Preparation of Polycrystalline Cds Thin Films by Chemical Bath Deposition

1995 ◽  
Vol 410 ◽  
Author(s):  
Eun A Lee ◽  
Bum-Soo Kim ◽  
Sung Ho Shin ◽  
Jung Il Park ◽  
Kwang Ja Park
Keyword(s):  
Thin Films ◽  
Heat Treatment ◽  
Optical Properties ◽  
Chemical Bath Deposition ◽  
Reaction Temperature ◽  
Ammonium Acetate ◽  
Cadmium Acetate ◽  
Structural And Optical Properties ◽  
Cds Thin Films

ABSTRACTWe prepared CdS thin films from a solution containing cadmium acetate, thiourea, ammonia, and ammonium acetate. We varied fabrication conditions such as the concentrations of reactants, reaction temperature, and heat treatment, to investigate the changes in structural and optical properties of the film. Effects of substrate on the properties were also investigated.

Effect of Ammonium Acetate Concentration on the Structural and Optical Properties of CdS Thin Film Grown by Chemical Bath Deposition Technique

MRS Advances ◽  
2016 ◽  
Vol 1 (37) ◽  
pp. 2603-2616
Author(s):  
Hamda A. Al-Thani ◽  
Abeer A. Al Yafeai ◽  
Falah S. Hasoon
Keyword(s):  
Thin Films ◽  
Optical Properties ◽  
Chemical Bath Deposition ◽  
Ammonium Acetate ◽  
Energy Dispersive Spectrometer ◽  
Chemical Properties ◽  
Cadmium Acetate ◽  
Deposition Process ◽  
Cds Thin Films ◽  
Cds Films

ABSTRACTThis study focuses on understanding the influence of incorporating Ammonium Acetate into the chemical bath used for the deposition of CdS thin films, on its optical, morphology, and microstructural properties. Thus, CdS thin films were deposited on 1” × 2” microscopic glass substrates using chemical bath deposition (CBD) technique. The deposition process was carried out in a double jacket beaker with fixed chemical bath temperature of 90°C for a deposition time of 40 min. The chemical bath solution consisted of fixed concentrations of Cadmium Acetate, Thiourea, and Ammonium Hydroxide; with corresponding values of 4.8×10-4M; 0.97×10-4M; and 0.2M, respectively. However, Ammonium Acetate was incorporated into the deposition bath with concentrations that were varied from 3.0 mM to 12.2 mM. Meanwhile, for comparison purposes associated to the initial physical and chemical properties of the CdS films; reference CdS films were deposited under the same above chemical bath conditions, but in the absence of Ammonium Acetate. The pH of the chemical bath was measured during the deposition process. The films’ morphology and the chemical composition were examined by Field Emission Scanning Electron Microscopy (FE-SEM), and the Energy Dispersive spectrometer (EDS), respectively. The X-Ray Diffraction (XRD) θ/2θ technique was applied to study the structure of the films, including the lattice parameters. Atomic Force Microscopy (AFM) was used to examine the films topography and to determine the root-mean-square (RMS) surface roughness of the films as well as the grain size. Dektak Surface Profilometer was used to determine the CdS films’ thickness, where the films’ optical properties were measured using UV-Vis-NIR spectrometer. Optical energy band gap (Eg), and absorption coefficient (α) were calculated from the transmission spectral data.

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