2010
DOI: 10.1016/j.tsf.2010.07.011
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Effect of CdCl2 annealing treatment on thin CdS films prepared by chemical bath deposition

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Cited by 56 publications
(45 citation statements)
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“…2(b). 22 It can be seen that the nano-crystalline size was decreased from 31.5 nm for the undoped CdS to a value of 27.4 nm for the 5% Cu doped CdS film. After the CdCl 2 -annealing, the characteristics hexagonal H(103) peak was observed for all the samples, see Fig.…”
Section: Resultsmentioning
confidence: 92%
See 1 more Smart Citation
“…2(b). 22 It can be seen that the nano-crystalline size was decreased from 31.5 nm for the undoped CdS to a value of 27.4 nm for the 5% Cu doped CdS film. After the CdCl 2 -annealing, the characteristics hexagonal H(103) peak was observed for all the samples, see Fig.…”
Section: Resultsmentioning
confidence: 92%
“…22,31 For the three CdS samples doped with different Cu doping concentrations, after the CdCl 2 -annealing, see Fig. 6(b), the V Cd -related defect emission intensity for the 0.1%-Cu-doped sample was much larger than that of the 0.3% and 0.5%-Cu-doped samples.…”
Section: Resultsmentioning
confidence: 94%
“…Oxides (CdO and CdSO 4 ) formed when a CdS film was heat treated without a CdCl 2 precoating in air. The detailed formation mechanism of the oxides and the CdS grain coalescence process was discussed in details in our previous work [9]. The presence of oxides in a CdS film heat treated without CdCl 2 in air prevented the clusters to be coalesced at high temperatures.…”
Section: Resultsmentioning
confidence: 98%
“…These oxides will also affect the performance of a CdTe/CdS solar cell. The presence of CdCl 2 on the surface of a CdS film protected it from oxidation during annealing in air and promoted formation of Cl S and V Cd point defects in CdS [9]. The anti-oxidation was attributed to the incorporation of a significant amount of Cl into CdS to form the Cl S , which prevented the oxygen in-diffusion and chemical bonding during the annealing.…”
Section: Resultsmentioning
confidence: 99%
“…The green band emission observed at 2.28 eV has been originated from the transition of the increased V s donors to recombine with S interstitials (I s ) acceptors in the valence band [25]. The yellow band emission observed at 2.04 eV is caused by a donor-acceptor pair [26]. Ahmad-Bitar [27] reported a similar band for CdS thin films which they attributed to recombination via surface localized states, a transition from cadmium interstitial (I Cd ) to valence band, and the transition from interstitial cadmium-cadmium vacancy complex I + Cd −V − Cd which acts as a donor to an acceptor level.…”
Section: Pl Studiesmentioning
confidence: 99%