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This study presents an innovative method for the synthesis of indium aluminum nitride (InAlN) layers by direct current (DC) co-sputtering at room temperature, with the aim of reducing production costs of optoelectronic devices. Indium and aluminum targets are used, varying the power applied to the aluminum target. The results show that increasing the target power favors the formation of aluminum nitride (AlN), which modifies the chemical composition of the material. The layers obtained present smooth surfaces with a roughness of less than 3 nm, which is beneficial for applications requiring interfaces with low defect density. Regarding the optical properties, it is observed that the optical bandgap varies between 1.8 eV and 2.0 eV, increasing with the target power. Hall effect measurements indicate a decrease in the free carrier concentration and an increase in the resistivity with increasing power. This approach allows for the synthesis of InAlN with properties suitable for optoelectronic applications, solar cells, photocatalysis, and photoelectrocatalysis at low cost. [ABSTRACT FROM AUTHOR]

Abstract The present work deals with developing a method for revalorizing steel residues to create sunlight-active photocatalysts based on iron oxides. Commercial-grade steel leftovers are oxidized under different combinations of pH and temperature (50–90 °C and 3 ≥ pH ≤ 5) in a low energy-intensive setup. The material with the highest production efficiency (yield > 12%) and magnetic susceptibility (χm = 387 × 10−6 m3/kg) was further explored and modified by diffusion of M2+ (Zn and Co) ions within the structure of the oxide using a hydrothermal method to create ZnFe2O4, CoFe2O4 and combined Co–Zn ferrite. (Co–Zn)Fe2O4 displayed a bandgap of 2.02 eV and can be activated under sunlight irradiation. Electron microscopy studies show that (Co–Zn)Fe2O4 consists of particles with diameters between 400 and 700 nm, homogeneous size, even distribution, and good dispersibility. Application of the developed materials in the sunlight catalysis of black liquors from cellulose extraction resulted in a reduction of the Chemical Oxygen Demand (− 15% on average) and an enhancement in biodegradability (> 0.57 BOD/COD) after 180 min of reaction. Since the presented process employs direct solar light, it opens the possibility to large-scale water treatment and chemical upgrading applications.

The present work deals with developing a method for revalorizing steel residues to create sunlight-active photocatalysts based on iron oxides. Commercial-grade steel leftovers are oxidized under different combinations of pH and temperature (50–90 °C and 3 ≥ pH ≤ 5) in a low energy-intensive setup. The material with the highest production efficiency (yield > 12%) and magnetic susceptibility (χm = 387 × 10−6 m3/kg) was further explored and modified by diffusion of M2+ (Zn and Co) ions within the structure of the oxide using a hydrothermal method to create ZnFe2O4, CoFe2O4 and combined Co–Zn ferrite. (Co–Zn)Fe2O4 displayed a bandgap of 2.02 eV and can be activated under sunlight irradiation. Electron microscopy studies show that (Co–Zn)Fe2O4 consists of particles with diameters between 400 and 700 nm, homogeneous size, even distribution, and good dispersibility. Application of the developed materials in the sunlight catalysis of black liquors from cellulose extraction resulted in a reduction of the Chemical Oxygen Demand (− 15% on average) and an enhancement in biodegradability (> 0.57 BOD/COD) after 180 min of reaction. Since the presented process employs direct solar light, it opens the possibility to large-scale water treatment and chemical upgrading applications. [ABSTRACT FROM AUTHOR]

Quest for efficient and lead-free perovskite absorber layer is the need of the hour. The less explored titanium-based halide perovskites might be the non-toxic answer for the efficient yet toxic, organic, lead-based halide perovskite. It is of great interest to synthesize cesium titanium iodide perovskite and to investigate their novel properties. We have reported the synthesis of vacancy-ordered double perovskite cesium titanium iodide (Cs2TiI6) at room temperature. Structural, electrical and optical properties are investigated. Broad photoluminescence spectrum is observed. Absorbance and stability of this compound are discussed in detail. Using the absorption data, we have simulated solar cells with different transport layers to give an insight into its application. [ABSTRACT FROM AUTHOR]

This study presents an innovative method for the synthesis of indium aluminum nitride (InAlN) layers by direct current (DC) co-sputtering at room temperature, with the aim of reducing production costs of optoelectronic devices. Indium and aluminum targets are used, varying the power applied to the aluminum target. The results show that increasing the target power favors the formation of aluminum nitride (AlN), which modifies the chemical composition of the material. The layers obtained present smooth surfaces with a roughness of less than 3 nm, which is beneficial for applications requiring interfaces with low defect density. Regarding the optical properties, it is observed that the optical bandgap varies between 1.8 eV and 2.0 eV, increasing with the target power. Hall effect measurements indicate a decrease in the free carrier concentration and an increase in the resistivity with increasing power. This approach allows for the synthesis of InAlN with properties suitable for optoelectronic applications, solar cells, photocatalysis, and photoelectrocatalysis at low cost.

The active layer of organic solar cells (OSCs) is composed of a p-type conjugated polymer as the donor and an n-type organic semiconductor as the acceptor. Since the report of bulk-heterojunction OSCs with soluble C60 derivative PCBM as the acceptor in 1995, fullerene derivatives, including PCBM and the C70 derivative PC71BM, have been the dominant acceptors in OSCs for 20 years. In 2015, the A–D–A structured small molecule acceptor (SMA) was developed, which possesses the advantages of a narrow bandgap, strong absorption in the long wavelength region, and suitable electronic energy levels, in contrast to the fullerene derivative acceptors. A–D–A SMAs boost the power conversion efficiency (PCE) of OSCs to the 10–14% level. Recently, benefiting from the innovation of A–DA′D–A structured SMAs, the PCE of OSCs has rapidly increased from 15% to 19%. In this review, the development history of n-type organic semiconductor acceptor materials is briefly introduced. The molecular structures and the physicochemical and photovoltaic properties of acceptors, including fullerene derivatives and narrow bandgap SMAs, are described. In particular, the effect of regulating the molecular packing and miscibility of SMAs on their photovoltaic performance is discussed. Finally, current challenges and prospects for n-type organic semiconductor acceptors are analyzed and discussed.

Nanoparticles can enhance the intensity of susceptible vibrational modes through electromagnetic or chemical enhancement mechanisms responsible for the SERS effect (Surface-enhanced Raman spectroscopy). In the present work, copper nanoparticles (CuNP) with diameters between 3 and 10 nm were obtained by a simple method using rongalite and gelatin. The UV–Vis spectrum showed a well-defined absorption band centered at 570 nm, attributed to the surface plasmon resonance (SPR) of CuNP in a colloidal solution. The SERS effect was analyzed on the pyridine (Py) molecule, observing an enhancement in the radial breathing mode of Py. Complementarily, Cu4n clusters (with n = 1–5) were modeled under the DFT (Density Functional Theory) framework at the B3LYP (Becke, 3-parameter, Lee–Yang–Parr) approximation level in combination with the LANL2DZ base set (Los Alamos National Laboratory 2 Double-Zeta). After analyzing the molecular descriptors, the Cu4n-Py interaction study provided hints of SERS behavior. [ABSTRACT FROM AUTHOR]

Perovskite solar cells deliver high efficiencies, but are often made from high‐cost bespoke chemicals, such as the archetypical hole‐conductor, 2,2′,7,7′‐tetrakis(N,N‐di‐p‐methoxy‐phenylamine)‐9‐9′‐spirobifluorene (spiro‐OMeTAD). Herein, new charge‐transporting carbazole‐based enamine molecules are reported. The new hole conductors do not require chemical oxidation to reach high power conversion efficiencies (PCEs) when employed in n‐type‐intrinsic‐p‐type perovskite solar cells; thus, reducing the risk of moisture degrading the perovskite layer through the hydrophilicity of oxidizing additives that are typically used with conventional hole conductors. Devices made with these new undoped carbazole‐based enamines achieve comparable PCEs to those employing doped spiro‐OMeTAD, and greatly enhanced stability under 85 °C thermal aging; maintaining 83% of their peak efficiency after 1000 h, compared with spiro‐OMeTAD‐based devices that degrade to 26% of the peak PCE within 24 h. Furthermore, the carbazole‐based enamines can be synthesized without the use of organometallic catalysts and complicated purification techniques, lowering the material cost by one order of magnitude compared with spiro‐OMeTAD. As a result, we calculate that the overall manufacturing costs of future photovoltaic (PV) modules are reduced, making the levelized cost of electricity competitive with silicon PV modules. [ABSTRACT FROM AUTHOR]

Copper (Cu) is a low cost and efficient filler for nanofluids. However, commercially available copper nanopowders are as costly as silver. A few methods are available for synthesis of copper nanopowder in the lab, but the amount of powder produced per batch is very small, and it is impractical to produce a large volume of nanofluid using these methods. Solution based high concentration synthesis for production of copper nanopowder using batch reactor has been reported in this work. Cost of production is minimal in this method and nanoparticles are separated from the suspension by a controlled flocculation process. The proposed method relies on the higher solubility of cuprammonium complex in an aqueous medium and its chemical reduction using hydrazine hydrate. The colloid has been stabilised using sodium citrate and obtained as sub 50 nm powder re-dispersible in water and ethylene glycol (EG). Continuous synthesis of this product using a Continuous Stirred Tank Reactor (CSTR) has also been demonstrated. The quality of particles from the CSTR is similar to that of the batch method. Stable nanofluids have been prepared by re-dispersing the nanopowder in water and EG. Moderate enhancement (∼5%) in thermal conductivity for Cu-EG nanofluids and small enhancement (∼2%) for Cu-water nanofluid have been observed with 0.6 vol% of copper loading. [ABSTRACT FROM AUTHOR]

In this study, zinc oxide (ZnO) nanoparticles were synthesized using a novel environmentally friendly hydroelectric cell without an electrolyte or external current source. The hydroelectric cell comprised a nanoporous Li substituted magnesium ferrite pellet in contact with two electrodes, with zinc as the anode and silver as an inert cathode. The surface unsaturated cations and oxygen vacancies in the nanoporous ferrite dissociated water molecules into hydronium and hydroxide ions when the hydroelectric cell was dipped into deionized water. Hydroxide ions migrated toward the zinc electrode to form zinc hydroxide and the hydronium ions were evolved as H 2 gas at the silver electrode. The zinc hydroxide collected as anode mud was converted into ZnO nanoparticles by heating at 250 °C. Structural analysis using Raman spectroscopy indicated the good crystallinity of the ZnO nanoparticles according to the presence of a high intensity E 2 -(high) mode. The nanoparticle size distribution was 5–20 nm according to high resolution transmission electron microscopy. An indirect band gap of 2.75 eV was determined based on the Tauc plot, which indicated the existence of an interstitial cation level in ZnO. Near band edge and blue emissions were detected in photoluminescence spectral studies. The blue emissions obtained from the ZnO nanoparticles could potentially have applications in blue lasers and LEDs. The ZnO nanoparticles synthesized using this method had a high dielectric constant value of 5 at a frequency of 1 MHz, which could be useful for fabricating nano-oscillators. This facile, clean, and cost-effective method obtained a significant yield of 0.017 g for ZnO nanoparticles without applying an external current source. [ABSTRACT FROM AUTHOR]

Abstract: The aim of this work was to explore the possibility of using nano PbO2 in commercial type tubular lead-acid battery positive electrodes. In that prospect, nanosized αPbO2 and βPbO2 have been synthesized at room temperature by a low-cost solution technique involving the chemical oxidation of lead nitrate with ammonium persulfate in concentrated alkaline medium. Mini-tubular electrodes were then prepared using the same type of gauntlet as the one used in commercial tubular electrodes. We show that the capacity and the cycling stability of the tubular electrode highly depend on the sulfuric acid concentration in the electrolyte and on the lead dioxide surface area. A percentage of utilization higher than 45% of the active mass with an excellent cycling stability was obtained when our nano βPbO2 was used as active material in a diluted H2SO4 electrolyte. [Copyright &y& Elsevier]

Low-cost catalysts are of great significance for the batch synthesis of carbon nanotubes. In this study, the low-cost red soil was directly used as a natural catalyst to catalyze the growth of multi-walled carbon nanotubes (MWCNTs). The results of SEM, TEM, Raman, TG and carbon yields of the products consistently showed that 400 °C calcined red soil lead to high quality MWCNTs growth, the Raman I G /I D of the product is 1.66, which indicates that the product has exceeded the graphitization of many industrially synthesized MWCNTs. The high catalyzation efficiency may be attributed to the fact of composition characteristics that red soil lacks alkali metals and alkaline earth metals but is rich in iron and aluminum oxide, making the composition of red soil similar to the catalyst composition used in the synthesis of carbon nanotubes by common chemical vapor deposition method. Meanwhile the impurity content is less than other natural catalytic materials. The porous structure formed after proper calcination has also played a positive role to the catalytic growth of MWCNTs, which improved catalyst utilization by facilitating the gas phase diffusion. We explored a technique for synthesis of high-quality MWCNTs at low cost using soil as a catalyst. Unlabelled Image • A low-cost synthesis of carbon nanotubes using the red soil as catalyst. • Red soil calcined at 400 °C lead to high quality MWCNTs growth. • The I G /I D of the product is 1.66,which was higher than that of many commercially prepared MWCNTs. • Red soil showed the most effective catalyst for the growth of CTNs compared with other soils. [ABSTRACT FROM AUTHOR]

Background: Nanoparticles have been applied to medicine, hygiene, pharmacy and dentistry, and will bring significant advances in the prevention, diagnosis, drug delivery and treatment of disease. Green synthesis of metal nanoparticles has a very important role in nanobiotechnology, allowing production of non-toxic and eco-friendly particles. Objectives: Green synthesis of silver nanoparticles (AgNPs) was studied using pine pollen as a novel, cost-effective, simple and non-hazardous bioresource. The antifungal activity of the synthesized AgNPs was investigated in vitro . Materials and Methods: Biosynthesis of AgNPs was conducted using pollen of pine (as a novel bioresource) acting as both reducing and capping agents. AgNPs were characterized using UV-visible spectroscopy, X-ray diffraction and transmission electron microscopy. In evaluation for antifungal properties, the synthesized AgNPs represented significant in vitro inhibitory effects on Neofusicoccum parvum cultures. Results: Pine pollen can mediate biosynthesis of colloidal AgNPs with an average size of 12 nm. AgNPs were formed at 22 °C and observed to be highly stable up to three months without precipitation or decreased antifungal property. AgNPs showed significant inhibitory effects against Neofusicoccum parvum . Conclusion: The first report for a low-cost, simple, well feasible and eco-friendly procedure for biosynthesis of AgNPs was presented. The synthesized AgNPs by pine pollen were nontoxic and eco-friendly, and can be employed for large-scale production. The nanoparticles showed strong effect on quantitative inhibition and disruption of antifungal growth.