Graphitic Carbon Nitride/Zinc Oxide-Based Z-Scheme and S-Scheme Heterojunction Photocatalysts for the Photodegradation of Organic Pollutants.

Graphitic carbon nitride (g-C3N4), a metal-free polymer semiconductor, has been recognized as an attractive photocatalytic material for environmental remediation because of its low band gap, high thermal and photostability, chemical inertness, non-toxicity, low cost, biocompatibility, and optical and electrical efficiency. However, g-C3N4 has been reported to suffer from many difficulties in photocatalytic applications, such as a low specific surface area, inadequate visible-light utilization, and a high charge recombination rate. To overcome these difficulties, the formation of g-C3N4 heterojunctions by coupling with metal oxides has triggered tremendous interest in recent years. In this regard, zinc oxide (ZnO) is being largely explored as a self-driven semiconductor photocatalyst to form heterojunctions with g-C3N4, as ZnO possesses unique and fascinating properties, including high quantum efficiency, high electron mobility, cost-effectiveness, environmental friendliness, and a simple synthetic procedure. The synergistic effect of its properties, such as adsorption and photogenerated charge separation, was found to enhance the photocatalytic activity of heterojunctions. Hence, this review aims to compile the strategies for fabricating g-C3N4/ZnO-based Z-scheme and S-scheme heterojunction photocatalytic systems with enhanced performance and overall stability for the photodegradation of organic pollutants. Furthermore, with reference to the reported system, the photocatalytic mechanism of g-C3N4/ZnO-based heterojunction photocatalysts and their charge-transfer pathways on the interface surface are highlighted.

Synthesis of metal nanoclusters and their application in Hg2+ ions detection: A review.

Mercuric (Hg2+) ions released from human activities, natural phenomena, and industrial sources are regarded as the global pollutant of world's water. Hg2+ ions contaminated water has several adverse effects on human health and the environment even at low concentrations. Therefore, rapid and cost-effective method is urgently required for the detection of Hg2+ ions in water. Although, the current analytical methods applied for the detection of Hg2+ ions provide low detection limit, they are time consuming, require expensive equipment, and are not suitable for in-situ analysis. Metal nanoclusters (MNCs) consisting of several to ten metal atoms are important transition missing between single atoms and plasmonic metal nanoparticles. In addition, sub-nanometer sized MNCs possess unique electronic structures and the subsequent unusual optical, physical, and chemical properties. Because of these novel properties, MNCs as a promising material have attracted considerable attention for the construction of selective and sensitive sensors to monitor water quality. Hence this review is focused on recent advances on synthesis strategies, and optical and chemical properties of various MNCs including their applications to develop optical assay for Hg2+ ions in aqueous solutions.

Towards the Enhancement in Photocatalytic Performance of Ag3PO4 Nanoparticles through Sulfate Doping and Anchoring on Electrospun Nanofibers.

Present work reports the enhancement in photocatalytic performance of Ag3PO4 nanoparticles through sulfate doping and anchoring on Polyacrylonitrile (PAN)-electrospun nanofibers (SO42--Ag3PO4/PAN-electrospun nanofibers) via electrospinning followed by ion-exchange reaction. Morphology, structure, chemical composition, and optical properties of the prepared sample were characterized using XRD, FESEM, FTIR, XPS, and DRS. The anchoring of SO42--Ag3PO4 nanoparticles on the surface of PAN-electrospun nanofibers was evidenced by the change in color of the PAN nanofibers mat from white to yellow after ion-exchange reaction. FESEM analysis revealed the existence of numerous SO42--Ag3PO4 nanoparticles on the surface of PAN nanofibers. Photocatalytic activity and stability of the prepared sample was tested for the degradation of Methylene blue (MB) and Rhodamine B (RhB) dyes under visible light irradiation for three continuous cycles. Experimental results showed enhanced photodegradation activity of SO42--Ag3PO4/PAN-electrospun nanofibers compared to that of sulfate undoped sample (Ag3PO4/PAN-electrospun nanofibers). Doping of SO42- into Ag3PO4 crystal lattice could increase the photogenerated electron-hole separation capability, and PAN nanofibers served as support for nanoparticles to prevent from agglomeration.

Enhanced Antibacterial Property of Sulfate-Doped Ag3PO4 Nanoparticles Supported on PAN Electrospun Nanofibers.

Heterojunction nanofibers of PAN decorated with sulfate doped Ag3PO4 nanoparticles (SO42--Ag3PO4/PAN electrospun nanofibers) were successfully fabricated by combining simple and versatile electrospinning technique with ion exchange reaction. The novel material possessing good flexibility could exhibit superior antibacterial property over sulfate undoped species (Ag3PO4/PAN electrospun nanofibers). FESEM, XRD, FTIR, XPS and DRS were applied to characterize the morphology, phase structure, bonding configuration, elemental composition, and optical properties of the as fabricated samples. FESEM characterization confirmed the successful incorporation of SO42--Ag3PO4 nanoparticles on PAN electrospun nanofibers. The doping of SO42- ions into Ag3PO4 crystal lattice by replacing PO43- ions can provide sufficient electron-hole separation capability to the SO42--Ag3PO4/PAN heterojunction to generate reactive oxygen species (ROS) under visible light irradiation and enhances its antibacterial performance. Finally, we hope this work may offer a new paradigm to design and fabricate other types of flexible self-supporting negative-ions-doped heterojunction nanofibers using electrospinning technique for bactericidal applications.

Novel preparation and characterization of human hair-based nanofibers using electrospinning process.

Human hair-based biocomposite nanofibers (NFs) have been fabricated by an electrospinning technique. Aqueous keratin extracted from human hair was successfully blended with poly(vinyl alcohol) (PVA). The focus here is on transforming into keratin/PVA nanofibrous membranes and insoluble property of electrospun NFs. The resulting hair-based NFs were characterized using Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning colorimetry (DSC), and thermogravimetric analysis (TGA). Toward the potential use of these NFs after cross-linking with various weight fractions of glyoxal, its physicochemical properties, such as morphology, mechanical strength, crystallinity, and chemical structure were investigated. Keratin/PVA ratio of 2/1 NFs with 6 wt%-glyoxal showed good uniformity in fiber morphology and suitable mechanical properties, and excellent antibacterial activity providing a potential application of hair-based NFs in biomedical field.

Effect of polymer molecular weight on the fiber morphology of electrospun mats.

In this work, different fractions of solvent-induced polymer degraded solution were mixed with freshly prepared solution of same polymer, and its effect on fiber morphology of electrospun mats was investigated. Nylon-6 solution in formic acid was allowed to degrade for 3 weeks and different fractions of it were mixed with freshly prepared nylon-6 solution to get the electrospun mats. FE-SEM images of the mats indicated that the a large amount of sub-nanofibers (<50 nm in diameter) in the form of spider-net like structures were achieved by tailoring the amount of solvent degraded polymer solution in the freshly prepared nylon-6 solution. Large quantity of these ultrafine sub-nanofibers present in electrospun nylon-6 mats could increase its hydrophilicity and mechanical strength. The decreased average pore diameter and increased BET surface area of the mat, caused by spider-net like structure, can make it as a potential candidate for air/water filtration.

Fabrication of highly porous poly (ɛ-caprolactone) fibers for novel tissue scaffold via water-bath electrospinning.

Highly porous fibers were prepared by water-bath electrospinning from pure poly(ɛ-caprolactone) (PCL), and its blends with methoxy poly(ethylene glycol) (MPEG). These fibers were further analyzed by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and gravimetric as well as contact angle measurement. SEM images showed that the fibers diameters as well as pores diameter on the fibers were affected by the weight ratio of MPEG/PCL. DSC and XRD not only revealed suppression of crystallinity of PCL but also indicated the presence of trace amount of MPEG in PCL water-bath collected fibers. The potential use of these hydrophilic porous electrospun fibrous mats as scaffolding materials was evaluated in vitro using mouse osteoblasts (MC3T3-E1) as reference cell lines. Cytotoxicity assessment of the fiber mats indicated that the porous electrospun mat containing trace amount of MPEG was nontoxic to the cell. Cell culture results showed that porous fibrous mats were good in promoting the cell attachment and proliferation. This novel electrospun matrix could be used as potential tissue scaffold material.