Solar Water Splitting Using Earth-Abundant Electrocatalysts Driven by High-Efficiency Perovskite Solar Cells.

Hydrogen is considered as the "holy grail" for the energy community. One of the most promising strategies to produce hydrogen is to split water using renewable energy such as solar radiation. The abundance of water and solar energy enables the potential of scaling-up of this new technology, if suitable electrocatalysts and solar cells are developed. In this work, a series of materials made of earth-abundant elements was investigated for hydrogen evolution or oxygen evolution reaction. Among the developed catalysts, MoS2 and NiFe showed the best activities for proton reduction and water oxidation, respectively. These catalysts were further integrated into an alkaline electrolyzer, which delivered a current density of 10 mA cm-2 at a cell voltage of 1.9 V for water splitting. Using two in-series-connected perovskite solar cells (PSCs) as a power source, a remarkable solar-to-hydrogen conversion efficiency of 12.67 % was achieved in an alkaline electrolyzer with a partial current density of 10.3 mA cm-2 for hydrogen production. The usage of earth-abundant catalysts in this study, together with the employment of low-cost perovskite light absorber, shows the potential of scaling up this type of photovoltaic electrolyzer for sustainable hydrogen production.

Synthesis of zero-valent Au nanoparticles on chitosan coated NiAl layered double hydroxide microspheres for the discoloration of dyes in aqueous medium.

The catalyst activity of the nano Au was largely dependent on the particle size and the structure of the supported matrix to avoid particle agglomeration. Chitosan (CS) and CS coated layered double hydroxide of NiAl (LDH) microsphere were designed through a simple and an economic casting method. The CS and LDH microsphere were used for the impregnation and support of Au NPs and represented as Au/CS and Au/LDH and used for the sole and concurrent discoloration of methylene blue (MB) and rhodamine B (RB) dyes. The aim of the incorporation of NiAl-LDH to the CS host polymer is to increase the binding capacity of CS with Au NPs to make it more stable. The Au/LDH displaying stronger catalyst activity for both dyes discoloration, while found highly selective for MB dye. The high catalyst activity of Au/LDH is due to their small crystallite size which is 1.02 nm compared to 6.75 nm in Au/CS derived from Scherer's equation. The kapp value based on zero-order kinetics was higher with Au/LDH against MB and RB dyes which are 3.5 × 10-1 and 1.4 × 10-1 min-1 respectively.

A new antibacterial dibenzofuran-type phloroglucinol from myrtus communis linn.

Our continuation on the bio-assay guided isolation from Myrtus communis Linn. led to the discovery of a new dibezofuran type phloroglucinol 1,1'-(1,3,7,9-tetrahydroxydibenzo[b,d]furan-2,8-diyl)bis(ethan-1-one) 1. The structure was established through detailed spectroscopic studies including one and two dimensional NMR spectroscopy and electrospray ionization high resolution mass spectrometer (ESI-HRMS). The crude acetone extract from M. communis (AMA), dichloromethane fraction (DCM), and the isolated pure compound 1 were tested against pathogenic bacteria. Compound 1 displayed higher antibacterial activity against the Gram-positive and Gram-negative Staphlocococus aureus and Escherichia coli respectively as compared to the crude extract and fractions.

Cellulose Acetate Based Nanocomposites for Biomedical Applications: A Review.

The development of polymer nanocomposites by incorporating variable nanofillers has attracted attention of scientists, researchers and industrial sectors due to their dramatic improvement in various properties. Cellulose acetate (CA) based nanocomposites have interesting history in the field of medical applications because CA meets a wide range of biomedical implant properties. Since cellulose acetate is considered as a biodegradable, renewable, non-corrosive, non-toxic and biocompatible material, it raised up the unique advantages over many other materials. This review is designed to provide a broad overview of cellulose acetate nanocomposites in the field of medical applications and medical devices.

Photoinduced atom transfer radical polymerization using semiconductor nanoparticles.

Photoinduced atom transfer radical polymerization of methyl methacrylate initiated by in situ generation of copper (I) complex from higher oxidation state species using neat zinc oxide and iron-doped zinc oxide nanoparticles is investigated. The polymerizations proceed in a well-controlled manner under UV light at room temperature as evidenced by kinetic and light on-off experiments. The evolution of molecular weight with conversion shows good correlations between experimental and theoretical molecular weights, which confirmed good control over polymerization along with a narrow molecular weight distribution.