Doping stability

Conceptually elegant, the SOFC nonetheless contains inherently expensive materials, such as an electrolyte made from zirconium dioxide stabilized with yttrium oxide, a strontium-doped lanthanum man-gaiiite cathode, and a nickel-doped stabilized zirconia anode. Moreover, no low-cost fabrication methods have yet been devised. 

Material Doping with Conductivity Maximum Doping Stability in Air... 

Random co-polymers of methyl and octyl thiophenes were prepared electrochemically by Pei et al. [101] with the purpose of checking the thermal dedoping behaviour of such materials, based on the idea that long and short side chains simultaneously present should create additional space for the dopant molecules. It was found that the doping stability is intermediate between that of the parent polymers, and depends on the composition. Sfructural studies of the materials were not performed. 

Despite the increased free volume of the PHT-POT mixture, their doping stability turns out to be not enhanced over the stability of the individual PHT and POT [101]. 

Recent research efforts have been focused on the synthesis of doped, stabilized zirconia powders, especially with nanometer-sized particles. Nanocrystalline stabilized powders are vital for the preparation of nanocrystalline materials, as their properties are fundamentally different from those of conventional powders, due to the extremely small crystalline dimension, superior phase homogeneity and low-temperature sinterabUity that significantly determines the later-stage processing and sintering properties of ceramics. 

Rahman MS, Pal U, Choudhury AK, Maiti S (1991) New conducting polymers, 3. Doping, stability, electrical, and optical characteristics of poly-(p-phenylphosphoethynediyl). Colloid Polym Sci 269 576-582... 

The polymer had a A ,ax of 546 nm in the solid state and 462 nm in a chloroform solution, and an of 1 X 1 O. The Amax values indicated that poly(43) was highly conjugated. Conductivity of iodine-doped polymer was 100 S cm and the doped state would be stable for 10-20 years. This high doping stability was explained in terms of free-volume theory by Inganas [42]. The third order susceptibility (3oj co, CO, (o) was measured to be (4.3 1) x 10 esu on an... 

SDZ scandium-doped zirconia (Zr02)i-x(Sc203) c YSZ yttrium-doped (stabilized) zirconia (Zr02)i- c(Y203) t ... 

The result is the formation of a dense and uniform metal oxide layer in which the deposition rate is controlled by the diffusion rate of ionic species and the concentration of electronic charge carriers. This procedure is used to fabricate the thin layer of soHd electrolyte (yttria-stabilized 2irconia) and the interconnection (Mg-doped lanthanum chromite). 

The performance of many metal-ion catalysts can be enhanced by doping with cesium compounds. This is a result both of the low ionization potential of cesium and its abiUty to stabilize high oxidation states of transition-metal oxo anions (50). Catalyst doping is one of the principal commercial uses of cesium. Cesium is a more powerflil oxidant than potassium, which it can replace. The amount of replacement is often a matter of economic benefit. Cesium-doped catalysts are used for the production of styrene monomer from ethyl benzene at metal oxide contacts or from toluene and methanol as Cs-exchanged zeofltes ethylene oxide ammonoxidation, acrolein (methacrolein) acryflc acid (methacrylic acid) methyl methacrylate monomer methanol phthahc anhydride anthraquinone various olefins chlorinations in low pressure ammonia synthesis and in the conversion of SO2 to SO in sulfuric acid production. 

Another application is in tire oxidation of vapour mixtures in a chemical vapour transport reaction, the attempt being to coat materials with a tlrin layer of solid electrolyte. For example, a gas phase mixture consisting of the iodides of zirconium and yttrium is oxidized to form a thin layer of ytnia-stabilized zirconia on the surface of an electrode such as one of the lanthanum-snontium doped transition metal perovskites Lai j.Srj.M03 7, which can transmit oxygen as ions and electrons from an isolated volume of oxygen gas. 

The polymers which have stimulated the greatest interest are the polyacetylenes, poly-p-phenylene, poly(p-phenylene sulphide), polypyrrole and poly-1,6-heptadiyne. The mechanisms by which they function are not fully understood, and the materials available to date are still inferior, in terms of conductivity, to most metal conductors. If, however, the differences in density are taken into account, the polymers become comparable with some of the moderately conductive metals. Unfortunately, most of these polymers also have other disadvantages such as improcessability, poor mechanical strength, instability of the doped materials, sensitivity to oxygen, poor storage stability leading to a loss in conductivity, and poor stability in the presence of electrolytes. Whilst many industrial companies have been active in their development (including Allied, BSASF, IBM and Rohm and Haas,) they have to date remained as developmental products. For a further discussion see Chapter 31. 

An alternative approach to stabilizing the metallic state involves p-type doping. For example, partial oxidation of neutral dithiadiazolyl radicals with iodine or bromine will remove some electrons from the half-filled level. Consistently, doping of biradical systems with halogens can lead to remarkable increases in conductivity and several iodine charge transfer salts exhibiting metallic behaviour at room temperature have been reported. However, these doped materials become semiconductors or even insulators at low temperatures. 

Singh, D.J., 1988, Electronic structure, magnetism and stability of Co-doped NiAl, Phys. Rev. B 46 14392. Vvedensky, D.D., 1992, Theory of X-ray absorption fine structure, in Unoccupied electronic states fundamentals ofXANES, EELS, IPS and BIS, Topics in Applied Physics, Vol. 69, J.C. Euggle and J.E. Inglesfiels, eds. Springer, Berlin. 

Polyacetylene is considered to be the prototypical low band-gap polymer, but its potential uses in device applications have been hampered by its sensitivity to both oxygen and moisture in its pristine and doped states. Poly(thienylene vinylene) 2 has been extensively studied because it shares many of the useful attributes of polyacetylene but shows considerably improved environmental stability. The low band gap of PTV and its derivatives lends itself to potential applications in both its pristine and highly conductive doped state. Furthermore, the vinylene spacers between thiophene units allow substitution on the thiophene ring without disrupting the conjugation along the polymer backbone. 

The investigation of the stability of P -alumina in ZEBRA cells, which always contain some iron, showed an increase of resistance under certain extreme conditions of temperature (370 °C) and of voltage. This is related to the interaction of the P alumina with iron and it was shown that iron enters / -alumina in the presence of an electric field when current is passing, if the cell is deliberately overheated. However, it was found that only the P -phase but not the P"-phase was modified by the incursion of iron. The resistance of the iron-doped regions was high. It was shown that the addition of NaF inhibits access of the iron to the / " -alumina ceramic. By doping practical cells these difficulties have now been overcome and lifetime experiments show that the stability of / "-alumina electrolytes are excellent in ZEBRA cells. 

The stoichiometry of the redox reactions of conducting polymers (n and m in reactions 1 and 2) is quite variable. Under the most widely used conditions, polypyrroles and polythiophenes can be reversibly oxidized to a level of one hole per ca. 3 monomer units (i.e., a degree of oxidation, n, of ca. 0.3).7 However, this limit is dictated by the stability of the oxidized film under the conditions employed (Section V). With particularly dry and unreactive solvents, degrees of oxidation of 0.5 can be reversibly attained,37 and for poly-(4,4 -dimethoxybithiophene), a value of n = 1 has been reported.38 Although much fewer data are available for n-doping, it appears to involve similar stoichiometries [i.e., m in Eq. (2) is typically ca. 0.3].34,39"41 Polyanilines can in principle be reversibly p-doped to one... 

Today, the term solid electrolyte or fast ionic conductor or, sometimes, superionic conductor is used to describe solid materials whose conductivity is wholly due to ionic displacement. Mixed conductors exhibit both ionic and electronic conductivity. Solid electrolytes range from hard, refractory materials, such as 8 mol% Y2C>3-stabilized Zr02(YSZ) or sodium fT-AbCb (NaAluOn), to soft proton-exchange polymeric membranes such as Du Pont s Nafion and include compounds that are stoichiometric (Agl), non-stoichiometric (sodium J3"-A12C>3) or doped (YSZ). The preparation, properties, and some applications of solid electrolytes have been discussed in a number of books2 5 and reviews.6,7 The main commercial application of solid electrolytes is in gas sensors.8,9 Another emerging application is in solid oxide fuel cells.4,5,1, n... 

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