Three solvents, that is, acetone, acetic acid, and dimethylacetamide (DMAc), with a range of solubility parameter ␦, surface tension ␥, viscosity and boiling temperature were used to generate mixtures for electrospinning cellulose acetate (CA) (degree of substitution, DS ϭ 2.45). Although none of these solvents alone enables continuous formation of fibers, mixing DMAc with either acetone or acetic acid produced suitable solvent systems. The 2:1 acetone:DMAc mixture is the most versatile mixture because it allows CA in the 12.5-20% concentration range to be continuously electrospun into fibrous membranes. These CA solutions have between 1.2 and 10.2 poise and ␥ around 26 dyne/cm and produce smooth fibers with diameters from 100 nm to ϳ1 m. Fiber sizes generally decrease with decreasing CA concentrations. The nature of the collectors affects the morphology as well as packing of fibers. Fibers collected on paper have more uniform sizes, smooth surfaces, and fewer defects, whereas fibers collected on water are more varied in size. Electrically conductive solid collectors, such as Al foil and water, favor more tightly packed and less porous membranes. Porous collectors, like paper and copper mesh, produce highly porous membranes. The pores in membranes collected on the Al foil and paper are much better interconnected in the planar directions than those in membranes collected on water. There is evidence that electrospinning induces order in the fibers. Deacetylation of CA membranes is more efficient and complete in NaOH/ethanol than in aqueous NaOH, producing DS values between 0.15 and 2.33 without altering fiber surfaces, packing, or organization. The fully regenerated cellulose membranes are similarly hydrophilic as commodity cellulose fibrous matrices but absorb nearly 10 times as much water.

We have used a nonlithographic deposition process to form single polymeric nanowire chemical sensors. Oriented polyaniline nanowires, with diameters on the order of 100 nm, were deposited on gold electrodes. The devices showed a rapid and reversible resistance change upon exposure to NH 3 gas at concentrations as low as 0.5 ppm. The well-defined single-wire geometry allows for the characterization of the wire material and the device response. The response times of nanowire sensors with various diameters correspond to radius-dependent differences in the diffusion time of ammonia gas into the wires. The nanowire deposition process, utilizing a scanned microfabricated electrospinning source, presents a general method for interfacing polymeric nanowire devices with microfabricated structures.

We report on a single nanofiber field-effect transistor made from electrospun regioregular poly(3-hexylthiophene). Nanofibers, with diameters of 100–500 nm, were deposited by electrospinning from chloroform solution onto electrodes on a SiO2∕Si substrate. The transistor exhibited a hole field-effect mobility of 0.03cm2∕Vs in the saturation regime, and a current on/off ratio of 103 in the accumulation mode. Electrospinning offers a simple means of fabricating one-dimensional polymer transistors.

The high conductive TiO(2) nanoneedles film is first employed as a support matrix for immobilizing model enzyme, cytochrome c (cyt c) to facilitate the electron transfer between redox enzymes and electrodes. Reversible and direct electron transfer of cyt c is successfully achieved at the nanostructured TiO(2) surface with the redox formal potential (E(0)') of 108.0 +/- 1.9 mV versus Ag|AgCl and heterogeneous electron transfer rate constant (k(s)) of 13.8 +/- 2.1 s(-1). Experimental data indicate that cyt c is stably immobilized onto the TiO(2) nanoneedles film and maintains inherent enzymatic activity toward H(2)O(2). On the basis of these results, the cyt c-TiO(2) nanocomposits film is capable of sensing H(2)O(2) at a suitable potential, 0.0 V (vs Ag|AgCl), where not only common anodic interferences like ascorbic acid, uric acid, 3,4-dihydroxyphenylacetic acid but also a cathodic interference, O(2), are effectively avoided. Besides high selectivity, the present biosensor for H(2)O(2) shows broad dynamic range and low detection limit. These remarkable analytical advantages, as well as the characteristic of TiO(2) nanoneedles film such as high conductivity, biocompatibility, and facile ability to miniaturize establishes a novel approach to detection of extracellular H(2)O(2) released from human liver cancer cells.

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A one-step, nontemplated, low-cost electrochemical method for the growth of gold nanostructures with different shapes is reported here. It is the first time that nanopyramidal, nanorod-like, and spherical gold nanostructures were fabricated on polycrystalline gold substrates through electrochemical overpotential deposition (OPD) by easily manipulating the deposited potentials and concentrations of HAuCl4. X-ray diffraction and electrochemical analyses revealed that the pyramidal structures are more extensively dominated by (111) facets in comparison with the other nanostructures. The nanopyramids, which have anisotropic structures, exhibited broad extinction over the visible region, most likely due to plasmon resonance. Oxygen reduction activity of a gold electrode with the pyramidal structures was lower than those of the electrodes with the other nanostructures since the activity at the gold (111) surface is lower than that at the (100) and (110) surfaces.

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Novel underwater tissue-selective adhesive hydrogels with adhesion energy to wet porcine skin of ∼1011 J m−2 were made by bio-mimicking Mfps.