined by angle-resolved photoemission spectroscopy (ARPES) using synchrotron radiation. Valence-band features shift to higher binding energy with Zn content, while the conduction band position does not depend strongly on Zn content. An increase of the indirect band gap with Zn-doping is larger than that of the direct band gap, reflecting a weaker hybridization between Zn 3d and O 2p than that between Cd 4d and O 2p. Two-dimensional electronic states due to the quantization along surface normal direction are formed in the surface accumulation layer and show non-parabolic dispersions. Binding energy of the quantized two-dimensional state is well reproduced using an accumulation potential with the observed surface band bending and the characteristic width of about 30 Å.