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Electrodes contact layers

Figure 2.105 Optically transparent thin layer electrochemical (OTTLE) cell. A = PTFE cell body, B = 13 x 2 mm window, (C and E) = PTFE spacers, D = gold minigrid electrode, F = 25 mm window, G = pressure plate, H = gold working electrode contact, 1 = reference electrode compartment, J = silver wire, K = auxiliary electrode and L = solution presaturator. From Ranjith... Figure 2.105 Optically transparent thin layer electrochemical (OTTLE) cell. A = PTFE cell body, B = 13 x 2 mm window, (C and E) = PTFE spacers, D = gold minigrid electrode, F = 25 mm window, G = pressure plate, H = gold working electrode contact, 1 = reference electrode compartment, J = silver wire, K = auxiliary electrode and L = solution presaturator. From Ranjith...
Electrolyte mixing is necessary to maintain the particles in suspension, unless the particles are neutrally buoyant, and to transport the particles to the surface of the electrode. The hydrodynamics of the electrodeposition system control the rate, direction, and force with which the suspended particles contact the electrode surface. Bringing the particles in contact with the electrode is a necessary step for the incorporation of particles into the metal matrix, although particle-electrode contact does not guarantee incorporation of the particle. Of course, an increase in flow can increase the plating rate as the thickness of the diffusion layer at the electrode surface decreases. [Pg.200]

Fig. 2.3. Schematic view of a porous nanocrystaUine sensing layer with a one-dimensional representation of the energetic conduction band. A inter-grain band bending, eVs, occms as a consequence of smTace phenomena, and a band bending, eVc, occurs at the grain-electrode contact. Eb denotes the minimmn conduction band energy in the bulk tin oxide, and Ep is the Fermi-energy in the electrode metal... Fig. 2.3. Schematic view of a porous nanocrystaUine sensing layer with a one-dimensional representation of the energetic conduction band. A inter-grain band bending, eVs, occms as a consequence of smTace phenomena, and a band bending, eVc, occurs at the grain-electrode contact. Eb denotes the minimmn conduction band energy in the bulk tin oxide, and Ep is the Fermi-energy in the electrode metal...
Hi) (Following from (ii)) The silver electrode contact itself is not strong, so solution can seep between the silver paint and the electrode, thus destroying all chance of reproducibility. A protective over-layer prevents such seepage. [Pg.284]

Generally in a nail penetration test, an instantaneous internal short would result the moment the nail is tucked into the battery. Enormous heat is produced from current flow (double layer discharge and electrochemical reactions) in the circuit by the metal nail and electrodes. Contact area varies according to depth of penetration. The shallower the depth, the smaller the contact area and therefore the greater the local current density and heat pro-... [Pg.200]

During SOFC operation, interconnects interact with surrounding gaseous environments on both the cathode and anode side, as well as with adjacent components such as sealing materials, electrodes, and electrical contact layers inserted between interconnects and electrodes. These interactions potentially cause corrosion of metallic interconnects and affect their stability and performance. [Pg.232]

The recent advent of semidry electrophoretic transfer (seevol. 3, Chapter 29) allows the rapid transfer of several gels simultaneously, in a stack of up to 6 gels/membrane sandwiches," each sandwich being separ rated from the others by a layer of dialyns membrane to prevent transfer of polypeptides from one sandwich to the next The technique uses relatively low power and small amounts of transfer buffer, and the electrodes consist of graphite plates several types of apparatus are now commercially available. However, in our experience, it is often difficult to exclude all air bubbles from the gel/membrane sandwich and to maintain even electrode contact throughout the transfer. [Pg.232]

Recent advances and progress in electrically contacted, layered enzyme electrodes in the potential applications for amperometric biosensors, sensor... [Pg.347]

Figure 1-1. Schematic drawing of a single-layer electroluminescent device. An applied electric field leads to injection of holes (positive charges the majortiy charge carriers in polymers such as PPV) and electrons (usually the minority charge carriers) into the light-emitting polymer film from the two electrode contacts. Formation of an electron-hole pair within the polymer may then result in the emission of a photon. Since holes migrate much more easily through PPV than electrons, electron-hole recombination takes place in the vicinity of the cathode. Figure 1-1. Schematic drawing of a single-layer electroluminescent device. An applied electric field leads to injection of holes (positive charges the majortiy charge carriers in polymers such as PPV) and electrons (usually the minority charge carriers) into the light-emitting polymer film from the two electrode contacts. Formation of an electron-hole pair within the polymer may then result in the emission of a photon. Since holes migrate much more easily through PPV than electrons, electron-hole recombination takes place in the vicinity of the cathode.
Freshly cleaved mica substrates (Spruce Pine Mica Co., Spruce, NC) were vacuum-coated with an approximately 500 A thick layer of gold at one end this served as the reference/counter electrode contact. In all experiments the tip was laterally positioned approximately 1 mm from the Au contact and the imaging process was operated in the constant current mode. In ac-admittance measurements, a small ac voltage (10 mV peak-to-peak amplitude, 10 kHz) was superimposed on the dc bias and the admittance was measured with a phase-sensitive detector. If not otherwise mentioned, the mica substrate was heated with one small drop (—10 /xL) of a phosphate... [Pg.125]

In evaporation-intercalation devices solar energy conversion would, at least in the more efficient case of a thermal system, not be converted by exciting electrons and rapidly separating them from holes, but by transferring atoms or molecules across a phase boundary by evaporation which is usually a very efficient process. It is, consequently, neither necessary to use materials which are well crystallized like those developed for photovoltaic cells nor is it necessary to prepare sophisticated junctions. A compacted polycrystalline sheet of a two-dimensional material which is on one side placed in contact with an electrolyte, sandwiched between the layer-type electrode and a porous counter electrode, as it is used in fuel cells, would constitute the central energy conversion unit. Some care would have to be taken to choose an electrolyte which is suitable for intercalation reactions and which is not easily evaporated through leaks in the electrodes. Thin layers of polymeric or solid electrolytes would seem to be promising. [Pg.171]

Auger techniques have also proven useful in the characterization of electrochemically induced changes in thin-film electrodes. An example concerns films (500-2000 A thick) of magnesium phthalocyanine (MgPc) deposited over a gold contact layer on a glass substrate (106) ... [Pg.717]

The line shape of the radical is a measure for the mobility of the spin probe and at least of the polymer chain where the label is fixed. Comparing the ESR spectra of spin labeled styrene maleic acid copolymer in solution (Fig.9a) and on the electrode surface layer of nickel micro mesh (Fig.9b) it can be concluded that the surface layer on the polymer modified electrode has two regions of different mobility. The more restricted mobility of one part of the polymer might be found in contact with the solid electrode and the mobile polymer chains in contact with the solution. This problem might be further studied by ESR tomography. [Pg.65]

The potentiostatic electrolysis at a platinum electrode at +1-0 V results in a polymer layer on the electrode surface. After an induction period the electrode surface layer gives an ESR signal with one line of 0.15 mT linewidth (Fig.lO). The linewidth is independent on the radical concentration and the type of the cation in the supporting electrolyte. If the polyaniline film is in contact with aniline in the abscence of an applied potential, the line intensity decrease with time indicating a further reaction of the polymer with the aniline. Under UV-irradiation the free spin can be renewed without reaching its initial intensity (Fig.lOb). [Pg.66]


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Contact layers

Electrodes layers

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