Ruthenium based metallopolymer grafted reduced graphene oxide as a new hybrid solar light harvester in polymer solar cells.

A new class of pyridyl benzimdazole based Ru complex decorated polyaniline assembly (PANI-Ru) was covalently grafted onto reduced graphene oxide sheets (rGO) via covalent functionalization approach. The covalent attachment of PANI-Ru with rGO was confirmed from XPS analysis and Raman spectroscopy. The chemical bonding between PANI-Ru and rGO induced the electron transfer from Ru complex to rGO via backbone of the conjugated PANI chain. The resultant hybrid metallopolymer assembly was successfully demonstrated as an electron donor in bulk heterojunction polymer solar cells (PSCs). A PSC device fabricated with rGO/PANI-Ru showed an utmost ~6 fold and 2 fold enhancement in open circuit potential (Voc) and short circuit current density (Jsc) with respect to the standard device made with PANI-Ru (i.e., without rGO) under the illumination of AM 1.5 G. The excellent electronic properties of rGO significantly improved the electron injection from PANI-Ru to PCBM and in turn the overall performance of the PSC device was enhanced. The ultrafast excited state charge separation and electron transfer role of rGO sheet in hybrid metallopolymer was confirmed from ultrafast spectroscopy measurements. This covalent modification of rGO with metallopolymer assembly may open a new strategy for the development of new hybrid nanomaterials for light harvesting applications.

Ultrasound-assisted mineralization of organic contaminants using a recyclable LaFeO3 and Fe3+/persulfate Fenton-like system.

A recyclable heterogeneous catalyst has been successfully developed for application in a Fenton-type advanced oxidation process without adding external H2O2. LaFeO3 was prepared from Fe(NO3)3·9H2O and La(NO3)·6H2O by a simple sol-gel method and its catalytic efficiency was evaluated for mineralization of 4-chlorophenol using a Fenton-like process. The mineralization process was carried out under ultrasonication in presence of heterogeneous LaFeO3 catalyst with H2O2 that was produced during ultrasonication. The mineralization process was monitored through total organic carbon (TOC) analysis. Very importantly, utmost 5-fold synergism was evidenced by the ultrasound mediated LaFeO3-catalyzed system. Besides, more than twofold synergism was observed by combining the ultrasound assisted LaFeO3 catalytic process and potassium persulfate (KPS) assisted advanced oxidation process. It is worth to mention that complete mineralization (∼96%) of 4-chlorophenol (initial concentration of 1.25×10-4M) was observed within 1h in the presence of LaFeO3 (0.5gL-1) and KPS (1.0mmol) under ultrasonication (40kHz). Even after four cycles, the activity of LaFeO3 remained intact which proved its recyclability. Extremely reusable heterogeneous LaFeO3 catalyst makes the system more interesting from both economic and environmental points of view.

Gold Nanoparticles Supported on Magnesium Oxide Nanorods for Oxidation of Alcohols.

Gold nanoparticles supported on magnesium oxide nanorods (Au-MgO) have been synthesised by a solution based chemical reduction method. Au-MgO nanorods were found to be an efficient heterogeneous catalyst for oxidation of alcohols with hydrogen peroxide in aqueous medium at room temperature. To find out the best reaction conditions for oxidation, optimization of catalyst quantity, solvent, mole equivalence of hydrogen peroxide were carried out. The scope of the reaction was extended to several aromatic and aliphatic alcohols, product yields were quantified by gas chromatography (GC) and GC/mass spectroscopy. Heterogeneity and reusability tests were performed. The use of water as a solvent and hydrogen peroxide as co-catalyst at room temperature makes the reaction interesting from sustainable development point of view.

Recyclable Mesoporous Ceria Supported Gold Nanoparticles Based Catalyst for O-Arylation of Phenols.

Ceria supported gold nanoparticles (Au-CeO2 NPs) were prepared by a simple deposition-precipitation method. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR) and Raman analysis indicated the formation of gold nanoparticles over phase pure cerianite ceria support. The presence of gold nanoparticles was well identified by UV-DRS study. In addition, the field emission scanning electron microscope (FESEM) and high resolution transmission electron microscope (HR-TEM) images revealed that the maximum number of particles having spherical shape were approximately 10 nm size. Subsequently, surface area of the catalyst determined from BET, Langmuir and DFT methods were found to be 83.1, 134 and 85.2 m2 g(-1) respectively. N2 absorption-desorption measurement revealed that Au-CeO2 NPs was mesoporous in nature. Au-CeO2 NPs proved to be an efficient catalyst for the O-arylation reactions. The reaction conditions were optimized using 2,6-dimethoxyphenol and 1-chloro-4-nitrobenzene as a model substrate by changing the solvent, base, quantity of catalyst, and temperature. The scope of the work was extended to various substituted phenols and aryl halides (F, Cl and Br) and reusability of catalyst was tested for four cycles which showed no loss in its activity.