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The anode contact

Anode contacts to hole transporting molecular layers were discussed briefly in Section 9.3.2. To reiterate, it is often found that metal phthalocyanine compounds effectively mediate the injection of holes from ITO into hole transport layers. (One could also say oxidation of carbocations in the HTL with net transfer of an electron from the HTL into the ITO.) Some experiments have suggested that multiple layers of phthalocyanines based on different metals, and hence having different HOMO state energies, can further reduce the injection barrier. The basic method in use in these cases is to provide a staircase of small barriers up which a hole can climb more easily than would be the case for a single large step. The low mobility of holes in the organic interlayers comes in handy here as it reduces the rate at which holes return to the contact. [Pg.439]

For polymer-based devices, conducting polymers such as polyanaline and polythiophene have been used extensively as anodes. These are naturally p-type (hole conducting) materials produced by oxidation of conjugated molecules and thus are naturally suited to mediating the hole injection problem. However, these materials are not ideal. The polymer devices have generally lagged behind the molecular-based devices, probably in part, because more intensive study and improvement of contacts has been pursued for the molecular materials. [Pg.439]


The electrochemical properties of zinc also have a large bearing on its corrosion behaviour. Zinc is negative to Eh /h2 and magnesium and aluminium excepted, to most other metals commonly encountered, including those found in the less pure forms of zinc. This means that when zinc is in contact with these metals sacrificial electrochemical action can take place, with zinc forming the anode. Contact with other metals and impurities can... [Pg.815]

Polyphenylene has been prepared from benzene in the presence of Lewis acid and oxidizing agent by Kovacic (26). It was surprising that the same polymers were electrolytically yielded at the interface of the benzene-HF mixture containing small amounts of HaO or KF, according to Shepard and Dannels (27). The mixture exhibited unusual electrical conductivity, the maximum of which was obtained with the anode contacting the interface between the phases and the cathode either contacting the interface or situated in the HF layer. [Pg.390]

Certainly, the period between servicing of the cell is determined either by disintegration of the anode or by corrosion of the anode contact and downtime is a constant problem with fluorine cells. [Pg.133]

The plate of a power tube resembles a copper cup with the upper-half of a plate contact ring welded to the mouth and cooling fins silver soldered or welded to the outside of the assembly. The lower-half of the anode contact ring is bonded to a base ceramic spacer. At the time of assembly, the two halves of the ring are welded together to form a complete unit, as shown in Fig. 5.34. [Pg.380]

What is the cell potential of a concentration cell that contains two hydrogen electrodes if the cathode contacts a solution with pH = 7.8 and the anode contacts a solution with [H+] = 0.05 M ... [Pg.848]

The second most used material is nickel oxide which is processed from nickel ore and used for the anode substrate and anode together with yttrium-stabilized zirkonia in form of a cermet and as a nickel mesh for the anode contact layer. Yttrium-stabilized zirconia is produced from rare earths and mineral sands. [Pg.768]

With the exception of the anode contact (where slight modification of the top/anode interface is necessary), materials for the cadmium/mercuric oxide cell are generally the same as for the zinc/mercuric oxide cell. However, because of the wide range of storage and operating conditions of most applications, cellulose and its derivatives are not used, and low-melting-point polymers are also avoided. Nickel is usually used on the anode side of the cell and also, conveniently, at the cathode. [Pg.278]

Electrons move through Ti02 toward the anode contact by a random walk process (essentially diffusion, as the Ti02 nanostructure under solar... [Pg.119]

The improvement in power conversion efficiency (PCE) of plasmonic solar cells is always an urgent problem and short circuit current density is one of the key factors for the PCE. The improvement in the Jsc of plasmonic solar cells is mainly achieved by the introduction of metallic nanoparticles, such as blending Au nanoparticles into the anodic buffer layer or the interconnecting layer that connects two subcells of the tandem plasmonic solar cells [86]. Compared with the metallic NPs, nanowires (NWs) are superior in terms of improving photocurrent, while most of the metallic NWs introducing in cells reported previously were used for the anodic contact of the cells [87]. The improvement of PCE in bulk heterojunction polymer solar cells with active layer P3HT PCBM by introducing 40 nm Au nanoparticles between ITO and PEDOT PSS layer with various concentrations is also observed by Gao et al. [88]. It has been found that both short-circuit current density and PCE increase from 3.50% to 3.81% with 0.9 wt. % Au NPs due to the localized surface plasmon excitation of Au NPs. [Pg.131]

G lv nic Corrosion. Galvanic corrosion is an electrochemical process with four fundamental requirements (/) an anode (magnesium), 2) a cathode (steel, brass, or graphite component), (J) direct anode to cathode electrical contact, and (4) an electrolyte bridge at the anode and cathode interface, eg, salt water bridging the adjacent surfaces of steel and magnesium components. If any one of these is lacking, the process does not occur (133,134). [Pg.334]

The cell for this process is unlike the cell for the electrolysis of aluminum which is made of carbon and also acts as the cathode. The cell for the fused-salt electrolysis is made of high temperature refractory oxide material because molten manganese readily dissolves carbon. The anode, like that for aluminum, is made of carbon. Cathode contact is made by water-cooled iron bars that are buried in the wall near the hearth of the refractory oxide cell. [Pg.496]


See other pages where The anode contact is mentioned: [Pg.125]    [Pg.500]    [Pg.13]    [Pg.508]    [Pg.517]    [Pg.349]    [Pg.55]    [Pg.483]    [Pg.412]    [Pg.255]    [Pg.255]    [Pg.692]    [Pg.127]    [Pg.439]    [Pg.125]    [Pg.500]    [Pg.13]    [Pg.508]    [Pg.517]    [Pg.349]    [Pg.55]    [Pg.483]    [Pg.412]    [Pg.255]    [Pg.255]    [Pg.692]    [Pg.127]    [Pg.439]    [Pg.2732]    [Pg.213]    [Pg.113]    [Pg.243]    [Pg.486]    [Pg.489]    [Pg.499]    [Pg.127]    [Pg.127]    [Pg.454]    [Pg.391]    [Pg.175]    [Pg.175]    [Pg.175]    [Pg.175]    [Pg.175]    [Pg.176]    [Pg.3]    [Pg.99]    [Pg.100]    [Pg.528]    [Pg.404]    [Pg.523]    [Pg.527]   


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Anode contact

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