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Electrode contacts

The second most widely used noble metal for preparation of electrodes is gold. Similar to Pt, the gold electrode, contacted with aqueous electrolyte, is covered in a broad range of anodic potentials with an oxide film. On the other hand, the hydrogen adsorption/desorption peaks are absent on the cyclic voltammogram of a gold electrode in aqueous electrolytes, and the electrocatalytic activity for most charge transfer reactions is considerably lower in comparison with that of platinum. [Pg.319]

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]

Metal housing Sensing electrode Reference electrode Courier electrode Electrolyte reservoir Electrode contacts... [Pg.513]

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...
Fig.4.4. Schematic of the functional elements of the microhotplate. Rheat denotes the heating resistance, Rs is the metal-oxide resistance measured between the electrode contacts E+ and E-, and Rr is the temperaturesensor resistance... Fig.4.4. Schematic of the functional elements of the microhotplate. Rheat denotes the heating resistance, Rs is the metal-oxide resistance measured between the electrode contacts E+ and E-, and Rr is the temperaturesensor resistance...
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]

For in situ x-ray diffraction measurements, the basic construction of an electrochemical cell is a cell-type enclosure of an airtight stainless steel body. A beryllium window, which has a good x-ray transmission profile, is fixed on an opening in the cell. The cathode material can be deposited directly on the beryllium window, itself acting as a positive-electrode contact. A glass fiber separator soaked in liquid electrolyte is then positioned in contact with the cathode followed by a metal anode (3). A number of variations and improvements have been introduced to protect the beryllium window, which is subject to corrosion when the high-voltage cathode is in direct contact with it. [Pg.239]

Conductivity detection is a universal detection mode in which the conductivity between two inert electrodes comprising the detector cell is measured. The different arrangements employed for the construction of these detectors include apparatus with a galvanic contact of the solution with the sensing electrodes (contact conductivity detection) [51] and detection systems without galvanic contact of the solution with the sensing electrodes (contactless conductivity detection) [1]. [Pg.168]

There are two main varieties of bulk conductivity detectors contact and contactless. In a contact conductivity detector, the electrodes contact the column effluent directly. The electrodes are usually made of stainless steel, platinum, or gold in order to minimize electrochemical reactions, but they are still subject to fouling over time. In the absence of electrochemical reactions, there is no charge transfer between the solution and the electrodes, so the conductivity measurement is made with an oscillating or alternating voltage. [Pg.220]

For kilohertz measnrement frequencies and above, the contribution of Qi can generally be neglected. McWhorter and Soper employed a simple two-electrode contact conductivity detector with reverse-phase ion pair chromatography, and achieved a detection limit of 3.46pg in a lOOnL volume (464nM) for KCl [54]. Four-electrode setups, in which two leads are nsed to measure current and the other pair to measure voltage, can also be nsed in order to eliminate the effect of the impedance of the electrical leads on the measnrement. [Pg.221]

The stability of silicon electrodes contacting an aqueous electrolyte is a severe problem in regenerative solar systems. As mentioned previously, the standard electrode potential of a silicon element is negative enough to induce an electrochemical reaction mechanism, giving rise to an insulating surface silicon oxide in the absence of complexing reactants. On the... [Pg.330]

While many of the issues remain controversial, it is clear that electrode contact will dominate transport under certain conditions and that the mechanistic issues involved once the electrode problems are understood relate closely to the same mechanistic issues involved in electron transfer experiments. While band structure calculations are very helpful for under-... [Pg.22]

Traps and recombination centers which depend on purity, crystal defects and preparation, can exert an influence, and electrode contacts, carrier injections, and other factors can interfere with measurements. Yet there is no doubt that the photoconductive gain (quantum yield) G can be reproduced by different methods. As in the case of dark conductivity, the photoconductivity properties are related to the electronic and structural behavior of pure and doped organic compounds, also those in the polycrystalline state. [Pg.105]

An RDE for use at high temperatures had been described [113]. For application to RDEs made of semiconductor crystals, some advantages are to be gained by having two electrode contacts, one for current and the other potentiometric [114]. [Pg.391]

Fig. 9. Typical wall-jet cell, A, Disc electrode contact B, ring electrode contact C, Ag/AgCl reference electrode D, Pt tube counter electrode E, cell inlet F, Kel-F cell body. (From ref. 44.)... Fig. 9. Typical wall-jet cell, A, Disc electrode contact B, ring electrode contact C, Ag/AgCl reference electrode D, Pt tube counter electrode E, cell inlet F, Kel-F cell body. (From ref. 44.)...

See other pages where Electrode contacts is mentioned: [Pg.175]    [Pg.175]    [Pg.175]    [Pg.131]    [Pg.50]    [Pg.267]    [Pg.113]    [Pg.296]    [Pg.332]    [Pg.80]    [Pg.93]    [Pg.228]    [Pg.477]    [Pg.48]    [Pg.48]    [Pg.127]    [Pg.69]    [Pg.69]    [Pg.283]    [Pg.82]    [Pg.66]    [Pg.220]    [Pg.296]    [Pg.311]    [Pg.4]    [Pg.113]    [Pg.308]    [Pg.334]    [Pg.2]    [Pg.223]    [Pg.50]    [Pg.254]   
See also in sourсe #XX -- [ Pg.105 ]




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