Comparison of thin epitaxial film silicon photovoltaics fabricated on monocrystalline and polycrystalline seed layers on glass

We fabricate thin epitaxial crystal silicon solar cells on display glass and fused silica substrates overcoated with a silicon seed layer. To confirm the quality of hot‐wire chemical vapor deposition epitaxy, we grow a 2‐µm‐thick absorber on a (100) monocrystalline Si layer transfer seed on display glass and achieve 6.5% efficiency with an open circuit voltage (V_OC) of 586 mV without light‐trapping features. This device enables the evaluation of seed layers on display glass. Using polycrystalline seeds formed from amorphous silicon by laser‐induced mixed phase solidification (MPS) and electron beam crystallization, we demonstrate 2.9%, 476 mV (MPS) and 4.1%, 551 mV (electron beam crystallization) solar cells. Grain boundaries likely limit the solar cell grown on the MPS seed layer, and we establish an upper bound for the grain boundary recombination velocity (S_GB) of 1.6x10⁴ cm/s. Copyright © 2014 John Wiley & Sons, Ltd.     

The rate of chloroacetic acid alkaline hydrolysis: Medium effect

Rate constant of chloroacetic acid alkaline hydrolysis in the mixed aqueous-organic solvents depends on the organic co-solvent nucleophilic solvation; however, the effect of the medium polarity on the rate constant is not clear. The rate constant can be reasonably estimated with a multi-parameter equation accounting for the organic co-solvent basicity as well as its density of cohesion energy and molar volume.     

Thermal studies of furosemide–caffeine binary system that forms a cocrystal

Thermal techniques, differential scanning calorimetry (DSC), and hot stage microscopy (HSM) have been used to study the interactions between furosemide and caffeine that are known to form a 1:1 cocrystal. This system has been used as an example to study the probable mechanism of cocrystal formation when the individual components, which are polymorphic, are heated. The study indicates that the phase transition of the low temperature stable polymorph of furosemide initiates cocrystal formation. This result suggests increased mass transfer rate can trigger cocrystal formation. The binary phase diagram (composition–temperature plots) of furosemide–cocrystal–caffeine system was determined from the DSC curves. The results imply that the cocrystal forms eutectic with caffeine but not with furosemide. This study has thus exemplified the use of DSC in understanding binary phase system where the two components form a cocrystal.     

Theoretical modeling of Cu(II), Sr(II), Gd(III), U(VI) sorption from nuclear effluent on PHA resin with experimental validation

Journal of Radioanalytical and Nuclear Chemistry - The sorption capacity of an in–house synthesized novel resin Polyhydraxamic acid(PHA) towards Cu(II), Sr(II), Gd(III), U(VI) ions was...     

α-Amidoaldehydes as Substrates in Rhodium-Catalyzed Intermolecular Alkyne Hydroacylation: The Synthesis of α-Amidoketones

We show that readily available α-amidoaldehydes are effective substrates for intermolecular Rh-catalyzed alkyne hydroacylation reactions. The catalyst [Rh(dppe)(C₆H₅F)][BAr^F₄] provides good reactivity, and allows a broad range of aldehydes and alkynes to be used as substrates, delivering α-amidoketone products. High yields and high levels of regioselectivity are achieved. The use of α-amidoaldehydes as substrates establishes that 1,4-dicarbonyl motifs can be used as controlling groups in Rh-catalyzed hydroacylation reactions.     

An Easy Access to Oxime Ethers by Pd‐Catalyzed C—O Cross‐Coupling of Activated Aryl Bromides with Ketoximes and Chalcone Oximes

An efficient Pd‐catalyzed method for C—O cross‐coupling of ketoximes and chalcone oximes with activated aryl bromides and bromo‐chalcones has been developed. All oxime ethers were obtained in good to excellent yields by [(π‐allyl)PdCl]₂/tBuXPhos ( L7 ) catalyst system. TrixiePhos ( L11 ) was also found to be effective for the oxime coupling. This method offers an easy and smooth coupling of chalcone oximes with activated aryl bromides and bromo‐chalcones, which has not been previously explored.     

Sustainable preparation of gold nanoparticles via green chemistry approach for biogenic applications

Novel premises of ‘Green Nanotechnology’ have tremendous impacts towards industrial scale revolution. The furtive extracted from natural precursors have driven to the generation of biogenic resources for the fabrication of cutting-edge nanomaterials in simple and cost-effective process. This inspection is an intension of the coupling hypothesis of Nanotechnology via ‘Green-Chemistry’ avenue. So, as to diminish the negative effects of technological applications in the health of human beings and the environment, society is focused towards a greener future. Nanoscience assures a promising future by its improvement in green chemistry to develop the 'Greenary Nanoscience and Nanotechnology'. The improvement and execution of chemical assisted processes in order to reduce the usage of harmful substances, the ‘Green Chemistry’ approach is one and only remarkable authentication, which attributed to long range surface area and higher pore volume of gold-nanoparticles. As of now, the efficient biogenic mechanism dramatically reduces the utilization and hazardous reagents have been employed to low-price natural and waste products to yield value-added nanomaterials with extensive relevance, suggesting an economical and green solution to environmental issues. In depth investigation of this critical review illustrates, novel biogenic screening platform was also conducted against antimicrobial strains and degradation of gold-nanoparticles products well explored-from selection precursors evolved from natural extracts, as well as eventually disintegration into bio-degradable yet potentially recyclable byproducts.