Multi-Functional Applications of H-Glass Embedded with Stable Plasmonic Gold Nanoislands.

Metal nanoparticles (MNPs) are synthesized using various techniques on diverse substrates that significantly impact their properties. However, among the substrate materials investigated, the major challenge is the stability of MNPs due to their poor adhesion to the substrate. Herein, it is demonstrated how a newly developed H-glass can concurrently stabilize plasmonic gold nanoislands (GNIs) and offer multifunctional applications. The GNIs on the H-glass are synthesized using a simple yet, robust thermal dewetting process. The H-glass embedded with GNIs demonstrates versatility in its applications, such as i) acting as a room temperature chemiresistive gas sensor (70% response for NO2 gas); ii) serving as substrates for surface-enhanced Raman spectroscopy for the identifications of Nile blue (dye) and picric acid (explosive) analytes down to nanomolar concentrations with enhancement factors of 4.8 × 106 and 6.1 × 105 , respectively; and iii) functioning as a nonlinear optical saturable absorber with a saturation intensity of 18.36 × 1015 W m-2 at 600 nm, and the performance characteristics are on par with those of materials reported in the existing literature. This work establishes a facile strategy to develop advanced materials by depositing metal nanoislands on glass for various functional applications.

H-Glass Supported Hybrid Gold Nano-Islands for Visible-Light-Driven Hydrogen Evolution.

Flat panel reactors, coated with photocatalytic materials, offer a sustainable approach for the commercial production of hydrogen (H2) with zero carbon footprint. Despite this, achieving high solar-to-hydrogen (STH) conversion efficiency with these reactors is still a significant challenge due to the low utilization efficiency of solar light and rapid charge recombination. Herein, hybrid gold nano-islands (HGNIs) are developed on transparent glass support to improve the STH efficiency. Plasmonic HGNIs are grown on an in-house developed active glass sheet composed of sodium aluminum phosphosilicate oxide glass (H-glass) using the thermal dewetting method at 550 °C under an ambient atmosphere. HGNIs with various oxidation states (Au0, Au+, and Au-) and multiple interfaces are obtained due to the diffusion of the elements from the glass structure, which also facilitates the lifetime of the hot electron to be ≈2.94 ps. H-glass-supported HGNIs demonstrate significant STH conversion efficiency of 0.6%, without any sacrificial agents, via water dissociation. This study unveils the specific role of H-glass-supported HGNIs in facilitating light-driven chemical conversions, offering new avenues for the development of high-performance photocatalysts in various chemical conversion reactions for large-scale commercial applications.

Assemble of Bi-doped TiO2 onto 2D MoS2: an efficient p-n heterojunction for photocatalytic H2 generation under visible light.

Fabrication of noble-metal-free, efficient and stable hybrid photocatalyst is essential to address the rapidly growing energy crisis and environmental pollution. Here, MoS2 has been used as the co-catalyst on Bi-doped TiO2 to form a novel heterostructure to increase the utilization of the photogenerated charge carriers for improving photocatalytic H2 evolution activity through water reduction. Significantly increased photocatalytic H2 generation has been achieved on the optimized MoS2/Bi-TiO2 nanocomposite (∼512 µmol g-1) after 4 h of visible light illumination, which is nine times higher than that of the pristine TiO2 (∼57 µmol g-1). The measurements of photocurrent, charge transfer resistance and photo-stability of MoS2/Bi-TiO2 photoanode imply that charge separation efficiency has been improved in comparison to the pure MoS2 and TiO2 photoanodes. Further, the Mott-Schottky study confirmed that a p-n heterojunction has been formed between n-type MoS2 and p-type Bi-doped TiO2, which provides a potential gradient to increase charge separation and transfer efficiency. On the basis of these experimental results, this enhanced photocatalytic activity of MoS2/Bi-TiO2 heterostructures could be ascribed to the significant visible light absorption and the efficient charge carrier separation. Thus, this work demonstrates the effect of p-n junction for achieving high H2 evolution activity and photoelectrochemical water oxidation under visible light illumination.

Highly active 3-dimensional cobalt oxide nanostructures on the flexible carbon substrates for enzymeless glucose sensing.

The demand for electrochemical sensors with high sensitivity and reliability, fast response, and excellent selectivity has stimulated intensive research on developing highly active nanomaterials. In this work, freestanding 3D/Co3O4 thorn-like and wire-like (nanowires) nanostructures are directly grown on a flexible carbon fiber paper (CFP) substrate by a single-step hydrothermal process without using surfactants or templates. The 3D/Co3O4 thorn-like nanostructures show higher electrochemical activity than wire-like because of their high conductivity, large specific surface areas, and mesopores on their surface. The characterization of 3D/Co3O4 nanostructures is performed by using high resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction analysis (XRD), and electrochemical methods. The 3D/Co3O4 thorn-like nanostructures displayed non-enzymatic higher catalytic activity towards the electrochemical detection of glucose, compared to the 3D/Co3O4 wire-like morphology. The 3D/Co3O4 thorn-like nanostructures show a wide linear range response of glucose concentration ranging from 1 to 1000 µM with a detection limit of 0.046 µM (S/N = 3). The 3D/Co3O4 thorn-like nanostructure-modified CFP electrode selectively detects glucose in the presence of 100-fold excess of interfering compounds. The 3D/Co3O4 thorn-like nanostructure-modified CFP electrode is tested with human blood serum samples and validated with commercial glucose sensors. The newly developed sensor material shows potential for glucose monitoring in clinical and food samples.

Conducting polymer nanostructures for photocatalysis under visible light.

Visible-light-responsive photocatalysts can directly harvest energy from solar light, offering a desirable way to solve energy and environment issues. Here, we show that one-dimensional poly(diphenylbutadiyne) nanostructures synthesized by photopolymerization using a soft templating approach have high photocatalytic activity under visible light without the assistance of sacrificial reagents or precious metal co-catalysts. These polymer nanostructures are very stable even after repeated cycling. Transmission electron microscopy and nanoscale infrared characterizations reveal that the morphology and structure of the polymer nanostructures remain unchanged after many photocatalytic cycles. These stable and cheap polymer nanofibres are easy to process and can be reused without appreciable loss of activity. Our findings may help the development of semiconducting-based polymers for applications in self-cleaning surfaces, hydrogen generation and photovoltaics.

A Peptide-Based Mechano-sensitive, Proteolytically Stable Hydrogel with Remarkable Antibacterial Properties.

A long-chain amino acid containing dipeptide has been found to form a hydrogel in phosphate buffer whose pH ranges from 6.0 to 8.8. The hydrogel formed at pH 7.46 has been characterized by small-angle X-ray scattering (SAXS), wide-angle powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy, field-emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM) imaging and rheological analyses. The microscopic imaging studies suggest the formation of a nanofibrillar three-dimensional (3D) network for the hydrogel. As observed visually and confirmed rheologically, the hydrogel at pH 7.46 exhibits thixotropy. This thixotropic property can be exploited to inject the peptide. Furthermore, the hydrogel exhibits remarkable antibacterial activity against Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa, which are responsible for many common diseases. The hydrogel has practical applicability due to its biocompatibility with human red blood cells and human fibroblast cells. Interestingly, this hydrogel shows high resistance toward proteolytic enzymes, making it a new potential antimicrobial agent for future applications. It has also been observed that a small change in molecular structure of the gelator peptide not only turns the gelator into a nongelator molecule under similar conditions, but it also has a significant negative impact on its bactericidal character.

Facile synthesis of reduced graphene oxide-gold nanohybrid for potential use in industrial waste-water treatment.

Here, we report a facile approach, by the photochemical reduction technique, for in situ synthesis of Au-reduced graphene oxide (Au-RGO) nanohybrids, which demonstrate excellent adsorption capacities and recyclability for a broad range of dyes. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) data confirm the successful synthesis of Au-RGO nanohybrids. The effect of several experimental parameters (temperature and pH) variation can effectively control the dye adsorption capability. Furthermore, kinetic adsorption data reveal that the adsorption process follows a pseudo second-order model. The negative value of Gibbs free energy (ΔG0) confirms spontaneity while the positive enthalpy (ΔH0) indicates the endothermic nature of the adsorption process. Picosecond resolved fluorescence technique unravels the excited state dynamical processes of dye molecules adsorbed on the Au-RGO surface. Time resolved fluorescence quenching of Rh123 after adsorption on Au-RGO nanohybrids indicates efficient energy transfer from Rh123 to Au nanoparticles. A prototype device has been fabricated using Au-RGO nanohybrids on a syringe filter (pore size: 0.220 µm) and the experimental data indicate efficient removal of dyes from waste water with high recyclability. The application of this nanohybrid may lead to the development of an efficient reusable adsorbent in portable water purification.

Radiation-induced synthesis of nanostructured conjugated polymers in aqueous solution: fundamental effect of oxidizing species.

Synthesis of conjugated poly(3,4-ethylenedioxythiophene) (PEDOT) polymers is achieved through the radiolysis of N2O-saturated aqueous solutions of 3,4-ethylenedioxythiophene by using two different oxidizing species: HO(·) (hydroxyl) and N3(·) (azide) radicals. Both oxidative species lead to self-assembled polymers that are evidenced in solution by cryotransmission electron microscopy and UV/Vis absorption spectroscopy and, after centrifugation and deposition, by scanning electron microscopy and attenuated total reflectance FTIR techniques. Whereas HO(·) radicals lead to PEDOT-OH globular nanostructures with hydrophilic properties, N3(·) radicals enable the formation of amphiphilic PEDOT-N3 fibrillar nanostructures. These results, which highlight the differences in the intermolecular interaction behaviors of the two kinds of PEDOT polymers, are discussed in terms of polymerization mechanisms.

Modulation of glyceraldehyde-3-phosphate dehydrogenase activity by surface functionalized quantum dots.

Enzymatic regulation is a fast and reliable diagnosis tool via identification and design of inhibitors for modulation of enzyme function. Previous reports on quantum dots (QDs)-enzyme interactions reveal a protein-surface recognition ability leading to promising applications in protein stabilization, protein delivery, bio-sensing and detection. However, the direct use of QDs to control enzyme inhibition has never been revealed to date. Here we show that a series of biocompatible surface-functionalized metal-chalcogenide QDs can be used as potent inhibitors for malignant cells through the modulation of enzyme activity, while normal cells remain unaffected. The in vitro activity of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), an enzyme involved critically in the glycolysis of cancer cells, is inactivated selectively in a controlled way by the QDs at a significantly low concentration (nM). Cumulative kinetic studies delineate that the QDs undergo both reversible and irreversible inhibition mechanisms owing to the site-specific interactions, enabling control over the inhibition kinetics. These complementary loss-of-function probes may offer a novel route for rapid clinical diagnosis of malignant cells and biomedical applications.

Tungsten-based Lindqvist and Keggin type polyoxometalates as efficient photocatalysts for degradation of toxic chemical dyes.

Photocatalytic dye degradation employing polyoxometalates (POMs) has been a research focus for several years. We report the facile synthesis of tungsten-based Lindqvist and Keggin-type POMs that degrade toxic chemical dyes, methyl orange (MO) and methylene blue (MB), respectively. The Lindqvist POM, sodium hexatungstate, Na2W6O19, degrades MO under 100 W UV light irradiation within 15 min, whereas the Keggin POM, Ag4PW11VO40, degrades MB under 20 W visible light source within 180 min. The effect of various operating parameters, such as photocatalyst concentration, pH, time, and initial dye concentration, were assessed in the degradation of both dyes. The photoelectrochemical performance of the as-synthesized polyoxometalates shows that the Ag4PW11VO40 shows 2.4 times higher photocurrent density than Na2W6O19 at a potential of 0.9 V vs. Ag/AgCl. Electrochemical impedance analysis reveals that Ag4PW11VO40 exhibits much lower charge transfer resistance as compared to Na2W6O19, which indicates facile charge transfer at the electrode-electrolyte interface. Further Mott-Schottky measurements reveal that both the catalysts possess n-type semiconductivity and the charge carrier concentration of Ag4PW11VO40 (5.89 × 1019 cm-3) is 1.4 times higher as compared to Na2W6O19 (4.25 × 1019 cm-3). This work offers a new paradigm for designing polyoxometalates suitable for efficient photocatalytic degradation of organic dyes.

Recent progress in chromium removal from wastewater using covalent organic frameworks - A review.

Covalent organic frameworks (COFs) offer a pivotal solution to urgently address heavy metal removal from wastewater due to their exceptional attributes such as high adsorption capacity, tunable porosity, controllable energy band structures, superior photocatalytic performance, and high stability-reusability. Despite these advantages, COFs encounter certain challenges, including inefficient utilization of visible light, rapid recombination of photogenerated carriers, and limited access to active sites due to close stacking. To enhance the photocatalytic and adsorptive performance of COF-based catalysts, various modification strategies have been reported, with a particular focus on molecular design, structural regulation, and heterostructure engineering. This review comprehensively explores recent advancements in COF-based photocatalytic and adsorptive materials for chromium removal from wastewater, addressing kinetics, mechanisms, and key influencing factors. Additionally, it sheds light on the influence of chemical composition and functional groups of COFs on the efficiency of hexavalent chromium [Cr (VI)] removal.

Band-structure tunability via the modulation of excitons in semiconductor nanostructures: manifestation in photocatalytic fuel generation.

Understanding the energetics of electron transfer at the semiconductor interface is crucial for the development of solar harvesting technologies, including photovoltaics, photocatalysis, and solar fuel systems. However, modern artificial photosynthetic materials are not efficient and limited by their fast charge recombination with high binding energy of excitons. Hence, reducing the exciton binding energy can increase the generation of charge carriers, which improve the photocatalytic activities. Extensive research has been dedicated to improving the exciton dissociation efficiency through rational semiconductor design via heteroatom doping, vacancy engineering, the construction of heterostructures, and donor-π-acceptor (D-π-A) interfaces to extend the charge carrier migration, promoting the dissociation of excitons. Consequently, functionalized photocatalysts have demonstrated remarkable photocatalytic performances for solar fuel production under visible light irradiation. This review provides the fundamental aspects of excitons in semiconductor nanostructures, having a high binding energy and ultrafast exciton formation together with promising photo-redox properties for solar to fuel conversion application. In particular, this review highlights the significant role of the excitonic effect in the photocatalytic activity of newly developed functional materials and the underlying mechanistic insight for tuning the performance of nanostructured semiconductor photocatalysts for water splitting, CO2 reduction, and N2 fixation reactions.

Role of Efficient Charge Transfer at the Interface between Mixed-Phase Copper-Cuprous Oxide and Conducting Polymer Nanostructures for Photocatalytic Water Splitting.

Photocatalytic hydrogen generation from water splitting is regarded as a sustainable technology capable of producing green solar fuels. However, the low charge separation efficiencies and the requirement of lowering redox potentials are unresolved challenges. Herein, a multiphase copper-cuprous oxide/polypyrrole (PPy) heterostructure has been designed to identify the role of multiple oxidation states of metal oxides in water reduction and oxidation. The presence of a mixed phase in PPy heterostructures enabled an exceptionally high photocatalytic H2 generation rate of 41 mmol h-1 with an apparent quantum efficiency of 7.2% under visible light irradiation, which is a 7-fold augmentation in contrast to the pure polymer. Interestingly, the copper-cuprous oxide/PPy heterostructures exhibited higher charge carrier density, low resistivity, and 6 times higher photocurrent density compared to Cu2O/PPy. Formation of a p-p-n junction between polymer and mixed-phase metal oxide interfaces induce a built-in electric field which influences directional charge transfer that improves the catalytic activity. Notably, photoexcited charge separation and transfer have been significantly improved between copper-cuprous oxide nanocubes and PPy nanofibers, as revealed by femtosecond transient absorption spectroscopy. Additionally, the photocatalyst demonstrates excellent stability without loss of catalytic activity during cycling tests. The present study highlights a superior strategy to boost photocatalytic redox reactions using a mixed-phase metal oxide in the heterostructure to achieve enhanced light absorption, longer charge carrier lifetimes, and highly efficient photocatalytic H2 and O2 generation.

A Ni(II) Metal-Organic Framework with Mixed Carboxylate and Bipyridine Ligands for Ultrafast and Selective Sensing of Explosives and Photoelectrochemical Hydrogen Evolution.

We report a Ni-MOF (nickel metal-organic framework), Ni-SIP-BPY, synthesized by using two linkers 5-sulfoisophthalic acid (SIP) and 4,4'-bipyridine (BPY) simultaneously. It displays an orthorhombic crystal system with the Ama2 space group: a = 31.425 Å, b = 19.524 Å, c = 11.2074 Å, α = 90°, ß = 90°, γ = 90°, and two different types of nickel(II) centers. Interestingly, Ni-SIP-BPY exhibits excellent sensitivity (limit of detection, 87 ppb) and selectivity toward the 2,4,6-trinitrophenol (TNP)-like mutagenic environmental toxin in the pool of its other congeners via "turn-off" fluorescence response by the synergism of resonance energy transfer, photoinduced electron transfer, intermolecular charge transfer, π-π interactions, and competitive absorption processes. Experimental studies along with corroborated theoretical experimentation, vide density functional theory studies, shed light on determining the plausible mechanistic pathway in selective TNP detection, which is highly beneficial in the context of homeland security perspective. Along with the sensing of nitroaromatic explosives, the moderately low band gap and the p-type semiconducting behavior of Ni-SIP-BPY make it suitable as a photoanode material for visible-light-driven water splitting. Highly active surface functionalities and sufficient conduction band minima effectively reduce the water and result in a seven times higher photocurrent density under visible-light illumination.

Conjugated polymer nanostructures displaying highly photoactivated antimicrobial and antibiofilm functionalities.

This work reports the use of conjugated polymer nanostructures (CPNs) as photoactivated antimicrobial compounds against Gram-positive and Gram-negative microorganisms. Two representative CPNs of polythiophene (PEDOT) and polyaniline (PANI) were prepared as nanofibres with an average diameter of 40 nm and length in the micrometer range. Both CPNs exhibited strong antimicrobial activity under UVA irradiation with the same fluence rate as the UVA component of the solar spectrum. The effect was tested using the Gram-positive bacteria Staphylococcus aureus and the Gram-negative bacteria Escherichia coli. The reduction of colony forming units (CFUs) reached >6 log for PEDOT concentrations as low as 33 ng mL-1. For PEDOT nanofibers, a complete inhibition of S. aureus and E. coli growth was reached at 883 ng mL-1 and 333 ng mL-1 respectively. The photoactivation effect of PANI nanofibres on S. aureus and E. coli was also high, with a CFU reduction of about 7 log and 4 log respectively for an exposure concentration of 33 ng mL-1. The antimicrobial activity was only high under light irradiation and was almost negligible for bulk PEDOT and PANI. The effect of polymeric nanofibers could be attributed to the photoinduced generation of reactive oxygen species, which may induce cell membrane damage, eventually leading to bacterial impairment and inhibition of their biofilm forming capacity. CPN PEDOT and PANI coatings were able to keep surfaces free of bacterial attachment and growth even after 20 h of previous contact with exponentially growing cultures in the dark. PEDOT and PANI CPNs demonstrated good cytocompatibility with human fibroblasts and the absence of hemolytic activity. The materials demonstrated advantages in terms of broad antibacterial spectrum, biofilm inhibition, and the absence of acute toxicity for biomedical applications.

Polymeric ruthenium precursor as a photoactivated antimicrobial agent.

Ruthenium coordination compounds have demonstrated a promising anticancer and antibacterial activity, but their poor water solubility and low stability under physiological conditions may limit their therapeutic applications. Physical encapsulation or covalent conjugation with polymers may overcome these drawbacks, but generally involve multistep reactions and purification processes. In this work, the antibacterial activity of the polymeric precursor dicarbonyldichlororuthenium (II) [Ru(CO)2Cl2]n has been studied against Escherichia coli and Staphylococcus aureus. This Ru-carbonyl precursor shows minimum inhibitory concentration at nanogram per millilitre, which renders it a novel antimicrobial polymer without any organic ligands. Besides, [Ru(CO)2Cl2]n antimicrobial activity is markedly boosted under photoirradiation, which can be ascribed to the enhanced generation of reactive oxygen species under UV irradiation. [Ru(CO)2Cl2]n has been able to inhibit bacterial growth via the disruption of bacterial membranes and triggering upregulation of stress responses as shown in microscopic measurements. The activity of polymeric ruthenium as an antibacterial material is significant even at 6.6 ng/mL while remaining biocompatible to the mammalian cells at much higher concentrations. This study proves that this simple precursor, [Ru(CO)2Cl2]n, can be used as an antimicrobial compound with high activity and a low toxicity profile in the context of need for new antimicrobial agents to fight bacterial infections.

Probing of ascorbic acid by CdS/dendrimer nanocomposites: a spectroscopic investigation.

The gamma irradiation method has provided a route for synthesis of highly water-soluble, good-quality luminescent CdS/dendrimer nanocomposites with amino- or carboxyl-terminated PAMAM dendrimer. An attempt has been made to probe ascorbic acid with the as-synthesized CdS/dendrimer nanocomposites (DNC). Ascorbic acid (AA) is an important biological antioxidant and marker for different diseases in clinical chemistry as well as in quality control in the food industry. Micromolar concentrations of AA significantly quenched the photoluminescence (PL) of both amino (-NH(2)) and carboxylic (-COOH) functionalized semiconductor nanocomposites. The quenching followed a linear Stern-Volmer equation and time-resolved photoluminescence spectroscopy confirmed its static nature. A strong size dependence of the quenching pattern was observed. The binding constants, and the corresponding thermodynamic parameters DeltaG(theta), DeltaH(theta), DeltaS(theta) at different temperatures were calculated. CdS DNC showed selectivity towards ascorbic acid even in the presence of possible interfering molecules, such as uric acid, tartaric acid and citric acid. Nanocomposites-based assay techniques could override the complications involved in multitudes of assay procedures, providing a simple and fast new strategy for the quantification of Ascorbic acid in the range of 16.6 to 100 microM (R=0.998, n=9). The proposed method was applied to the detection of ascorbic acid in Vitamin C tablets with satisfactory results.

Conducting Polymer-Based Nanohybrids for Fuel Cell Application.

Carbon materials such as carbon graphitic structures, carbon nanotubes, and graphene nanosheets are extensively used as supports for electrocatalysts in fuel cells. Alternatively, conducting polymers displayed ultrahigh electrical conductivity and high chemical stability havegenerated an intense research interest as catalysts support for polymer electrolyte membrane fuel cells (PEMFCs) as well as microbial fuel cells (MFCs). Moreover, metal or metal oxides catalysts can be immobilized on the pure polymer or the functionalized polymer surface to generate conducting polymer-based nanohybrids (CPNHs) with improved catalytic performance and stability. Metal oxides generally have large surface area and/or porous structures and showed unique synergistic effects with CPs. Therefore, a stable, environmentally friendly bio/electro-catalyst can be obtained with CPNHs along with better catalytic activity and enhanced electron-transfer rate. The mass activity of Pd/polypyrrole (PPy) CPNHs as an anode material for ethanol oxidation is 7.5 and 78 times higher than that of commercial Pd/C and bulk Pd/PPy. The Pd rich multimetallic alloys incorporated on PPy nanofibers exhibited an excellent electrocatalytic activity which is approximately 5.5 times higher than monometallic counter parts. Similarly, binary and ternary Pt-rich electrocatalysts demonstrated superior catalytic activity for the methanol oxidation, and the catalytic activity of Pt24Pd26Au50/PPy significantly improved up to 12.5 A per mg Pt, which is approximately15 times higher than commercial Pt/C (0.85 A per mg Pt). The recent progress on CPNH materials as anode/cathode and membranes for fuel cell has been systematically reviewed, with detailed understandings into the characteristics, modifications, and performances of the electrode materials.

Soft Materials for Wearable/Flexible Electrochemical Energy Conversion, Storage, and Biosensor Devices.

Next-generation wearable technology needs portable flexible energy storage, conversion, and biosensor devices that can be worn on soft and curved surfaces. The conformal integration of these devices requires the use of soft, flexible, light materials, and substrates with similar mechanical properties as well as high performances. In this review, we have collected and discussed the remarkable research contributions of recent years, focusing the attention on the development and arrangement of soft and flexible materials (electrodes, electrolytes, substrates) that allowed traditional power sources and sensors to become viable and compatible with wearable electronics, preserving or improving their conventional performances.

Nitrogen photofixation ability of g-C3N4 nanosheets/Bi2MoO6 heterojunction photocatalyst under visible-light illumination.

In this study, we combined bismuth molybdate with graphitic carbon nitride nanosheets with different percentages of 10%, 20%, 30%, and 40%, in which noticeable N2 photoreduction under visible-light illumination was seen for the binary g-C3N4 nanosheets/Bi2MoO6 photocatalysts, denoted as NCN/BMO. The XPS, HRTEM, TEM, XRD, EDX, UV-vis DRS, N2 adsorption-desorption, FT-IR, TGA, PL, photocurrent, and EIS instruments were utilized to characterize the fabricated photocatalysts. The results displayed the construction of type-II heterojunction between the NCN and BMO components for the easy charge transfer. Under mild conditions and using ethanol as a hole scavenger, the NCN/BMO (30%) nanocomposite showed the maximum capability for ammonia generation by 3271 µmol/L g, which is 1.9 and 9.2 times higher than the NCN and BMO components, respectively. The effects of solvent type, pH of solution, and electron scavenger on the rate of NH4+ production were also studied and conversed. Finally, the stability of the NCN/BMO (30%) nanocomposite was evaluated for four cycles, in which the results were desirable.