We have found that poly(benzobisimidazobenzophenanthroline) (BBL) nanobelts can be prepared by a simple high-yield, solution-phase process, which enables dispersions of the nanobelts in a large number of solvents including environmentally benign solvents such as methanol and water. Characterization of the nanobelts by transmission electron and atomic force microscopies, electron diffraction, and X-ray diffraction showed that the BBL polymer chains are oriented parallel to the long axis of each nanobelt. This unique packing motif is unlike the reported packing of polymer chains in other nanostructures, such as poly(3-hexylthiophene) nanowires, where the polymer backbone packs face-to-face along the nanowire direction. This unusual molecular packing in BBL nanobelts is explained by the rather strong intermolecular interactions, which are a result of the rigid and planar polymer chains. We investigated electron transport in single nanobelts and nanobelt networks via field-effect transistors and observed mobilities up to ∼7 × 10−3 cm2 V−1 s−1 and on/off current ratios of ∼1 ×104. The n-channel nanobelt transistors showed stability and repeatability in air for more than 6 months, which is the most stable among current n-channel polymer transistors. These results demonstrate that the BBL nanobelts are promising for organic electronics and nanoelectronics.

Bioglass, which has a composition of sodium carbonate, calcium carbonate, phosphorous pentoxide and silica, has been shown to bond to living bone. This ability is dependent on controlled surface reactions. Investigators with 45S5 bioglass have demonstrated that the formation of a SiO2-rich layer and a calcium phosphate film on its surface in an aqueous environment is associated with the film bonding the bioglass to bone. The objects of this research were: 1. To study SiO2 dependence on the formation of a silica-rich layer and calcium phosphate films on a bioglass surface in a simulated physiological solution, and 2. To establish a correlation between in vitro surface reactions and in vivo bonding ability. It was discovered that three types of reactions occur in a simulated physiological solution depending on bioglass composition: 1. A calcium phosphate film and SiO2-rich layer form simultaneously and the reaction rate is fast for bioglasses which have a lower content of SiO2 (approximately 46 mol% SiO2). 2. A SiO2-rich layer forms first and a calcium phosphate film develops later between the aqueous environment and the SiO2-rich layer for bioglasses whose SiO2 content is between 46--55 mol %. 3. A calcium phosphate film does not form for glasses whose SiO2 content is more than 60 mol %.

A variation on molecular beam epitaxy (MBE), called van der Waals epitaxy, is described where a material with primarily two-dimensional (2D) bonding is grown on a substrate which also has a 2D structure. Lattice matching difficulties, which limit the choice of materials in MBE of 3D systems, are circumvented since the interlayer bonding is from weak van der Waals interactions. The title system shows a lattice mismatch of 10% yet high quality epitaxial films can be grown. The films were characterized in situ with reflection high energy electron diffraction, Auger electron spectroscopy, and low energy electron loss spectroscopy. Additional characterization after exposure to ambient by x-ray photoelectron spectroscopy, low energy electron diffraction, transmission electron microscopy confirmed the highly ordered nature of the films. Scanning tunneling microscopy provided real space images of the morphology of the epitaxial layer and showed unusual structures attributed to lattice mismatch.

In this paper, we report on n-alkyl phosphonic acid (PA) self-assembled monolayer (SAM)/hafnium oxide (HfO(2)) hybrid dielectrics utilizing the advantages of SAMs for control over the dielectric/semiconductor interface with those of high-k metal oxides for low-voltage organic thin film transistors (OTFTs). By systematically varying the number of carbon atoms of the n-alkyl PA SAM from six to eighteen on HfO(2) with stable and low leakage current density, we observe how the structural nature of the SAM affects the thin-film crystal structure and morphology, and subsequent device performance of low-voltage pentacene based OTFTs. We find that two primary structural factors of the SAM play a critical role in optimizing the device electrical characteristics, namely, the order/disorder of the SAM and its physical thickness. High saturation-field-effect mobilities result at a balance between disordered SAMs to promote large pentacene grains and thick SAMs to aid in physically buffering the charge carriers in pentacene from the adverse effects of the underlying high-k oxide. Employing the appropriate n-alkyl PA SAM/HfO(2) hybrid dielectrics, pentacene-based OTFTs operate under -2.0 V with low hysteresis, on-off current ratios above 1 x 10(6), threshold voltages below -0.6 V, subthreshold slopes as low as 100 mV dec(-1), and field-effect mobilities as high as 1.8 cm(2) V(-1) s(-1).