Optical design of multilayer antireflection coatings for indoor solar cell applications.

Multilayer antireflection coatings (ARCs) for solar cells are conventionally designed to enhance the photocurrent level obtained at normal incidence. This is mainly because outdoor solar panels are usually placed such that they can receive strong midday sunlight at a nearly vertical angle. However, in the case of indoor photovoltaic devices, the direction of light changes considerably with changes in the relative position and angle between the device and light sources; therefore, it is often difficult to predict the incident angle. In this study, we explore a method to design ARCs suitable for indoor photovoltaics by essentially taking into account the indoor lighting environment, which is different from the outdoor conditions. We propose an optimization-based design strategy that aims to enhance the average level of the photocurrent generated when a solar cell receives irradiance randomly from all directions. We apply the proposed method to design an ARC for organic photovoltaics, which are expected to be promising indoor devices, and numerically compare the resultant performance with that obtained using a conventional design method. The results demonstrate that our design strategy is effective for achieving excellent omnidirectional antireflection performance and allows the realization of practical and efficient ARCs for indoor devices.

Oxygen vacancy mediated room-temperature ferromagnetism and band gap narrowing in DyFe0.5Cr0.5O3 nanoparticles.

We report on the magnetic and optical properties of DyFe0.5Cr0.5O3 nanoparticles synthesized by a sol-gel method. Rietveld refinement of a powder X-ray diffraction (XRD) pattern confirms the formation of an orthorhombic disordered phase with the Pnma space group. The formation of nano-sized particles, with an average size of 42(±12) nm, was approximated by the transmission electron microscopy (TEM) image analysis. X-ray photoelectron spectroscopy (XPS) of this compound reveals the presence of Fe2+/Fe3+ and Cr2+/Cr3+ mixed-valence states as a consequence of oxygen vacancies present at the surface of nanoparticles. The temperature-dependent magnetization (M-T) shows a finite non-zero magnetization up to 300 K and the field-dependent magnetization (M-H) curve exhibits a weak ferromagnetic (WFM) nature at 300 K with a clear hysteresis loop, which is quite appealing compared to that of the previously reported micron-sized DyFe0.5Cr0.5O3. These observations indicate that the large concentration of uncompensated surface spin of nanoparticles could be responsible for the observed room-temperature ferromagnetism. Moreover, DyFe0.5Cr0.5O3 nanoparticles show a significantly narrow band gap (Eg ∼ 2.0 eV). Meanwhile, the oxygen vacancies may generate shallow trap energy levels within the band gap as observed from photoluminescence (PL) spectroscopy. The observed band gap narrowing by Fe doping and the effect of oxygen vacancies on the band gap are consistent with the predictions of density functional theory (DFT) calculations. The evidence of room-temperature ferromagnetism in DyFe0.5Cr0.5O3 nanoparticles compared to their bulk counterparts and the significantly narrow band gap in the visible range manifest the potential of this material in spintronic and optical applications.

Does open-beach ship-breaking affect the mineralogical composition of soil more adversely than typical industrial activities?

In Bangladesh, India, and Pakistan the ship breaking (SB) sector dismantles end-of-life ships on open beaches, exposing the environment to the resulting pollution, especially the soil and water. Because SB occurs in the vicinity of other poorly-regulated activities in industrial zones (IZ) in these countries, there is some ambiguity concerning the relative roles played by SB and IZ in the accumulation of hazardous materials in the soil. In the absence of comparative studies, this study investigated the relative levels of soil contamination due to SB or IZ in the same geographic region by taking soil samples from SB and unrelated IZs in Chittagong, Bangladesh. The technogenic input of sixty-four chemical elements into the soil at the SB or IZ were compared with off-site reference values or the natural content of these elements in the Earth's crust and surface. The magnitude of soil contamination by ecotoxic elements, the corresponding bioavailability, and the ecological risks were assessed based on the regulatory reference values (RRVs) and with other approaches using data aggregation. Among the different potentially toxic elements, Cr, Cu, Ni, Pb, and Zn were found to be above the maximum allowable concentration (p < 0.05) in both SB and IZ. Moderate-to-high soil contamination from SB and moderate-to-considerable soil contamination in the IZ were observed. However, the element-bioavailability as ascertained via solid-phase speciation or weak-acid induced leaching, and the evaluation of associated ecological risk both indicated a low hazard quotient for soils from both SB and IZ. The outcome of the current research marked both SB and IZ soils as contaminated but not polluted, yet remediation is suggested. The level of contamination in SB soils was relatively higher than that of IZ. The comparative results presented in this study for the first time will hopefully be useful as a reference for future ecological and geochemical studies concerning the environmental contamination associated with both ship recycling on open beaches and other typical industrial activities.

Synthesis, Characterization of α-GaOOH Self-Assembly and Its Application in Removal of Perfluorinated Compounds.

This article discusses the hydrothermal synthesis of well-dispersed faceted α-GaOOH in the presence of sodium acetate by the self-assembly method. The synthesized α-GaOOH possesses a mixture of hexagonal and rectangular plates, cubic and diamond-like morphologies. The presence of ethanol as a co-solvent with water (1:1) facilitates scroll-like cylindrical morphology. The influences of sodium acetate concentration, hydrothermal temperatures, time and solvent on the formation of the above-mentioned morphologies were investigated. The synthesized α-GaOOH was characterized using X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM) and High-Resolution Transmission Electron Microscopy (HR-TEM), thermal analysis and nitrogen adsorption analysis. The XRD pattern confirmed the formation of orthorhombic α-GaOOH. The increase of the sodium acetate concentration from 0.031 mol/L to 0.250 mol/L facilitates the formation of more cubic and diamond-shaped particles than plate-like particles. The formation of faceted α-GaOOH is slow at 150 degrees C, and a further increase in hydrothermal temperature from 175 degrees C to 225 degrees C had no appreciable effect. Similarly, an increase in hydrothermal time from 5 h to 20 h at 200 degrees C facilitates hexagonal to cubic shaped plates. The solution pH strongly influenced the aspect ratio of the nanoplates. Hydrothermal temperature and time had no appreciable effect from 175 degrees C to 225 degrees C. The removal perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) using the synthesized α-GaOOH was studied. A plausible mechanism for the formation of nanoplates is proposed.

Simple top-down preparation of magnetic Bi0.9Gd0.1Fe1-xTixO3 nanoparticles by ultrasonication of multiferroic bulk material.

We present a simple technique to synthesize ultrafine nanoparticles directly from bulk multiferroic perovskite powder. The starting materials, which were ceramic pellets of the nominal compositions Bi0.9Gd0.1Fe1-xTixO3 (x = 0.00-0.20), were prepared initially by a solid state reaction technique, then ground into micrometer-sized powders and mixed with isopropanol or water in an ultrasonic bath. The particle size was studied as a function of sonication time with transmission electron microscopic imaging and electron diffraction that confirmed the formation of a large fraction of single-crystalline nanoparticles with a mean size of 11-13 nm. A significant improvement in the magnetic behavior of Bi0.9Gd0.1Fe1-xTixO3 nanoparticles compared to their bulk counterparts was observed at room temperature. This sonication technique may be considered as a simple and promising route to prepare ultrafine nanoparticles for functional applications.

Recent developments in heterogeneous catalyzed environmental remediation processes.

This article reports on recent developments in heterogeneous AOP processes such as photocatalysis, Fenton-like process and catalytic ozonation. The principle, mechanism, and influence of experimental conditions on the degradation of pollutants in heterogeneous catalytic ozonation and the photocatalytic process were discussed. Introducing solid catalysts substantially increased the efficiency of the ozonation process by producing hydroxyl radicals in the degradation process. The different types of catalyst, catalyst dosage, solution pH, ozone flow rate, water matrix and catalytic reusability and stability are reported on here. The list of various semiconductor materials used as photocatalysts, their light absorption properties, various light sources and surface properties such as surface area, pore size and pore volume as a factor in the photocatalytic degradation of various pollutants are discussed. The review article also discussed the pollutants degraded using these three processes.

Nanospace-enhanced photoreduction for the synthesis of copper(I) oxide nanoparticles under visible-light irradiation.

Nanoparticles of copper(I) oxide (cuprous oxide; Cu2O) were able to be synthesized from nano-restricted copper acetate (Cu(OAc)2) in micropores of single-wall carbon nanotubes (SWNTs) by visible-light photoreduction. The specific structure of confined Cu(OAc)2 in the micropore is indispensable for the reduction process to Cu2O by the irradiation, because, in general, aqueous solution of Cu(OAc)2 can be reduced under UV-light irradiated conditions. The present results strongly suggest that the micropore of SWNTs whose pore width is in the micropore-size range can play as nanoreactor space for the synthesis of Cu2O through the nano-restricted precursor whose reactivity is different from that in the bulk phase.

Structure of hydrated cobalt ions confined in the nanospace of single-walled carbon nanotubes.

The structure of hydrated Co ions confined in the nanospace of single-walled carbon nanotubes (SWNTs) has been studied using the X-ray absorption fine structure (XAFS) technique. Water adsorption isotherms on Co-impregnated SWNTs indicate a high affinity of Co ions to water molecules. The results of XAFS analysis provided the information on the proportion of dissolved species in nanospaces against the total amount of cobalt ions adsorbed on the open-pored SWNT. The structural information of the first shell around a Co ion was expressed in terms of the hydration number, Co-O distance and Debye-Waller factor. The actual coordination number and the interatomic distance of Co-O for the dissolved species were remarkably reduced compared to the bulk aqueous solution indicating the dehydration of water molecules from Co ions and a compact hydrated structure in the micropore of SWNTs.

Highly compressed nanosolution restricted in cylindrical carbon nanospaces.

We shed light on the specific hydration structure around a zinc ion of nanosolution restricted in a cylindrical micropore of single-wall carbon nanotube (SWNT) by comparison with the structure restricted in a cylindrical mesopore of multi-wall carbon nanotube (MWNT) and that of bulk aqueous solution. The average micropore width of open-pore SWNT was 0.87 nm which is equivalent to the size of a hydrated zinc ion having 6-hydrated water molecules. We could impregnate the zinc ions into the micropore of SWNT with negligible amounts of ion-exchanged species on surface functional groups by the appropriate oxidation followed by heat treatment under an inert condition. The results of X-ray absorption fine structure (XAFS) spectra confirmed that the proportion of dissolved species in nanospaces against the total adsorbed amounts of zinc ions on the open-pore SWNT and MWNT were 44 and 61%, respectively, indicating the formation of a dehydrated structure in narrower nanospaces. The structure parameters obtained by the analysis of XAFS spectra also indicate that the dehydrated and highly compressed hydration structure can be stably formed inside the cylindrical micropore of SWNT where the structure is different from that inside the slit-shaped micropore whose pore width is less than 1 nm. Such a unique structure needs not only a narrow micropore geometry which is equivalent to the size of a hydrated ion but also the cylindrical nature of the pore.

Template-free synthesis of self-assembled Co3O4 micro/nanocrystals.

In this article, we have reported the fabrication of various morphological porous Co3O4 by thermal decomposition of cobalt oxalate at open atmospheric conditions. Uniform cobalt oxalate microrods and microneedles were synthesized without using any surfactants or templates in large scale. The cobalt oxalate preparation method was played a crucial role on the crystal structure and its morphology. The as prepared cobalt oxalates and its corresponding cobalt oxides were characterized by using the thermogravimetric analysis, X-ray diffraction (XRD), field-emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM) and nitrogen adsorption analysis. The XRD results indicated that the orthorhombic and monoclinic cobalt oxalates were formed in different experimental conditions. The influence of preparation method of cobalt oxalates and cobalt precursors on the final morphology has been investigated. The M-H loop of the Co3O4 porous microrods and microneedles showed the presence of paramagnetic properties at room temperatures. A plausible mechanism of both cobalt oxalates and Co3O4 formation was proposed based on the experimental results.

In situ green synthesis of biocompatible ginseng capped gold nanoparticles with remarkable stability.

We report herein an unprecedented one-step green synthesis of gold nanoparticles (G-AuNps), using naturally occurring Korean red ginseng root (Panax ginseng C.A. Meyer) without any special reducing/capping agents. The AuNps generated through this ginseng-mediated process did not aggregate suggesting that the phytochemicals present in them serve as excellent coatings on the nanoparticles and thus, provide robust shielding from aggregations. The ginseng-generated AuNps exhibit remarkable in vitro stability in various buffers including: cysteine, histidine, saline, sodium chloride and a host of pH ranges. Furthermore, the phytochemical coatings on the G-AuNps rendered them nontoxic as demonstrated through detailed cytotoxicity assays using WST-8 counting kit, performed on normal cervical cells lines. The present study opens up a new possibility of conveniently synthesizing AuNps using natural products which will be useful in optoelectronic and biomedical applications.

Template-free synthesis of beta-In2S3 superstructures and their photocatalytic activity.

In this article, we have successfully fabricated various morphological beta-Indium sulfide (In2S3) superstructures by using indium thiocyanate complex at acidic pH. All the synthesis has been performed by a template-free, hydrothermal method at 195 degrees C for 3 h. The photocatalytic activity of synthesized In2S3 have been investigated by using UV-B (lamda = 365 nm) light with Methyl Orange dye as a model pollutant. The synthesized photocatalyst was characterized by using XRD, FE-SEM, HR-TEM, DRS spectra and nitrogen adsorption analysis. The influence of indium precursors and solvents on the morphology as well as the surface properties has also been discussed. The XRD result shows that cubic phase beta-In2S3 formed under all experimental conditions. A plausible mechanism of the In2S3 microsphere formation has been discussed based on experimental observations.

Plasmon-induced photothermal cell-killing effect of gold colloidal nanoparticles on epithelial carcinoma cells.

Gold colloidal nanoparticles were prepared by the liquid laser ablation of a gold metal plate in water and also by the citrate reduction of HAuCl(4).4H2O. The gold colloidal nanoparticles with the plasmonic band strongly absorb light, which is converted to the photothermal energy. This photothermal energy gives a cytotoxic effect on epithelial carcinoma cells. Interestingly, we found that the size and shape of the nanoparticles are changed by light during the photothermal process in vitro. The cervical carcinoma cell line (HeLa cell) was incubated with the colloidal gold nanoparticles and then exposed to continuous visible light at 400-600 nm with UV- and heat-cutoff filters. The distinct cell-killing effect was observed by this procedure. In the absence of the gold colloidal nanoparticles, only a small amount of cells were photothermally destroyed.

Photophysical and photochemical studies of chlorophyll a and cobalt(II)tetraphenylporphyrin in poly(L-glutamate)-decylammonium ion complex.

Spectroscopic studies were carried out on chlorophyll a and cobalt(II)tetraphenylporphyrin solubilized in a poly(L-glutamate) (Poly(Glu))-decylammonium chloride (DeAC) complex system, in the presence of methylviologen (MV2+). The cooperative binding occurred between the anionic Poly(Glu) and the cationic DeAC, leading to the formation of micelle-like hydrophobic clusters of DeAC and also the change in conformation of the Poly(Glu) from the random coil to the alpha-helix. All of the absorption spectra, the fluorescence quantum yields and the fluorescence lifetimes indicated the existence of equilibrium between the aggregated biofunctional molecules in the bulk phase and the monomeric species in the complex phase of the Poly(Glu)-DeAC solution. The fluorescence quenching of the biofunctional molecules by methylviologen indicates that the conformation-dependent electron transfer occurs in the complex phase.

Visible-light induced hydrogen production using a polypeptide-chlorophyll complex with alpha-helix conformation.

Hydrogen production was accomplished under visible-light irradiation by using a system consisting of a biomolecule (chlorophyll a), methylviologen, ethylenediaminetetraacetic acid disodium salt and Pt-loaded poly(l-glutamate) (Poly(Glu)), in aqueous decylammonium chloride (DeAC) solution. Spectroscopic studies revealed that chlorophyll a is solubilized in the hydrophobic clusters of Pt-loaded Poly(Glu)-decylammonium chloride. In the Poly(Glu)-DeAC complex, the electron transfer occurred between chlorophyll a and methylviologen leading to hydrogen production. The most noticeable result is that the rate of hydrogen evolution depends on the change from the random coil to the alpha-helix in conformation of Poly(Glu) induced by the cooperative binding with DeAC.