Optical and electrical properties of Sn-doped CdO thin films obtained by pulse laser deposition

Transparent tin-doped cadmium oxide (Sn-CdO) thin films with different Sn concentration were deposited on quartz glass substrates by pulse laser deposition (PLD) at 400 °C. The film’s crystallographic structure, optical and electrical properties were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), UV-VIS spectrophotometer and Hall system. Results show that doping of Sn enhances the film’s [111] preferred orientation and causes slight shift in the (200) Bragg angle towards higher value. The optical band gaps (E_g) of the Sn-doped films were found to increase with the increase of Sn doping concentration. In addition, proper doping of Sn evidently improves the electrical properties of CdO, such as the resistivity of the CdO film with 2.9 at% Sn doping is about one-twelfth of that of the CdO film, while the carrier concentration is about 13 times of that of the undoped. The improvements both in optical and electrical properties endow that the Sn-CdO thin films have potential application as TCO material for different optoelectronic device applications.     

Effects of alternating and direct current in electrocoagulation process on the removal of cadmium from water

In practice, direct current (DC) is used in an electrocoagulation processes. In this case, an impermeable oxide layer may form on the cathode as well as corrosion formation on the anode due to oxidation. This prevents the effective current transfer between the anode and cathode, so the efficiency of electrocoagulation processes declines. These disadvantages of DC have been diminished by adopting alternating current (AC) in electrocoagulation processes. The main objective of this study is to investigate the effects of AC and DC on the removal of cadmium from water using aluminum alloy as anode and cathode. The results showed that the removal efficiency of 97.5 and 96.2% with the energy consumption of 0.454 and 1.002 kWh kl⁻¹ was achieved at a current density of 0.2 A/dm² and pH of 7.0 using aluminum alloy as electrodes using AC and DC, respectively. For both AC and DC, the adsorption of cadmium was preferably fitting Langmuir adsorption isotherm, the adsorption process follows second order kinetics and the temperature studies showed that adsorption was exothermic and spontaneous in nature.     

Effects of dissolved organic matter from the rhizosphere of the hyperaccumulator Sedum alfredii on sorption of zinc and cadmium by different soils

Pot experiments were conducted to investigate the changes of the dissolved organic matter (DOM) in the rhizosphere of hyperaccumulating ecotype (HE) and non-hyperaccumulating ecotype (NHE) of Sedum alfredii and its effects on Zn and Cd sorption by soils. After planted with HE, soil pH in the rhizosphere reduced by 0.5-0.6 units which is consistent with the increase of DOM. The hydrophilic fractions (51%) in DOM from the rhizosphere of HE (HE-DOM) was much greater than NHE-DOM (35%). In the presence of HE-DOM, Zn and Cd sorption capacity decreased markedly in the following order: calcareous clay loam > neutral clay loam > acidic silty clay. The sorption isotherms could be well described by the Freundlich equation (R² > 0.95), and the partition coefficient (K) in the presence of HE-DOM was decreased by 30.7-68.8% for Zn and 20.3-59.2% for Cd, as compared to NHE-DOM. An increase in HE-DOM concentration significantly reduced the sorption and increased the desorption of Zn and Cd by three soils. DOM derived from the rhizosphere of the hyperaccumulating ecotype of S. alfredii could significantly reduce metal sorption and increase its mobility through the formation of soluble DOM-metal complexes.     

Phytochelatin synthase activity as a marker of metal pollution

The synthesis of phytochelatins is catalyzed by γ-Glu-Cys dipeptidyl transpeptidase called phytochelatin synthase (PCS). Aim of this study was to suggest a new tool for determination of phytochelatin synthase activity in the tobacco BY-2 cells treated with different concentrations of the Cd(II). After the optimization steps, an experiment on BY-2 cells exposed to different concentrations of Cd(NO₃)₂ for 3 days was performed. At the end of the experiment, cells were harvested and homogenized. Reduced glutathione and cadmium (II) ions were added to the cell suspension supernatant. These mixtures were incubated at 35 °C for 30 min and analysed using high performance liquid chromatography coupled with electrochemical detector (HPLC-ED). The results revealed that PCS activity rises markedly with increasing concentration of cadmium (II) ions. The lowest concentration of the toxic metal ions caused almost three fold increase in PCS activity as compared to control samples. The activity of PCS (270 fkat) in treated cells was more than seven times higher in comparison to control ones. K_m for PCS was estimated as 2.3 mM.     

Characteristics of the CdZnS thin film doped by thermal diffusion of vacuum evaporated indium films

Effects of the thickness of indium films and the annealing temperature on structural, optical and electrical properties of chemically deposited cadmium zinc sulfide (CdZnS) films were investigated. X-ray diffraction patterns of CdZnS films indicate that the minimum thickness and annealing temperature for the formation of an In₂O₃ layer, which acts as a barrier preventing the out-diffusion of indium, are 20 nm and 350°C, respectively. In₂O₃ layers give the high optical transmittance due to their transparent properties. As the thickness of indium film and the annealing temperature increase, the conductivity of CdZnS films improves and the lowest resistivity of 0.3 Ω cm is attained for CdZnS films with 40 nm indium coating and annealed at 450°C.     

Biosorptive removal of Pband Cd onto novel biosorbent: Defatted Carica papaya seeds

Carica papaya seeds, an agricultural waste in Nigeria, were defatted to obtain defatted C. papaya seed biosorbent. The Fourier Transformed Infrared spectrum of defatted C. papaya seed biosorbent suggests the presence of CO, OH of carboxylic acid, lactonic and amide band functional groups. The adsorption of metal ion onto defatted C. papaya seed biosorbent led to small shifts in the IR bands. The adsorption capacity of defatted C. papaya seed biosorbent was evaluated to be 1666.67 mg/g for Pb²⁺ and 1000.00 mg/g for Cd²⁺. In binary metal ion solution, the defatted C. papaya seeds showed decreased adsorption capacity for either metal ion. The influence of different particle sizes was found to have negative impact on the adsorption capacity of C. papaya seed biosorbent in the removal of Pb²⁺ and Cd²⁺ from aqueous solution. The adsorption of both metal ions was observed to follow the Freudlich model better than the Langmuir model suggesting that the adsorption of both metal ions was on multisites on the defatted C. papaya seed biosorbent. The adsorption was found to be highly feasible, spontaneous and exothermic in nature. Optimization results suggests 5 m³ of 100 mg/L of Pb²⁺ and Cd²⁺ requires 43.3 and 49.2 kg of defatted C. papaya seeds to remove 95% of the metal ions from aqueous solution.     

Investigation of the excitonic luminescence band of CdTe solar cells by photoluminescence and photoluminescence excitation spectroscopy

The excitonic luminescence band of polycrystalline cadmium telluride layers has been investigated by Photoluminescence (PL) and Photoluminescence excitation spectroscopy (PLE). CdTe was deposited by means of close space sublimation and the samples were activated by different chlorine containing compounds, i.e. cadmium chloride, hydrochloric acid, and sodium chloride as well as by simple air activation or received no post deposition treatment. In the PL spectra, four different peaks within the excitonic luminescence band were resolved. These include the free-exciton peak and two transitions of excitons bound to defects. Furthermore, free excitons and band to band transitions were detected by means of PLE. The PL and PLE spectra are discussed with respect to the post deposition treatments.     

Efficiency simulations of thin film chalcogenide photovoltaic cells for different indoor lighting conditions

Photovoltaic (PV) energy is an efficient natural energy source for outdoor applications. However, for indoor applications, the efficiency of PV cells is much lower. Typically, the light intensity under artificial lighting conditions is less than 10 W/m² as compared to 100-1000 W/m² under outdoor conditions. Moreover, the spectrum is different from the outdoor solar spectrum. In this context, the question arises whether thin film chalcogenide photovoltaic cells are suitable for indoor use. This paper contributes to answering that question by comparing the power output of different thin film chalcogenide solar cells with the classical crystalline silicon cell as reference. The comparisons are done by efficiency simulation based on the quantum efficiencies of the solar cells and the light spectra of typical artificial light sources i.e. an LED lamp, a “warm” and a “cool” fluorescent tube and a common incandescent and halogen lamp, which are compared to the outdoor AM 1.5 spectrum as reference.     

Chemical bath deposition of CdS highly-textured, columnar films

Chemical bath deposition (CBD) is one of the most common techniques for depositing CdS films. While there have been many studies on these films, and considerable characterization of their morphologies, most of this characterization has been by either X-ray diffraction or plan-view electron microscopy. With the exception of epitaxial films deposited on single crystal substrates, there has been little characterization of the cross-sectional structure of CBD CdS films. We show how, using a CdSO₄ bath and ethylenediamine as complexant, dense, columnar films of predominantly cubic CdS can be very reproducibly obtained. The initial growth is disordered, but preferential growth perpendicular to the polar face results in highly textured growth. A similar, if somewhat less ordered, morphology is obtained from a commonly-used ammonia bath using CdCl₂ as the source of Cd. Although not explicitly recognized, chloride baths in the literature exhibited sharp X-ray diffraction peaks and this is now connected with the growth mode these baths have in common with ethylenediamine baths.     

Optical spectroscopy of single Cd0.6Zn0.4Te/ZnTe quantum dots on Si substrate

Microphotoluminescence (μ-PL) measurements were carried out to investigate the optical properties of single Cd_0.6Zn_0.4Te/ZnTe quantum dots (QDs) grown on Si (001) substrate by using molecular beam epitaxy. The high quality of single Cd_0.6Zn_0.4Te/ZnTe QDs is witnessed by resolution-limited emission, negligible background and absence of measurable spectral jitter or blinking. Polarization-dependent and power-dependent μ-PL spectroscopy measurements were performed to identify the exciton, the biexciton, and the charged exciton in the emission spectra of single QDs. Furthermore a weak linearly polarized line is observed on the low energy side of the neutral exciton and is ascribed to dark exciton recombination.