Photocatalytic degradation effect of CdSe nanoparticles for textile wastewater effluents at low cost and proves to be efficient method.

Semiconductor nanoparticles and nanocrystals have a great impact due to its contribution in the diverse fields including electronics, solar energy, biological imaging, and photonics. Among these semiconductor nanoparticles, cadmium selenide of II-VI group binary semiconductor nanoparticles were synthesized using solvothermal process for the different reaction temperatures. The XRD pattern of the synthesized samples confirms the crystalline nature of the samples and showed increase in its crystallite size with rise in temperature. The morphology of the samples was analysed with TEM images and found that the nanoparticles synthesized at different temperatures were varied in size and shape indicating the increase in the size of the particles with the raise in temperature. The optical properties of the samples pointed out that they exhibit a blue shift owing to quantum confinement. Photocatalytic activity was carried out for the synthesized samples under visible light radiation using methylene blue (MB) as a model pollutant and it proved to be a good photocatalyst achieving the efficiency of 75% which is promising for future application with good optimization. The efficiency could be increased when these semiconductor CdSe nanoparticles are doped with metal particles due to an increase in the absorption edge wavelength and a decrease in bandgap energy were reported in detail.

An efficient and magnetically recoverable g-C3N4/ZnS/CoFe2O4 nanocomposite for sustainable photodegradation of organic dye under UV-visible light illumination.

Effective improvement of an easily recoverable photocatalyst is equally vital to its photocatalytic performance from a practical application view. The magnetically recoverable process is one of the easiest ways, provided the photocatalyst is magnetically strong enough to respond to an external magnetic field. Herein, we prepared graphitic carbon nitride nanosheet (g-C3N4), and ZnS quantum dots (QDs) supported ferromagnetic CoFe2O4 nanoparticles (NPs) as the gC3N4/ZnS/CoFe2O4 nanohybrid photocatalyst by a wet-impregnation method. The loading of CoFe2O4 NPs in the g-C3N4/ZnS nanohybrid resulted in extended visible light absorption. The ferromagnetic g-C3N4/ZnS/CoFe2O4 nanohybrid exhibited better visible-light-active photocatalytic performance (97.11%) against methylene blue (MB) dye, and it was easily separable from the aqueous solution by an external bar magnet. The g-C3N4/ZnS/CoFe2O4 nanohybrid displayed excellent photostability and reusability after five consecutive cycles. The favourable band alignment and availability of a large number of active sites affected the better charge separation and enhanced photocatalytic response. The role of active species involved in the degradation of MB dye during photocatalyst by g-C3N4/ZnS/CoFe2O4 nanohybrid was also investigated. Overall, this study provides a facile method for design eco-friendly and promising g-C3N4/ZnS/CoFe2O4 nanohybrid photocatalyst as applicable in the eco-friendly dye degradation process.

Visible light driven reduced graphene oxide supported ZnMgAl LTH/ZnO/g-C3N4 nanohybrid photocatalyst with notable two-dimension formation for enhanced photocatalytic activity towards organic dye degradation.

In this study, 2D/2D/2D heterostructured r-GO/LTH/ZnO/g-C3N4 nanohybrid were synthesized through hydrothermal method. The strong electrostatic interaction between the negatively charged g-C3N4 and r-GO nanosheets with positively charged layered triple hydroxide (LTH) nanosheets are effectively influences the successful formation of heterojunction. The LTH nanosheets are well spread on the g-C3N4 nanosheets combined with r-GO. In particular, the as prepared heterojunction shows a better photocatalytic degradation activity compared to pristine samples and the significant enhancement in the photocatalytic performance is mainly accredited to the large interfacial charge transition of photogenerated charge carriers under the visible light irradiation. Although the 2D/2D/2D heterojunction effectively hinders the charge carrier recombination resulting high photocatalytic activity with good stability. In addition, the r-GO supported LTH/ZnO/g-C3N4 heterojunction shows high photo-stability after sequential experimental runs with no obvious change in the dye degradation process. Consequently, the role of active species was investigated over the r-GO/LTH/ZnO/g-C3N4 heterojunction with the help of different scavengers.

Construction of magnetically recoverable ZnS-WO3-CoFe2O4 nanohybrid enriched photocatalyst for the degradation of MB dye under visible light irradiation.

Easily recyclable photocatalysts have received considerable attention for their practical application, in order to address the wastewater treatments. Here, we report efficient and magnetically recyclable ZnS-WO3-CoFe2O4 nanohybrid prepared through wet impregnation method. The photophysical and optical properties of as-prepared photocatalysts was investigated by different spectroscopic techniques. The photocatalytic activity of as synthesized samples were assessed by the photodegradation of methylene blue (MB) dye under visible light irradiation. Amongst, ZnS-WO3-CoFe2O4 nanohybrid exhibit higher photodegradation activity than the other bare and hybrid samples. The enhanced light absorption and lower emission intensity provide the improved photocatalytic activity of ZnS-WO3-CoFe2O4 nanohybrid. The ZnS-WO3-CoFe2O4 nanohybrid exhibit excellent photostability after four consecutive cycles. The ferromagnetic behavior of the hybrid sample using easily recover from the dye solution using an external bar magnet.

In-situ development of metal organic frameworks assisted ZnMgAl layered triple hydroxide 2D/2D hybrid as an efficient photocatalyst for organic dye degradation.

Metal organic framework (MOF) supported layered triple hydroxide (LTH) 2D/2D hybrid material was prepared by a simple hydrothermal method. The photophysical properties of the prepared samples were investigated through a set of analytical methods such as X-ray diffraction, Fourier-transform infrared spectroscopy, field emission scanning electron microscope, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy and mapping. The photocatalytic degradation activity of as prepared 2D/2D MOF-5/LTH hybrid sample was investigated against methylene blue (MB) dye under the UV-visible light irradiation. The degradation efficiency of the MOF-5/LTH hybrid sample was twice a time greater than that of pristine MOF-5, particularly degradation efficiency of the MOF-5, LTH and MOF-5/LTH hybrid samples are 43.3, 57.7 and 98.1% respectively. The Pseudo first order rate and the reusing investigation was further used to study the catalytic activity and stability of the as-synthesized 2D/2D photocatalyst. The observed improvement in the photocatalytic activity of the hybrid samples were owed to enhance visible light absorption, efficient separation and transportation of photoinduced electrons and holes.

Designed assembly of Ni/MAX (Ti3AlC2) and porous graphene-based asymmetric electrodes for capacitive deionization of multivalent ions.

The contamination of aquatic ecosystems by fluoride and heavy metal ions constitute an environmental hazard and has been proven to be harmful to human health. This study explores the feasibility of using asymmetric capacitive deionization (CDI) electrodes to remove such toxic ions from wastewater. An asymmetric CDI cell was fabricated using 2D Ni/MAX as an anode and 3D porous reduced graphene oxide (pRGO) as a cathode for the electrosorption of F-, Pb2+, and As(III) ions. A simple microwave process was used for the synthesis of Ni/MAX composite using fish sperm DNA (f-DNA) as a cross-linker between MAX nanosheets (NSs) and the metallic Ni nanoparticles (NPs). Further, pRGO anode was prepared through effective reduction of RGO using lemon juice as green reducing agent with the assist of f-DNA as a structure-directing agent for the formation of 3D network. With this tailored nanoarchitecture, pRGO and Ni/MAX electrodes exhibited a high specific capacitance of 760 and 385 F g-1, respectively. The fabricated Ni/MAX and pRGO based CDI system demonstrated a high electrosorption capacity of 68, 76, and 51 mg g-1 for the monovalent F-, divalent Pb2+, and trivalent As(III) ions at 1.4 V in neutral pH. Furthermore, Ni/MAX//pRGO system was successfully applied for the removal of total F(T), Pb(T), and As(T) ions from real industrial wastewater and contaminated groundwater. The present findings indicate that the fabricated Ni/MAX//pRGO electrode has excellent electrochemical properties that can be exploited for the removal of anionic and cationic metal ions from aqueous solutions in a CDI based system.