Nickel oxide doping with

The fuel cell analyzed in the present section is a disk-shaped anode-supported SOFC, currently produced by H.C. Starck/InDEC B.V As illustrated in Figure 4.1 [1], the anode material is a cermet of nickel oxide doped with yttrium stablilized zir-conia (NiO/8YSZ). The cathode is composed of two layers one made of 8YSZ with strontium-doped LaMnC>3 (8YSZ/LSM) and one of LSM. The electrolyte consists of a dense 8YSZ material. 

Within the periodic Hartree-Fock approach it is possible to incorporate many of the variants that we have discussed, such as LFHF or RHF. Density functional theory can also be used. I his makes it possible to compare the results obtained from these variants. Whilst density functional theory is more widely used for solid-state applications, there are certain types of problem that are currently more amenable to the Hartree-Fock method. Of particular ii. Icvance here are systems containing unpaired electrons, two recent examples being the clci tronic and magnetic properties of nickel oxide and alkaline earth oxides doped with alkali metal ions (Li in CaO) [Dovesi et al. 2000]. 

Acceptor doping, as in lithium oxide doping of nickel oxide, produces p-type thermistors. The situation in nickel-oxide-doped Mn304 is similar but slightly more complex. This oxide has a distorted spinel structure (Supplementary Material SI), with Mn2+ occupying tetrahedral sites and Mn3+ occupying octahedral sites in the crystal, to give a formula Mn2+[Mn3+]204, where the square parentheses enclose the ions in octahedral sites. The dopant Ni2+ ions preferentially occupy... 

Relative densities of extended defects were evaluated by X-Ray Small Angle Scattering method (SAXS) using Cu K radiation with a nickel filter and an amplitude analyzer [4,8] Mossbauer spectra of Fe (including experiments with oxides doped with this ion tracer) were acquired using an NF-640 spectrometer in the temperature range 298-4.2 K [7, 10]. 

Recently, in the new ReRAM non-volatile memory, a nickel oxide film with titanium (Ti NiO) was doped to increase voltage for memory erasures. Operations required only 5 ns, about 10,000 times faster than before, and with resistance fluctuations reduced to 1/10 that of conventional ReRAMs. Optimizing the voltage applied to a transistor reduced the current need to erase memory to <100 pA. 

Figure 9.8. The resistivity of lithium-doped nickel oxide. Published with permission from the Journal of Materials Education.

The anode material in SOF(7s is a cermet (rnetal/cerarnic composite material) of 30 to 40 percent nickel in zirconia, and the cathode is lanthanum rnanganite doped with calcium oxide or strontium oxide. Both of these materials are porous and mixed ionic/electronic conductors. The bipolar separator typically is doped lanthanum chromite, but a metal can be used in cells operating below 1073 K (1472°F). The bipolar plate materials are dense and electronically conductive. 

The transition from non-protective internal oxidation to the formation of a protective external alumina layer on nickel aluminium alloys at 1 000-1 300°C was studied by Hindam and Smeltzer . Addition of 2% A1 led to an increase in the oxidation rate compared with pure nickel, and the development of a duplex scale of aluminium-doped nickel oxide and the nickel aluminate spinel with rod-like internal oxide of alumina. During the early stages of oxidation of a 6% A1 alloy somewhat irreproducible behaviour was observed while the a-alumina layer developed by the coalescence of the rodlike internal precipitates and lateral diffusion of aluminium. At a lower temperature (800°C) Stott and Wood observed that the rate of oxidation was reduced by the addition of 0-5-4% A1 which they attributed to the blocking action of internal precipitates accumulating at the scale/alloy interface. At higher temperatures up to 1 200°C, however, an increase in the oxidation rate was observed due to aluminium doping of the nickel oxide and the inability to establish a healing layer of alumina. 

The catalytic activity of doped nickel oxide on the solid state decomposition of CsN3 decreased [714] in the sequence NiO(l% Li) > NiO > NiO(l% Cr) > uncatalyzed reaction. While these results are in qualitative accordance with the assumption that the additive provided electron traps, further observations, showing that ZnO (an rc-type semi-conductor) inhibited the reaction and that CdO (also an rc-type semi-conductor) catalyzed the reaction, were not consistent with this explanation. It was noted, however, that both NiO and CdO could be reduced by the product caesium metal, whereas ZnO is not, and that the reaction with NiO yielded caesium oxide, which is identified as the active catalyst. Detailed kinetic data for these rate processes are not available but the pattern of behaviour described clearly demonstrates that the interface reactions were more complicated than had been anticipated. 

Fig. 22. Differential heats of adsorption of oxygen at 30°C on four different samples of pure and doped nickel oxide, (a) NiO (200), (b) NiO(Li) (250), (c) NiO (250), (d) NiO(Ga) (250). Reprinted from (8) with permission. Copyright 1969 by Academic Press, Inc. New York.

Fig. 25. Differential heats of adsorption of carbon monoxide at 30°C on fresh (A) or oxygenated (B) samples of a gallium-doped nickel oxide. Reprinted from (63) with permission J. Chim. Phys.

Thermochemical Cycles Testing the Formation of Gaseous (Cycle 1) or Adsorbed (Cycle 2) Carbon Dioxide by the Interaction of Carbon Monoxide with Oxygen Preadsorbed on Gallium-Doped Nickel Oxide ... 

Fig. 26. Differential heats of interaction of carbon monoxide at 30°C with a sample of gallium-doped nickel oxide, containing a limited amount (0.4 cm3 02 gm l) of preadsorbed oxygen.

Nickel oxide, NiO, is doped with lithium oxide, Li20, to form Li Ni, xO with the sodium chloride structure, (a) Derive the form of the Heikes equation for the variation of Seebeck coefficient, a, with the degree of doping, x. The following table gives values of a versus log[(l-x)/x] for this material, (b) Are the current carriers holes or electrons (c) Estimate the value of the constant term k/e. 

Molten Carbonate Fuel Cell The electrolyte in the MCFC is a mixture of lithium/potassium or lithium/sodium carbonates, retained in a ceramic matrix of lithium aluminate. The carbonate salts melt at about 773 K (932°F), allowing the cell to be operated in the 873 to 973 K (1112 to 1292°F) range. Platinum is no longer needed as an electrocatalyst because the reactions are fast at these temperatures. The anode in MCFCs is porous nickel metal with a few percent of chromium or aluminum to improve the mechanical properties. The cathode material is hthium-doped nickel oxide. 

Finally, Al (/= 5/2) and Co NMR spectroscopy have been used to probe AP+ in Al-doped lithium cobalt oxides and lithium nickel oxides. A Al chemical shift of 62.5 ppm was observed for the environment Al(OCo)e for an AP+ ion in the transition-metal layers, surrounded by six Co + ions. Somewhat surprisingly, this is in the typical chemical shift range expected for tetrahedral environments (ca. 60—80 ppm), but no evidence for occupancy of the tetrahedral site was obtained from X-ray diffraction and IR studies on the same materials. Substitution of the Co + by AF+ in the first cation coordination shell leads to an additive chemical shift decrease of ca. 7 ppm, and the shift of the environment A1(0A1)6 (20 ppm) seen in spectra of materials with higher A1 content is closer to that expected for octahedral Al. The spectra are consistent with a continuous solid solution involving octahedral sites randomly occupied by Al and Co. It is possible that the unusual Al shifts seen for this compound are related to the Van-Vleck susceptibility of this compound. 

Aluminium dissolves with H2 evolution, and this hydrogen remains chemisorbed on nickel, presumably in a dissociated form. Raney nickel catalysts are often doped with other metals in order to improve the catalytic activity the selectivity decreases in the order. Mo > Cr > Fe > Cu > Co. These metals are fused with the Ni-Al alloy and remain on the final catalyst, probably as oxides. It is believed that the role of the doping metals is to strengthen the selective adsorption of nitrogenous substrates. 

This is practically total above 300°C and, even at atmospheric pressure, lowers the residual CO content to less than 20 ppm and to a few ppm under pressure. It takes place in the presence of nickel base catalysts deposited on alumina and doped with chrominm oxide. The exothennicity of the reaction (Ar from 70 to 80 C/per cent CO converted) requires operation with two catalyst beds and intermediate effluent cooling. 

---