J. Appl. Cryst.の発刊に際して

Solar energy is an alternative, sustainable energy source for mankind. Finding a convenient way to convert sunlight energy into chemical energy is a key step towards realizing large-scale solar energy utilization. Owing to their structural regularity and synthetic tunability, metal–organic frameworks (MOFs) provide an interesting platform to hierarchically organize light-harvesting antennae and catalytic centers to achieve solar energy conversion. Such photo-driven catalytic processes not only play a critical role in the solar to chemical energy conversion scheme, but also provide a novel methodology for the synthesis of fine chemicals. In this review, we summarize the fundamental principles of energy transfer and photocatalysis and provide an overview of the latest progress in energy transfer, light-harvesting, photocatalytic proton and CO2 reduction, and water oxidation using MOFs. The applications of MOFs in organic photocatalysis and degradation of model organic pollutants are also discussed.

Metal–organic frameworks for artificial photosynthesis and photocatalysis

Graphene-based materials are gaining heightened attention as novel materials for environmental applications The unique physicochemical properties of graphene, notably its exceptionally high surface area, electron mobility, thermal conductivity, and mechanical strength, can lead to novel or improved technologies to address the pressing global environmental challenges This critical review assesses the recent developments in the use of graphene-based materials as sorbent or photocatalytic materials for environmental decontamination, as building blocks for next generation water treatment and desalination membranes, and as electrode materials for contaminant monitoring or removal The most promising areas of research are highlighted, with a discussion of the main challenges that we need to overcome in order to fully realize the exceptional properties of graphene in environmental applications

Environmental applications of graphene-based nanomaterials.

In the present review we try to give a comprehensive and most up to date view to the field, with an emphasis on the currently most investigated anodic TiO2 nanotube arrays. We will first give an overview of different synthesis approaches to produce TiO2 nanotubes and TiO2 nanotube arrays, and then deal with physical and chemical properties of TiO2 nanotubes and techniques to modify them. Finally, we will provide an overview of the most explored and prospective applications of nanotubular TiO2.

One-dimensional titanium dioxide nanomaterials: nanotubes.

The world is recently witnessing an explosive development of novel electronic and optoelectronic devices that demand more-reliable power sources that combine higher energy density and longer-term durability. Supercapacitors have become one of the most promising energy-storage systems, as they present multifold advantages of high power density, fast charging-discharging, and long cyclic stability. However, the intrinsically low energy density inherent to traditional supercapacitors severely limits their widespread applications, triggering researchers to explore new types of supercapacitors with improved performance. Asymmetric supercapacitors (ASCs) assembled using two dissimilar electrode materials offer a distinct advantage of wide operational voltage window, and thereby significantly enhance the energy density. Recent progress made in the field of ASCs is critically reviewed, with the main focus on an extensive survey of the materials developed for ASC electrodes, as well as covering the progress made in the fabrication of ASC devices over the last few decades. Current challenges and a future outlook of the field of ASCs are also discussed.

Asymmetric Supercapacitor Electrodes and Devices.

Layers of high silica zeolites, synthesized with an organic structure directing agent (OSDA) and grown onto porous support structures, frequently suffer from the thermal stress during the removal of OSDA via the calcination process. The different thermal expansion coefficients of the zeolite and the support material, especially when stainless steel is used as a support, causes enormous tension resulting in defect formation in the zeolite layer. However, the calcination is an easy procedure to decompose the OSDA in the pore system of the zeolite. Recently, methods to synthesize zeolite beta without the use of an organic structure directing agent have been described. In the present study, a seed-directed synthesis is used to prepare OSDA-free zeolite beta layers on stainless steel supports via an in situ preparation route. For the application as membrane, a porous stainless steel support has been chosen. The beta/stainless steel composites are characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). To prove its possible application as a membrane, the beta/stainless steel composites were also tested by single gas permeances of H₂, He, CO₂, N₂, and CH₄.

Supported Zeolite Beta Layers via an Organic Template-Free Preparation Route.

Present work reviews the synthesis of Schiff base ligand derived from N-(1-Naphthyl) ethylenediamine with 1,2diphenylethane-1,2-dione in the ratio of 1:2 and its metal complexes. The colored complexes prepared were of type [M 2+ L]X2, where M 2+ = Cu, Co, Zn, L= Synthesised schiff base ligand and X= Cl. The chelation of the ligand to metal ions occurs through the four nitrogen atoms of the ligand. The structure of the obtained ligand and their respective metal complexes were elucidated by FTIR, elemental analysis, ultraviolet–visible spectra, conductometric measurements, magnetic susceptibility measurements and also 1 HNMR spectral studies. The metal complex exhibits octahedral coordination geometrical arrangement. From spectral studies and molar conductance measurements, octahedral geometry was confirmed for Co(II) and square planar for Zn(II) complexes. Schiff base ligand and its metal complexes were screened against bacterial and fungal strains and their preliminary results showed that these complexes inhibited bacterial/fungal growth to a greater extent than the ligand.

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Design, Characterization and antimicrobial activity of Cu(II), Co(II) and Zn(II) complexes with Schiff base from 1,2-diphenylethane-1,2-dione and N-(1-Naphthyl) ethylenediamine

Removing organic pollutants, textile dyes, and pharmaceutical wastes from the water bodies has become an essential requirement for a safe environment. Therefore, the present study aimed to prepare semiconductor zinc oxide nanoparticles (ZnO NPs) and plasmonic Ag-supported ZnO nanocomposite (ZnO–Ag) using an environmentally friendly bio-approach as an alternative to hazardous synthesis approaches. ZnO NPs and ZnO–Ag nanocomposite were characterized by using UV–Vis diffuse reflectance spectroscopy (UV–DRS) (the Ag-supported ZnO nanocomposite exhibited an absorption band between 450–550 nm, attributed to the Ag NPs surface plasmon resonance (SPR)), Photoluminescence (PL) spectral investigation, which revealed the PL emission intensity of ZnO–Ag NPs was lower than pure ZnO NPs, describing an extended electron-hole pair (e--h+) lifespan of photogenerated charge carriers, Fourier transform infrared spectroscopy (FTIR), FT-Raman, and X-ray diffraction (XRD) analyses were deduced. In addition, energy dispersive X-ray spectroscopy (SEM-EDX), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA) were performed and further ascertained the successful biosynthesis and thermally stable ZnO Nps and ZnO–Ag nanocomposite. The as-prepared ZnO–Ag nanocomposite displayed increased photocatalytic characteristics due to the decline in the bandgap energy from 3.02 eV (ZnO NPs) to 2.90 eV (ZnO–Ag nanocomposite). The photocatalytic activity of the developed nanocomposite for the degradation of methylene blue (MB) dye, a primary textile industry released water-pollutant, was conducted under UV light irradiation. Meanwhile, the maximum % degradation of MB dye molecules was attained by 98.0 % after 60 min exposure of UV-light irradiation. Increased photocatalytic activity of ZnO–Ag nanocomposites and a faster rate of MB degradation were achieved by the deposition of plasmonic Ag NPs and the surface plasmon resonance (SPR) effect possessed by Ag NPs. The primary oxidative route that resulted in MB degradation was the production of hydroxyl radicals (OH•). The SPR effect of the photocatalyst induced the synergistic enhancement of the optical response and separation of the photo-induced charge carriers. The combined study gives comprehensive information and directions for future research on noble metal-modified nanocatalysts for direct applications in the photocatalytic degradation of textile and organic wastes in water.

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Shaeel A. Al-Thabaiti

Papers

Supported Zeolite Beta Layers via an Organic Template-Free Preparation Route.

Design, Characterization and antimicrobial activity of Cu(II), Co(II) and Zn(II) complexes with Schiff base from 1,2-diphenylethane-1,2-dione and N-(1-Naphthyl) ethylenediamine

Facile Green Synthesis of ZnO NPs and Plasmonic Ag-Supported ZnO Nanocomposite for Photocatalytic Degradation of Methylene Blue

Bioactive Macrocyclic Ni(II) Metal Complex: Synthesis, Spectroscopic Elucidation, and Antimicrobial Studies

Effects of electrolytes and surfactants on the morphology and stability of advanced silver nano-materials