Anisotropy of the Mobility of Pentacene from Frustration

The bandstructure of pentacene is calculated using first-principles density functional theory. A large anisotropy of the hole and electron effective masses within the molecular planes is found. The band dispersion of the HOMO and the LUMO is analyzed with the help of a tight-binding fit. The anisotropy is shown to be intimately related to the herringbone structure.Comment: Accepted for publication in Synthetic Metal

Highly Efficient Rubrene–Graphene Charge-Transfer Interfaces as Phototransistors in the Visible Regime

This is the final version of the article. Available from Wiley via the DOI in this record.Atomically thin materials such as graphene are uniquely responsive to charge transfer from adjacent materials, making them ideal charge-transport layers in phototransistor devices. Effective implementation of organic semiconductors as a photoactive layer would open up a multitude of applications in biomimetic circuitry and ultra-broadband imaging but polycrystalline and amorphous thin films have shown inferior performance compared to inorganic semiconductors. Here, the long-range order in rubrene single crystals is utilized to engineer organic-semiconductor–graphene phototransistors surpassing previously reported photogating efficiencies by one order of magnitude. Phototransistors based upon these interfaces are spectrally selective to visible wavelengths and, through photoconductive gain mechanisms, achieve responsivity as large as 10^7 A/W and a detectivity of 9 × 10^11 Jones at room temperature. These findings point toward implementing low-cost, flexible materials for amplified imaging at ultralow light levels.S.R. and M.F.C. acknowledge financial support from EPSRC (Grant 464 Nos. EP/J000396/1, EP/K017160/1, EP/K010050/1, EP/G036101/1, EP/M001024/1, and 465 EP/M002438/1), from Royal Society international Exchanges Scheme 2012/R3 and 466 2013/R2 and from European Commission (No. FP7-ICT-2013-613024-GRASP)

A study of the reaction of Portland cement with certain acids

Portland cement was treated with various concentrations of hydrochloric, acetic, and sulfuric acids. The reaction products, mixed gels of SiO2, Al203, and Fe2O3, were examined for commercial possibilities. Liquid absorption of organic dyes was used as a criterion of surface activity. When 10gm cement was reacted with 100m.l. of acid solution, it was found that the reaction went to completion at 3 molar HCl, 3 normal H2SO4, and about 7-9 molar HAc. The best absorbers for methylene blue were formed by the reaction of 2.5-3 molar HCl and 6-9 molar HAc. The absorption of some of these gels were carefully dried and washed compared favorably with commercial products. Other characteristics such as color, apparent density, microscopic appearance, chemical composition, pH of filtrate solutions, and appearance during reaction were also studied. The absorbents were found to follow the Freundlich Isotherm but not the Langmuir Equation, showing that absorption at their surfaces is probably multi-moleculalr. Over one hundred and fifty separate samples at twenty-five different concentrations of acid were prepared, and many scored of absorption tests were performed

Face-selective electrostatic control of hydrothermal zinc oxide nanowire synthesis

Rational control over the morphology and the functional properties of inorganic nanostructures has been a long-standing goal in the development of bottom-up device fabrication processes. We report that the geometry of hydrothermally grown zinc oxide nanowires can be tuned from platelets to needles, covering more than three orders of magnitude in aspect ratio (~0.1–100). We introduce a classical thermodynamics-based model to explain the underlying growth inhibition mechanism by means of the competitive and face-selective electrostatic adsorption of non-zinc complex ions at alkaline conditions. The performance of these nanowires rivals that of vapour-phase-grown nanostructures and their low-temperature synthesis (<60 °C) is favourable to the integration and in situ fabrication of complex and polymer-supported devices. We illustrate this capability by fabricating an all-inorganic light-emitting diode in a polymeric microfluidic manifold. Our findings indicate that electrostatic interactions in aqueous crystal growth may be systematically manipulated to synthesize nanostructures and devices with enhanced structural control.National Science Foundation (U.S.) (MIT Center for Bits and Atoms (NSF CCR0122419))Massachusetts Institute of Technology. Media LaboratoryKorea Foundation for Advanced StudiesSamsung Electronics Co. (research internship)Harvard University. Society of FellowsWallace H. Coulter Foundation (Early Career Award)Brain & Behavior Research Foundation (Young Investigator Award)National Science Foundation (U.S.)National Institutes of Health (U.S.) (Director’s New Innovator Award

Structure of Na_3NdSi_6O_(15)._2H_2O - A Layered Silicate with Paths for Possible Fast Ion Conductor

Hydrothermal investigations of the high silica region of the Na₂0-Nd₂0₃-SiO₂ system, carried out in the search for new fast-ion conductors (FIC's), yielded the compound Na₃NdSi₆O₁₅.2H₂0 (sodium neodymium silicate). Single-crystal X-ray methods provided lattice constants of a=7.385(2), b=30.831(7) and c= 7.1168 (13)Å, space group Cmm2, and 22 atoms in the asymmetric unit. With four formula units per unit cell, the calculated density is 2.68gcm⁻³. Refinement was carried out with 1113 independent structure factors to a weighted residual wR(F) of 2.63% [8.09% for wR(F²)] using anisotropic temperature factors for all atoms. The structure, based on corrugated Si₆O₁₅ layers containing four-, five-, six- and eight-membered rings, is related to that of a model previously reported for a compound assigned the composition NaNdSi₆O₁₃(OH)₂.nH₂0. Our structure differs in the placement of sodium ions and water molecules, and contains no hydroxyl groups. We believe that both studies examined the same phase

Formation and physicochemical properties of crystalline and amorphous salts with different stoichiometries formed between ciprofloxacin and succinic acid

YesMulti-ionizable compounds, such as dicarboxylic acids, offer the possibility of forming salts of drugs with multiple stoichiometries. Attempts to crystallize ciprofloxacin, a poorly water-soluble, amphoteric molecule with succinic acid (S) resulted in isolation of ciprofloxacin hemisuccinate (1:1) trihydrate (CHS-I) and ciprofloxacin succinate (2:1) tetrahydrate (CS-I). Anhydrous ciprofloxacin hemisuccinate (CHS-II) and anhydrous ciprofloxacin succinate (CS-II) were also obtained. It was also possible to obtain stoichiometrically equivalent amorphous salt forms, CHS-III and CS-III, by spray drying and milling, respectively, of the drug and acid. Anhydrous CHS and CS had melting points at ∼215 and ∼228 °C, while the glass transition temperatures of CHS-III and CS-III were ∼101 and ∼79 °C, respectively. Dynamic solubility studies revealed the metastable nature of CS-I in aqueous media, resulting in a transformation of CS-I to a mix of CHS-I and ciprofloxacin 1:3.7 hydrate, consistent with the phase diagram. CS-III was observed to dissolve noncongruently leading to high and sustainable drug solution concentrations in water at 25 and 37 °C, with the ciprofloxacin concentration of 58.8 ± 1.18 mg/mL after 1 h of the experiment at 37 °C. This work shows that crystalline salts with multiple stoichiometries and amorphous salts have diverse pharmaceutically relevant properties, including molecular, solid state, and solubility characteristics.Solid State Pharmaceutical Cluster (SSPC), supported by Science Foundation Ireland under grant number 07/SRC/ B1158

Structure of Na_3YSi_6O_(15) - a Unique Silicate Based on Discrete Si_6O_(15) Units, and a Possible Fast-Ion Conductor

Hydrothermal investigations in the high silica region of the Na₂O-Y₂0₃-Si₆O₁₅ system, carried out in a search for novel fast-ion conductors (FIC's), yielded the new compound trisodium yttrium hexasilicate, Na₃YSi₆O₁₅. Single-crystal X-ray methods revealed that Na₃YSi₆O₁₅ crystallizes in space group Ibmm, has lattice constants a=10.468 (2), b=15.2467 (13) and c=8.3855 (6) Å, Z=4, and 11 atoms in the asymmetric unit. Refinement was carried out to a weighted residual of 3.53% using anisotropic temperature factors for all atoms. The structure is unique in that the silica tetrahedra form isolated SiSi₆O₁₅⁶⁻ double dreier-rings, rather than layers as might be expected from the Si to O ratio of 0.4. No isomorphs to Na₃YSi₆O₁₅ have been reported

Optical Properties of GaSb Nanofibers

Amorphous GaSb nanofibers were obtained by ion beam irradiation of bulk GaSb single-crystal wafers, resulting in fibers with diameters of ~20 nm. The Raman spectra and photoluminescence (PL) of the ion irradiation-induced nanofibers before and after annealing were studied. Results show that the Raman intensity of the GaSb LO phonon mode decreased after ion beam irradiation as a result of the formation of the amorphous nanofibers. A new mode is observed at ~155 cm-1 both from the unannealed and annealed GaSb nanofiber samples related to the A1g mode of Sb–Sb bond vibration. Room temperature PL measurements of the annealed nanofibers present a wide feature band at ~1.4–1.6 eV. The room temperature PL properties of the irradiated samples presents a large blue shift compared to bulk GaSb. Annealed nanofibers and annealed nanofibers with Au nanodots present two different PL peaks (400 and 540 nm), both of which may originate from Ga or O vacancies in GaO. The enhanced PL and new band characteristics in nanostructured GaSb suggest that the nanostructured fibers may have unique applications in optoelectronic devices

High Electron Mobility in Vacuum and Ambient for PDIF-CN2 Single-Crystal Transistors

We have investigated the electron mobility on field-effect transistors based on PDIF-CN$_{2}$ single crystals. The family of the small molecules PDI8-CN$_{2}$ has been chosen for the promising results obtained for vapour-deposited thin film FETs. We used as gate dielectric a layer of PMMA (spinned on top of the SiO$_{2}$), to reduce the possibility of electron trapping by hydroxyl groups present at surface of the oxide. For these devices we obtained a room temperature mobility of 6 cm$^{2}$/Vs in vacuum and 3 cm$^{2}$/Vs in air. Our measurements demonstrate the possibility to obtain n-type OFETs with performances comparable to those of p-type devices.Comment: published online in JAC