Effects of deposition time and post-deposition annealing on the physical and chemical properties of electrodeposited CdS thin films for solar cell application

CdS thin films were cathodically electrodeposited by means of a two-electrode deposition system for different durations. The films were characterised for their structural, optical, morphological and compositional properties using x-ray diffraction (XRD), spectrophotometry, scanning electron microscopy (SEM) and energy dispersive x-ray (EDX) respectively. The results obtained show that the physical and chemical properties of these films are significantly influenced by the deposition time and post-deposition annealing. This influence manifests more in the as-deposited materials than in the annealed ones. XRD results show that the crystallite sizes of the different films are in the range (9.4 – 65.8) nm and (16.4 – 66.0) nm in the as-deposited and annealed forms respectively. Optical measurements show that the absorption coefficients are in the range (2.7×104 – 6.7×104) cm-1 and (4.3×104 – 7.2×104) cm-1 respectively for as-deposited and annealed films. The refractive index is in the range (2.40 – 2.60) for as-deposited films and come to the value of 2.37 after annealing. The extinction coefficient varies in the range (0.1 – 0.3) in asdeposited films and becomes 0.1 in annealed films. The estimated energy bandgap of the films is in the range (2.48 – 2.50) eV for as-deposited films and becomes 2.42 eV for all annealed films. EDX results show that all the films are S-rich in chemical composition with fairly uniform Cd/S ratio after annealing. The results show that annealing improves the qualities of the films and deposition time can be used to control the film thickness. Keywords: Electrodeposition; two-electrode system; CdS; annealing; deposition time; thin-film

Scientific complications and controversies noted in the field of CdS/CdTe thin film solar cells and the way forward for further development

Cadmium telluride-based solar cell is the most successfully commercialised thin film solar cell today. The laboratory-scale small devices have achieved ~ 22%, and commercial solar panels have reached ~ 18% conversion efficiencies. However, there are various technical complications and some notable scientific contradictions that appear in the scientific literature published since the early 1970s. This review paper discusses some of these major complications and controversies in order to focus future research on issues of material growth and characterisation, post-growth processing, device architectures and interpretation of the results. Although CdTe can be grown using more than 14 different growth techniques, successful commercialisation has been taken place using close-space sublimation and electrodeposition techniques only. The experimental results presented in this review are mainly based on electrodeposition. Historical trends of research and commercial successes have also been discussed compared to the timeline of novel breakthroughs in this field. Deeper understanding of these issues may lead to further increase in conversion efficiencies of this solar cell. Some novel ideas for further development of thin film solar cells are also discussed towards the end of this paper

A comparative study of microstructural stability and sulphur diffusion in CdS/CdTe photovoltaic devices

The role of CdCl2 activation in the production of high quality CdTe-based photovoltaic devices remains a subject of much debate. In this study, CdTe-based cells produced in three independent laboratories using different device fabrication technologies are investigated before and after CdCl2 activation with regard to structural changes (recrystallisation and grain growth) and sulphur out-diffusion. Using scanning transmission electron microscopy (STEM) and x-ray diffraction it is demonstrated that CdCl2 activation of the investigated cells produces no statistical structural changes to the CdTe. Additionally, energy dispersive spectrometry (EDS) performed in the STEM on the same samples illustrates that the change in sulphur diffusion following activation is more limited than expected from previous studies; no change is detectable when the thermal budget for CdTe deposition is significantly greater than that for activation. This suggests that the efficiency enhancement during CdCl2 treatment is not due to sulphur out-diffusion. Lastly, cathodoluminescence microscopy is used to demonstrate in two dimensions how sulphur diffuses into a model sample and the results are found to be consistent with STEM–EDS. Some spectroscopic evidence for enhanced sulphur diffusion along grain boundaries is also observed