Indigo dyes: Toxicity, teratogenicity, and genotoxicity studies in zebrafish embryos.

Wastewater released by textile dyeing industries is a major source of pollution. Untreated wastewater released from indigo dyeing operations affects aquatic ecosystems and threatens their biodiversity. We have assessed the toxicity of natural and synthetic indigo dye in zebrafish embryos, using the endpoints of teratogenicity, genotoxicity, and histopathology. The zebrafish embryo toxicity test (ZFET) was conducted, exposing embryos to ten concentrations of natural and synthetic indigo dyes; the 96-hour LC50 values were approximately 350 and 300 mg/L, respectively. Both dyes were teratogenic, causing egg coagulation, tail detachment, yolk sac edema, pericardial edema, and tail bend, with no significant difference in effects between the natural and synthetic dyes. Both dyes were genotoxic (using comet assay for DNA damage). Real-time RT-PCR studies showed upregulation of the DNA-repair genes FEN1 and ERCC1. Severe histological changes were seen in zebrafish larvae following exposure to the dyes. Our results show that indigo dyes may be teratogenic and genotoxic to aquatic organisms, underscoring the need for development of sustainable practices and policies for mitigating the environmental impacts of textile dyeing.

A review on potential sulfide-based ternary chalcogenides for emerging photo-assisted water purification applications.

Sulfide-based ternary chalcogenides have been recognized widely as exceptional photocatalysts, thanks to their narrow band gap enabling them to harvest solar energy to the maximum extent. They provide excellent optical, electrical, and catalytic performance and are of abundant use as a heterogeneous catalyst. Among sulfide-based ternary chalcogenides, compounds exhibiting AB2X4 structure form a new class of materials with excellent stability in photocatalytic performance. In the AB2X4 family of compounds, ZnIn2S4 is one of the top performing photocatalyst for energy and environmental applications. However, to date, only limited information is available on the mechanism behind the photo-induced migration of charge carriers in ternary sulfide chalcogenides. Ternary sulfide chalcogenides with their visible region activity and substantial chemical stability greatly depend on crystal structure, morphology, and optical characteristics for their photocatalytic activity. Hence, in this review, a comprehensive assessment of the reported strategies for enhancement of the photocatalytic efficiency of this compound is presented. In addition, a meticulous investigation of the applicability of ternary sulfide chalcogenide compound ZnIn2S4, in particular, has been delivered. Also, the photocatalytic behavior of other sulfide-based ternary chalcogenides for water remediation applications has also been briefed. Finally, we conclude with an insight into the challenges and future advancements in the exploration of ZnIn2S4-based chalcogenide as a photocatalyst for various photo-responsive applications. It is believed that this review could contribute to a better understanding of ternary chalcogenide semiconductor photocatalysts for solar-driven water treatment applications.

Immobilization of a TiO2-PEDOT:PSS hybrid heterojunction photocatalyst for degradation of organic effluents.

Heterojunction photocatalysts have recently emerged for use in degradation of organic pollutants, typically being suspended in effluent solution to degrade it. Post degradation, the catalyst must be removed from the treated solution, which consumes both energy and time. Moreover, the separation of nano catalysts from the treated solution is challenging. In the present work, we explore fabrication of immobilized TiO2-PEDOT:PSS hybrid heterojunction catalysts with the support of a PVA (polyvinyl alcohol) matrix. These photocatalytic films do not require any steps to separate the powdered catalyst from the treated water. While the PVA-based films are unstable in water, their stability could be significantly enhanced by heat treatment, enabling efficient removal of organic effluents like methylene blue (MB) and bisphenol-A (BPA) from the aqueous solution under simulated sunlight irradiation. Over 20 cycles, the heterojunction photocatalyst maintained high photocatalytic activity and showed excellent stability. Hence, an immobilization of the TiO2-PEDOT:PSS hybrid heterojunction is suggested to be beneficial from the viewpoint of reproducible and recyclable materials for simple and efficient wastewater treatment.

Solar-driven hybrid photo-Fenton degradation of persistent antibiotic ciprofloxacin by zinc ferrite-titania heterostructures: degradation pathway, intermediates, and toxicity analysis.

Present work puts forward an efficient strategy to degrade one of the persistent antibiotic contaminants, ciprofloxacin (CIP). Hybrid advanced oxidation process (HAOP) is tailored with a synergy effect between photocatalysis and photo-Fenton catalysis on zinc ferrite-titania heterostructured composite (ZFO-TiO2). The ZFO-TiO2 heterostructured composite enables heterogenous surfaces for enhanced charge separation where HAOP is implemented for CIP degradation with the aid of class AAA solar simulator. The results reveal an enhanced degradation rate of CIP (kobs = 0.255 min-1), noticeably higher than the conventional TiO2-based photocatalysis. The HAOP system strongly enhances the reaction rates showing five times higher performance as compared to TiO2-based photocatalysis. The substitution reactions for degradation of CIP into its intermediates were analyzed by LC-MS/MS, and the plausible degradation pathways have been graphically modeled identifying 3-phenyl-1-propanol and phenol molecules as less toxic end products. Toxicity of the photodegraded samples reveal 18.1 ± 1.24% inhibition of V. fischeri at the end of 60-min treatment indicating reduced toxicity of CIP contaminated samples. Antimicrobial inhibition studies on E. coli also corroborate an effective CIP removal (~ 100%) in less than 90 min. The study puts forward a novel ZFO-TiO2 composite HAOP system for efficient and rapid mineralization of an antibiotic pollutant, extendable towards wide range of pharmaceutical drug degradation studies.

Ga based Sillenite-TiO2 composite for efficient sunlight induced photo reduction of Cr (VI) and photo degradation of ampicillin.

This work reports the design and development of an efficient sillenite based visible light photoactive Bi24Ga2O39-TiO2 (BGT) heterostructure. Structural and morphological studies based on X-ray diffraction (XRD) and high-resolution scanning electron microscopy (HRSEM) confirm the formation of combined phase as well the overall morphology of composite BGT. Additionally, X-ray photoelectron spectroscopy (XPS) results confirm the presence of Bi3+, Ga3+, Ti4+ & O2-. The composite exhibits a shift in the absorbance edge towards visible region of electromagnetic spectrum when compared to that of TiO2. Suitable band edge positions in the composite facilitate the formation of type-1 heterojunction enhancing visible light photocatalytic property. The photocatalytic activity is evident from photo reduction of Cr (VI) (95% reduction in 180 min). The composite also plays an improved and effective role in the degradation of persistent drug ampicillin-cloxacillin (AMC) with a rate constant of 0.02 min-1. Photocatalytic experiments conducted at different pH values showed higher performance at lower pH ∼3. Trapping experiments performed on the sample confirm the role of holes as the main active species during photocatalysis. Appreciable recyclability of BGT composite was noted with respect to AMC drug degradation.

Synergy of photocatalysis and fuel cells: A chronological review on efficient designs, potential materials and emerging applications.

The rising demand of energy and lack of clean water are two major concerns of modern world. Renewable energy sources are the only way out in order to provide energy in a sustainable manner for the ever-increasing demands of the society. A renewable energy source which can also provide clean water will be of immense interest and that is where Photocatalytic Fuel Cells (PFCs) exactly fit in. PFCs hold the ability to produce electric power with simultaneous photocatalytic degradation of pollutants on exposure to light. Different strategies, including conventional Photoelectrochemical cell design, have been technically upgraded to exploit the advantage of PFCs and to widen their applicability. Parallel to the research on design, researchers have put an immense effort into developing materials/composites for electrodes and their unique properties. The efficient strategies and potential materials have opened up a new horizon of applications for PFCs. Recent research reports reveal this persistently broadening arena which includes hydrogen and hydrogen peroxide generation, carbon dioxide and heavy metal reduction and even sensor applications. The review reported here consolidates all the aspects of various design strategies, materials and applications of PFCs. The review provides an overall understanding of PFC systems, which possess the potential to be a marvellous renewable source of energy with a handful of simultaneous applications. The review is a read to the scientific community and early researchers interested in working on PFC systems.

Characterization of mitochondrial genome of Indian Ocean blue-spotted maskray, Neotrygon indica and its phylogenetic relationship within Dasyatidae Family.

The present study characterized complete mitochondrial genome of Blue-spotted maskray, Neotrygon indica and studied the evolutionary relationship of the species within the Dasyatidae family. The total length of the mitogenome was 17,974 bp including 37 genes and a non-coding control region. The average frequency of nucleotides in protein-coding genes was A: 29.1 %, T: 30.2 %, G: 13.0 % and C: 27.7 % with AT content of 59.3 %. The values of AT and GC skewness were -0.018 and -0.338, respectively. Comparative analyses showed a large number of average synonymous substitutions per synonymous site (Ks) in gene NADH4 (5.07) followed by NADH5 (4.72). High values of average number of non-synonymous substitutions per non-synonymous site (Ka) were observed in genes ATPase8 (0.54) and NADH2 (0.44). Genes NADH4L and NADH2 showed high interspecific genetic distance values of 0.224 ± 0.001 and 0.213 ± 0.002, respectively. Heat map analysis showed variation in codon usage among different species of the Dasyatidae family. The phylogenetic tree showed a sister relationship between the Dasyatinae and the Neotrygoninae subfamilies. Neotrygon indica formed as a sister species to the clade consisting of N. varidens and N. orientalis. Based on the present results, Neotrygon indica could have diverged from the common ancestor of the two latter in the Plio-Pleistocene. The present study showed distinct characteristics of N. indica from its congeners through comparative mitogenomics.

Enhanced photo-fenton and photoelectrochemical activities in nitrogen doped brownmillerite KBiFe2O5.

Visible-light-driven photo-fenton-like catalytic activity and photoelectrochemical (PEC) performance of nitrogen-doped brownmillerite KBiFe2O5 (KBFO) are investigated. The effective optical bandgap of KBFO reduces from 1.67 to 1.60 eV post N-doping, enabling both enhancement of visible light absorption and photoactivity. The photo-fenton activity of KBFO and N-doped KBFO samples were analysed by degrading effluents like Methylene Blue (MB), Bisphenol-A (BPA) and antibiotics such as Norfloxacin (NOX) and Doxycycline (DOX). 20 mmol of Nitrogen-doped KBFO (20N-KBFO) exhibits enhanced catalytic activity while degrading MB. 20N-KBFO sample is further tested for degradation of Bisphenol-A and antibiotics in the presence of H2O2 and chelating agent L-cysteine. Under optimum conditions, MB, BPA, and NOX, and DOX are degraded by 99.5% (0.042 min-1), 83% (0.016 min-1), 72% (0.011 min-1) and 95% (0.026 min-1) of its initial concentration respectively. Photocurrent density of 20N-KBFO improves to 8.83 mA/cm2 from 4.31 mA/cm2 for pure KBFO. Photocatalytic and photoelectrochemical (PEC) properties of N-doped KBFO make it a promising candidate for energy and environmental applications.

g-C3N4/Ca2Fe2O5 heterostructures for enhanced photocatalytic degradation of organic effluents under sunlight.

g-C3N4/Ca2Fe2O5 heterostructures were successfully prepared by incorporating g-C3N4 into Ca2Fe2O5 (CFO). As prepared g-C3N4/CFO heterostructures were initially utilized to photodegrade organic effluent Methylene blue (MB) for optimization of photodegradation performance. 50% g-C3N4 content in CFO composition showed an enhanced photodegradation efficiency (~ 96%) over g-C3N4 (48.15%) and CFO (81.9%) due to mitigation of recombination of photogenerated charge carriers by Type-II heterojunction. The optimized composition of heterostructure was further tested for degradation of Bisphenol-A (BPA) under direct sunlight, exhibiting enhanced photodegradation efficiency of about 63.1% over g-C3N4 (17%) and CFO (45.1%). The photoelectrochemical studies at various potentials with and without light illumination showed significant improvement in photocurrent response for g-C3N4/Ca2Fe2O5 heterostructures (~ 1.9 mA) over CFO (~ 67.4 µA). These studies revealed efficient solar energy harvesting ability of g-C3N4/Ca2Fe2O5 heterostructures to be utilized for organic effluent treatment.

Characterization of the complete mitochondrial genome of Neolissochilus hexastichus (McClelland, 1839).

The complete mitochondrial genome of the near threatened mahseer fish, Neolissochilus hexastichus, was characterized for the first-time using Ion Torrent NGS platform. The total length of the mitogenome was 16,538 bp including a standard set of 22 transfer RNAs (tRNAs), 2 ribosomal RNAs (rRNAs), 13 protein-coding genes and a non-coding control region. Twenty-eight of the 37 genes are located on the light strand and, the remaining nine genes are situated on the heavy strand. Phylogenetic analysis showed the sister relationship between N. hexastichus and N. hexagonolepis. The mitogenome could be useful for phylogenetics, population genetics, and conservation of the mahseers.

Growth of sillenite Bi12FeO20 single crystals: structural, thermal, optical, photocatalytic features and first principle calculations.

Ideal sillenite type Bi12FeO20 (BFO) micron sized single crystals have been successfully grown via inexpensive hydrothermal method. The refined single crystal X-ray diffraction data reveals cubic Bi12FeO20 structure with single crystal parameters. Occurrence of rare Fe4+ state is identified via X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). The lattice parameter (a) and corresponding molar volume (Vm) of Bi12FeO20 have been measured in the temperature range of 30-700 °C by the X-ray diffraction method. The thermal expansion coefficient (α) 3.93 × 10-5 K-1 was calculated from the measured values of the parameters. Electronic structure and density of states are investigated by first principle calculations. Photoelectrochemical measurements on single crystals with bandgap of 2 eV reveal significant photo response. The photoactivity of as grown crystals were further investigated by degrading organic effluents such as Methylene blue (MB) and Congo red (CR) under natural sunlight. BFO showed photodegradation efficiency about 74.23% and 32.10% for degrading MB and CR respectively. Interesting morphology and microstructure of pointed spearhead like BFO crystals provide a new insight in designing and synthesizing multifunctional single crystals.

Nitrogen Incorporated Photoactive Brownmillerite Ca2Fe2O5 for Energy and Environmental Applications.

Ca2Fe2O5 (CFO) is a potentially viable material for alternate energy applications. Incorporation of nitrogen in Ca2Fe2O5 (CFO-N) lattice modifies the optical and electronic properties to its advantage. Here, the electronic band structures of CFO and CFO-N were probed using Ultraviolet photoelectron spectroscopy (UPS) and UV-Visible spectroscopy. The optical bandgap of CFO reduces from 2.21 eV to 2.07 eV on post N incorporation along with a clear shift in the valence band of CFO indicating the occupation of N 2p levels over O 2p in the valence band. Similar effect is also observed in the bandgap of CFO, which is tailored upto 1.43 eV by N+ ion implantation. The theoretical bandgaps of CFO and CFO-N were also determined by using the Density functional theory (DFT) calculations. The photoactivity of these CFO and CFO-N was explored by organic effluent degradation under sunlight. The feasibility of utilizing CFO and CFO-N samples for energy storage applications were also investigated through specific capacitance measurements. The specific capacitance of CFO is found to increase to 224.67 Fg-1 upon N incorporation. CFO-N is thus found to exhibit superior optical, catalytic as well as supercapacitor properties over CFO expanding the scope of brownmillerites in energy and environmental applications.

Photoactive Brownmillerite Multiferroic KBiFe2O5 and Its Potential Application in Sunlight-Driven Photocatalysis.

KBiFe2O5 (KBFO) is an upcoming promising brownmillerite-structured multiferroic photoactive material for next-generation photovoltaic and photocatalytic applications. In the present work, KBFO has been developed using multistep thermal treatment method to reduce the volatility of constituent elements and improve the stability of compound. The band gap of KBFO (found to be ∼1.68 eV) extends to the near-infrared region compared to traditional perovskite-structured multiferroics. The magnetic and dielectric transitions occur in the same temperature range (740 K-800 K), reflecting the existence of magneto-dielectric effect in the as-synthesized sample. It also shows promising photocatalytic activity by degrading organic effluents under natural sunlight compared to regular perovskite BiFeO3 photocatalyst (operating under visible light). A new application of brownmillerite multiferroic KBFO photocatalyst in environmental and energy applications has been explored by integrating the structural, optical, magnetic, and dielectric properties of the same.

Microstructural study of assorted ZnO nanostructures: nanocombs, nanocones and microspheres.

We report the microstructural study of ZnO nanostructures: nanocombs, nanocones and microspheres, synthesized using a simple thermal evaporation technique. While nanocombs require the presence of a catalyst, nanocones and hollow ZnO microspheres have been synthesized on silicon substrate in absence of any catalyst or template material. ZnO hexagonal nanocones have been synthesized on Si(100) substrates by directly evaporating zinc acetate dihydrate, at a low temperature of 400 degrees C, without using any carrier gas. The possible mechanism of formation of these structures has been discussed in brief. Chemical composition analysis by energy dispersive X-ray spectroscopy shows an O rich condition of ZnO nanocones and oxygen deficient condition of nanocombs.

Structure and physical properties of undoped ZnO and vanadium doped ZnO films deposited by pulsed laser deposition.

Undoped ZnO films were deposited using pulsed laser deposition technique on Si and glass substrates in different O2 partial pressures (ranging from 10(-5) mbar to 3 mbar) and substrate temperatures. When the substrate temperature is 500 degrees C and O2 partial pressure (pp) approximately 3 mbar, randomly oriented ZnO hexagons were observed on glass substrate, whereas, dense ZnO hexagonal rod like structures (diameter ranging from 200-500 nm) were observed on Si substrate. The photoluminescence (PL) characterization of ZnO film grown on Si exhibited an intense defect free narrow excitonic emission in the UV region (Full width half maximum (FWHM) approximately 11.26 nm) as compared to broad emission (FWHM approximately 57.06 nm) from that grown on glass. The parent film emission was found to shift from UV to blue region on doping ZnO with Vanadium.