Bioengineered sustainable phytofabrication of anatase TiO2 -adorned g-C3N4 nanocomposites and unveiling their photocatalytic potential towards advanced environmental remediation.

The ecologically friendly properties, low-cost, and readily available titanium dioxide (TiO2) materials have made them a subject of considerable interest for numerous promising applications. Anatase TiO2 nanoparticles were synthesized in the current study through the utilization of a hibiscus leaf extract and the advent of TiO2-doped g-C3N4(TiCN) nanocomposites (varying 0.5 mM, 1.0 mM, 1.5 mM, and 2.0 mM) by thermal polymerization. Here, the proposed study utilized multiple analytical techniques, including UV-Vis spectroscopy, a diffraction pattern (XRD), SEM coupled with EDX analysis, TGA, and EPR, to characterize the as-prepared TiO2 nanoparticles and TiCN nanocomposites. BET analysis the adsorption-desorption isotherms of the TiCN(1.5 mM) nanocomposite, the surface area of the prepared nanocomposite is 112.287 m2/g, and the pore size is 7.056 nm. The XPS spectra support the development of the TiCN(1.5 mM) nanocomposite by demonstrating the presence of C and N elements in the nanocomposite in addition to TiO2. HRTEM images where the formation of stacked that indicates a planar, wrinkled graphitic-like structure is clearly visible. The TiCN (1.5 mM) specimen exhibited enhanced morphology, enhanced surface area, greater capacity to take in visible light, and lowered band gap when compared to g-C3N4 following z-scheme heterojunction. The sample denoted as TiCN (1.5 mM) exhibited superior performance in terms of adsorption and photocatalytic activity using rhodamine B and Bisphenol A. Furthermore, the TiCN (1.5 mM) composite exhibited satisfactory stability over four cyclic runs, indicating its potential application in minimizing the impact of organic wastewater contaminants when compared to g-C3N4.

Unleashing the visible light-exposed photocatalytic potential of V2O5/g-C3N4 nanocomposites for dye industries wastewater cleaner production.

Dealing harmful dye-containing effluent from the textile sector significantly contributes to water contamination. The persistence of these dyes in wastewater complicates traditional treatment approaches, emphasizing the necessity for efficient photocatalytic materials for dye pollution degradation. Due to its unique features, V2O5/g-C3N4 nanocomposites are discovered as promising photocatalysts in this area. The V205 nanoparticles act as electron acceptors, while g-C3N4 acts as electron donors, thus encouraging charge separation and increasing photocatalytic activity. The V2O5/g-C3N4 nanocomposites are characterized using XRD, FTIR spectroscopy, SEM, TEM, XPS, and UV-DRS. Cationic dyes, anionic dyes and mix dyes (1:1 mixture of cationic and anionic dyes) are used to test the photocatalytic activity of the nanocomposites. Photocatalytic activity shows that V2O5/g-C3N4 nanocomposites are more active than their precursors. The V5G-2 nanocomposite degrades anionic (Rose Bengal (85.1%) and Xylenol Orange (77.6%), cationic (Auramine O (75% and Crystal Violet (79.5%), and mixed dyes (81%), after 120 min of irradiation. This study introduces a novel technique for synthesizing V2O5/g-C3N4 nanocomposites using solvothermal and ultrasonic processes. The findings of this research provide significant knowledge for the development of photocatalysts with enhanced efficiency in the degradation of dye pollutants.

Ppy/TiO2-SiO2 nanohybrid series: synthesis, characterization, photocatalytic activity, and antimicrobial potentiality.

A series of polypyrrole doped TiO2-SiO2 nanohybrids (Ppy/TS NHs) were synthesized thru in-situ oxidation polymerization by varying weight ratio of pyrrole. The structural analysis of NHs were characterized by X-ray Diffraction (XRD) spectra, UV-visible (UV-Vis) spectra and X-ray Photoelectron spectra (XPS) confirmed synthesis of nanomaterials. Surface and morphological study done by adopting, Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), Transmittance Electron Microscopy (TEM) and Brunauer-Emmett-Teller (BET) analysis confirmed the homogenous distribution, nano range size formation and mesoporous nature of nanohybrids. Further, electrochemical behavior of synthesized NHs investigated by adopting Electrochemical Impedance Spectroscopy (EIS) showed good kinetic behaviour and electron transport tendency. The nanohybrids and precursors were examined for photocatalytic degradation of methylene blue (MB) dye and revealed enhanced degradation tendency for the NHs series photocatalysts. It was found that variation of pyrrole (0.1 to 0.3 g) to TS nanocomposites (TS Nc) increased the photocatalytic potential of TS Nc. The maximum photodegradation efficacy was found to be 90.48% in 120 min for Ppy/TS0.2 NHs under direct solar light. Additionally, Ppy/TS0.2 NHs performed appreciably towards antibacterial studies against some Gram-positive and Gram-negative deleterious bacteria, Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, Shigella flexneri microbes.

Visible light enhanced photocatalytic degradation of organic pollutants with SiO2/g-C3N4 nanocomposite for environmental applications.

The development of eco-friendly photocatalysts is gaining attention as an effective approach for degrading organic pollutants. In the present study, the composite materials are composed of various components with varying structures that combine to enhance their characteristics and widen their applications. This work uses the hydrothermal method for the fabrication of a novel and steady SiO2/g-C3N4 photocatalyst. The amount of SiO2 was fixed, and graphitic carbon nitride (g-C3N4) was varied in the ratio (1:x, where x = 1, 2, 3) and abbreviated as SCN1, SCN2, and SCN3. The optical properties, surface morphology, and structural analysis of the prepared nanocomposites were studied using various techniques such as FTIR, TGA, X-ray diffraction, and ultraviolet-visible spectroscopy. The results show that SCN2 nanocomposites significantly improved the photocatalytic activity, with a degradation efficiency of 70% for auramine O and 84.6% for xylenol orange dye under visible light irradiation, which is a result of their large surface area and efficient electron-hole separation rate.

Photocatalytic dye degradation and antibacterial activities of CeO2/g-C3N4 nanomaterials for environmental applications.

The uncontrolled dumping of synthetic dyes into water sources has posed severe hazards to the ecosystem. For decades, several materials with low cost and high efficiency have been investigated for dye degradation. Photocatalytic degradation is regarded as a successful strategy since it utilizes sunlight to transform harmful pollutants into nontoxic compounds without using oxidative agents. The photocatalytic potentials of CeO2/g-C3N4 (CG) were investigated in this work using a simplistic ultrasonication process. Here, the amount of CeO2 was fixed, and g-C3N4 was varied in the ratio (1:x, where x = 1, 2, and 3) and abbreviated as CG1, CG2, and CG3. Characterization techniques such as Fourier transforms-infrared spectroscopy, thermal gravimetric analysis (TGA), powdered X-ray diffraction, ultraviolet-visible spectroscopy, etc. were used to characterize structural analysis, optical properties, particle size, and chemical bonds of the prepared nanocomposites. The photocatalytic results showed that CG2 effectively degraded rose bengal (RB) and crystal violet (CV) dyes when exposed to visible light irradiation as compared to pure GCN and CeO2. The antibacterial activity analysis further supported the potential application of prepared photocatalyst as a disinfectant agent against both gram-positive (Staphylococcus aureus and Bacillus cereus) and gram-negative (Salmonella abony and Escherichia coli) pathogenic strains of bacteria.