RESUMEN
Compositional and structural elucidation of the materials is important to know their properties, chemical stability, and electro-photoactivity. The heterojunction electrocatalyst and photocatalyst activity could open a new window for solving the most urgent environmental and energy problems. Here, for the first time, we have designed and fabricated Bi2O3/bismuth titanates modified with MOF-In2S3/CdIn2S4 materials by a stepwise process. The detailed structural elucidation and formation of mixed composite phases were studied in detail. It has been found that the formed composite was efficiently utilized for the electrocatalytic H2 production reaction and the photocatalytic degradation of tetracycline. XRD patterns for the metal-organic framework-In2S3 showed a main compound of MOF, and it was assigned to a MIL-53 MOF phase, with a monoclinic structure. The addition of CdCl2 onto the MOF-In2S3 phase effectively produced a CdIn2S4 flower platform on the MOF rods. The uniform dispersion of the bismuth titanates in MOF-In2S3/CdIn2S4 materials is detected by mapping of elements obtained by dark-field HAADF-STEM. Finally, the predictions of how to integrate experiments and obtain structural results more effectively and their common development in new heterojunctions for electro-/photocatalytic applications are presented.
RESUMEN
Novel KTO/BiOCl nanostructured photocatalysts with various weight proportions were synthesized using a simple hydrothermal process. The as-prepared nanostructured composite catalysts were characterized by powder X-ray diffraction, Fourier transform infrared spectroscopy, UV-vis diffused reflectance spectroscopy, Raman spectroscopy, field emission scanning electron microscopy, transmission electron microscopy with high resolution, X-ray photoelectron spectroscopy, and photoluminescence (PL). The photocatalytic activity of prepared catalysts was examined using Rhodamine B (RhB) and Congo Red (CR) as the aimed pollutants. BiOCl nanoparticles were distributed uniformly on the surface of the K2Ti4O9 nanobelts. The optical properties showed that the layered titanate with BiOCl nanostructured photocatalyst displayed improved photoresponsivity due to the narrowed bandgap. The PL results showed that the greater inhibition of the electron-hole recombination process and KTO/BiOCl with a mass proportion of 20% revealed the most favorable photocatalytic behavior. The rate constant of RhB and CR degradation was five times as high as that of the bare BiOCl and titanate. The superior photocatalytic performance was attributed to the advancement of heterojunction between the KTO nanobelt and BiOCl. The KTO/BiOCl nanostructure is a promising visible, active photocatalyst, and the photocatalytic mechanism is discussed using the possible band structures of BiOCl and KTO.
Asunto(s)
Colorantes , Nanoestructuras , Catálisis , Luz , Nanoestructuras/química , Espectroscopía de FotoelectronesRESUMEN
Pristine TiO2 and x% Ru/TiO2 catalysts with different wt.% of Ru (x%= 1.5%, 2%, 2.5% and 3%) were synthesized using sol-gel and simple impregnation methods. Different characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), High-resolution transmission electron microscope (HR-TEM), Inductively coupled plasma-optical emission spectrometry (ICP-OES) and Thermogravimetry/Differential thermal analysis (TG/DTA) were used to study the physicochemical and morphological properties. The XRD patterns of the as-prepared pristine TiO2 catalyst showed high crystalline nature. The HR-TEM images revealed that the Ru nanoparticles (NPs) were evenly dispersed on the TiO2 surface. The prepared catalysts were evaluated for their catalytic activity towards the liquid phase hydrogenation of ethyl levulinate under mild reaction conditions (ambient H2 pressure). Among the various catalysts, 2.5% Ru/TiO2 catalyst showed the maximum catalytic activity of 79% ethyl levulinate (EL) conversion with 82% selectivity of γ-valerolactone (GVL). The recyclability test revealed that the most active 2.5% Ru/TiO2 also showed the highest stability of the catalyst under optimized experimental conditions.
Asunto(s)
Hidrogenación , Catálisis , Ácidos Levulínicos , Espectroscopía Infrarroja por Transformada de Fourier , TitanioRESUMEN
Nitrogen doped titania over reduced form of graphene oxide (N-TiO2/rGO) catalysts were synthesized by adopting single step hydrothermal route. All the prepared photocatalysts were thoroughly characterized by using different analytical tools such as XRD, Raman, UV-DRS, FE-SEM and HRTEM. The photocatalytic activities of bare and composite catalysts were evaluated towards the photocatalytic decolourisation/degradation of Methylene blue dye (MB) and Metronidazole antibiotic (MTZ) under visible electromagnetic radiation. Among all the synthesized catalysts, N-TiO2/rGO composite catalyst showed the highest decolourisation/degradation activity towards both the dye and the antibiotic. The most active catalyst was also tested under UV and solar light irradiations which showed promising results. The stability of the most active catalyst (N-TiO2/rGO) was examined by recyclability test. The possible photocatalytic mechanism was proposed for the composite catalyst.
RESUMEN
Value added chemicals, fuels, and fuel additives can be obtained from cheap bio masses such as levulinic acid. Levulinic acid is the dehydration and hydrolysis products of pentoses and hexoses. The present work deals with the synthesis of sulphobenzylated Al-SBA-15, [SO3H-Bz-Al-SBA-15], characterization by various analytical techniques such as XRD, BET, FT-IR, TGA, DTA, FE-SEM/EDS and HR-TEM/EDX techniques and evaluation of catalytic activity towards esterifi-cation of levulinic acid to ethyl levulinate under mild and non corrosive conditions. Sulphonation of the aromatic ring of the benzyl group has been done in different amounts to get nanoporous x% SO3H-Bz-Al-SBA-15 catalysts where (x â 0.02, 0.04, 0.06, 0.08 and 0.10% w/w). Among them 0.08% SO3H-Bz-Al-SBA-15 catalyst showed the highest conversion of levulinic acid (100%) with the highest selectivity towards ethyl levulinate (100%). Esterification of levulinic acid has been carried out with different primary alcohols and all of them yielded 100% selectivity towards alkyl levulinate. However conversion level of levulinic acid was found to be different with different alcohols. Reaction conditions have been optimized. The results were compared with other supported catalysts and discussed.
RESUMEN
In this study, we report the synthesis of NiWO4/nitrogen doped reduced graphene oxide nano composite by one-pot hydrothermal method. The NiWO4 nano particles were dispersed uniformly on graphene sheets. The as prepared NiWO4, NiWO4/5% rGO and NiWO4/N-5% rGO composites were analytically characterized by Powder X-ray diffraction (XRD), Raman spectroscopy, Diffuse reflectance spectroscopy (DRS-UV), Scanning electron microscopy (SEM) and N2 adsorption-desorption isotherm. The photocatalytic performances of the synthesized composites were evaluated towards the photo degradation of congo red (CR) under visible light radiation. The synthesized catalysts showed remarkable photocatalytic activity in the degradation of CR. Among the catalysts NiWO4/N-5% rGO showed the highest decolourization of congo red (92%) under visible light irradiation. This high activity is attributed to its high e- transport property. Our results provide an invaluable methodology for designing high-performance photo-catalysts for new energy applications.
RESUMEN
Herein, we report the synthesis of novel nitrogen doped reduced graphene oxide/ BiVO4 photo catalyst by single step hydrothermal method. The physicochemical properties of the catalysts were characterized using XRD, N2 adsorption-desorption, Raman, XPS, SEM TEM, DRS-UV and EIS techniques. The synthesized catalysts were tested for their catalytic activity in the photo degradation of some harmful textile dyes (methylene blue & congo red) and antibiotics (metronidazole and chloramphenicol) under visible light irradiation. Reduced charge recombination and enhanced photocatalytic activity were observed due to the concerted effect between BiVO4 and nitrogen-rGO. The degradation efficiency of BiVO4/N-rGO in the degradation of CR and MB was remarkably high i.e 95% and 98% under visible light irradiation. Similarly 95% of MTZ and 93% of CAP were degraded under visible light irradiation. HPLC studies implied that both the dyes and antibiotics were degraded to the maximum extent. The plausible photocatalytic mechanism on the basis of experimental results was suggested.