Direct laser printing for high efficiency silicon solar cells fabrication

Silicon solar cells still require cost reduction and improved efficiency to become more competitive. New architectures can provide a significant increase in efficiency, but today most of the approaches need additional fabrication steps. In this context, laser processing offers a unique way to replace technological steps like photolithography that is not compatible with the requirements of the photovoltaic industry. In particular laser induced thermal effects can be used to activate or re-organise dopants at the silicon surface to design new emitter geometries. In this paper dopant diffusion using a nanosecond UV laser on phosphorous-doped silicon emitters is studied. The presence of a phosphosilicate glass underneath a silicon nitride layer leads to a local decrease of the emitter sheet resistance from 100 Ω/sq to 20 Ω/sq. Laser induced damage, phosphorus diffusion profile and electrical shunt are assessed in the perspective of selective emitter silicon solar cells fabrication compatible with electrochemical metal contacts deposition.     

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An Enantiopure Cyclometallated Iridium Complex Displaying Long‐Lived Phosphorescence both in Solution and in the Solid State

A new enantiopure cyclometallated iridium complex bearing a [4]helicenic ‐coordinating and two ‐coordinating dfppy (2‐(2,4‐difluorophenyl)‐pyridyl) ligands was prepared. This complex displayed long‐lived phosphorescence both in solution and in the solid state. Its chiroptical properties, namely electronic circular dichroism and circularly polarized luminescence, were also examined. Comparison with former chiral complexes enabled assignment of the Δ_Ir‐(?) and Λ_Ir‐(+) absolute configurations.     

Hydrodynamic limit for the Ginzburg–Landau ∇ϕ interface model with non-convex potential

The hydrodynamic limit of the Ginzburg–Landau $??$ interface model was derived in Funaki and Spohn (1997) and Nishikawa (2003) for strictly convex potentials. This paper deals with non-convex potentials under suitable assumptions on the free energy and identification of the extremal Gibbs measures which have been recently established at sufficiently high temperature in Cotar and Deuschel (2012). Because of the non-convexity, many difficulties arise, especially, on the identification of equilibrium states. We show the equivalence between the stationarity and the Gibbs property under quite general settings, and we complete the identification of equilibrium states. We also establish some uniform estimates for variances of extremal Gibbs measures.     

Synthesis and Properties of Partially Saturated Fluorenyl-Derived [n]Helicenes Featuring an Overcrowded Alkene

The straightforward, multigram-scale synthesis of the partially saturated H₆-fluoreno[n]helicenes (n=5 or 7) featuring a central, overcrowded alkene is described. The key cyclization step was based on an intramolecular McMurry reaction from the corresponding 1,5-diketones. Chiral stationary phase HPLC analysis and isomer separation indicate that each helicenic compound is constituted of three diastereoisomers at room temperature, i. e. the configurationally stable (R,R,P)/(S,S,M) pair of enantiomers and an apparently achiral compound resulting from the rapid interconversion between the (R,S,P) and (S,R,M) enantiomers. The partially saturated H₆-fluoreno[n]helicenes are oxidatively aromatized to give an efficient access to the corresponding fluoreno[n]helicenes. The chiroptical properties (vibrational and electronic circular dichroism) of the chiral, enantiopure compounds have been measured and analyzed by quantum-chemical calculations, confirming their helicoidal nature.     

Weinreb Amide,Ketone and Amine as Potential and Competitive Secondary Molecular Stations for Dibenzo-[24]Crown-8 in [2]Rotaxane Molecular Shuttles

This paper reports the synthesis and study of new pH-sensitive DB24C8-based [2]rotaxane molecular shuttles that contain within their axle four potential sites of interaction for the DB24C8: ammonium, amine, Weinreb amide, and ketone. In the protonated state, the DB24C8 lay around the best ammonium site. After either deprotonation or deprotonation-then-carbamoylation of the ammonium, different localizations of the DB24C8 were seen, depending on both the number and nature of the secondary stations and steric restriction. Unexpectedly, the results indicated that the Weinreb amide was not a proper secondary molecular station for the DB24C8. Nevertheless, through its methoxy side chain, it slowed down the shuttling of the macrocycle along the threaded axle, thereby partitioning the [2]rotaxane into two translational isomers on the NMR timescale. The ketone was successfully used as a secondary molecular station, and its weak affinity for the DB24C8 was similar to that of a secondary amine.     

Intramolecular cyclisation of isosorbide by dimethylcarbonate chemistry

In this work the synthesis of a tricyclic isosorbide derivative in moderate yield directly from the dicarboxymethyl isosorbide in a continuous-flow apparatus is reported. The tricyclic structure has been isolated as pure and fully characterized. This product confirms the potentiality of dimethylcarbonate (DMC) as dehydrating agent also for complicated structure and opens up further investigation and application of DMC chemistry on renewable starting materials.     

The Chemoselective Cleavage of Acylthioaryltioacetals with Tributyltin Hydride

Acylthioarylthioacetals are cleaved selectively by tributyltin hydride/AIBN affording thioacyls radicals, which can react with tethered carbon-carbon double or triple bond to form functionalized cyclopentanes.