An overview on ZnO-based sonophotocatalytic mitigation of aqueous phase pollutants.

Over the past several decades, the increase in industrialization provoked the discharge of harmful pollutants into the environment, affecting human beings and ecosystems. ZnO-based photocatalysts seem to be the most promising photocatalysts for treating harmful pollutants. However, fast charge carrier recombination, photo corrosion, and long reaction time are the significant factors that reduce the photoactivity of ZnO-based photocatalysts. In order to enhance the photoactivity of such photocatalysts, a combined process i.e., sonocatalysis + photocatalysis = sonophotocatalysis was used. Sonophotocatalysis is one of several different AOP methods that have recently drawn considerable interest, as it produces high reactive oxygen species (ROS) which helps in the oxidation of pollutants by acoustic cavitation. This combined technique enhanced the overall efficiency of the individual method by overcoming its limiting factors. The current review aims to present the theoretical and fundamental aspects of sonocatalysis and photocatalysis along with a detailed discussion on the benefits that can be obtained by the combined process i.e., US + UV (sonophotocatalysis). Also, we have provided a comparison of the excellent performance of ZnO to that of the other metal oxides. The purpose of this study is to discuss the literature concerning the potential applications of ZnO-based sonophotocatalysts for the degradation of pollutants i.e., dyes, antibiotics, pesticides, phenols, etc. That are carried out for future developments. The role of the produced ROS under light and ultrasound stimulation and the degradation mechanisms that are based on published literature are also discussed. In the end, future perspectives are suggested, that are helpful in the development of the sonophotocatalysis process for the remediation of wastewater containing various pollutants.

Recent advances in Metal Organic Framework (MOF)-based hierarchical composites for water treatment by adsorptional photocatalysis: A review.

Architecting a desirable and highly efficient nanocomposite for applications like adsorption, catalysis, etc. has always been a challenge. Metal Organic Framework (MOF)-based hierarchical composite has perceived popularity as an advanced adsorbent and catalyst. Hierarchically structured MOF material can be modulated to allow the surface interaction (external or internal) of MOF with the molecules of interest. They are well endowed with tunable functionality, high porosity, and increased surface area epitomizing mass transfer and mechanical stability of the fabricated nanostructure. Additionally, the anticipated optimization of nanocomposite can only be acquired by a thorough understanding of the synthesis techniques. This review starts with a brief introduction to MOF and the requirement for advanced nanocomposites after the setback faced by conventional MOF structures. Further, we discussed the background of MOF-based hierarchical composites followed by synthetic techniques including chemical and thermal treatment. It is important to rationally validate the successful nanocomposite fabrication by characterization techniques, an overview of challenges, and future perspectives associated with MOF-based hierarchically structured nanocomposite.

Photo-Fenton assisted AgCl and P-doped g-C3N4 Z-scheme photocatalyst coupled with Fe3O4/H2O2 system for 2, 4-dimethylphenol degradation.

In this study graphitic carbon nitride (g-C3N4 or GCN) and phosphorus doped graphitic carbon nitride (p-g-C3N4 or PCN) were prepared using facile thermal polycondensation method. Phosphorus doping was employed to preserve the non-metallic nature of GCN. The AgCl/PCN/Fe3O4 heterojunction was synthesized using a simple in-situ route. The photocatalytic performance of the GCN, PCN, Fe3O4 and AgCl/PCN/Fe3O4 was tested towards 2, 4-dimethylphenol (DMP) pollutant. The work explored improvement in physiochemical properties and reduction of band gap of GCN after P doping (through Tauc's plot method). Coupling with AgCl (silver halide) also enhanced photoinduced charge carriers' separation and migration ability due to apt band alignment among both AgCl and PCN photocatalysts which resulted in formation of direct Z-scheme charge transfer mechanism. Similarly, the incorporation of ferrimagnetic material i.e. Fe3O4 enhanced the generation of hydroxyl (•OH) radicals via photo-Fenton process and facilitated photocatalysts easy separation from the aqueous medium. Through PL and EIS analysis the enhanced charge separation and migration ability in AgCl/PCN/Fe3O4 nanocomposite was validated. The attained DMP degradation efficiency of photo-Fenton assisted AgCl/PCN/Fe3O4/H2O2 Z-scheme nanocomposite was much higher i.e. 99% compared to other photocatalysts within 60 min of visible light irradiation following pseudo-first-order kinetics. Electron paramagnetic resonance (EPR) and scavenging tests confirmed the substantial role of •OH and •O2- radicals in the photo-Fenton reaction. Furthermore, liquid chromatography-mass spectrometry (LC-MS) analysis detected the generated oxidative products and mineralization pathways associated with DMP degradation. The proposed direct Z-scheme charge transfer route presented efficient charge separation and migration ability in AgCl/PCN/Fe3O4 nanocomposite. Recycle ability of the fabricated AgCl/PCN/Fe3O4 photocatalyst was tested up to 5 cycles with 90% removal efficacy, confirming the excellent reusability and stability of AgCl/PCN/Fe3O4 photocatalyst.

Insertion of metal cations into hybrid organometallic halide perovskite nanocrystals for enhanced stability: eco-friendly synthesis, lattice strain engineering, and defect chemistry studies.

In this work, we developed a facile and environmentally friendly synthesis strategy for large-scale preparation of Cr-doped hybrid organometallic halide perovskite nanocrystals. In the experiment, methylammonium lead bromide, CH3NH3PbBr3, was efficiently doped with Cr3+ cations by eco-friendly method at low temperatures to grow crystals via antisolvent-crystallization. The as-synthesized Cr3+ cation-doped perovskite nanocrystals displayed ∼45.45% decrease in the (100) phase intensity with an enhanced Bragg angle (2θ) of ∼15.01° compared to ∼14.92° of pristine perovskites while retaining their cubic (221/Pm-cm, ICSD no. 00-069-1350) crystalline phase of pristine perovskites. During synthesis, an eco-friendly solvent, ethanol, was utilized as an antisolvent to grow nanometer-sized rod-like crystals. However, Cr3+ cation-doped perovskite nanocrystals display a reduced crystallinity of ∼67% compared to pristine counterpart with ∼75% crystallinity with an improved contact angle of ∼72° against water in thin films. Besides, as-grown perovskite nanocrystals produced crystallite size of ∼48 nm and a full-width-at-half-maximum (FWHM) of ∼0.19° with an enhanced lattice-strain of ∼4.52 × 10-4 with a dislocation-density of ∼4.24 × 1014 lines per m2 compared to pristine perovskite nanocrystals, as extracted from the Williamson-Hall plots. The as-obtained stable perovskite materials might be promising light-harvesting candidates for optoelectronic applications in the future.

Recent progress on elemental sulfur based photocatalysts for energy and environmental applications.

The growing needs of the rising population and blatant misuse of resources have contributed enormously to environmental problems. Among the various methods, photocatalysis has emerged as one of the effective remediation methods. The continuous search for effective photocatalysts that can be made from abundant, cheap, non-toxic materials is going on. Although sulfur is a known insulator, recent sulfur use as a visible light photocatalyst has ushered a new era in this direction. Sulfur is a non-toxic, cheap, and abundant photocatalyst, exhibiting significant photocatalytic properties. But, hydrophobicity, poor light-harvesting and high recombination rate of charge carriers in elemental sulfur photocatalyst are some of the major drawbacks of the elemental sulfur photocatalyst. The photocatalytic activity of sulfur as a single element was low, but various methods such as nanoscaling, heterojunction formation, doping and surface modifications have been used to enhance it. The review highlights sulfur's crystal structure, electronic and optical properties, and morphological changes, making it an excellent visible light photocatalyst. The article points to the limitations of sulfur as a single photocatalyst and various strategies to improve the shortcomings. More recently, there has been an emphasis on the synthesis of metal-free photocatalysts. This review provides its readers with a comprehensive detail of sulfur being used as a dopant in improving the photocatalytic properties of metal-free photocatalysts and their environmental remediation use. Finally, the conclusion and future perspectives for sulfur-based nanostructures are presented.

Green aspects of photocatalysts during corona pandemic: a promising role for the deactivation of COVID-19 virus.

The selection of a facile, eco-friendly, and effective methodology is the need of the hour for efficient curing of the COVID-19 virus in air, water, and many food products. Recently, semiconductor-based photocatalytic methodologies have provided promising, green, and sustainable approaches to battle against viral activation via the oxidative capabilities of various photocatalysts with excellent performance under moderate conditions and negligible by-products generation as well. Considering this, recent advances in photocatalysis for combating the spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are inclusively highlighted. Starting from the origin to the introduction of the coronavirus, the significant potential of photocatalysis against viral prevention and -disinfection is discussed thoroughly. Various photocatalytic material-based systems including metal-oxides, metal-free and advanced 2D materials (MXenes, MOFs and COFs) are systematically examined to understand the mechanistic insights of virus-disinfection in the human body to fight against COVID-19 disease. Also, a roadmap toward sustainable solutions for ongoing COVID-19 contagion is also presented. Finally, the challenges in this field and future perspectives are comprehensively discussed involving the bottlenecks of current photocatalytic systems along with potential recommendations to deal with upcoming pandemic situations in the future.

Graphitic carbon nitride based immobilized and non-immobilized floating photocatalysts for environmental remediation.

In solar photocatalysis, light utilization and recycling of powder from reaction solution are the main obstructions that hinder the photocatalytic efficacy of any photocatalyst. In this respect, a floatable system is effective for efficient solar photocatalysis by light utilization. Due to the maximum solar light absorption property, floating nanocomposite photocatalyst is an appealing substitute for effective wastewater treatment. Floating photocatalysts are a non-oxygenated and non-stirred solution that is a good light harvester, stable, non-toxic, biodegradable, naturally abundant in nature. They also have low density, a simple preparation process, no need to stir, and high porosity. Due to these characteristics, floating photocatalysts are widely favored and ideal candidates for practical environmental remediation. Several researchers have come up with new and innovative ways for immobilizing capable photocatalyst on a floatable substrate to produce floating nanocomposite photocatalytic material. In recent decades, g-C3N4-based floating photocatalysts have gained a lot of attention as g-C3N4 is a visible light active photocatalyst with unique and exceptional properties. It also has good photocatalytic activity in waste water treatment and environmental remediation. Many previous reports have studied the logical design and manufacturing method for heterojunction floating photocatalysts and immobilized floating photocatalysts. Based on those studies, we have focused on the g-C3N4 based immobilized and non-immobilized floating photocatalysts for pollutant degradation. We have also categorized immobilized floating photocatalyst based on several lightweight substrates such as expanded perlite and glass microbead. In addition, future challenges have been discussed to maximize solar light absorption and to improve the efficiency of broadband response floating photocatalysts. Floating photocatalysis is an advanced technique in energy conversion and environmental remediation thus requires special consideration.

Emerging architecture titanium carbide (Ti3C2Tx) MXene based photocatalyst toward degradation of hazardous pollutants: Recent progress and perspectives.

MXenes family has aroused marvelous consideration as a frontier photoactive candidate for solar energy transformation and environmental remediation. 2D Ti3C2 exhibit a unique layered microstructure, large surface functional groups (-F, -OH, -O), substantial sorption selectivity, superior reduction efficiency, and electrical conductivity. Electronically conductive Ti3C2Tx with tunable energy band gap (0.92-1.75eV) makes it one of the most potential photoactive materials for photodegradation. The present review paper aims to design cost-effective heterojunctions and Schottky junctions of Ti3C2 with transition metal oxides, sulfides, g-C3N4, and other organic frameworks. The discussion mainly involves different aspects related to its tunable electronic structure, stability problems, and surface morphology control. In addition, the advantages of Ti3C2 in fabricating highly efficient Ti3C2 based catalytic junctions exhibiting suppressed charge carrier recombination are discussed with particular emphasis on their adsorption and redox properties for the removal of toxic dyes, heavy metal ions, and various pharmaceuticals. Finally, current challenges and research directions are outlined and prospected for the future development of Ti3C2 based photocatalytic systems.

Strategies based review on near-infrared light-driven bismuth nanocomposites for environmental pollutants degradation.

Recently, solar energy has been considered the most vulnerable source to resolve environmental pollution and energy scarcity problems. Researchers have made intense research efforts to convert solar energy into chemical energy through photocatalysis processes as it is a green, clean and renewable energy source. Numerous discovered photocatalysts show absorption in the ultraviolet-visible (UV∼5% and visible ∼43%) region and are devoid of near-infrared (NIR ∼52%) light utilization. As infrared (IR) light contains a top portion of the solar spectrum; therefore, many alluring and attractive practical strategies have been explored to improve photocatalytic reactions and to harness full solar spectrum (including NIR light). Among those strategies, bandgap engineering, coupling with carbon quantum dots, heterostructure formation, mingling with plasmonic and upconversion (UC) NPs are more worthwhile. In different visible light-assisted photocatalysts, bismuth typically covers a distinctive, favorable, and earth-abundant group of freshly discovered innovative photocatalytic nanomaterials. Bi-based photocatalysts have suitable/good optoelectronic properties, crystalline geometric conformations, amendable electronic structure, and outstanding visible-light responsive range, helpful in environmental remediation and energy transformation. Due to the outstanding photo-oxidization/photodegradation capability of NIR-driven photocatalysts, bismuth-based nanomaterials have been considered suitable photocatalysts for inclusive solar energy utilization. Henceforth, keeping in mind the benefits of bismuth nanomaterials, the present review is focused on NIR-based modification strategies to upgrade solar light absorption of bismuth-based photocatalysts in the NIR region by making it NIR responsive photocatalyst. We have also discussed the photocatalytic applications of bismuth-based NIR responsive photocatalysts in pollutant degradation.

Fabrication of a lead ion selective membrane based on a polycarbazole Sn(iv) arsenotungstate nanocomposite and its ion exchange membrane (IEM) kinetic studies.

A polycarbazole-Sn(iv) arsenotungstate (Pcz-SnAT) nanocomposite cation exchanger membrane (CEM) was prepared via the casting solution technique utilizing polycarbazole-Sn(iv) arsenotungstate and PVC (polyvinyl chloride) as a binder. The synthesis of the Pcz-SnAT membrane was confirmed via various characterization methods such as EDX, SEM, TGA, XRD, and FTIR spectroscopy. This membrane having a 4.5 : 1 composition ratio of composite by PVC exhibited the most effective outcomes for swelling, thickness, porosity, and water content. Our research indicates that the present ion selective membrane electrode is selective towards Pb(ii) ions, with the detection limit ranging from 1 × 10-7 mol L-1 to 1 × 10-1 mol L-1 where 20 s is the response time and 3-7 is the working value pH. The mechanism of the Pcz SnAT ion exchange membrane was obtained by kinetic studies by utilizing the equation given by Nernst Planck at 40-80 °C. As a result, activation energy and thermodynamic studies were done. The analytical utility of this electrode is conventional by utilizing it as an electrode indicator within the potentiometric titration.