Higher Degradation Research Articles

High photocatalytic degradation of methylene blue and enhancing the magnetization, AC conductivity of Dy3+ and Ce3+ doped CdCoFe2O4 nano ferrites

Photocatalysts that combine with dielectric and magnetic properties are vital because of a wide variety of applications for these combinations, and nanostructured magnetic semiconductive materials have attracted significant interest due to their potential applications. A series of Cd0.4Co0.6DyXCeXFe2-2XO4 spinel nano ferrites (nFs) were synthesized by using a highly efficient low-temperature method of citrate sol-gel auto-combustion for Methylene Blue (MB) dye degradation photocatalysts under visible light irradiation that combines with dielectric and magnetic properties are vital because of a wide variety of applications for these combinations, and nanostructured magnetic semiconductive materials have attracted significant interest due to their potential applications. The recycled MB is one of the hazardous textile dyes that is used extensively but causes risks for both humans and the environment. The prepared Dy3+ and Ce3+ doped Cd–Co nFs were polycrystalline with cubic structure, and crystalline size was increased from 15.78 to 21.02 nm with higher crystallinity, and the surface morphology changes from a spherical shape to a hexagonal shape with higher doping concentrations. The direct optical band gap values are increased. FTIR spectra reveal the stretching vibrations along the [M↔O] bond tetrahedral (A) and octahedral (B) sites. HRTEM results revealed that the prepared Cd–Co nFs have higher crystalline nature and high porosity. VSM indicates the sample's soft magnetic action and hysteresis loops showed the highest saturation magnetization (Ms) is 12.243 emu/g, and retentivity increases around 6.038 emu/g, decreasing the dielectric tangent loss, dielectric constant and dielectric loss. The AC conductivity raised with applied frequency. The PL gives a blue emission, and photocatalytic has the highest degradation activity 40.93 % of MB would be successful after 120 min irradiation of X = 0.07 Dy3+ and Ce3+ doped Cd–Co nFs.

Single-Atom Iron Can Steer Atomic Hydrogen toward Selective Reductive Dechlorination: Implications for Remediation of Chlorinated Solvents-Impacted Groundwater.

Atomic hydrogen (H*) is a powerful and versatile reductant and has tremendous potential in the degradation of oxidized pollutants (e.g., chlorinated solvents). However, its application for groundwater remediation is hindered by the scavenging side reaction of H2 evolution. Herein, we report that a composite material (Fe0@Fe-N4-C), consisting of zerovalent iron (Fe0) nanoparticles and nitrogen-coordinated single-atom Fe (Fe-N4), can effectively steer H* toward reductive dechlorination of trichloroethylene (TCE), a common groundwater contaminant and primary risk driver at many hazardous waste sites. The Fe-N4 structure strengthens the bond between surface Fe atoms and H*, inhibiting H2 evolution. Nonetheless, H* is available for dechlorination, as the adsorption of TCE weakens this bond. Interestingly, H* also enhances electron delocalization and transfer between adsorbed TCE and surface Fe atoms, increasing the reactivity of adsorbed TCE with H*. Consequently, Fe0@Fe-N4-C exhibits high electron selectivity (up to 86%) toward dechlorination, as well as a high TCE degradation kinetic constant. This material is resilient against water matrix interferences, achieving long-lasting performance for effective TCE removal. These findings shed light on the utilization of H* for the in situ remediation of groundwater contaminated with chlorinated solvents, by rational design of earth-abundant metal-based single-atom catalysts.

Green synthesis structural, morphological and sonocatalytic properties of CuO nanoparticles assisted by Camellia sinensis (Tea) extract

In this green synthesis approach for copper oxide (CuO) nanoparticles (NPs), the reducing agent obtained from Camellia sinensis (Tea) extract was used. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet visible (UV-Vis) spectroscopy, field emission scanning electron microscope (FESEM) with energy-dispersive X-ray (EDX), high resolution transmission electron microscope (HRTEM) and Selected Area Electron Diffraction (SAED) techniques were used for as-prepared sample characterization. From XRD result, the crystallite size estimated by Scherrer method was found to be 35 nm. Morphological results reveals that the CuO NPs possesses small particle size with the range of 40–45 nm, led to high surface area, which enhances the absorption of more number of dye molecules, which results in high degradation efficiency. Present work reveals that degradation of malachite green (MG) dye in aqueous solutions under sonocatalytic treatment. CuO NPs exhibit excellent degradation efficiency against MG dye (95 % removal in 70 min). Moreover, the rate constant for the degradation efficiency was investigated with pseudo- first and second order kinetics. Moreover, CuO NPs possesses potential antibacterial activity against human pathogens such as Gram-positive (Staphylococcus pyogenes) and Gram-negative (Pseudomonas aeruginosa).

Effect of physical and chemical co-application of biochar and sulfidated nano scale zero valent iron on the NB degradation in soil: Key roles of biochar

Sulfidated nano zero-valent iron (S-nZVI) can efficiently degrade nitrobenzene (NB) in water. However, its practical application in soil remediation is constrained by limited contact with soil-sorbed NB, leading to sparse research. Herein, Biochar (BC), with its notable adsorption capacity, was coupled with S-nZVI to assess the role of physical (S-nZVI + BC) and chemical (S-nZVI@BC) co-application of BC and S-nZVI, respectively, on enhancing NB degradation in soil. Regardless of the physical or chemical co-application, there was a remarkable advantage after addition of BC relative to S-nZVI alone. In physical co-application, the NB degradation rate of S-nZVI + BC increased as the increasing BC concentration from 0 to 3.5 g·L−1, attributed to enhanced NB desorption via the solubilization effect of BC, facilitating interaction with S-nZVI. Beyond this concentration, no significant improvement was observed, possibly due to BC obstructing reactive sites on S-nZVI surface. In chemical co-application, the S-nZVI@BC (S-nZVI/BC mass ratio of 1:1) exhibited a high NB degradation rate constant (1.097 h−1) during reaction. Apart from solubilization effect, BC in S-nZVI@BC endowed S-nZVI with a higher anti-oxidation property, hydrophobicity, electron transfer capacity, and dispersion effect, accounting for the higher reactivity of S-nZVI@BC over S-nZVI + BC. Besides, the water/soil ratio and initial soil pH significantly affected NB degradation rate, with the optimum water/soil ratio and initial soil pH being 3 and 5, respectively. Our finding broadens the applicability of BC and may offer a highly effective way in soil remediation.

Photocatalytic films with high ethylene degradation efficiency for strawberry preservation

The preservation of fruits has always been a research hotspot. In this research, titanium dioxide(TiO2) exhibiting diffraction peaks characteristic of both anatase and rutile phases was synthesized. Subsequently, photocatalytic films loaded with the TiO2 were fabricated using a twin-screw extruder combined with an extrusion casting technique. The films demonstrated a highest ethylene photocatalytic degradation efficiency of 88.57 %. The addition of TiO2 significantly enhanced the hydrophilicity of the films, with a maximum increase of 8.08 %. The tensile strength and elongation at break of the films were also improved. The optical properties, barrier properties and mechanical properties revealed that the film may make contributions to slowing down light aging, reducing weight loss of strawberries and increasing the load-bearing property. Furthermore, fresh-keeping experiment proved that the photocatalytic films could markedly slow down the appearance change, reduce weight loss and TBARS accumulation while decelerating the decline of TSS and antioxidant capacity in strawberries.

Overcome the trade-off in electro-fenton chemistry for in situ H2O2 generation-activation by tandem CoFe bimetallic single-atom configuration

Dual-atomic catalysts (DACs) demonstrated remarkable potential in addressing key challenges in electro-Fenton (EF) processes. In this study, we synthesized an EF DACs comprising both CoN4 and FeN4 sites, which was achieved a high H2O2 generation rate (1.68 mM−1h−1) and 100 % bisphenol A degradation efficiency via successive two-electron oxygen reduction and one-electron Fenton reactions (2e− ORR + 1e− Fenton). Our findings indicated that the single-atom nitrogen coordination of CoN4 and FeN4 sites plays crucial roles in regulating the adsorption of key intermediates of *OOH and *H2O2. The bimetallic sites independently regulated the binding energies of *OOH on CoN4 (pyrrole-type) for favorable H2O2 generation and its subsequent activation on adjacent FeN4 (pyridine-type). Thus, the dual-site engineering addresses the trade-off of in situ H2O2 generation-activation in EF chemistry, realizing high electron utilization efficiency and fast pollutant degradation toward efficient and sustainable water treatment.

Impacts of climate change in taxonomic, phylogenetic and functional diversity in snakes in largest dry forest ecoregion, the Gran Chaco

The impacts of anthropogenic activities have significantly contributed to recent and future climate changes worldwide. The future effects of climate change on biodiversity have been intensively studied globally over the past two decades. Currently, dry ecoregions are among the most threatened ecosystems in the world. In South America, three such seasonal dry ecoregions stand out: the Cerrado, Caatinga, and the Gran Chaco. Among these, the Chaco has experienced high deforestation rates and landscape degradation over the last decade, making it a top priority for conservation efforts. In this study, we employed ecological niche modeling to estimate the present and future distribution of snakes in the Chaco region. Our goal was to assess how snake diversity will change with projected climate changes across this geographic area. Our findings suggest that snake assemblages in the Chaco will undergo significant changes under future climatic conditions, with a clear trend toward biotic homogenization of the ecoregion and a decrease in species richness. These negative changes will likely extend to the protected areas within the Chaco, resulting in biotic homogenization and a loss of species richness.

Performance of UV/TiO2/PS, US/TiO2/PS and UV/US/TiO2/PS processes on the diazinon degradation from aqueous solutions and toxicity assay

Diazinon is a highly dangerous organophosphorus pesticide that conventional treatment methods cannot remove from wastewater. This study aims to investigate ultrasound-chemical-photocatalysis as an eco-friendly method for the effective decomposition of diazinon. The combination of ultrasound and ultraviolet leads to the formation of higher oxidizer agents and faster diazinon decomposition. To assess the efficiency of processes, experiments with AOP based on ultrasound, AOP based on ultraviolet, and a sonophotocatalytic process were conducted. The experiments were done in a glass photoreactor equipped with a UVC lamp and an ultrasonic device. The residual diazinon and intermediates were read by GC-MS. The results indicate that the highest degradation in all processes occurred at Time = 30 min, PS = 3 mmol, and pH = 3. Notably, the sonophotocatalyst process required the lowest catalyst usage. Since the efficiency of photocatalytic processes is significantly influenced by the amount and rate of generation of strong oxidizer radicals; consequently, the highest efficiency was observed in the UV/US/TiO2/PS process. Moreover, the electric energy consumption followed the order US/TiO2/PS> UV/US/TiO2/PS > UV/TiO2/PS. Additionally, with ATU < 1, the toxicity of the wastewater to the environment was found to be low.

Iron-based metal organic framework (Fe-MOF)-doped sesame stalk biochar enhances antibiotic degradation: Important role of free radicals and comparison of multiple degradation processes

A novel iron-based metal organic framework-doped sesame stalk biochar (Fe-MOF@SBC) composite was successfully synthesized using sonication and used for the degradation of sulfamethoxazole (SMX), norfloxacin (NOR), erythromycin (ERY) and tetracycline (TC) in aqueous solution. The characterization results indicated that Fe oxide was successfully loaded on the biochar. The Fe-MOF@SBC composite presented a porous structure enriched in micropores and mesopores. Adsorption mechanisms, including pore filling, π–π electron donor–acceptor (EDA) interactions, hydrophobic interactions, hydrogen bonding and electrostatic interactions, and the catalytic effect of the Fe-MOF@SBC composite facilitated antibiotic degradation. Specifically, single-layer and multilayer adsorption occurred, and abundant oxygen-containing functional groups were involved in the degradation of NOR, which might be one reason for the high degradation rate of NOR by the Fe-MOF@SBC composite. Scavenging experiments combined with electron paramagnetic resonance (EPR) analysis indicated that free radicals such as •OH, O2−• and 1O2 played vital roles in the degradation of SMX, NOR, ERY and TC. Furthermore, the proposed degradation pathways and possible intermediates of SMX, NOR, ERY and TC were identified, which indicated that the adsorption properties and free radical (•OH, O2−• and 1O2) activity of the Fe-MOF@SBC composite strongly promoted the removal of SMX, NOR, ERY and TC.

Influence of Nd3+ ions modified CoAl2O4 nanomaterials for high efficiency dye degradation application

This study aims to elucidate the possible application of cobalt aluminate nanoparticles (CoAl2O4) as a photocatalyst for the removal of organic dyes. The sol-gel method was employed to synthesise Ndx/CoAl2O4 nanoparticles with varying weight percentages (x = 0.0, 0.2, 0.4, and 0.6 wt %). The experimental investigation focused on the photocatalytic destruction of colour, employing a visible light irradiation source. The structural and optical properties of the synthesised nanoparticle were examined through various analytical techniques, including X-Ray Diffraction (XRD), Ultra Violet-Diffuse Reflectance Spectroscopy (UV-DRS), Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray spectroscopy (EDX), Tunnelling Electron Microscopy (TEM), and X-ray Photoelectron Spectroscopy (XPS). The cubic spinel structure was confirmed through the study of the X-ray diffraction (XRD) pattern of the Ndx/CoAl2O4 nanoparticles. For the compositions x = 0.0, 0.2, 0.4, and 0.6, the nanoparticles exhibited average crystallite sizes of 23.73, 22.99, 21.69, and 21.65 nm, respectively. The synthesised nanoparticle exhibited heterogeneous photocatalytic potential when employed as a model pollutant for the oxidative destruction of crystal violet dye. The experimental findings validated that the CoAl2O4 nanoparticle exhibited a dye degradation rate of 64 % during a 100-min timeframe. Additionally, the 0.6 wt % Nd CoAl2O4 nanoparticle shows a quick dye degradation rate of 91 % for crystal violet dyes when exposed to visible light sources. Hence, the synthesised nanoparticle exhibits catalytic activity and holds potential for utilisation in the treatment of hazardous contaminants in industrial wastewater.

Unravelling the mechanisms of organic micropollutant removal in bio-electrochemical systems: Insights into sorption, electrochemical degradation, and biodegradation processes

Bio-electrochemical systems (BESs) have recently been proposed as an efficient treatment technology to remove organic micropollutants from water treatment plants. In this study, we aimed to differentiate between sorption, electrochemical transport/degradation, and biodegradation. Using electro-active microorganisms and electrodes, we investigated organic micropollutant removal at environmentally relevant concentrations, clarifying the roles of sorption and electrochemical and biological degradation. The role of anodic biofilms on the removal of 10 relevant organic micropollutants was studied by performing separate sorption experiments on carbon-based electrodes (graphite felt, graphite rod, graphite granules, and granular activated carbon) and electrochemical degradation experiments at two different electrode potentials (−0.3 and 0 V).Granular activated carbon showed the highest sorption of micropollutants; applying a potential to graphite felt electrodes increased organic micropollutant removal. Removal efficiencies >80 % were obtained for all micropollutants at high anode potentials (+0.955 V), indicating that the studied compounds were more susceptible to oxidation than to reduction. All organic micropollutants showed removal when under bio-electrochemical conditions, ranging from low (e.g. metformin, 9.3 %) to exceptionally high removal efficiencies (e.g. sulfamethoxazole, 99.5 %). The lower removal observed under bio-electrochemical conditions when compared to only electrochemical conditions indicated that sorption to the electrode is key to guarantee high electrochemical degradation. The detection of transformation products of chloridazon and metformin indicated that (bio)-electrochemical degradation occurred. This study confirms that BES can treat some organic micropollutants through several mechanisms, which merits further investigation.

Green Synthesis, Characterization, and Evaluation of Photocatalytic and Antibacterial Activities of Co3O4-ZnO Nanocomposites Using Calpurnia aurea Leaf Extract.

The green synthesis of transition metal oxide nanocomposites using plant extracts is a new and effective method that avoids the involvement of hazardous chemicals. Nondegradable organic pollutants and antibiotic drug resistance have become serious public health issues worldwide. Hence, the main objective of this study is to synthesize Co3O4-ZnO nanocomposites using Calpurnia aurea leaf extract and evaluate its photocatalytic and antibacterial activities. The green synthesized particles were characterized using UV-vis spectra, Fourier transform infrared spectroscopy, X-ray diffraction techniques, and scanning electron microscopy combined with energy-dispersive X-ray studies. The synthesized particles were found to be crystalline in nature with average crystallite sizes of 23.82, 14.79, 15.99, 16.46, and 21.73 nm. Scanning electron microscopy shows the spherical morphology of Co3O4-ZnO NCs, and energy-dispersive X-ray analysis confirms the formation of highly pure ZnO NPs and Co3O4-ZnO NCs. The photocatalytic activity was performed under natural sunlight using malachite green as an organic dye pollutant. The green synthesized ZnO NPs, Co3O4 NPs, 1:4, 1:3, and 1:2 Co3O4-ZnO NCs showed high degradation efficiency after 60 min of irradiation. The synthetic material showed good potential against Staphylococcus aureus and Escherichia coli, with the highest growth inhibition recorded by 1:2 Co3O4-ZnO NCs. The kinetics study of the photocatalytic degradation was confirmed as pseudo first order, and the possible mechanisms for both photocatalytic and antibacterial activities were clearly determined.

Construction of a gelatin aerogel catalyst functionalized with LaCoO3 and g-C3N5 for efficient ciprofloxacin degradation via adsorption and peroxymonosulfate activation

Three-dimensional porous gelatin-based aerogels functionalized with LaCoO3 and nitrogen-rich graphitic carbon nitride (g-C3N5) were successfully fabricated via a freeze-drying approach. Herein, the gelatin-based aerogels served as excellent adsorbents and catalysts activating peroxymonosulfate (PMS) to efficiently degrade ciprofloxacin (CIP) from aqueous solutions. In comparison to the pristine gelatin aerogel (GA), the optimized functionalized aerogel (GA–LCCN-1.5) demonstrated a 17.0% superior CIP adsorption performance. Remarkably, GA–LCCN-1.5 exhibited 95.7% removal efficiency for CIP, attributed to the effective generation of •OH, SO4•−, and 1O2 via PMS activation. In addition, high degradation efficiencies over 84.1% were maintained throughout a broad pH range of 3–9. Notably, GA–LCCN-1.5 demonstrated outstanding stability and reusability, with 93.2% CIP removal efficiency even after five reuse cycles indicating significant promise in real applications. Radical quenching and electron spin resonance (ESR) analysis suggest that CIP degradation was dominated by radical and non-radical routes through GA–LCCN-1.5 catalyzed PMS decomposition. Besides, the plausible CIP degradation mechanisms were systemically analyzed and proposed. The toxicities of CIP and the intermediate by-products were evaluated and reported. The findings of this study and insights demonstrate a facile construction of a biopolymer-based aerogel catalyst for synergistic and efficient PMS activation for the removal of antibiotics in water.

Design of degradable hybrid dual-crosslinked polymer for high-efficiency profile control in high temperature reservoirs

Profile control and water plugging are key technologies to enhance oil and gas recovery. Traditional plugging materials, due to short gelation time, low mechanical strength, and difficulty in balancing plugging and protection, thus limiting application in high temperature reservoirs. Herein, a degradable hybrid dual-crosslinked polymer was prepared by employing a copolymerization - dual-grafting and physical adsorption design strategy. The dual-crosslinked process and reaction mechanism were analyzed using infrared spectroscopy and differential scanning calorimetry. The mechanical properties, water dilution resistance, aging stability and degradability of the dual cross-linked composite were also investigated. The solvation forces enable silica particles to exhibit excellent suspension stability in a PEG solvent. The temperature ranges from normal atmospheric temperature (20 °C) to reservoir temperature (140 °C), with the apparent viscosity falling within the range of 10–1200 mPa·s, meeting the requirements for mixing and injection. The combination of free radical copolymerization and click reaction is utilized to control the gelation time (2–10 h) in high temperature environment (140 °C), which is favorable for regulating the action position of the plugging agent in the reservoir. The cured material exhibits excellent mechanical strength owing to the presence of dual-crosslinking and inorganic hybridization, with a compressive strength of 0.221 MPa and a peak strain of 55.3 %. Furthermore, this composite material undergoes hydrolysis through an addition-elimination reaction, transitioning from a solid to a liquid state within 24 h, thereby aiding in the restoration of productivity in the temporarily shielded target layer. Compared to traditional materials, this dual-crosslinked composite system have the advantages of controllable gelation time, high mechanical strength, aging resistance, and degradability, making it suitable for profile control in high temperature reservoirs (140 ℃, 21.81×104 mg/L).

Fe-Ce based metal-organic framework as a novel heterogeneous catalyst accelerating redox cycle for efficient degradation of sulfamethoxazole in wide pH ranges

The electro-Fenton (EF) technology holds immense potential for wastewater treatment. However, there persist certain factors that affect its degradation efficiency, such as the restricted pH range, production of iron sludge and sluggish conversion rate between Fe2+ and Fe3+. Herein, 2,3,6,7,10,11-hexahydroxytriphenyl (HHTP) was introduced as the organic ligand to synthesize a series of efficient iron-based MOF catalysts (FexCe1-HHTP (x = 1, 2, 3, 4)) with different molar ratios for sulfamethoxazole (SMX) degradation in heterogeneous EF system. HHTP with electron-rich functional groups is beneficial to enhance performance of oxygen evolution reaction. Among these catalysts, Fe3Ce1-HHTP catalyst achieved 97.3 % degradation efficiency in 30 min and mineralization rate was 89.7 % at 1 h. The introduction of Ce promoted the transition of Fe3+ and Fe2+ in heterogeneous EF reaction. The synergistic effects between Fe3+/Fe2+ and Ce4+/Ce3+ further catalyzed the generation of hydroxyl radicals and it was proved as the main active species. The heterogeneous catalyst showed good performance in wide pH range, good stability, and high degradation efficiency to other pollutants. Three possible SMX degradation routes are suggested on basis of intermediates detected by mass spectrum analysis and theoretical calculations. The toxicity of these intermediates was assessed using Toxicity Estimation Software Tool (T.E.S.T.). This work provides valuable guidance for the design of highly efficient and stable heterogeneous EF catalyst for antibiotic degradation and expand the application potential in wastewater treatment of organic pollutants.

Smart Doped Polyaniline Coating for Wireless Anodic Protection of AISI 304 Stainless Steel in a Corrosive Medium Containing Sulfate and Chloride Ions: Electrochemical and DFT Evaluations.

Polyaniline (PANI) coatings have the capability of in situ anodic protection of stainless steels (SSs). However, these coatings have a high degradation rate in sulfuric acid. Also, the protection of SSs in a medium contaminated with chloride ions is an unsolved challenge. Therefore, the present work aims to modify the electrodeposited PANI coating with different dopants to find the optimal coating for the anodic protection of 304 SS in chloride-contaminated sulfuric acid. Thus, CH3COO-, HSO4-, NO3-, H2PO4-, and NaSO4- were doped electrochemically in PANI to determine the most effective corrosion depressor. Density functional theory (DF)T calculations determined that the lowest Gibbs free energy (more spontaneous doping) is for HSO4- doping by 24 kcal/mol. The band gap energy is <0.5 eV for the PANI/H2SO4 coating, indicating the very high conductivity of this coating. Monte Carlo simulation revealed that the highest deformation energy is related to PANI/H2SO4 at 1877 kcal/mol (stronger adsorption). Mott-Schottky and energy-dispersive spectroscopy (EDS) results showed that PANI doped with sulfuric acid creates a p-type semiconductor (Ni-rich), while the rest of the dopants lead to the formation of an n-type semiconductor passive film (Fe/Cr-rich). Despite the relatively low corrosion resistance of PANI/H2SO4 in the early days, its resistance improved over time by more than 1 order of magnitude. Therefore, this seems to be a more favorable option for long-term anodic protection. Thus, in this work, the corrosion behavior of the passive film formed at the interface of PANI and SS was comprehensively evaluated.

A biogenic geodesic dome of the silica skeleton in Phaeodaria

Unique architectures of microbial skeletons are viewed as a model for the architectural design of artificial structural materials. In particular, the specific geometric arrangement of a spherical skeleton 0.5–1.5 mm in diameter of shell-bearing protists, Phaeodaria (Aulosphaera sp.), is remarkably interesting because of its similarity to a geodesic polyhedron, which is a hollow framework with 6-branched nodes that requires minimal building material for maximal strength. A phaeodarian skeleton composed of silica rods 5–10 µm in diameter was characterized as a distorted dome that is based on an icosahedron sectioned with a 7-frequency subdivision. The major difference of the biogenic architecture from the ideal geodesic dome is the coexistence of 7- and 5-branched nodes with the distortion of the frames and the presence of radial spines. From a microscopic perspective, the frames and radial spines were revealed to be hollow tubes having inner fibers and lamellar walls consisting of silica nanoparticles 4–8 nm in diameter with interlayer organic matter. The high degradability of the silica skeleton in seawater after cell mortality is ascribed to the specific nanometric composite structure. The biological architectonics sheds light on the production of environmentally friendly, lightweight structural materials and microdevices.

Exploring Flower-Structured Bifunctional VCu Layered Double Hydroxide and its Nanohybrid with g-C3N4 for Electrochemical and Photoelectrochemical Seawater Electrolysis.

Seawater electrolysis holds great promise for sustainable green hydrogen generation, but its implementation is hindered by high energy consumption and electrode degradation. Two dimensional (2D) layered double hydroxide (LDH) exhibits remarkable stability, high catalytic activity, and excellent corrosion resistance in the harsh electrolytic environment. The synergistic effect between LDH and seawater ions enhances the oxygen evolution reaction, enabling efficient and sustainable green hydrogen generation. Here, we report a synthesis of low cost, novel 2D Vanadium Copper (VCu) LDH first time in the series of LDH's as a highly efficient bifunctional electrocatalyst. The electrochemical (EC) and photoelectrochemical (PEC) study of VCu LDH and VCu LDH/Graphite Carbon Nitride (g-C3N4) nanohybrid was performed in 0.5 M H2SO4 (acidic), 1 M KOH (basic), 0.5 M NaCl (artificial seawater), 0.5 M NaCl+1 M KOH (artificial alkaline seawater), real seawater and 1 M KOH+real seawater (alkaline real seawater) electrolyte medium. It was found that VCu LDH shows a remarkable lower overpotential of 72 mV hydrogen evolution reaction (HER) and 254 mV oxygen evolution reaction (OER) at current density of 10 mA/cm2 under alkaline real seawater electrolysis exhibiting bifunctional activity and also showing better stability.

Improved high voltage operation of amorphous In–Ga–Zn–O thin film transistor by carrier density enhancement

We report on improved high voltage operation of amorphous-In–Ga–Zn–O (a-IGZO) thin film transistors (TFTs) by increasing carrier density and distributing the high bias field over the length of the device which utilizes an off-set drain structure. By decreasing the O2 partial pressure during sputter deposition of IGZO, the channel carrier density of the high voltage a-IGZO TFT (HiVIT) was increased to ∼1018 cm−3. Which reduced channel resistance and therefore the voltage drop in the ungated offset region during the on-state. To further decrease the electric field in the offset region, we applied Ta capping and subsequent oxidation to locally increase the oxygen vacancy levels in the offset region thereby increasing local carrier density. The reduction of the drain field in the offset region from 1.90 V μm−1 to 1.46 V μm−1 at 200 V drain voltage, significantly improved the operational stability of the device by reducing high field degradation. At an extreme drain voltage of 500 V, the device showed an off-state current of ∼10−11 A and on-state current of ∼1.59 mA demonstrating that with further enhancements the HiVIT may be applicable to thin-film form, low leakage, high voltage control applications.

2D–2D g-C3N4/WS2 Z-scheme heterojunction: Comparison of the photocatalytic degradation of tetracycline and sulfamethoxazole

In recent years, 2D–2D layered heterojunctions have emerged as promising photocatalytic platforms for the sustainable destruction of refractory pollutants because of their distinct advantages. Herein, we have rationally synthesized an organic–inorganic g-C3N4/WS2 heterojunction, with intimate interfacial contact, via a facile hydrothermal-driven self-assembling approach. Systematic investigations involving electrochemical impedance spectroscopy measurements and Mott–Schottky analysis reveal that the internal electric field between g-C3N4 and WS2 induces a Z-scheme charge transfer mechanism. Under visible light irradiation, the optimized photocatalyst exhibits a high degradation efficiencytowards two broad-spectrum antibiotics, i.e., tetracycline (TC) (89%) and sulfamethoxazole (SMX) (97%), with the apparent reaction rate constants several folds higher than that of bulk g-C3N4 and pristine WS2 nanosheets. Further, the g-C3N4/WS2 photocatalyst exhibits a favorable reusability of four operation cycles. Additionally, the impacts of different reaction variables are explored and the probable routes of photocatalytic dissociation of TC and SMX by g-C3N4/WS2 are proposed. The present findings not only validate the feasibility of g-C3N4/WS2 to eliminate consumer-derived micropollutants from the aqueous phase without creating secondary pollutants but also provide important insights for designing highly efficient 2D material-based heterojunction photocatalysts for decentralized wastewater treatment.