Detection of acetaminophen using cyclic voltammetry on MnFe2O4/polyaniline

A novel sensing material, MnFe₂O₄/polyaniline (PANI), was fabricated by doping PANI to MnFe₂O₄ on a modified glassy carbon electrode (GCE). This sensing material was characterized using X‐ray diffraction (XRD), scanning electron microscopy (SEM), and high‐resolution transmission electron microscopy (HR‐TEM). Using a cyclic voltammetry electrochemical‐sensing method, we tested MnFe₂O₄/PANI, and an acetaminophen concentration of 0.0625–5 mM was recorded. Furthermore, the sensor responses were 2.05–22.44. The detection limit was 2.23 × 10^?7 M. Strong selectivity was observed for MnFe₂O₄/PANI, which is a possible sensing mechanism.     

Lithium intercalation and conduction in Fe-containing tantalum oxide films synthesized with an atmospheric pressure plasma jet

Journal of Solid State Electrochemistry - Lithium ionic intercalation and conduction performance of tantalum oxides films improved by adding with iron oxides using an atmospheric pressure plasma...     

Redox Communication within Multinuclear Iron–Sulfur Complexes Related to Electronic Interplay in the Active Site of [FeFe]Hydrogenase

The one‐electron oxidations of a Fe₂ complex lead to the formation of a persistent metal‐stabilized thiyl radical Fe₂ species, mixed‐valent Fe₄, and Fe₈ complexes. The unpaired spin in the Fe₂ radical species delocalizes over the Fe₂ and the aromatic dithiolate, mostly on the terminal sulfur. The subsequent dimerization of the singly oxidized Fe₂ to the Fe₄ retains the partial thiyl radical character. For an analogue with less steric hindrance, the π–π stacking interaction between the dithiolato aromatic rings induces generation of the Fe₈, in which process electronic structures of the species are modulated through reducing the thiyl radical to the thiolate. Electronic reorganization repeats when the Fe₈ is converted to Fe₄. Electronic interplay in the complexes decreases the energy gap of frontier MOs and buffers electronic impacts upon redox events. Easier accessible redox potentials and increased stability of the species are facilitated. The results demonstrate that electronic versatility of the benzenedithiolate exerts pronounced influences on electronic and coordination structure of the metal complexes.     

Enhanced lithium-ion intercalation and conduction of transparent tantalum oxide films by lithium addition with an atmospheric pressure plasma jet

An investigation is conducted on enhancing lithium-ion intercalation and conduction performance of transparent organo tantalum oxide (TaO _y C _z ) films, by addition of lithium via a fast co-synthesis onto 40 Ω/□ flexible polyethylene terephthalate/indium tin oxide substrates at the short exposed durations of 33–34 s, using an atmospheric pressure plasma jet (APPJ) at various mixed concentrations of tantalum ethoxide [Ta(OC₂H₅)₅] and lithium tert-butoxide [(CH₃)₃COLi] precursors. Transparent organo-lithiated tantalum oxide (Li _x TaO _y C _z ) films expose noteworthy Li⁺ ion intercalation and conduction performance for 200 cycles of reversible Li⁺ ion intercalation and deintercalation in a 1 M LiClO₄-propylene carbonate electrolyte, by switching measurements with a potential sweep from ?1.25 to 1.25 V at a scan rate of 50 mV/s and a potential step at ?1.25 and 1.25 V, even after being bent 360° around a 2.5-cm diameter rod for 1000 cycles. The Li⁺ ionic diffusion coefficient and conductivity of 6.2?×?10^?10 cm²/s and 6.0?×?10^?11 S/cm for TaO _y C _z films are greatly progressed of up to 9.6?×?10^?10 cm²/s and 7.8?×?10^?9 S/cm for Li _x TaO _y C _z films by co-synthesis with an APPJ.     

Low-temperature solution route to macroscopic amounts of hydrogen terminated silicon nanoparticles

A new solution route for preparing gram-scale, hydrogen terminated silicon nanoparticles is presented. Dimethoxyethane and diocytl ether have been used to prepare silicon nanoparticles via a solution reaction between sodium silicide and ammonium bromide. The reaction products are isolated as a clear yellow-orange solution and a dark black powder. Both the solution and the powder have been characterized.     

Prediction of Gear Dynamics Using Fast Fourier Transform of Static Transmission Error*

ABSTRACT

An analytical computer simulation procedure for dynamic modeling of low-contact-ratio spur gear systems is presented. The procedure computes the gear static transmission error and uses a Fast Fourier Transform (FFT) to generate its frequency spectrum at various tooth profile modifications. The dynamic loading response of an unmodified (perfect involut) gear pair is compared with that of gears with profile modifications. Correlations are found between several profile modifications and the resulting dynamic loads. An effective error, obtained from frequency domain anal     

Multielectron Redox Chemistry of a Neutral,NIR‐Active,Indigo‐Pillared ReI‐Based Triangular Metalloprism

Self‐assembled, hexarhenium(I), triangular metalloprism compound [{(CO)₃Re(μ‐ 2 )Re(CO)₃}₃(μ₃‐ 1 )₂] ( 3 ) featuring three bis‐chelating pillarlike indigo dianions (μ‐ 2 ), each of which connects two fac‐Re(CO)₃ cores, which are interconnected by a tritopic N donor, that is, a 2,4,6‐tris(4‐pyridyl)‐1,3,5‐triazine (μ₃‐ 1 , tPyTz) ligand, has been synthesized in high yield and characterized. Metalloprism 3 exhibits a strong absorption in the near‐infrared (NIR) region. The reversible, multielectron redox properties of the electrogenerated 3 ⁿ species, where n=3+, 0, 3?, 4?, 5?, 8?, in the visible and especially in the NIR region were investigated in THF solution by cyclic voltammetry (CV), chronocoulometry, EPR spectroscopy, and thin‐layer UV/Vis/NIR spectroelectrochemistry (SEC). Stepwise, site‐specific electrochemical reductions lead to the formation of a series of highly stable ion (radical) species in which electrons associated with μ‐ 2 or μ₃‐ 1 components of the molecule can be clearly distinguished. An EPR investigation revealed interaction of unpaired electrons with the metal nuclei (^185,187Re, I=5/2) in the reduced intermediates. The framework has C₂ symmetry, and accidental degeneracies suffice. Detailed theoretical calculations by structure‐based DFT confirm that the triply degenerate HOMO has ≥70 % indigo character with a sizable dπ‐Re character, while the LUMO is dominated by the triply degenerate indigo ligands, and the LUMO+1 by doubly degenerate tPyTz ligands. A comparison of 3 and previously reported 2,2′‐bis‐benzimidazolate‐ (BiBzlm) or alkoxy‐pillared Re^I metalloprisms indicates a very low switching potential with a potential window of less than 1 V and reversibly accessible optical properties with higher stability of the intermediates. The properties exhibited by 3 appear to be due to the slight tuning of the bridging ligand from N,N^? to N,O^?.     

Preparation and Application of Immobilized Fullerene C60‐Heparin for Anticoagulation of Blood

The interaction between fullerene C60 and heparin was studied using a fullerene C60‐coated piezoelectric quartz crystal sensor. The irreversible response of the piezoelectric quartz crystal was found which could be attributed to the quite strong adsorption of heparin onto the C60 molecule. Immobilized fullerene C60‐Heparin was prepared and successfully applied as a good inhibitor for blood clotting. Like solvated heparin, both wet and dry C60‐heparin solid all demonstrated excellent ability of anticoagulation of blood. The blood clotting time with C60‐heparin solid was found to be > 7 days, while only 17.9 min required for blood clotting time in the absence of C60‐heparin solid. Furthermore, the C60‐heparin coated artificial PVC blood vessels were prepared by coating fullerene C60 onto the surface of artificial PVC blood vessels, followed by the adsorption of water solvated heparin onto the fullerene C60 molecule to form C60‐heparin coating. The blood clotting time of blood in artificial PVC blood vessels with C60‐heparin coating was found to be > 30 days, while only ≤ 30 min. of blood clotting time without the C60‐Heparin coating was observed. The C60‐heparin coated artificial PVC blood vessels can be expected to be employed in human body for the anticoagulation of blood.     

Influence of polymer dielectric surface energy on thin‐film transistor performance of solution‐processed triethylsilylethynyl anthradithiophene (TES‐ADT)

This study investigates the correlation between surface energy of polymer dielectrics and the film morphology, microstructure, and thin‐film transistor performance of solution‐processed 5,11‐bis(triethylsilylethynyl) anthradithiophene (TES‐ADT) films. The low surface energy polyimide (PI) dielectric induced large grains with strong X‐ray reflections for spin‐cast TES‐ADT films in comparison to high surface en‐ ergy poly(4‐vinyl phenol) (PVP) dielectric. Furthermore, thin‐film transistors based on spin‐cast TES‐ADT films on PI dielectric exhibited enhanced electrical performance, small hysteresis, and high stability under bias stress with carrier mobility as high as 0.43 cm²/Vs and a current on/off ratio of 10⁷. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)