Effect of precursors on structure, optical and electrical properties of chemically deposited nanocrystalline ZnO thin films

被引:31
|
作者
Prajapati, C. S. [1 ]
Sahay, P. P. [1 ]
机构
[1] Motilal Nehru Natl Inst Technol, Dept Phys, Allahabad 211004, Uttar Pradesh, India
关键词
Zinc oxide; Nanocrystalline thin films; Structural properties; Optical Properties; Activation energy; SPRAY-PYROLYSIS TECHNIQUE; GAS SENSOR APPLICATIONS; ETHANOL SENSORS; TRANSPARENT; BATH;
D O I
10.1016/j.apsusc.2011.10.141
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanocrystalline ZnO thin films were chemically deposited on glass substrates using two different precursors namely, zinc sulphate and zinc nitrate. XRD studies confirm that the films are polycrystalline zinc oxide having hexagonal wurtzite structure with crystallite size in the range 25-33 nm. The surface morphology of film prepared using zinc sulphate exhibits agglomeration of small grains throughout the surface with no visible holes or faulty zones, while the film prepared using zinc nitrate shows a porous structure consisting of grains with different sizes separated by empty spaces. The film prepared using zinc sulphate shows higher reflectance due to its larger refractive index which is related to the packing density of grains in the film. Further, the film prepared using zinc sulphate is found to have normal dispersion for the wavelength range 550-750 nm, whereas the film prepared using zinc nitrate has normal dispersion for the wavelength range 450-750 nm. The direct optical band gaps in the two films are estimated to be 3.01 eV and 3.00 eV, respectively. The change in film resistance with temperature has been explained on the basis of two competing processes, viz. thermal excitation of electrons and atmospheric oxygen adsorption, occurring simultaneously. The activation energies of the films in two different regions indicate the presence of two energy levels - one deep and one shallow near the bottom of the conduction band in the bandgap. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2823 / 2828
页数:6
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