Cu2ZnSnS4 (CZTS)‐based materials have a useful band gap and a high absorption coefficient; however, their power conversion efficiency is low compared with that of CdTe and Cu(In,Ga)Se2‐based solar cells. Two of the factors that strongly affect CZTS solar cell characteristics are the MoS2 layer and the presence of defects. In this study, Mo back‐contact layers were annealed to control MoS2 layer formation and the Na content in the Mo layer before the absorber precursor layer was deposited. The increase in oxygen content in the Mo layer suppressed MoS2 layer formation. In addition, the increase in Na diffusion during the initial stage of the absorber precursor deposition decreased the defect density in the absorber layer and in the absorber–buffer interface. These results were verified through measurements of the external quantum efficiency, the temperature dependence of the open‐circuit voltage (VOC), and admittance spectra. The current densities (JSC) and VOC, as well as the power conversion efficiencies, improved as the annealing temperature of the Mo layer increased, which suggests that CZTS solar cell characteristics can be improved by suppressing MoS2 layer formation and increasing Na content in the Mo layer before deposition of the absorber precursor layer. Copyright © 2014 John Wiley & Sons, Ltd.

Objectives:This study is designed to analyze the penetration performance into ceiling materials containing asbestos of scattering prevention agents and investigate the change in penetration depth and viscosity according to the dilution rate of anti-scattering agents diluted with distilled water. Methods: Five different types of scattering prevention agents were spread on plate-type asbestos ceiling materials. The penetration depth of each coated ceiling material was measured by energy dispersive spectroscopy (EDS) analysis, based on X-ray fluorescence (XRF) results of the non-coated ceiling materials. Test equipment installed the ceiling materials and 60 minutes were collected at a flow rate of 10 ℓ/min at a filter of 25 mm. Results: An EDS analysis of the cross-section of ceiling materials constructed with a scattering prevention agent revealed that potassium is detected in the process of penetrating hardener solidification and this element could be an indicator for infiltration. When anti-scattering agents with different viscosities were constructed and the penetration depth was analyzed by potassium detection assessment using EDS, the depth results with viscosities of 5.0, 2.5, and 1.9 cP were 98.5, 103, and 147 μm, respectively. Penetration performance improved with decrease in viscosity. Conclusions: For asbestos ceiling materials, it is concluded that a higher dilution rate of the scattering prevention agent leads to lower viscosity, and hence a deeper penetration depth from 156 ㎛ to 3 mm. The asbestos anti-scattering properties according to the penetration depth will be confirmed through further study.

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The effect of diluting asbestos stabilizer on its performance of suppressing the asbestos fibre release has been investigated in terms of its penetrability into ceiling materials containing asbestos fibres. The performance of a silicate stabilizer was determined for cases where the ceiling material was damaged by external factors. The higher dilution rate of the stabilizer resulted in lower viscosities and hence greater penetration depths into asbestos ceiling materials. In addition, for cases in which the diluted stabilizer was sprayed several times onto the ceiling materials, the released asbestos fibre concentration was shown to be reduced by approximately 89% compared to the case of damaged ceiling material. Furthermore, this held true in cases where treated ceiling materials were damaged. The optimum condition, considering both performance and efficiency, is for a stabilizer with distilled water to be applied onto the damaged asbestos ceiling materials several times.