High efficient catalytic degradation of tetracycline and ibuprofen using visible light driven novel Cu/Bi2Ti2O7/rGO nanocomposite::Kinetics, intermediates and mechanism

The photoexcited charge carriers trapping was an effective way to generate a large number of active species like O-2(center dot-) and (OH)-O-center dot radicals to oxidize pharmaceutical molecules. In ternary Cu/Bi2Ti2O7/rGO composite Cu nanoparticles and rGO sheets act as charge carrier trappers and the suppression of e(-)-h(+) pair recombination was confirmed by Photoluminescence analysis. The Cu/Bi2Ti2O7/rGO composite exhibited higher photocatalytic degradation efficiency for degradation of ibuprofen and tetracycline molecules under visible light irradiation within 90 min. Therefore, this research designates a promising strategy for higher photoexcited charge carrier trapping photocatalyst design for efficient degradation of pharmaceutical molecules. (C) 2019 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved

Effects of Single Metal-Ion Doping on the Visible-Light Photoreactivity of TiO_2

Titanium dioxide (M-TiO_2), which was doped with 13 different metal ions (i.e., silver (Ag^+), rubidium (Rb^+), nickel (Ni^(2+)), cobalt (Co^(2+)), copper (Cu^(2+)), vanadium (V^(3+)), ruthenium (Ru^(3+)), iron (Fe^(3+)), osmium (Os^(3+)), yttrium (Y^(3+)), lanthanum (La^(3+)), platinum (Pt^(4+), Pt^(2+)), and chromium (Cr3+, Cr6+)) at doping levels ranging from 0.1 to 1.0 at. %, was synthesized by standard sol−gel methods and characterized by X-ray diffraction, BET surface area measurement, SEM, and UV−vis diffuse reflectance spectroscopy. Doping with Pt(IV/II), Cr(III), V(III), and Fe(III) resulted in a lower anatase to rutile phase transformation (A−R phase transformation) temperature for the resultant TiO_2 particles, while doping with Ru(III) inhibited the A−R phase transformation. Metal-ion doping also resulted in a red shift of the photophysical response of TiO_2 that was reflected in an extended absorption in the visible region between 400 and 700 nm. In contrast, doping with Ag(I), Rb(I), Y(III), and La(III) did not result in a red shift of the absorption spectrum of TiO_2. As confirmed by elemental composition analysis by energy dispersive X-ray spectroscopy, the latter group of ions was unable to be substituted for Ti(IV) in the crystalline matrix due to their incompatible ionic radii. The photocatalytic activities of doped TiO_2 samples were quantified in terms of the photobleaching of methylene blue, the oxidation of iodide (I^(−)), and the oxidative degradation of phenol in aqueous solution both under visible-light irradiation (λ > 400 nm) and under broader-band UV−vis irradiation (λ > 320 nm). Pt- and Cr-doped TiO_2, which had relatively high percentages of rutile in the particle phase, showed significantly enhanced visible-light photocatalytic activity for all three reaction classes

TiO2-doped resorcinol–formaldehyde (RF) polymer and carbon gels with photocatalytic activity

Resorcinol-formaldehyde (RF) polymer gels offer a relatively easy and versatile route for incorporating metals into a carbon aerogel matrix. The hybrid materials thus obtained are ideal candidates for applications involving enhanced adsorption or catalysis. This paper presents a detailed study of Ti-doped RF and carbon aerogels. The metal was introduced into the system at three different stages of the preparation process: during polymerization, by impregnation of the RF gel, or by impregnation of the carbon gel. The structure and morphology of the samples are compared using low temperature N2 adsorption, SEM, and small and wide angle X-Ray scattering (SAXS/WAXS) methods. The TiO2-doped carbon aerogels display photocatalytic activity in breaking down aromatic compounds

Photocatalytic degradation of ketorolac tromethamine (KTC) drug in aqueous phase using prepared Ag-doped ZnO microplates

In this study, Ag-doped ZnO microplates were prepared via precipitation technique and further characterized by FESEM, EDS, XRD, FTIR, TGA, XPS, UV-DRS and RT-PL techniques. The outcomes indicated that Ag+ ions were well incorporated into ZnO lattice leading to the absorption of ZnO in visible region as well as effective charge separation. The photocatalytic experiments showed that Ag-doped ZnO microplates show higher catalytic activity (91%) than bare ZnO (71%) for the degradation of KTC drug under solar illumination. The photocatalytic degradation of KTC drug over Ag doped ZnO microplates obeyed pseudo first-order kinetics model. Also, the role of active species was examined by the addition of several scavengers in the photocatalytic degradation system. The results indicated that h+, •OHs, 1O2 and •OH were considered as prime reactive species in photocatalytic degradation process

Charge Transfer Induced Molecular Hole Doping into Thin Film of Metal-Organic-Frameworks

Despite the highly porous nature with significantly large surface area, metal organic frameworks (MOFs) can be hardly used in electronic, and optoelectronic devices due to their extremely poor electrical conductivity. Therefore, the study of MOF thin films that require electron transport or conductivity in combination with the everlasting porosity is highly desirable. In the present work, thin films of Co3(NDC)3DMF4 MOFs with improved electronic conductivity are synthesized using layer-by-layer and doctor blade coating techniques followed by iodine doping. The as-prepared and doped films are characterized using FE-SEM, EDX, UV/Visible spectroscopy, XPS, current-voltage measurement, photoluminescence spectroscopy, cyclic voltammetry, and incident photon to current efficiency measurements. In addition, the electronic and semiconductor property of the MOF films are characterized using Hall Effect measurement, which reveals that in contrast to the insulator behavior of the as-prepared MOFs, the iodine doped MOFs behave as a p-type semiconductor. This is caused by charge transfer induced hole doping into the frameworks. The observed charge transfer induced hole doping phenomenon is also confirmed by calculating the densities of states of the as-prepared and iodine doped MOFs based on density functional theory. Photoluminescence spectroscopy demonstrate an efficient interfacial charge transfer between TiO2 and iodine doped MOFs, which can be applied to harvest solar radiations.Comment: Main paper (19 pages, 6 figures) and supplementary information (15 pages, 10 figures), accepted in ACS Appl. Materials & Interface

AgandCuloadedonTiO2/graphite as a catalyst for �Escherichia coli- contaminated water disinfection

TiO2 film was synthesized by means of the chemical bath deposition (CBD) method from TiCl4 as a precursor and surfactant cetyl trimethyl ammonium bromide (CTAB) as a linking and assem- bling agent of the titanium hydroxide network on a graphite substrate. Ag and Cu were loaded on the TiO2 film by means of electrodeposition at various applied currents. Photoelectrochemical testing on the composite of Ag–TiO2/G and Cu–TiO2/G was used to define the composite for Escherichia coli-contaminated water disinfection. Disinfection efficiency and the rate of disinfection of E. coli-contaminated water with Ag–TiO2/G as a catalyst was higher than that observed for Cu–TiO2/G in all disinfection methods including photocatalysis (PC), electrocatalysis (EC), and photoelectrocatalysis (PEC). The highest rate constant was achieved by the PEC method using Ag–TiO2/G, k was 6.49 × 10−2 CFU mL−1 min−1 . Effective disinfection times of 24 h (EDT24) and 48 h (EDT48) were achieved in all methods except the EC method using Cu–TiO2/G. Keywords: Ag–TiO2/G, Cu–TiO2/G, Escherichia coli, disinfectio

Visible light driven photoanodes for water oxidation based on novel r-GO/\u3b2-Cu2V2O7/TiO2 nanorods composites

This paper describes the preparation and the photoelectrochemical performances of visible light driven photoanodes based on novel r-GO/-Cu2V2O7/TiO2 nanorods/composites. -Cu2V2O7 was deposited on both fluorine doped tin oxide (FTO) and TiO2 nanorods (NRs)/FTO by a fast and convenient Aerosol Assisted Spray Pyrolysis (AASP) procedure. Ethylenediamine (EN), ammonia and citric acid (CA) were tested as ligands for Cu2+ ions in the aerosol precursors solution. The best-performing deposits, in terms of photocurrent density, were obtained when NH3 was used as ligand. When -Cu2V2O7 was deposited on the TiO2 NRs a good improvement in the durability of the photoanode was obtained, compared with pure -Cu2V2O7 on FTO. A further remarkable improvement in durability and photocurrent density was obtained upon addition, by electrophoretic deposition, of reduced graphene oxide (r-GO) flakes on the -Cu2V2O7/TiO2 composite material. The samples were characterized by X-ray Photoelectron Spectroscopy (XPS), Raman, High Resolution Transmission Electron Microscopy (HR-TEM), Scanning Electron Microscopy (SEM), Wide Angle X-ray Diffraction (WAXD) and UV\u2013Vis spectroscopies. The photoelectrochemical (PEC) performances of -Cu2V2O7 on FTO, -Cu2V2O7/TiO2 and r-GO/-Cu2V2O7/TiO2 were tested in visible light by linear voltammetry and Electrochemical Impedance Spectroscopy (EIS) measurements

Electrochemical CO₂ Reduction to CO Catalyzed by 2D Nanostructures

Electrochemical CO₂ reduction towards value-added chemical feedstocks has been extensively studied in recent years to resolve the energy and environmental problems. The practical application of electrochemical CO₂ reduction technology requires a cost-effective, highly efficient, and robust catalyst. To date, vigorous research have been carried out to increase the proficiency of electrocatalysts. In recent years, two-dimensional (2D) graphene and transition metal chalcogenides (TMCs) have displayed excellent activity towards CO₂ reduction. This review focuses on the recent progress of 2D graphene and TMCs for selective electrochemical CO₂ reduction into CO