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Industrial activities generate enormous quantities of polluted effluents, necessitating advanced methods of wastewater treatment to prevent potential environmental threats. Thus, the design of a novel photocatalytic reactor for industrial water decontamination, purification, and reuse is proposed as an efficient advanced oxidation technology. In this work, the development of the active reactor components is described, utilizing a two-step sol–gel technique to prepare a silica-titania trilayer coating on 3D-printed polymeric filters. The initial dip-coated SiO2 insulator further protects and enhances the stability of the polymer matrix, and the subsequent TiO2 layers endow the composite architecture with photocatalytic functionality. The structural and morphological characteristics of the modified photocatalytic filters are extensively investigated, and their performance is assessed by studying the photocatalytic degradation of the Triton X-100, a common and standard chemical surfactant, presented in the contaminated wastewater of the steel metal industry. The promising outcomes of the innovative versatile reactor pave the way for developing scalable, cost-effective reactors for efficient water treatment technologies.

Perovskite solar cells (PSCs) are third-generation photovoltaic technology that has gained a lot of attention due to its technological and economic advantages. The PSCs are characterized with low cost, high absorption, long carrier diffusion length, and low fabrication temperature. To model the performance of PSCs, a new dynamic model is proposed to track the cells hysteresis by adding a variable voltage capacitor to the single, double, and triple diode models. The aim with adding the variable capacitor is to emulate the effect of charge accumulation at the interfaces of the device. Three modified models are presented based on one or more variable capacitors at single, double, and triple diode models. Where, the triple diode model with third order variable voltage capacitor model is the best among all models by 74.9% enhancement in comparison with single diode model. Also, the Equilibrium optimization algorithm (EOA) is proposed to determine the parameters of the proposed dynamic model based on the triple diode model. In comparison with the experimental data, for both forward and reverse scans, the findings showed that the suggested model accurately reflects cell performance. Added to that, the EOA finds well the optimal model parameters considering the root mean square as primary objective function. Based on the simulation results, it was proved that the proposed model gives very close results to reality.

The disinfection properties of photocatalysis on liquid digestate derived from biogas plants have been investigated for the first time. The study presents the physiological characteristics of liquid digestate retrieved from various biogas plants based in northern Greece, revealing the heterogeneity of this matrix. Preliminary photocatalysis experiments conducted on inoculated liquid digestate samples showed that disinfection was possible when a pre-treated digestate underwent a combination of centrifuge–flocculation–μfiltration after 5.5 h with 0.7 g/L suspended TiO2 under UVA illumination. To explore the feasibility of an industrial application based on this concept, a novel design photocatalytic nanofiltration reactor was implemented for disinfection experiments on pre-treated liquid digestate. The synergistic action of photocatalysis during nanofiltration alleviated the leakage phenomena, and both the retentate and permeate effluents had lower concentrations of pathogens by approximately 1–2 log10 cfu/mL. This work sets out the basis for the efficient operation and engineering application of collaborative technology, with photocatalysis as the final step for liquid digestate sanitation and reusable water recovery.

The addition of biocarriers can improve biological processes in bioreactors, since their surface allows for the immobilization, attachment, protection, and growth of microorganisms. In addition, the development of a biofilm layer allows for the colonization of microorganisms in the biocarriers. The structure, composition, and roughness of the biocarriers’ surface are crucial factors that affect the development of the biofilm. In the current work, the aluminosilicate zeolites 13X and ZSM-5 were examined as the main building components of the biocarrier scaffolds, using bentonite, montmorillonite, and halloysite nanotubes as inorganic binders in various combinations. We utilized 3D printing to form pastes into monoliths that underwent heat treatment. The 3D-printed biocarriers were subjected to a mechanical analysis, including density, compression, and nanoindentation tests. Furthermore, the 3D-printed biocarriers were morphologically and structurally characterized using nitrogen adsorption at 77 K (LN2), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The stress–strain response of the materials was obtained through nanoindentation tests combined with the finite element analysis (FEA). These tests were also utilized to simulate the lattice geometries under compression loading conditions to investigate their deformation and stress distribution in relation to experimental compression testing. The results indicated that the 3D-printed biocarrier of 13X/halloysite nanotubes was endowed with a high specific surface area of 711 m2/g and extended mesoporous structure. Due to these assets, its bulk density of 1.67 g/cm3 was one of the lowest observed amongst the biocarriers derived from the various combinations of materials. The biocarriers based on the 13X zeolite exhibited the highest mechanical stability and appropriate morphological features. The 13X/halloysite nanotubes scaffold exhibited a hardness value of 45.64 MPa, which is moderate compared to the rest, while it presented the highest value of modulus of elasticity. In conclusion, aluminosilicate zeolites and their combinations with clays and inorganic nanotubes provide 3D-printed biocarriers with various textural and structural properties, which can be utilized to improve biological processes, while the most favorable characteristics are observed when utilizing the combination of 13X/halloysite nanotubes.

Among key issues in municipal wastewater treatment plants (MWTP) is the existence of pathogenic bacteria in the discarded effluents. Conventional disinfectants (ozone, UV irradiation, chlorine) have been insufficient in providing safe water due to the development of undesirable and noxious by-products. TiO2 comprises an attractive alternative to conventional methods because of its versatility and recently explored biocidal efficiency. As a result, within the framework of this study, chemically modified, visible active nanocrystalline TiO2 powders (N-TiO2, N,S-TiO2, and Ag@N-TiO2) were prepared via a low-cost, feasible sol-gel method for the treatment of real municipal wastewater effluents. Wastewater samples were acquired from the outlet of the treatment of Antiparos (Cyclades, Greece) MWTP during the summer period in which a great number of seasonal habitants and tourists usually visit the island, resulting in at least a doubling of the population. All synthesized powders were thoroughly characterized using various morphological and spectroscopic techniques, such as FE-SEM, XRD, micro-Raman, FTIR, DLS, UV-DRS, and XPS. Photocatalytic evaluation experiments were initially conducted towards Rhodamine B degradation under visible light irradiation. Among all studied powders, Ag@N-TiO2 indicated the highest efficiency, reaching total degradation (100%) of RhB within 240 min due to its smaller crystallite size (1.80 nm), enhanced surface area (81 m2g−1), and reduced energy band gap (Eg = 2.79 eV). The effect of the produced powders on the disinfection as assessed in terms of fecal indicator microorganisms (E. coli and total coliforms) inactivation was also examined in a semi-pilot scale-up photocatalytic reactor. Ag@N-TiO2 nanopowder was also found substantially more active for both groups of bacteria, leading to complete inactivation in less than 35 min, probably due to the higher production of H2O2/•OH, as emerged from the photocatalytic mechanism study. In addition, Ag@N-TiO2 nanoparticles demonstrated excellent photocatalytic and disinfection stability even after five subsequent recycling trials (8.34% activity loss and complete inactivation, respectively). The results of the present study demonstrate the feasibility for Ag@N-TiO2 to be utilized as a viable, eco-friendly approach for the photocatalytic pathogenic bacteria inactivation as an alternative disinfection approach for municipal wastewater treatment plant effluents with intense seasonal fluctuations in volume.

Ternary TiO2/g-C3N4@Ag nanocomposites with controlled composition were synthesized and used as highly effective bifunctional photocatalysts. TiO2 nanoparticles were initially prepared via a sol-gel method and afterwards combined with optimum amounts of graphitic carbon nitride (g-C3N4) by a hydrothermal procedure to finally produce TiO2/g-C3N4 heterostructures. TiO2/g-C3N4 was impregnated with a silver nitrate aqueous solution containing sodium citrate as a reducing agent resulting in elemental silver nanoparticle (Ag0 NP) integration, as confirmed by x-ray photoelectron spectroscopy (XPS). Following crystallographic, electron-microscopy and spectroscopic characterization, the prepared nanocomposites presented high photocatalytic activity for both oxidation and reduction reactions. The photodegradation of model organic pollutants: methylene blue (MB) and rhodamine B (RhB) dyes and oxytetracycline (OTC) pharmaceutical, together with decomposition of 4-nitrophenol (4-NP) and Cr(VI), was investigated and the reaction constants were determined. An optimum component ratio was determined, which leads to the effective elimination of pollutants under UV light, with degradation percentages up to 95% for MB and 89% for RhB and 90% removal efficiency of the OTC pharmaceutical. The degradation of both dyes was also confirmed under artificial solar light. Furthermore, the ternary TiO2/g-C3N4@Ag NCs were highly effective for the photocatalytic reduction of 4-NP to aminophenol (>95%) and Cr(VI) to Cr(III) (80%), under UV illumination.

Pesticide residues, when present in agricultural wastewater, constitute a potential risk for the environment and human health. Hence, focused actions for their abatement are of high priority for both the industrial sectors and national authorities. This work evaluates the effectiveness of the photocatalytic process to decompose two frequently detected pesticides in the water effluents of the fruit industry: thiamethoxam-a neonicotinoid compound and flonicamid-a pyridine derivative. Their photocatalytic degradation and mineralization were evaluated in a lab-scale photocatalytic batch reactor under UV-A illumination with the commercial photocatalyst Evonik P25 TiO2 by employing different experimental conditions. The complete degradation of thiamethoxam was achieved after 90 min, when the medium was adjusted to natural or alkaline pH. Flonicamid was proven to be a more recalcitrant substance and the removal efficiency reached ~50% at the same conditions, although the degradation overpassed 75% in the acidic pH medium. Overall, the pesticides’ degradation follows the photocatalytic reduction pathways, where positive charged holes and hydroxyl radicals dominate as reactive species, with complete mineralization taking place after 4 h, regardless of the pH medium. Moreover, it was deduced that the pesticides’ degradation kinetics followed the Langmuir-Hinshelwood (L-H) model, and the apparent rate constant, the initial degradation rate, as well as the L-H model parameters, were determined for both pesticides.

Nowadays, the increased agro-industrial activities and the inability of traditional wastewater treatment plants (WWTPs) to eliminate recalcitrant organic contaminants are raising a potential worldwide risk for the environment. Among the various advanced water treatment technologies that are lately proposed for addressing this challenge, the development and optimization of an innovative hybrid photocatalytic nanofiltration reactor (PNFR) prototype emerges as a prominent solution that achieves synergistic beneficial effects between the photocatalytic degradation activity and size exclusion capacity for micropollutant molecules. Both these features can be contemporarily endued to a multitude of membrane monoliths. The physicochemical and the photoinduced decontamination properties of the titania materials were firstly determined in the powder form, and subsequently, the structural and morphological characterization of the obtained titania-modified membrane monoliths were accomplished. The PNFR unit can operate at high water recovery and low pressures, exhibiting promising removal efficiencies against Acetamiprid (ACT) and Thiabendazole (TBZ) pesticides and achieving the recycling of 15 m3/day of real agro-wastewater. The obtained results are very encouraging, demonstrating the integration of titania photocatalysts in a photocatalytic membrane reactor as a feasible technological solution for the purification of agricultural wastewater.

We investigate super-hydrophilic TiO _2 (titania) films for concentrated solar-thermal power applications. Reactive magnetron sputtering has been used to deposit 8 to 12 nm thick titania thin films onto borosilicate microscope glass slides, low-Fe extra-clear architectural glass, or Si(100) wafers with a 500 nm thick thermal SiO _2 layer. The effects of deposition temperature and O _2 fraction of the O _2 /Ar working gas were investigated. We demonstrate the importance of the O _2 fraction for obtaining optically transparent, super-hydrophilic (contact angle below 1°) thin films. In particular, we show that as the O _2 fraction increases, contact angle decreases, obtaining super-hydrophilic titania thin films at deposition temperatures as low as 120 °C. Our work enables to develop low thermal budget cost-efficient industrial synthesis processes, paving the way for commercial applications.

In this work, a proposed high-efficiency and low-cost photovoltaic water-pumping system based on semitransparent dye-sensitized solar cells (DSSCs) is presented. DSSCs are low-cost third-generation photovoltaics that have gained a lot of interest as a promising alternative for silicon solar cells. DSSCs are fabricated at low cost and low temperature and present power conversions with high efficiency, exceeding 14%, thanks to high transparency, a variety of colors, and high efficiency, even in low light conditions. The DSSC modules used in this study were tested under different working conditions, and their characteristics were determined experimentally and simulated theoretically via MATLAB. A complete laboratory infrastructure is constructed to test the proposed photovoltaic water-pumping system based on the DSSC module array. The system contains a synchronous reluctance motor driving a water pump and feeding from the DSSCs via an inverter without DC–DC converters or batteries. The proposed system has many merits, such as high efficiency and low cost. The DSSCs’ maximum available power is obtained via a maximum power point tracking technique (perturb-and-observe). Moreover, a control system for driving the motor via the inverter was also implemented. The maximum torque per ampere strategy is also considered in the proposed control system to drive the motor efficiently using the inverter. Finally, experimental validation of the complete system via laboratory measurements is implemented.

The reliable mathematical model construction of dye-sensitized solar cells (DSSCs) using the triple-diode model (TDM) is proposed but it is a challenge due to its complexity. This work implements a novel method incorporating a recent meta-heuristic optimizer called the heterogeneous marine predators algorithm (H-MPA) to identify the nine parameters of the triple-diode equivalent circuit of DSSCs. In the optimization procedure, the nine unknown parameters of TDM are employed as decision variables, but the objective function to be minimized is the root mean square error (RMSE) between the experimental data and the estimated data. To prove the superiority of the H-MPA, the obtained results are compared with the slime mold algorithm (SMA), Transient search optimizer (TSO), Manta-Ray Foraging Optimization algorithm (MRFO), Forensic-Based Investigation (FBI), Equilibrium optimizer (EO), and Artificial ecosystem-based optimizer. The primary findings demonstrated the superiority of the proposed strategy in building a consistent model of the triple-diode model of DSSCs.

Nowadays, water pumping systems based on photovoltaics as a source of electricity have widely increased. System cost and efficiency still require enhancement in order to spread their application. Perovskite solar cells (PSCs) are the most hopeful third-generation photovoltaic for replacing the silicon-based photovoltaic thanks to their high power conversion efficiency, reaching 25.8%; tunable band-gap; long diffusion length; low fabrication temperature; and low cost. In this work, for the first time, we proposed a high-power-density hybrid perovskite solar cell thermoelectric generator (TEG) array for feeding a synchronous reluctance motor (SynRM) driving a water pump for use in an irrigation system. A control technique was used to achieve two functions. The first function was driving the motor to obtain the maximum torque/ampere. The second was harvesting the maximum perovskite solar cell array output power on the basis of the maximum power point tracking (MPPT) algorithm using the perturbation and observation approach. Thus, the proposed hybrid perovskite solar cell–thermoelectric generator feeds the motor via an inverter without DC–DC converters or batteries. Accordingly, the short life problems and the high replacement cost are avoided. The proposed complete system was simulated via the MATLAB package. Moreover, a complete laboratory infrastructure was constructed for testing the proposed high-power-density hybrid perovskite solar cell–TEG array for the water pumping system. The results revealed that using the high-power-density hybrid perovskite solar cell–TEG array, both the motor’s output power and the pump’s flow rate were improved by 11% and 14%, respectively, compared to only using the perovskite solar cell array. Finally, both the simulation and experimental results proved the high-performance efficiency of the system in addition to showing its system complexity and cost reduction.

In this study, we developed highly sensitive substrates for Surface-Enhanced-Raman-Scattering (SERS) spectroscopy, consisting of silicon nanowires (SiNWs) decorated by silver nanostructures using single-step Metal Assisted Chemical Etching (MACE). One-step MACE was performed on p-type Si substrates by immersion in AgNO3/HF aqueous solutions resulting in the formation of SiNWs decorated by either silver aggregates or dendrites. Specifically, dendrites were formed during SiNWs’ growth in the etchant solution, whereas aggregates were grown after the removal of the dendrites from the SiNWs in HNO3 aqueous solution and subsequent re-immersion of the specimens in a AgNO3/HF aqueous solution by adjusting the growth time to achieve the desired density of silver nanostructures. The dendrites had much larger height than the aggregates. R6G was used as analyte to test the SERS activity of the substrates prepared by the two fabrication processes. The silver aggregates showed a considerably lower limit of detection (LOD) for SERS down to a R6G concentration of 10−13 M, and much better uniformity in terms of detection in comparison with the silver dendritic structures. Enhancement factors in the range 105–1010 were calculated, demonstrating very high SERS sensitivities for analytic applications.

Perovskite solar cells (PSCs) have attracted great research interest in the scientific community due to their extraordinary optoelectronic properties and the fact that their power conversion efficiency (PCE) has increased rapidly in recent years, surpassing other 3rd generation photovoltaic (PV) technologies. Graphitic carbon nitride (g-C3N4) presents exceptional optical and electronic properties and its use was recently expanded in the field of PSCs. The addition of g-C3N4 in the perovskite absorber and/or the electron transport layer (ETL) resulted in PCEs exceeding 22%, mainly due to defects passivation, improved conductivity and crystallinity as well as low charge carriers’ recombination rate within the device. Significant performance increase, including stability enhancement, was also achieved when g-C3N4 was applied at the PSC interfaces and the observed improvement was attributed to its wetting (hydrophobic/hydrophilic) nature and the fine tuning of the corresponding interface energetics. The current review summarizes the main innovations for the incorporation of graphitic carbon nitride in PSCs and highlights the significance and perspectives of the g-C3N4 approach for emerging highly efficient and robust PV devices.

Photonic crystal structuring has emerged as an advanced method to enhance solar light harvesting by metal oxide photocatalysts along with rational compositional modifications of the materials’ properties. In this work, surface functionalization of TiO2 photonic crystals by blue luminescent graphene quantum dots (GQDs), n–π* band at ca. 350 nm, is demonstrated as a facile, environmental benign method to promote photocatalytic activity by the combination of slow photon-assisted light trapping with GQD-TiO2 interfacial electron transfer. TiO2 inverse opal films fabricated by the co-assembly of polymer colloidal spheres with a hydrolyzed titania precursor were post-modified by impregnation in aqueous GQDs suspension without any structural distortion. Photonic band gap engineering by varying the inverse opal macropore size resulted in selective performance enhancement for both salicylic acid photocatalytic degradation and photocurrent generation under UV–VIS and visible light, when red-edge slow photons overlapped with the composite’s absorption edge, whereas stop band reflection was attenuated by the strong UVA absorbance of the GQD-TiO2 photonic films. Photoelectrochemical and photoluminescence measurements indicated that the observed improvement, which surpassed similarly modified benchmark mesoporous P25 TiO2 films, was further assisted by GQDs electron acceptor action and visible light activation to a lesser extent, leading to highly efficient photocatalytic films.

Novel V2O5 bifunctional photocatalysts were prepared following a wet chemical process with the addition of anionic or non-ionic surfactants into the precursor solution and further heating under reflux. Detailed characterization and investigation of the relevant light-matter interactions proved that surfactants addition had a strong impact on the morphology, while also affecting the crystallinity, the optoelectronic properties, and the surface chemistry of the novel photocatalysts. The most efficient photocatalyst (T80) was based on tween 80, a surface-active agent employed for the first time in the synthesis of vanadium oxide materials. T80 presented crystalline nature without structural defects, which are usually centers of e− − h+ recombination. This material also exhibited small crystal size, high porosity, and short migration paths for the charge carriers, enabling their effective separation during photocatalysis. Under UV light illumination, T80 was capable to reduce hexavalent chromium to trivalent up to 70% and showed high yields in degrading methylene blue azo-dye and tetracycline antibiotic water pollutants. This remarkably high bifunctional performance defines T80 as a promising and capable photocatalytic material for both advanced oxidation and reduction processes (AOPs-ARPs).

A bifunctional thin film photocatalyst consisting of graphitic carbon nitride on tungsten trioxide (g-C3N4/WO3) is introduced for the improvement of photocatalytic activity concerning hexavalent chromium reduction and methylene blue dye removal in water, compared to the bare, widely used WO3 semiconductor. A bilayered structure was formed, which is important for the enhancement of the charge carriers’ separation. The characterization of morphological, structural, optoelectronic, and vibrational properties of the photocatalysts permitted a better understanding of their photocatalytic activity for both dye degradation and Cr+6 elimination in water and the analysis of the photocatalytic kinetics permitted the determination of the corresponding pseudo-first-order reaction constants (k). Trapping experiments performed under UV illumination revealed that the main active species for the photocatalytic reduction of Cr+6 ions are electrons, whereas in the case of methylene blue azo-dye (MB) oxidation, the activation of the corresponding photocatalytic degradation comes via both holes and superoxide radicals.

In this work, we prepared oriented mesoporous thin films of silica on various solid substrates using the pluronic block copolymer P123 as a template. We attempted to insert guest iron oxide (FexOy) nanoparticles into these films by two different methods: (a) by co-precipitation—where iron precursors are introduced in the synthesis sol before deposition of the silica film—and subsequent oxide production during the film calcination step; (b) by preparing and calcining the silica films first then impregnating them with the iron precursor, obtaining the iron oxide nanoparticles by a second calcination step. We have examined the structural effects of the guest nanoparticles on the silica film structures using grazing incidence X-ray scattering (GISAXS), high-resolution transmission electron spectroscopy (HRTEM), spectroscopic ellipsometry, X-ray photoelectron spectroscopy (XPS), and Raman microscopy. Formation of nanoparticles by co-precipitation may induce substantial changes in the film structure leading, in our adopted process, to the appearance of lamellar ordering in the calcination stage. On the contrary, impregnation-based approaches perturb the film structures much more weakly, but are also less efficient in filling the pores with nanoparticles.

Solution-processed organic-inorganic halide perovskites are currently established as the hottest area of interest in the world of photovoltaics, ensuring low manufacturing cost and high conversion efficiencies. Even though various fabrication/deposition approaches and device architectures have been tested, researchers quickly realized that the key for the excellent solar cell operation was the quality of the crystallization of the perovskite film, employed to assure efficient photogeneration of carriers, charge separation and transport of the separated carriers at the contacts. One of the most typical methods in chemistry to crystallize a material is anti-solvent precipitation. Indeed, this classical precipitation method worked really well for the growth of single crystals of perovskite. Fortunately, the method was also effective for the preparation of perovskite films by adopting an anti-solvent dripping technique during spin-coating the perovskite precursor solution on the substrate. With this, polycrystalline perovskite films with pure and stable crystal phases accompanied with excellent surface coverage were prepared, leading to highly reproducible efficiencies close to 22%. In this review, we discuss recent results on highly efficient solar cells, obtained by the anti-solvent dripping method, always in the presence of Lewis base adducts of lead(II) iodide. We present all the anti-solvents that can be used and what is the impact of them on device efficiencies. Finally, we analyze the critical challenges that currently limit the efficacy/reproducibility of this crystallization method and propose prospects for future directions.

cis-[Ru(bpy)2(Ln)]Cl2(n = 1, L1= 4-carboxy-2-(2′-pyridyl)quinoline (2); n = 2, L2= 2,2′-pyridine-4,4′-dicarboxylic acid (4)); and cis-[Ru(bpy)2(L′)2)]Cl2(L′ = 4-pyridinecarboxylic acid (6)) complexes, with surface anchoring groups, are prepared from the reaction of cis-[Ru(bpy)2Cl2] (1) with the appropriate ligand (L1, L2, L′). Ion exchange in aqueous solution with NH4PF6gives the corresponding bis(hexafluorophosphate) derivatives cis-[Ru(bpy)2(L1)](PF6)2(3), cis-[Ru(bpy)2(L2)](PF6)2(5) and cis-[Ru(bpy)2(L′)2](PF6)2(7), respectively. The photo-electrochemical properties of the dyes (2–7) are investigated and the efficiency of the corresponding dye sensitized solar cells is compared to a N719 sensitized device, under similar fabrication and testing conditions. [ABSTRACT FROM AUTHOR]