The immobilization of DNA molecules to electrodes in confined channels at physiological pH

Large numbers of DNA molecules are immobilized to electrodes at the physiological pH of 8.0, and the length of the immobilized DNA molecules is controlled using an ac voltage. Efficient DNA immobilization at physiological pH has been demonstrated by integrating electrodes in confined channels 500?nm wide and 100?nm deep. The low volume of the channels allows large numbers of DNA molecules to access the electrode surfaces, leading to efficient immobilization.     

ZnO films and nanorod/shell arrays electrodeposited on PET-ITO electrodes

In this work, ZnO films, nanorod and nanorod/shell arrays were synthesized on the surface of PET-ITO electrodes by electrochemical methods. ZnO films with high optical transmittance were prepared from a zinc nitrate solution using a pulsed current technique with a reduced pulse time (3 s). The X-ray diffraction pattern of ZnO film deposited on PET-ITO electrode showed that it has a polycrystalline structure with preferred orientations in the directions [0 0 2] and [1 0 3]. ZnO nanorods were synthesized on electrochemical seeded substrate in an aqueous solution containing zinc nitrate and hexamethylenetetramine. In order to increase the stability of PET-ITO electrode to electrochemical and chemical stresses during ZnO nanorods deposition the surface of the electrode was treated with a 17 wt% NH₄F aqueous solution. Electrochemical stability of PET-ITO electrode was evaluated in a solution containing nitrate ions and hexamethylenetetramine. ZnO nanorod/shell arrays were fabricated using eosin Y as nanostructuring agent. Photoluminescence spectra of ZnO nanorod and ZnO nanorod/shell arrays prepared on the surface of PET-ITO electrode were discussed comparatively. By employing the 1.5 μm-length ZnO nanorod/shell array covered with a Cu₂O film a photovoltaic device was fabricated on the PET-ITO substrate.     

Catalytic oxidation and flow detection of carbohydrates at ruthenium dioxide modified electrodes

Ruthenium dioxide (RuO2) containing carbon paste electrodes exhibiting electrocatalytic response toward carbohydrates are described. The electrocatalytic behavior is exploited for developing a highly stable and sensitive flow detection scheme for carbohydrates at a low and fixed potential (+0.4 V vs Ag/AgCl). The effects of pH, flow rate, operating potential, surface "loading", concentration, and other variables are explored. The electrode response was stable for more than 48 h, with a signal loss of less than 10% over this period. The detection limits at the picomole level and a relative standard deviation of 1.2% (n = 72) are reported. Electrocatalytic oxidation is described also for related polyhydroxyl compounds (aldonic and aldaric acids and alditols).     

Micro-capacitors based on electrochemically grown vertical arrays of gold nanowires as electrodes

This paper describes the development of micro-capacitors with electrodes based on electrochemically grown vertical gold nanowire arrays. A high aspect-ratio anodized aluminum oxide template integrated on silicon dioxide/silicon substrates was exploited for fabricating a vertical array of nanowires with a high surface to volume ratio. Bismuth ferric oxide thin films were deposited to create high dielectric material between the electrodes using room temperature electrodeposition. This nanofabrication process may be compatible with a complementary metal-oxide-semiconductor (CMOS) process, therefore, this capacitor can be used for protecting and regulating the surge voltage biased to the CMOS circuits. This capacitor achieved a high density capacitance of 3.1 μF/m² at 1 MHz, which was measured using a parallel plate set-up.     

Solution-processed top-contact electrodes strategy for organic crystalline field-effect transistor arrays

Organic crystals,especially ultra-thin two-dimensional(2D)ones such as monolayer molecular crystals,are fragile and vulnerable to traditional vacuum deposition.Up to now,most of the methods reported for fabricating organic field-effect transistors(OFETs)with top-electrodes on the 2D molecular crystals are based on mechanical-transfer method.Nondestructive method for large scale in-situ electrode deposition is urgent.In this work,the silver mirror reaction(SMR)is introduced to construct top-contact electrodes on 2D organic crystalline thin films.OFETs based on bilayer crystalline films with solution-processed silver electrodes show comparable performance to devices with transferred gold electrodes.In addition to that,OFETs with SMR fabricated silver electrodes show lower contact resistance than the ones with evaporated silver electrodes.Furthermore,the temperature under which SMR electrodes annealed is relatively low(60℃),making this approach applicable to varies of organic semiconductors,such as spin-coated polymer films,vacuum evaporated films,2D and even monolayer crystalline films.Besides,OFETs with sub-micrometer channel width and 25μm channel length are realized which might find practical application in the ultra-small pixel mini/micro-LEDs.     

三电极体系制备TiO2纳米管

利用电化学阳极氧化法在乙二醇和氟化铵溶液三电极体系中阳极氧化纯钛箔,制备出具有双面结构的TiO2阵列纳米管。研究了不同电压和电解液含水量对纳米管形貌的影响,通过扫描电子显微镜(SEM)和X射线衍射仪(XRD)分析了TiO2纳米管阵列的微观形貌及物相。     

Periodically porous top electrodes on vertical nanowire arrays for highly sensitive gas detection

Nanowires of various materials and configurations have been shown to be highly effective in the detection of chemical and biological species. In this paper, we report a novel, nanosphere-enabled approach to fabricating highly sensitive gas sensors based on ordered arrays of vertically aligned silicon nanowires topped with a periodically porous top electrode. The vertical array configuration helps to greatly increase the sensitivity of the sensor while the pores in the top electrode layer significantly improve sensing response times by allowing analyte gases to pass through freely. Herein, we show highly sensitive detection to both nitrogen dioxide (NO(2)) and ammonia (NH(3)) in humidified air. NO(2) detection down to 10 parts per billion (ppb) is demonstrated and an order-of-magnitude improvement in sensor response time is shown in the detection of NH(3).     

Voltammetry at micropipet electrodes

The use of micropipet electrodes for quantitative voltammetric measurements of ion-transfer (IT) and electron-transfer (ET) reactions at the interface between two immiscible electrolyte solutions (ITIES) requires knowledge of geometry of the liquid interface. The shape of the meniscus formed at the pipet tip was studied in situ by video microscopy under controlled pressure. The shape of the interface can be changed from a complete sphere to a concave spherical cap by varying the pressure applied to the pipet, and the diffusion current to the pipet changes accordingly. With no external pressure applied, the water/organic interface turned out to be flat, and the voltammetric response of a pipet must follow the well-known theory for a microdisk electrode. The large deviations from this theory observed previously can be attributed to a small amount of the filling aqueous solution which escapes from the pipet and forms a thin layer on its outer wall. This effect can be eliminated by making the outer pipet wall hydrophobic. Procedures have been developed for independent silanization of the inner and outer walls of the pipet. Pipets with a silanized inner wall can be filled with an organic solvent (e.g., 1,2-dichloroethane) and be used for voltammetric measurements in aqueous solutions. Another mode of voltammetry is based on trapping of a thin layer of organic solvent in the narrow shaft of a pipet between the filling solution and the aqueous outer phase. This arrangement is potentially useful for electrochemical catalysis and sensor applications.     

Olefin-vapor conductivities below 0.1 MPa at 220–680 K

A curve has been fitted to measurements on the thermal conductivities of olefin vapors at 220–680 K, which is based on the corresponding-state theory. Measurements have been made on the thermal conductivity of non-1-ene at 303–372 K.Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 57, No. 3, pp. 480–485, September, 1989.     

Thermal and electrical conductivities of exfoliated graphite at low temperatures

The thermal and electrical conductivities of exfoliated graphite foils have been measured along the rolling direction and across it.     

Carbon electrodes modified with ruthenium metallodendrimer multilayers for the mediated oxidation of methionine and insulin at physiological pH

A pentaerythritol-based metallodendrimer with ruthenium(II) terpyridine units, Ru(II)Den, catalyzed the oxidation of L-methionine and insulin at pH 7.0. The Ru(II)Den was immobilized on a carbon surface through layer-by-layer electrostatic deposition; the negatively charged polymer, poly(styrene sulfonate), was its counterpart. These bilayers were assembled on a glassy carbon electrode that was first modified by deposition of a layer of the conjugate base of sulfanilic acid and then with quaternized poly(4-vinylpyridine). Reversible voltammetry for the Ru(II/III) redox couple was observed, the current for which increased linearly with layer number, n, of Ru(II)Den up to n = 12. Cyclic voltammetry was used to demonstrate the mediation of L-methionine oxidation by a Ru(II)Den-containing multilayer assembly. Flow injection amperometric determination of insulin at pH 7.0 at this modified electrode yielded a calibration curve with the following characteristics: linear dynamic range, 6 nM-0.4 microM; sensitivity, 225 nA microM(-1); detection limit (k = 3 criterion), 2 nM. Of particular importance was that the sensitivity was proportional to the number of Ru(II)Den layers.     

Electrochemical flow injection analysis study of ion partitioning at high surface area carbon fiber electrodes

Charge-selective electrochemistry was previously shown to occur at high surface area carbon fibers that were produced by fracturing the outer periphery with anodic current or positive potential. The cyclic voltammetric behavior of electroactive species observed at these fibers exhibited a distinct pH dependence related to the protonation/deprotonation of oxygen-containing functional groups at the surface of the carbon fiber. In this paper, electrochemical flow injection analysis (EC-FIA) is used to probe ion partitioning in to and out of the interior microstructure of the treated carbon fiber, for both electroactive and electroinactive species. It was found that the extent of partitioning was the result of both ion charge and hydrated ionic radius, in addition to the level of fracture. It was further observed that the direction of movement for an injected ionic species could be controlled relative to the ion concentration, the pH of the carrier solution, or both. EC-FIA allowed the simultaneous observation of current due to ion movement and that due to electron transfer to a redox-active species. The results presented are consistent with a model in which fixed negatively charged sites in the interior of fractured fibers govern ion partitioning with positively charged ions in the carrier solution, with counterions located in the interior "free" volume.     

Cyclic biamperometry at micro-interdigitated electrodes

Cyclic biamperometry was studied as an analytical method for use with commercially available, comb-type, coplanar microinterdigitated electrodes (μIDEs), using the ferri-/ferrocyanide redox couple as a model analyte. The μIDEs studied in this work were made of gold that had been deposited onto a Ti/W adhesion layer on borosilicate glass chips and had 5 and 10 μm bands with equal gap sizes. Close proximity of the two working electrodes, and their interdigitation, resulted in signal amplification by redox cycling. Results were compared with those obtained by cyclic voltammetry, where one of the two IDE electrodes was used as the working electrode and external reference and auxiliary electrodes were used. Amplification factors of almost 20 were achieved due to redox cycling. Attempts to apply cyclic voltammetry to the μIDEs, with one of the combs as the working and the other as the auxiliary electrode, were unsuccessful due to corrosion of the auxiliary electrode comb. Results of this study, and the electrochemically unique feature of biamperometry to probe but not change the net contents of the medium under examination, suggest the applicability of scanning biamperometry at μIDEs to the very small volumes and electrochemical cell dimensions that are now of great interest.     

Pulse voltammetry at microcylinder electrodes.

Microcylindrical electrodes are easier to construct and maintain than microdisk electrodes. In the normal-pulse mode, ranges of time parameters and electrode sizes can be found such that depletion of reactant is unimportant and the response to the analysis pulse is predicted by theory for planar conditions. Similarly, ranges of parameters are found for reverse-pulse voltammetry such that the potential-dependent response can be treated as a sequence of individual double-pulse responses. Cylindrical diffusion and convection act to replenish reactant quickly near the electrode and thus permit overall experiment times in the range of seconds. For square-wave voltammetry the shape and position of the net current response are independent of the extent of cylindrical diffusion.     

Hierarchical ferric-cobalt-nickel ternary oxide nanowire arrays supported on graphene fibers as high-performance electrodes for flexible asymmetric supercapacitors

Fiber-based supercapacitors (FSCs) are new members of the energy storage family. They present excellent flexibility and have promising applications in lightweight, flexible, and wearable devices. One of the existing challenges of FSCs is enhancing their energy density while retaining the flexibility. We developed a facile and cost-effective method to fabricate a highly capacitive positive electrode based on hierarchical ferric-cobalt-nickel ternary oxide nanowire arrays/graphene fibers and a negative electrode based on polyaniline-derived carbon nanorods/graphene fibers. The elegant microstructures and excellent electrochemical performances of both electrodes enabled us to construct a highperformance flexible asymmetric graphene fiber-based supercapacitor device with an operating voltage of 1.4 V, a specific capacitance up to 61.58 mF·cm^–2, and an energy density reaching 16.76 μW·h·cm^–2. Moreover, the optimal device presents an outstanding cycling stability with 87.5% initial capacitance retention after 8,000 cycles, and an excellent flexibility with a capacitance retention of 90.9% after 4,000 cycles of repetitive bending.

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The electrical and thermal conductivities of dilute copper-chromium alloys at low temperatures

Electrical and thermal conductivity measurements are reported on dilute copper-chromium alloys containing 32 and 50 at. ppm chromium, in their unannealed state and also after annealing at 530–550°C for 16 and 66 h in each case, under fore-vacuum. From the electrical resistivity measurements evidence of a possible cluster formation is obtained in the annealed sample. The electronic Lorenz number of the alloys increases with decrease of temperature in the temperature range 4.2–1.6 K. Lower temperature measurements might show a maximum around the Kondo temperature (～1 K) as predicted by the available theories on dilute magnetic alloys.