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Deep eutectic solvents (DES) consisting of EG-(ChCl: C

Antibiotics are essential medications for human and animal health, as they are used to battle urinary infections and bacterial diseases. Therefore, the rapid determination of antibiotic drugs in biological samples is necessary to address the current clinical challenge. Here, we developed a heterojunction ternary composite of BiOCl/BiVO

Hierarchical nano-/microstructured photocatalysts have drawn attention for enhanced photocatalytic performance. Deep eutectic solvents (DESs) have been used as a green sustainable media to act as both solvent and structure-inducing agent in the synthesis of hierarchical nanomaterials. In this work, the DESs-assisted synthesis of flower-structured BiOCl/BiVO4 (BOC/BVO) with g-C3 N4 (BOC/BVO/g-CN) ternary heterojunctions was achieved by using a simple wet-chemical method, providing good acidic and alkaline oxygen evolution reaction (OER) catalysts. BOC/BVO/g-CN-15 achieved an enhanced photocatalytic activity for OER with an overpotential of 570 mV in 1 m H2 SO4 and 220 mV in 1 m KOH electrolyte at a current density of 10 mA cm-2 with excellent stability and extraordinary durability of the catalyst. The ternary heterojunctions displayed extended lifetimes for photogenerated charges and enhanced the separation efficiency of photogenerated electron-hole pairs, which is helpful to enhance the photocatalytic OER. Furthermore, the photocatalytic performance of the ternary heterojunctions in aqueous solution was demonstrated through photocatalytic dye degradation of methyl orange (MO) as a model pollutant, resulting in 95 % degradation of 20 ppm of MO in 210 min under the irradiation of a 35 W Xe arc lamp. This work not only provides new insight into the design of catalysts by using green solvents but also into the design of highly efficient metal-free OER photocatalysts for applications in acidic and alkaline media.

In this work we propose a study to determine the structure of Fe and Co doped TiO2 by using the Fe K-edge, Co K-edge and Ti K- edge X-ray absorption near edge spectroscopy. The detailed analysis of Fe and Co-doped TiO2 before and after Methylene blue (MB) treatment was examined under the irradiation of 35 W xenon arc lamp for 3 h. The materials treated with MB were studied by X-ray absorption spectroscopy, EPR and FT-IR which revealed that the oxidation state of Co2+ was photo-oxidized to Co3+ and Fe3+ was photo-reduced to Fe2+ or less. Thermodynamic, kinetic properties were studied at different reaction temperature and the activation energy (Ea), enthalpy (ΔH), entropy (ΔS) and free energy (ΔG) of activation were calculated for the reaction. The activation energy has been found for TiO2, Fe TiO2 and Co TiO2 as 24.771, 11.413 and 15.801 kJ mol−1 respectively. The structure, morphology and optical properties were studied by XRD, UV-diffuse reflectance spectra, FESEM, TEM and PL. Moreover, electrochemical studies were carried out to demonstrate the oxygen evolution reaction (OER) activity on TiO2, Fe TiO2 and Co TiO2 in 1 M of H2SO4 electrolyte, with a scan rate of 50 mV s−1 and the as-prepared photocatalysts could act as the promising electrode materials for water splitting.

Anion doping into the oxygen site as a new plan for tuning the physical and chemical properties of metal oxides and adjusting their catalytic behavior has been studied. Herein, we report a Cl− anion-doped CuO (Cl-CuO) preparation method using deep eutectic solvents (DESs) as a green solvent, and the Cl-CuO/g-C3N4 heterostructure was successfully prepared in various weight ratios via a simple ultrasonication and mixing method for the oxygen evolution reaction (OER) in acidic media and the photocatalytic degradation of 4-nitrophenol. Cl− was doped into the CuO crystal lattice, as revealed by the XRD and XPS studies. The as-prepared Cl-CuO/g-C3N4 (1 : 2) exhibited a low overpotential of 0.77 V on the glassy carbon electrode with a current density of 33 mA cm−2 at 2.4 V for OER in an acidic solution. Also, about 92% degradation of 20 ppm of 4-nitrophenol was achieved for Cl-CuO/g-C3N4 (1 : 2) in 100 minutes under the irradiation of a 35 W Xe arc lamp. We also evaluated the effect of thermal energy on degradation kinetics by tuning the temperature, which led us to the quantification of various thermodynamic parameters. To the best of knowledge, this is one of the new methods of green synthesis to fabricate photocatalysts for energy and environmental studies.

An efficient Bi2WO6 catalyst with Co2+ substitution was synthesized via a facile hydrothermal route, and the materials were characterized by P-XRD, FT-IR, FE-SEM, XPS, DRS, BET and PL techniques. The obtained Co2+ substituted Bi2WO6 materials displayed high photocatalytic activity for organic dye degradation; 97.5% of the dye was photodegraded by 5 mol% of Co2+ substituted Bi2WO6 within 240 min induced by the visible light, which was remarkably better than the degradation of the bare and Co2+ substituted Bi2WO6 (1, 3, 7 and 9% Co2+ concentration). Based on the structural, optical and elemental characterization, it was determined that the substitution of the Co2+ ions in the Bi2WO6 lattice to replace the W6+ ion sites occurred without substantial changes in the crystal structure. The substituent Co2+ played a strategic role, which narrowed the band gap, leading to an enlargement in visible light absorption ability and suppressing the recombination of photogenerated electron–hole pairs credited to the Co2+ inner energy state. Additionally, the photocatalytic mechanism was elucidated by performing the radical trapping experiments, which disclosed that holes (h+) were the main species responsible for the RhB degradation. In addition, the stability of the catalysts was tested by performing recycling experiments. After the four repeating cycles, the degradation efficiency was not dramatically reduced. The results of this study disclosed that Co2+ substitution of W6+ may offer an alternative approach to enhance the Bi2WO6 photocatalytic activity.

Graphene oxide-based composites have been developed as cheap and effective photocatalysts for dye degradation and water splitting applications. Herein, we report reduced graphene oxide (rGO)/Ag/Fe-doped TiO2 that has been successfully prepared using a simple process. The resulting composites were characterized by a wide range of physicochemical techniques. The photocatalytic activities of the composite materials were studied under visible light supplied by a 35 W Xe arc lamp. The rGO/Ag/Fe-doped TiO2 composite demonstrated excellent degradation of methylene blue (MB) in 150 min and 4-nitrophenol (4-NP) in 210 min under visible light irradiation, and trapping experiments were carried out to explain the mechanism of photocatalytic activity. Moreover, electrochemical studies were carried out to demonstrate the oxygen evolution reaction (OER) activity on rGO/Ag/Fe-doped TiO2 in 1 M of H2SO4 electrolyte, with a scan rate of 50 mV s−1. The reductions in overpotential are due to the d-orbital splitting in Fe-doped TiO2 and rGO as an electron collector and transporter.

Noble metals are very well known for their surface plasmon resonance property that facilitate of better light absorption in the visible region particularly for gold and silver. Nevertheless, unlike semiconductors, noble metals are commonly considered lacking the ability to accelerate reactions by way of photogenerated electron-hole pairs due to their continuous energy band structure. Here, we report a one dimensional (1D) AgNWs combined with BiOCl/BiVO4 photocatalysts have been synthesized at room temperature. BiOCl/BiVO4 photocatalysts have been synthesized in the presence of deep eutectic solvents (DESs), also known as deep eutectic ionic liquids (DEILs).The synthesized product was characterized using various techniques. Surface morphology was analyzed using SEM and TEM, which shows a sheet like shaped structure from sol–gel method. The structural, optical properties were investigated by X-ray diffraction (XRD), UV–vis spectrophotometer, and Photoluminescence (PL) spectroscopy measurements. The BiOCl/BiVO4@AgNWs shows a better degradation of methylene blue (MB) and rhodamine B (RhB) than pure BiVO4 illuminated under a Xe arc lamp with 35 W and color temperature of 6000 K. Also, the significant enhancement of visible-light-driven photocatalytic activity should be ascribed to the formation of the BiOCl/BiVO4 heterojunction, which can result in the high separation and transfer efficiency of photogenerated charge carriers. It was verified by electrochemical impedance spectra (EIS) and linear sweep voltammetry (LSV).

Heterostructured nanomaterials can paid more significant attention in environmental safety for the detection and degradation/removal of hazardous toxic chemicals over a decay. Here, we report the preparation of hierarchically nanostructured shuriken like bismuth vanadate (BiVO4) as a bifunctional catalyst for photocatalytic degradation and electrochemical detection of highly toxic hexavalent chromium (Cr(VI)) using the green deep eutectic solvent reline, which allows morphology control in one of the less energy-intensive routes. The SEM results showed a good dispersion of BiVO4 catalyst and the HR-TEM revealed an average particle size of ca. 5–10 nm. As a result, the BiVO4 exhibited good photocatalytic activity under UV-light about 95% reduction of Cr(VI) to Cr(III) was observed in 160 min. The recyclability of BiVO4 catalyst exhibited an appreciable reusability and stability of the catalyst towards the photocatalytic reduction of Cr(VI). Also, the BiVO4-modified screen printed carbon electrode (BiVO4/SPCE) displayed an excellent electrochemical performance towards the electrochemical detection of Cr(VI). Besides, the BiVO4/SPCE demonstrated tremendous electrocatalytic activity, lower linear range (0.01–264.5 μM), detection limit (0.0035 μM) and good storage stability towards the detection of Cr(VI). Importantly, the BiVO4 modified electrode was also found to be a good recovery in water samples for practical applications.

The development of perovskite-based materials with a narrow bandgap for oxygen evolution reactions (OER) and wastewater treatment have much attention in recent years. Herein, a narrow bandgap of Ca-doped BiFeO3 (BCFO) is synthesized by a simple auto combustion method. To create oxygen vacancies by doping Ca2+ the place of Bi3+, the amount of Fe3+ valence state is changed as well. 0.15% of Ca doped BiFeO3 (BCFO-15) indicate a high content of Fe4+ state with a conduction band and valence band located at 0.615 V and 2.46 V vs. NHE, respectively. The electrochemical OER of BCFO-15 observed a lower onset potential of 2.13 V vs. RHE, in acidic with a current density of 25.64 mA cm−2. In alkaline electrolyte, onset potential was observed at 2.10 V vs. RHE, with a current density of 65.87 mA cm−2. Furthermore, the photocatalytic performance of the perovskites in aqueous solution was demonstrated through photocatalytic reduction of Cr(VI) as a model pollutant, resulting in an 89.92% reduction of 50 ppm of Cr(VI) in 210 min under the irradiation of a 35 W Xe arc lamp. These findings suggest that simple divalent doping of Ca into pure BiFeO3 results in excellent photocatalytic and electrocatalytic perovskites.

Graphene oxide-based composites have been developed as cheap and effective photocatalysts for dye degradation and water splitting applications. Herein, we report reduced graphene oxide (rGO)/Ag/Fe-doped TiO