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Solar radiation is a sustainable, unlimited source of energy for electricity and chemical reactions, yet the conversion efficiency of actual processes is limited and controlled by photocarriers migration and separation. Enhancing the conversion efficiency would require to suppress the recombination of photogenerated electron–hole pairs and improve the low redox potentials. This can be done during the growth of step-scheme (S-scheme) heterojunctions. Here we review the charge transfer of S-scheme heterojunctions involving a reduction and oxidation photocatalyst in staggered band arrangement with Fermi level differences. We present factors determining the validation of the S-scheme mechanism with respective characterization techniques, including in situ and ex situ experiments, and theoretical studies. We show mechanistic drawbacks of traditional photocatalytic systems to highlight the advantages of S-scheme photocatalysts. We describe co-catalyst loading, bandgap tuning, and interfacial optimization that ultimately achieve highly efficient photocatalysis. Last, application for water splitting, CO2 conversion, pollutant degradation, bacterial inactivation and others is discussed.

Photocatalytic hybrid carbon nanotubes (CNTs)–mediated Ag-CuBi 2 O 4 /Bi 2 WO 6 photocatalyst was fabricated using a hydrothermal technique to effectively eliminate organic pollutants from wastewater. The as-prepared samples were characterized via Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction patterns (XRD), high-resolution transmission electron microscope (HR-TEM), UV–vis Diffuse Reflectance spectrum (UV–Vis DRS), and photoluminescence (PL) studies. The photocatalytic performance of fabricated pristine and hybrid composites was examined by photo-degradation of toxic dye viz. Rhodamine B (RhB) under visible light. Photo-degradation results revealed that the fabricated Ag-CuBi 2 O 4 /CNTs/Bi 2 WO 6 semiconductor photocatalyst followed pseudo-first-order kinetics and displayed a higher photocatalytic rate, which was found to be approximately 3.33 and 2.35 times higher than the pristine CuBi 2 O 4 and Bi 2 WO 6 semiconductor photocatalyst, respectively. Re-cyclic results demonstrated that the formed composite owns excellent stability, even after five consecutive cycles. As per the matched Fermi level of CNTs in between Ag-CuBi 2 O 4 and Bi 2 WO 6 , carbon nanotubes severed as electron transfer-bridge, Ag doping on CuBi 2 O 4 surface successfully increased photon absorption all across CuBi 2 O 4 surface. Also, it hindered the assimilation of photoinduced electron–hole pairs. The increased photocatalytic efficiency is contributed to the uniform dispersion of photo-generated electron–hole pairs via the construction of an S-scheme system. ROS trapping and ESR experiments suggested that (∙OH) and (O 2 − ∙) were the main radical species for enhanced photo-degradation of RhB dye. The current investigation, from our perspective, highlights the new insights for the fabrication of practical CNTs-mediated S-scheme–based semiconductor photocatalyst for the resolution of environmental issues based on practical considerations.

Solar illumination is a promising source of primary energy to reduce global warming and to clean polluted waters, thus fostering research of the design of efficient photocatalysts for hydrogen production by water splitting and for contaminant degradation. In particular, photocatalysis by indium sulfide (In2S3) is drawing attention due to its suitable narrow bandgap of 2.0–2.3 eV for visible light harnessing, yet large-scale application of unmodified In2S3 is limited. Here we review the photocatalyst criteria for water splitting, the synthesis and morphological manipulations of In2S3, the synthesis of heterojunctions by coupling semiconductors to increase performance, and doping In2S3. In2S3-based heterojunctions, i.e., traditional type II, all-solid-state, and direct Z-scheme photocatalytic systems show benefits such as larger charge separation, broad solar spectrum absorption, and amended conduction band and valence band edge potentials for maximum pollutant removal and H2 production. The effect of dopant incorporation on electronic modulations of In2S3 is explained by the density functional theory.

Since it was first discovered, thousands of years ago, silkworm silk has been known to be an abundant biopolymer with a vast range of attractive properties. The utilization of silk fibroin (SF), the main protein of silkworm silk, has not been limited to the textile industry but has been further extended to various high-tech application areas, including biomaterials for drug delivery systems and tissue engineering. The outstanding mechanical properties of SF, including its facile processability, superior biocompatibility, controllable biodegradation, and versatile functionalization have allowed its use for innovative applications. In this review, we describe the structure, composition, general properties, and structure-properties relationship of SF. In addition, the methods used for the fabrication and modification of various materials are briefly addressed. Lastly, recent applications of SF-based materials for small molecule drug delivery, biological drug delivery, gene therapy, wound healing, and bone regeneration are reviewed and our perspectives on future development of these favorable materials are also shared.

Bismuth vanadate, BiVO4, is a visible-light response semiconductor for photocatalysis applications such as organic pollutants degradation, oxygen production and carbon dioxide reduction. However, as a single-phase photocatalyst, BiVO4 efficiency is limited by the unpreferable recombination of the photoexcited electron (e−) and hole (h+). Thus, strategies have been designed to enhance the photocatalytic efficiency by promoting the separation of electrons and holes. This can be done by controling the morphology and crystallographic facets of BiVO4, and by building p–n junction photocatalytic systems with a combination of n-type semiconductors (BiVO4) and p-type semiconductors or a monoclinic–tetragonal heterostructure of BiVO4. In particular, a direct p–n junction photocatalytic system with tetragonal zircon-structured BiVO4 (t-z) and monoclinic scheelite-structured BiVO4 (m-s) combination has recently attracted attention. Here we review the synthesis of the monoclinic–tetragonal heterostructured BiVO4 photocatalyst (m–t BiVO4) by calcination, hydrothermal, microwave-assisted hydrothermal and solvothermal methods. m–t BiVO4 formation and the transmission phase between t-z and m-s are controlled by the calcining temperature, precursor pH, metal doping content, type of solvent, implementation of precursors and reaction conditions. We discuss m–t BiVO4 crystal structure, optical characteristics and photocatalytic principles. Successful formation of BiVO4 crystals with a m-s/t-z heterostructure is based on data from X-ray diffraction (XRD), Raman and ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS). In the m–t BiVO4 heterostructure, a direct p–n junction photocatalytic system is established. When this system is exposed to visible light, the electrons in the conduction band of m-s BiVO4, a n-type semiconductor, migrate easily to the conduction band of t-z BiVO4, while the holes on valence band of t-z BiVO4, a p-type semiconductor, move to the valence band of m-s BiVO4 through an internal electric field. As a result, the e−/h+ charge carriers are spatially separated.

In this work, we present an ecofriendly, non-hazardous, green synthesis of zinc oxide nanoparticles (ZnO NPs) by leaf extract of Crotalaria verrucosa (C. verrucosa). Total phenolic content, total flavonoid and total protein contents of C. verrucosa were determined. Further, synthesized ZnO NPs was characterized by UV–visible spectroscopy (UV-vis), X-ray diffractometer (XRD), Fourier transform infra-red (FTIR) Spectra, transmission electron microscope (TEM), and Dynamic light scattering (DLS) analysis. UV-vis shows peak at 375 nm which is unique to ZnO NPs. XRD analysis demonstrates the hexagonal phase structures of ZnO NPs. FTIR spectra demonstrates the molecules and bondings associated with the synthesized ZnO NPs and assures the role of phytochemical compounds of C. verrucosa in reduction and capping of ZnO NPs. TEM image exhibits that the prepared ZnO NPs is hexagonal shaped and in size ranged between 16 to 38 nm which is confirmed by DLS. Thermo-gravimetric analysis (TGA) was performed to determine the thermal stability of biosynthesized nanoparticles during calcination. The prepared ZnO NPs showed significant antibacterial potentiality against Gram-positive (S. aureus) and Gram-negative (Proteus vulgaris, Klebsiella pneumoniae, and Escherichia coli) pathogenic bacteria and SEM image shows the generalized mechanism of action in bacterial cell after NPs internalization. In addition, NPs are also found to be effective against the studied cancer cell lines for which cytotoxicity was assessed using MTT assay and results demonstrate highest growth of inhibition at the concentration of 100 µg/mL with IC50 value at 7.07 µg/mL for HeLa and 6.30 µg/mL for DU145 cell lines, in contrast to positive control (C. verrucosa leaf extract) with IC50 of 22.30 µg/mL on HeLa cells and 15.72 µg/mL on DU145 cells. Also, DAPI staining was performed in order to determine the effect on nuclear material due to ZnO NPs treatment in the studied cell lines taking leaf extract as positive control and untreated negative control for comparison. Cell migration assay was evaluated to determine the direct influence of NPs on metastasis that is potential suppression capacity of NPs to tumor cell migration. Outcome of the synthesized ZnO NPs using C. verrucosa shows antimicrobial activity against studied microbes, also cytotoxicity, apoptotic mediated DNA damage and antiproliferative potentiality in the studied carcinoma cells and hence, can be further used in biomedical, pharmaceutical and food processing industries as an effective antimicrobial and anti-cancerous agent.

This work successfully fabricated graphitic carbon nitride and magnetically recoverable α-Fe 2 O 3 /g-C 3 N 4 /SiO 2 photo-Fenton catalysts using thermal polycondensation and in situ-simple precursor drying-calcination process, respectively, was examined for model synthetic rhodamine B (RhB) dye in the presence of H 2 O 2 and acidic pH under simulated visible light irradiation. An aqueous suspension of the reaction mixture of dye-containing wastewater was fully degraded and reached 97% of photo-Fenton degradation efficiency within 120 min followed by the production of hydroxyl radical ( • OH). The dominant hydroxyl radical position generated surface charge, electrostatic potential distribution, and average local ionization potential, which contributed to the complete mineralization of RhB dye, according to the density functional theory (DFT) calculations. HPLC and GCMS experiments were performed to examine the degradation fragments of RhB and draw a plausible mechanistic pathway which showed that RhB degradation generated a series of N-deethylated products, followed by a one-time ring-opening, which indicated that photosensitization induced a photocatalysis reaction mechanism. Graphical Abstract

The rising energy conflicts and environmental pollution are calling for the rapid development of advanced techniques such as photoelectrocatalysis to transform waste into energy and to clean contaminated media. Here we review photoelectrocatalysis for removing wastewater contaminants and recovering energy such as electricity and hydrogen (H 2 ), with focus on the basics of photoelectrocatalysis, charge kinetics, selecting a photoelectrode, and performance. Modification strategies such as heterostructure formation and doping are discussed. We present applications such a hydrogen production coupled with wastewater treatment, carbon dioxide reduction coupled with pollutant degradation, energy production coupled with wastewater treatment, and microbial fuel cells for electricity generation and pollutant degradation.

Scaffolds are important to tissue regeneration and engineering because they can sustain the continuous release of various cell types and provide a location where new bone-forming cells can attach and propagate. Scaffolds produced from diverse processes have been studied and analyzed in recent decades. They are structurally efficient for improving cell affinity and synthetic and mechanical strength. Carbon nanotubes are spongy nanoparticles with high strength and thermal inertness, and they have been used as filler particles in the manufacturing industry to increase the performance of scaffold particles. The regeneration of tissue and organs requires a significant level of spatial and temporal control over physiological processes, as well as experiments in actual environments. This has led to an upsurge in the use of nanoparticle-based tissue scaffolds with numerous cell types for contrast imaging and managing scaffold characteristics. In this review, we emphasize the usage of carbon nanotubes (CNTs) and CNT–polymer composites in tissue engineering and regenerative medicine and also summarize challenges and prospects for their potential applications in different areas.

Low dimensional transition metal carbide and nitride (MXenes) have been emerging as frontier materials for energy storage and conversion. Ti3C2Tx was the first MXenes that discovered and soon become the most widely investigated among the MXenes family. Interestingly, Ti3C2Tx exhibits ultrahigh catalytic activity towards the hydrogen evolution reaction. In addition, Ti3C2Tx is electronically conductive, and its optical bandgap is tunable in the visible region, making it become one of the most promising candidates for the photocatalytic hydrogen evolution reaction (HER). In this review, we provide comprehensive strategies for the utilization of Ti3C2Tx as a catalyst for improving solar-driven HER, including surface functional groups engineering, structural modification, and cocatalyst coupling. In addition, the reaming obstacle for using these materials in a practical system is evaluated. Finally, the direction for the future development of these materials featuring high photocatalytic activity toward HER is discussed.