Facet-Dependent Competitive Adsorption Mechanisms of Chromate and Oxalic Acid on γ-FeO(OH) Nanocrystals.

Facet-dependent toxic metal adsorption of iron oxides widely occurred in natural environments. It is known that organic acids can alter the adsorption behaviors of trace elements by cooperative or competitive effects. However, the coadsorption mechanisms of the specific facets are still not fully understood. In the current investigation, Cr(VI) adsorption onto the lepidocrocite (γ-FeO(OH))-exposed facets in the presence of oxalic acid (OA) was studied using macroexperiments, in situ attenuated total reflectance Fourier transform infrared spectroscopy, X-ray adsorption fine structure, and density functional theory calculations. Rod-like lepidocrocite (R-LEP) with a high ratio of {001}/{010} facet showed excellent Cr(VI) adsorption capacity than that of plate-like lepidocrocite (P-LEP, the dominant facet is {010}) in the absence/presence of OA. Interestingly, OA reacted with R-LEP would be easier to diminish Cr(VI) adsorption than with P-LEP. The competitive adsorption occurred on the {001} facet due to the formation of inner-sphere OA configurations (monodentate mononuclear and bidentate mononuclear structures) and a bidentate binuclear Cr(VI) complex. However, OA coordinated with {010} facets via the outer-sphere complexes, while Cr(VI) could form a protonated monodentate binuclear configuration. These observations suggest that the competitive adsorption processes between OA and Cr(VI) exhibit facet dependence. Furthermore, lepidocrocite-exposed facets determine the interfacial interactions and geochemical behaviors of Cr(VI) in polluted environments.

Formation and transformation of reactive species in the Fe2+/peroxydisulfate/Cl- system.

The influence of Cl- on the formation mechanism of active components is often neglected in the Fe2+/peroxydisulfate (PDS) system containing a large amount of ferryl ion reactive specie (Fe(Ⅳ)). In the current investigation, the effects of Cl- concentration on the removal of methyl phenyl sulfoxide (PMSO), the formation of methyl phenyl sulfone (PMSO2), the transformation of reactive species and oxidation products were investigated under different reaction conditions that included Fe2+ dosage, PDS dosage, and pH0. The results showed that Cl- complexing Fe2+ increased the formation path of sulfate radical (SO4·-) in the Fe2+/PDS system. Fe2+ dosage and pH0 value affected the content and morphology of Fe2+-Cl- complex, thus affecting the composition of reactive species. According to the experiment of free radical steady-state concentration, it was found that low concentration of Cl- reacted with SO4·- and increased the steady-state concentration of chlorine radicals (8.09 × 10-13 M [·Cl]ss at 1.41 mM Cl-), while at high concentration of Cl-, the contents of SO4·-, hydroxyl radical (·OH) and dichloride anion radicals (Cl2·-) increased and the contents of Fe(Ⅳ) and ·Cl decreased. ·Cl had strong reactivity with PMSO, and PMSO and its oxidation products were chlorinated under the combined action of ·Cl and Cl2·-. This work reveals the reaction mechanism and environmental application risks of Fe2+/PDS technology and lays the groundwork for subsequent industrial application of Fe2+/PDS system.

Antimicrobial TiO2 nanocomposite coatings for surfaces, dental and orthopaedic implants.

Engineering of self-disinfecting surfaces to constrain the spread of SARS-CoV-2 is a challenging task for the scientific community because the human coronavirus spreads through respiratory droplets. Titania (TiO2) nanocomposite antimicrobial coatings is one of the ideal remedies to disinfect pathogens (virus, bacteria, fungi) from common surfaces under light illumination. The photocatalytic disinfection efficiency of recent TiO2 nanocomposite antimicrobial coatings for surfaces, dental and orthopaedic implants are emphasized in this review. Mostly, inorganic metals (e.g. copper (Cu), silver (Ag), manganese (Mn), etc), non-metals (e.g. fluorine (F), calcium (Ca), phosphorus (P)) and two-dimensional materials (e.g. MXenes, MOF, graphdiyne) were incorporated with TiO2 to regulate the charge transfer mechanism, surface porosity, crystallinity, and the microbial disinfection efficiency. The antimicrobial activity of TiO2 coatings was evaluated against the most crucial pathogenic microbes such as Escherichia coli, methicillin-resistant Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis, Legionella pneumophila, Staphylococcus aureus, Streptococcus mutans, T2 bacteriophage, H1N1, HCoV-NL63, vesicular stomatitis virus, bovine coronavirus. Silane functionalizing agents and polymers were used to coat the titanium (Ti) metal implants to introduce superhydrophobic features to avoid microbial adhesion. TiO2 nanocomposite coatings in dental and orthopaedic metal implants disclosed exceptional bio-corrosion resistance, durability, biocompatibility, bone-formation capability, and long-term antimicrobial efficiency. Moreover, the commercial trend, techno-economics, challenges, and prospects of antimicrobial nanocomposite coatings are also discussed briefly.

UV and Visible Light-Driven Production of Hydroxyl Radicals by Reduced Forms of N, F, and P Codoped Titanium Dioxide.

The photocatalytic activities of reduced titanium dioxide (TiO2) materials have been investigated by measuring their ability to produce hydroxyl radicals under UV and visible light irradiation. Degussa P25 TiO2 was doped with nitrogen (N), fluorine (F), and/or phosphorus (P) and then subjected to surface modification employing a thermo-physicochemical process in the presence of reducing agent sodium borohydride (NaBH4). The reduced TiO2 materials were characterized by a number of X-ray, spectroscopic and imaging methods. Surface doping of TiO2 was employed to modulate the band gap energies into the visible wavelength region for better overlap with the solar spectrum. Hydroxyl radical generation, central to TiO2 photocatalytic water purification applications, was quantitated using coumarin as a trap under UV and visible light irradiation of the reduced TiO2 materials. At 350 nm irradiation, the yield of hydroxyl radicals generated by the reduced forms of TiO2 was nearly 90% of hydroxyl radicals generated by the Degussa P25 TiO2. Hydroxyl radical generation by these reduced forms of TiO2 was also observed under visible light irradiation (419 and 450 nm). These results demonstrated that simple surface modification of doped TiO2 can lead to visible light activity, which is important for more economical solar-driven applications of TiO2 photocatalysis.

Novel microwave assisted synthesis of ZnS nanomaterials.

A novel ambient pressure microwave assisted technique is developed in which silver and indium-modified ZnS is synthesized. The as-prepared ZnS is characterized by x-ray diffraction, UV-vis spectroscopy, x-ray photoelectron spectroscopy and luminescence spectroscopy. This procedure produced crystalline materials with particle sizes below 10 nm. The synthesis technique leads to defects in the crystal which induce mid-energy levels in the band gap and lead to indoor light photocatalytic activity. Increasing the amount of silver causes a phase transition from cubic blende to hexagonal phase ZnS. In a comparative study, when the ZnS cubic blende is heated in a conventional chamber furnace, it is completely converted to ZnO at 600 °C. Both cubic blende and hexagonal ZnS show excellent photocatalytic activity under irradiation from a 60 W light bulb. These ZnS samples also show significantly higher photocatalytic activity than the commercially available TiO(2) (Evonik-Degussa P-25).

Directed morphology engineering of 2D MoS2 nanosheets to 1D nanoscrolls with enhanced hydrogen evolution and specific capacitance.

1D-molybdenum disulfide (MoS2) nanoscrolls displayed enhanced electrochemical properties compared to 2D-MoS2 nanosheet counterparts. Rolling of nanosheets is the main fabrication route to nanoscrolls. However, owing to the conflict between chemical stability and multiple bending, the morphology transition from nanosheets to nanoscrolls is quite challenging. Herein we describe a reversible morphology transition from nanosheets to nanoscrolls by utilizing non-covalent interactions between MoS2 nanosheets and phenothiazine based organic dye. Interestingly, nanoscrolls can easily be opened back into nanosheets by destroying the non-covalent interactions with organic solvents. The prepared nanoscrolls exhibited enhanced electrochemical properties than nanosheets. Compared to nanosheets, nanoscrolls exhibited comparatively lower overpotential with a Tafel slope of 141 mV dec-1 and high specific capacitance of 1868 F g-1. Hydrogen evolution by the Volmer-Heyrovsky mechanism being superior for the nanoscrolls is envisaged by the relatively increased availability of Hads sites at MoS2 edges induced by scrolling. Whereas the high specific capacitance value of nanoscrolls is ascribed to the enhanced electrical double-layer capacitance mediated charge storage, which arises due to the synergistic effect of both scrolled structure and the electron-rich phenothiazine-based dye.

Activated peroxydisulfate by sorghum straw-based biochar for enhanced tartrazine degradation: Roles of adsorption and radical/nonradical processes.

Biochar obtained from biomass waste through pyrolysis has significant potential in wastewater treatment due to its large specific surface area and multi-functional active sites. In current study, sorghum straw (SS) was pyrolyzed to prepare various biochar under nitrogen atmosphere. Adsorption kinetics of prepared biochar toward tartrazine (TTZ) was systematically investigated, and the biochar was also characterized by using multiple techniques to explore the contribution of physicochemical properties to adsorption. Then, the biochar with optimum TTZ adsorption performance, was also applied as a catalyst for peroxydisulfate (PDS) activation to degrade TTZ. Factors including PDS concentration, solution pH, and reaction temperature were examined. The optimized degradation rate constant of TTZ (1.1627 min-1) was achieved under the conditions at 2 mM PDS, pH of 3, and 23 °C. In addition, the free radical trapping experiments and EPR spectra revealed that the reactive substances of electron (e-), 1O2, SO4•-, O2•-, and •OH contributed to TTZ degradation. Density Functional Theory (DFT) also concluded that the atoms C(6), O(12), N(16), N(17), C(18) and N(22) in TTZ molecule showed larger f0 values which are vulnerable to radical attack. Therefore, the synergistic mechanism embodying adsorption and radical/non-radical processes were proposed. Besides, the degradation pathways of TTZ were identified with the aid of HPLC/MS technique, indicating that multiple reaction processes containing the symmetrical cleavage of azo bonds, the asymmetrical cleavage of C-N, desulfonation, and benzene-like structure cracking were involved. Therefore, this study provides a simple and effective catalytic system for TTZ degradation, and also realizes the resource utilization of solid waste.

Nanostructured Ti(1-x)S(x)O(2-y)N(y) heterojunctions for efficient visible-light-induced photocatalysis.

Highly visible-light-active S,N-codoped anatase-rutile heterojunctions are reported for the first time. The formation of heterojunctions at a relatively low temperature and visible-light activity are achieved through thiourea modification of the peroxo-titania complex. FT-IR spectroscopic studies indicated the formation of a Ti(4+)-thiourea complex upon reaction between peroxo-titania complex and thiourea. Decomposition of the Ti(4+)-thiourea complex and formation of visible-light-active S,N-codoped TiO(2) heterojunctions are confirmed using X-ray diffraction, Raman spectroscopy, transmission electron microscopy, and UV/vis spectroscopic studies. Existence of sulfur as sulfate ions (S(6+)) and nitrogen as lattice (N-Ti-N) and interstitial (Ti-N-O) species in heterojunctions are identified using X-ray photoelectron spectroscopy (XPS) and FT-IR spectroscopic techniques. UV-vis and valence band XPS studies of these S,N-codoped heterojunctions proved the fact that the formation of isolated S 3p, N 2p, and Π* N-O states between the valence and conduction bands are responsible for the visible-light absorption. Titanium dioxide obtained from the peroxo-titania complex exists as pure anatase up to a calcination temperature as high as 900 °C. Whereas, thiourea-modified samples are converted to S,N-codoped anatase-rutile heterojunctions at a temperature as low as 500 °C. The most active S,N-codoped heterojunction 0.2 TU-TiO(2) calcined at 600 °C exhibits a 2-fold and 8-fold increase in visible-light photocatalytic activities in contrast to the control sample and the commercial photocatalyst Degussa P-25, respectively. It is proposed that the efficient electron-hole separation due to anatase to rutile electron transfer is responsible for the superior visible-light-induced photocatalytic activities of S,N-codoped heterojunctions.

Electrode materials for stretchable triboelectric nanogenerator in wearable electronics.

Stretchable Triboelectric Nanogenerators (TENGs) for wearable electronics are in significant demand in the area of self-powered energy harvesting and storage devices. Designing a suitable electrode is one of the major challenges in developing a fully wearable TENG device and requires research aimed at exploring new materials and methods to develop stretchable electrodes. This review article is dedicated to presenting recent developments in exploring new materials for flexible TENGs with special emphasis on electrode components for wearable devices. In addition, materials that can potentially deliver properties such as transparency, self-healability and water-resistance are also reviewed. Inherently stretchable materials and a combination of soft and rigid materials including polymers and their composites, inorganic and ceramic materials, 2D materials and carbonaceous nanomaterials are also addressed. Additionally, various fabrication strategies and geometrical patterning techniques employed for designing highly stretchable electrodes for wearable TENG devices are also explored. The challenges reflected in the present approaches as well as feasible suggestions for future advancements are discussed.

Insights into the mechanism of low-temperature H2S oxidation over Zn-Cu/Al2O3 catalyst.

Odor pollution caused by toxic chemicals with low human olfactory thresholds, such as hydrogen sulfide (H2S), has become a major cause of environmental grievance world-wide. Although the low-temperature (<180 °C) catalytic oxidation of H2S using metal oxides has received widespread attention, desulfurization performance is not ideal. Herein, a series of Zn-Cu/Al2O3 catalysts were developed using an impregnation method based on the Al2O3 hydrophilicity and the effects of zinc loading on the catalyst physicochemical properties and performance were systematically studied. The catalysts were characterized using inductively coupled plasma-optical emission spectrometry (ICP-OES), N2 adsorption-desorption isotherms, scanning electron microscopy with energy dispersive spectrometry (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR) and electron paramagnetic resonance (EPR). It was found that optimization of zinc doping could improve the hydrophilicity of the catalyst, and hence its activity. Catalytic activity was also dependent on operational parameters such as temperature, humidity and space velocity. The Zn3Cu3 catalyst exhibited the highest breakthrough capacity of 353.91 mg/g at 50 °C and at a relative humidity of 50%. The excellent desulfurization performance was attributed to oxygen vacancies contributed by CuO, Cu2O and ZnO, which facilitated the conversion of H2O into hydroxyl radicals. Consequently, a hydroxyl radical-induced desulfurization mechanism over Zn-Cu/Al2O3 is proposed. This work provides a potential green and efficient catalyst for the selective oxidation of H2S.

COVID-19: Rapid prototyping and production of face shields via flat, laser-cut, and 3D-printed models.

The use of personal protective equipment (PPE) has become essential to reduce the transmission of coronavirus disease 2019 (COVID-19) as it prevents the direct contact of body fluid aerosols expelled from carriers. However, many countries have reported critical supply shortages due to the spike in demand during the outbreak in 2020. One potential solution to ease pressure on conventional supply chains is the local fabrication of PPE, particularly face shields, due to their simplistic design. The purpose of this paper is to provide a research protocol and cost implications for the rapid development and manufacturing of face shields by individuals or companies with minimal equipment and materials. This article describes a best practice case study in which the establishment of a local manufacturing hub resulted in the swift production of 12,000 face shields over a seven-week period to meet PPE shortages in the North-West region of Ireland. Protocols and processes for the design, materials sourcing, prototyping, manufacturing, and distribution of face shields are described. Three types of face shields were designed and manufactured, including Flat, Laser-cut, and 3D-printed models. Of the models tested, the Flat model proved the most cost-effective (€0.51/unit), while the Laser-cut model was the most productive (245 units/day). The insights obtained from this study demonstrate the capacity for local voluntary workforces to be quickly mobilised in response to a healthcare emergency, such as the COVID-19 pandemic.

Face masks and respirators in the fight against the COVID-19 pandemic: An overview of the standards and testing methods.

The COVID-19 outbreak has resulted in a shortage of personal protective equipment (PPE) throughout the world. This shortage has resulted in an increase in production of PPE to meet the demand, and as a result, several substandard equipment has entered the market. With face masks and respirators now beginning to see widespread use throughout the world, the standards and test with which they are required to undertake have become points of interest. The filtration efficiency of the masks is a key testing element that examines its ability to filter particles, bacteria and viruses; this examines the penetration efficiency percentage of each with lower results being preferable. Masks are also subjected to NaCl testing method, which allows a range of particle sizes to be examined and their penetration to be observed. The masks must also show considerable resistance to fluids and flames, to prevent the penetration of liquids and to be non-flammable. Various PPE testing protocols such as biological, chemical, fluid and flame resistances, protective ensemble, facepiece fit testing, NIOSH NaCl method and impact protection have been discussed. In addition, various tests involving bacterial and viral filtration efficiencies are also discussed. Differential pressure is examined to ascertain the comfort, airflow and breathability of the masks, whilst fit testing is examined to ensure a correct fit of the mask.

Heterogeneous Fenton catalysts: A review of recent advances.

Heterogeneous Fenton catalysts are emerging as excellent materials for applications related to water purification. In this review, recent trends in the synthesis and application of heterogeneous Fenton catalysts for the abatement of organic pollutants and disinfection of microorganisms are discussed. It is noted that as the complexity of cell wall increases, the resistance level towards various disinfectants increases and it requires either harsh conditions or longer exposure time for the complete disinfection. In case of viruses, enveloped viruses (e.g. SARS-CoV-2) are found to be more susceptible to disinfectants than the non-enveloped viruses. The introduction of plasmonic materials with the Fenton catalysts broadens the visible light absorption efficiency of the hybrid material, and incorporation of semiconductor material improves the rate of regeneration of Fe(II) from Fe(III). A special emphasis is given to the use of Fenton catalysts for antibacterial applications. Composite materials of magnetite and ferrites remain a champion in this area because of their easy separation and reuse, owing to their magnetic properties. Iron minerals supported on clay materials, perovskites, carbon materials, zeolites and metal-organic frameworks (MOFs) dramatically increase the catalytic degradation rate of contaminants by providing high surface area, good mechanical stability, and improved electron transfer. Moreover, insights to the zero-valent iron and its capacity to remove a wide range of organic pollutants, heavy metals and bacterial contamination are also discussed. Real world applications and the role of natural organic matter are summarised. Parameter optimisation (e.g. light source, dosage of catalyst, concentration of H2O2 etc.), sustainable models for the reusability or recyclability of the catalyst and the theoretical understanding and mechanistic aspects of the photo-Fenton process are also explained. Additionally, this review summarises the opportunities and future directions of research in the heterogeneous Fenton catalysis.

Carbonaceous cathode materials for electro-Fenton technology: Mechanism, kinetics, recent advances, opportunities and challenges.

Electro-Fenton (EF) technique has gained significant attention in recent years owing to its high efficiency and environmental compatibility for the degradation of organic pollutants and contaminants of emerging concern (CECs). The efficiency of an EF reaction relies primarily on the formation of hydrogen peroxide (H2O2) via 2e─ oxygen reduction reaction (ORR) and the generation of hydroxyl radicals (●OH). This could be achieved through an efficient cathode material which operates over a wide pH range (pH 3-9). Herein, the current progresses on the advancements of carbonaceous cathode materials for EF reactions are comprehensively reviewed. The insights of various materials such as, activated carbon fibres (ACFs), carbon/graphite felt (CF/GF), carbon nanotubes (CNTs), graphene, carbon aerogels (CAs), ordered mesoporous carbon (OMCs), etc. are discussed inclusively. Transition metals and hetero atoms were used as dopants to enhance the efficiency of homogeneous and heterogeneous EF reactions. Iron-functionalized cathodes widened the working pH window (pH 1-9) and limited the energy consumption. The mechanism, reactor configuration, and kinetic models, are explained. Techno economic analysis of the EF reaction revealed that the anode and the raw materials contributed significantly to the overall cost. It is concluded that most reactions follow pseudo-first order kinetics and rotating cathodes provide the best H2O2 production efficiency in lab scale. The challenges, future prospects and commercialization of EF reaction for wastewater treatment are also discussed.

Biomedical Applications of Electrospun Graphene Oxide.

Graphene oxide (GO) has broad potential in the biomedical sector. The oxygen-abundant nature of GO means the material is hydrophilic and readily dispersible in water. GO has also been known to improve cell proliferation, drug loading, and antimicrobial properties of composites. Electrospun composites likewise have great potential for biomedical applications because they are generally biocompatible and bioresorbable, possess low immune rejection risk, and can mimic the structure of the extracellular matrix. In the current review, GO-containing electrospun composites for tissue engineering applications are described in detail. In addition, electrospun GO-containing materials for their use in drug and gene delivery, wound healing, and biomaterials/medical devices have been examined. Good biocompatibility and anionic-exchange properties of GO make it an ideal candidate for drug and gene delivery systems. Drug/gene delivery applications for electrospun GO composites are described with a number of examples. Various systems using electrospun GO-containing therapeutics have been compared for their potential uses in cancer therapy. Micro- to nanosized electrospun fibers for wound healing applications and antimicrobial applications are explained in detail. Applications of various GO-containing electrospun composite materials for medical device applications are listed. It is concluded that the electrospun GO materials will find a broad range of biomedical applications such as cardiac patches, medical device coatings, sensors, and triboelectric nanogenerators for motion sensing and biosensing.

Graphene coupled TiO2 photocatalysts for environmental applications: A review.

Nanostructured photocatalysts have always offered opportunities to solve issues concerned with the environmental challenges caused by rapid urbanization and industrialization. These materials, due to their tunable physicochemical characteristics, are capable of providing a clean and sustainable ecosystem to humanity. One of the current thriving research focuses of visible-light-driven photocatalysts is on the nanocomposites of titanium dioxide (TiO2) with carbon nanostructures, especially graphene. Coupling TiO2 with graphene has proven more active by photocatalysis than TiO2 alone. It is generally considered that graphene sheets act as an electron acceptor facilitating the transfer and separation of photogenerated electrons during TiO2 excitation, thereby reducing electron-hole recombination. This study briefly reviews the fundamental mechanism and interfacial charge-transfer dynamics in TiO2/graphene nanocomposites. Design strategies of various graphene-based hybrids are highlighted along with some specialized synthetic routes adopted to attain preferred properties. Importantly, the enhancing interfacial charge transfer of photogenerated e¯CB through the graphene layers by morphology orientation of TiO2, predominated exposure of their high energy crystal facets, defect engineering, enhancing catalytic sites in graphene, constructing dedicated architectures, tuning the nanomaterial dimensionality at the interface, and employing the synergism adopted through various modifications, are systematically compiled. Portraying the significance of these photocatalytic hybrids in environmental remediation, important applications including air and water purification, self-cleaning surfaces, H2 production, and CO2 reduction to desired fuels, are addressed.

Efficient degradation of diclofenac sodium by periodate activation using Fe/Cu bimetallic modified sewage sludge biochar/UV system.

Iron/copper bimetallic nanoparticles based sludge biochar (Fe/Cu-SBC) was prepared by using a modified co-precipitation route. The Fe/Cu-SBC system prepared was subsequently applied to activate periodate (IO4-) to degrade diclofenac sodium (DCF) by using UV light at room temperature (25 °C). The physicochemical properties of both SBC and Fe/Cu-SBC such as morphology, physical properties, crystal structures and functional groups were examined. The type and number of surface functional groups were found to be increased and the catalytic performance was improved by the modification of Fe/Cu bimetallic nanoparticles. The influence of various parameters to evaluate the catalytic efficiency such as periodate (PI) concentration, dosage of catalysts, UV power, initial pH and coexisting anions were investigated. Under the optimized conditions (pH 6.9, UV-power 60 W, PI concentration of 5 mM and 0.1 g Fe/Cu-SBC), it was observed that 99.7% of DCF was degraded with a pseudo-first-order kinetics reaction constant 9.39 × 10-2 min-1. The radical scavenging experiments showed that IO3 radicals were the predominantly reactive oxidants in the Fe/Cu-SBC/UV system. Therefore, this investigation provides a feasible alternative for the degradation of PPCPs in wastewater.

Ternary Metal Chalcogenide Heterostructure (AgInS2-TiO2) Nanocomposites for Visible Light Photocatalytic Applications.

Hybrid nanoarchitectures of AgInS2 and TiO2 photocatalysts were prepared by using a modified sol-gel method. The experimental results reveal that these nanocomposites display enhanced visible light absorption and effective charge carrier separation compared to their pristine parent samples (AgInS2 or TiO2). 0.5 wt % AgInS2 loading was found to be the optimum concentration for photocatalytic applications. More than 95% of doxycycline degradation was achieved within 180 min of solar light illumination. Similarly, the dopant concentrations at lower values (<2 wt %) exhibited 300 times higher H2 generation rate under visible light irradiation compared to AgInS2 and TiO2. The microbial strains (Escherichia coli and Staphylococcus aureus) exhibited a 99.999% reduction within half an hour of simulated solar light illumination. The computational investigation was employed to understand the structural, electronic, and the dielectric properties of AgInS2 and TiO2 composites. The improved photocatalytic results are explained as a result of the decreased rate of exciton recombination. The current investigation opens up new insights into the use of novel ternary heterostructure nanocomposites for improved visible light activity.

Visible light photocatalytic degradation of tetracycline with porous Ag/graphite carbon nitride plasmonic composite: Degradation pathways and mechanism.

Ag/g-C3N4 plasmonic photocatalysts with porous structure (Ag/PCN) were successfully synthesized via a thermal exfoliation strategy and photo-reduction method. Owing to the combined merits of porous structure and surface plasmon resonance effect of silver nanoparticles, the Ag/PCN catalysts exhibited excellent photocatalytic performance for the degradation of antibiotic agents. With the optimal Ag loading, the Ag/PCN-2 catalyst exhibited the optimal catalytic activity for TC degradation under visible light, which shows about 11.8 times enhancement in the photocatalytic removal efficiency as compared to pure g-C3N4, respectively. This phenomenon can be attributed to the increased specific surface area, broadened visible light absorption and improved charge separation. The radical quenching results confirmed that h+ and O2- radicals were the major active species during removal of TC. The degradation of TC is increased with the increment of Ag/PCN-2 catalysts, and the optimum catalyst was found to be 1.67 g/L. The hindering effect of selected of anions (Cl-, CO3-, H2PO4-) was found to follow the order H2PO4- > CO3- > Cl-. Ag/PCN-2 sample also possessed high stability after six cycles of reuses. Furthermore, the possible degradation pathways of TC and photocatalytic mechanism over Ag/PCN-2 were proposed in detail.

A conceptual change in crystallisation mechanisms of oxide materials from solutions in closed systems.

Atomic and molecular level interactions in solutions dictate the structural and functional attributes of crystals. These features clearly dictate the properties of materials and their applicability in technologies. However, the microscopic phenomena of particle formation-nucleation and growth-in real systems are still not fully understood. Specifically, crystallisation occurring in closed systems are largely unproven. Combining coherent experimental data, we here demonstrate a fundamental nucleation-growth mechanism that occurs in a model zinc oxide system when particles are formed under continuous, rapid heating under closed reaction conditions. Defying all previous reports, we show that the nucleation commences only when the heating is terminated. A prenucleation clusters pathway is observed for nucleation, followed by crystallite assembly-growth. We show that the nucleation-growth processes result from temporal and dynamic activity of constituent ions and gaseous molecules in solution and by the irreversible expulsion of the dissolved gaseous molecules. We suggest that this nucleation process is generic to most closed systems that go through precipitation, and, therefore, important for the crystallisation of a variety of metal oxides, composites and minerals. We anticipate that the work may be a platform for future experimental and theoretical investigation promoting deeper understanding of the nucleation-growth phenomena of a variety of practical systems.