Nickel oxide electrical conductivity

Further improvements in anode performance have been achieved through the inclusion of certain metal salts in the electrolyte, and more recently by dkect incorporation into the anode (92,96,97). Good anode performance has been shown to depend on the formation of carbon—fluorine intercalation compounds at the electrode surface (98). These intercalation compounds resist further oxidation by fluorine to form (CF ), have good electrical conductivity, and are wet by the electrolyte. The presence of certain metals enhance the formation of the intercalation compounds. Lithium, aluminum, or nickel fluoride appear to be the best salts for this purpose (92,98). 

Almost all the methods described for the nickel electrode have been used to fabricate cadmium electrodes. However, because cadmium, cadmium oxide [1306-19-0], CdO, and cadmium hydroxide [21041-95-2], Cd(OH)2, are more electrically conductive than the nickel hydroxides, it is possible to make simple pressed cadmium electrodes using less substrate (see Cadmium and cadmium alloys Cadmium compounds). These are commonly used in button cells. 

Good results are obtained with oxide-coated valve metals as anode materials. These electrically conducting ceramic coatings of p-conducting spinel-ferrite (e.g., cobalt, nickel and lithium ferrites) have very low consumption rates. Lithium ferrite has proved particularly effective because it possesses excellent adhesion on titanium and niobium [26]. In addition, doping the perovskite structure with monovalent lithium ions provides good electrical conductivity for anodic reactions. Anodes produced in this way are distributed under the trade name Lida [27]. The consumption rate in seawater is given as 10 g A ar and in fresh water is... 

Methods. The differential heats of adsorption of reagents and the differential heat of their interaction on the nickel oxide surface were measured in a Calvet microcalorimeter with a precision of 2 kcal. per mole. The apparatus has been described (18). For each adsorption of a single gas, small doses of gas are allowed to interact with a fresh nickel oxide sample (100 to 200 mg.) placed in the calorimeter cell maintained at 30°C. At the end of the adsorption of the last dose, the equilibrium pressure is, in all cases, 2 torr. Duplication of any adsorption experiment on a new sample gives the same results within 2 kcal. per mole of heat evolved and 0.02 cc. of gas adsorbed per gram. Electrical conductivities of the nickel oxide sample are measured in an electrical conductivity cell with platinum electrodes (1) by a d.c. bridge. 

Sequence II O2—CO. Oxygen is first adsorbed on NiO(250) at 30°C. The sample is then evacuated at 30°C. (amount of irreversibly adsorbed oxygen, 1.9 cc. per gram), and carbon monoxide is adsorbed at the same temperature (Figure 3). The electrical conductivity of nickel oxide containing preadsorbed oxygen 1.8 X 10 5 (ohm cm.)"1 decreases during the adsorption of CO, and at the end of the adsorption, is identical to the conductivity of the pure oxide. Moreover, carbon dioxide is condensed in the cold trap. This shows that all ionized species are transformed into neutral species at the end of the interaction. 

Raman and Mossbauer studies.97 Thus the compounds are partially oxidized and should be more correctly expressed as [M(DPG)2KIs)o.2 with the nickel in a formal oxidation state of 2.20.97 The electrical conductivity in the Ni atom chain direction is 10-2 fi 1 cm-1, 105 times that of the unoxidized parent compound.97 98 The temperature dependence of the conductivity indicates that the compound is a semiconductor with AE = 0.19+0.01 eV. Table 3 indicates that changing the halide has little effect on the conductivity but that the Ni complex is more conducting than the Pd analogue. 

The electrical conductivity was measured by W. H. Ross, who found that in all cases the conductivity of the salt soln. was increased with time, especially with the more dil. soln. This is due to the decomposition of the salts under the influence of the platinum-black of the electrodes with polished electrodes, the effect is considerably smaller. The base itself is oxidized even more rapidly than the salts. The soln. are in all cases decomposed by the platinum electrodes, and G. M. J. MacKay showed that tin does not decompose the soln. at all, while copper decomposes the soln. completely. The order in which the metals were found to decompose the soln. is tin, platinum, silver, nickel, mercury, and copper. The electrical conductivity of hydroxylamine, using tin electrodes, in terms of mercury at 18°, with v vols. of soln. per mol, is as follows ... 

In the most important series of polymers of this type, the metallotetraphenylporphyrins, a metalloporphyrin ring bears four substituted phenylene groups X, as is shown in 7.19. The metals M in the structure are typically iron, cobalt, or nickel cations, and the substituents on the phenylene groups include -NH2, -NR2, and -OH. These polymers are generally insoluble. Some have been prepared by electro-oxidative polymerizations in the form of electroactive films on electrode surfaces.79 The cobalt-metallated polymer is of particular interest since it is an electrocatalyst for the reduction of dioxygen. Films of poly(trisbipyridine)-metal complexes also have interesting electrochemical properties, in particular electrochromism and electrical conductivity.78 The closely related polymer, poly(2-vinylpyridine), also forms metal complexes, for example with copper(II) chloride.80... 

Another alloy discovery that transformed an industry was that of nichrome, invented in 1905 by the young American engineer Albert Marsh (1877-1944). Nichrome is an alloy of nickel and chromium that is tough and ductile (capable of being drawn into wires), and very resistant to oxidation and melting with a very low electrical conductivity. These properties make the alloy ideal for a very special application use as wires in a toaster. 

Shim, J. Lee, H.-K. Improved performance of Raney nickel electrode by the addition of electrically conductive materials for hydrogen oxidation reaction. Materials Chemistry and Physics 2001 69(1-3) 72-76. 

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