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Perovskite disordered

There is often a wide range of crystalline soHd solubiUty between end-member compositions. Additionally the ferroelectric and antiferroelectric Curie temperatures and consequent properties appear to mutate continuously with fractional cation substitution. Thus the perovskite system has a variety of extremely usehil properties. Other oxygen octahedra stmcture ferroelectrics such as lithium niobate [12031 -63-9] LiNbO, lithium tantalate [12031 -66-2] LiTaO, the tungsten bron2e stmctures, bismuth oxide layer stmctures, pyrochlore stmctures, and order—disorder-type ferroelectrics are well discussed elsewhere (4,12,22,23). [Pg.205]

The ternary Ge halides, MGeX3 (M = Rb, Cs X = Cl, Br, I) are polymorphic with various distorted perovskite-like (p. 963) structures which reflect the influence of the nonbonding pair of electrons on the Ge" centre. Thus, at room temperature, rhombohedral CsGel3 has three Ge-I at 275 pm and three at 327 pm whereas in the high-temperature cubic form (above 277°C) there are six Ge-I distances at 320 pm as a result of position changes of the Ge atoms (reversible order-disorder transition). Again, RbGel3 has a lemon-yellow, orthorhombic form below —92° an intermediate, bordeaux-red orthorhombic perovskite form (—92° to —52°) a black rhombohedral form (—52° to —29°) and... [Pg.376]

Blinc R (2007) Order and Disorder in Perovskites and Relaxor Ferroelectrics. 124 51-67 Boca R (2005) Magnetic Parameters and Magnetic Functions in Mononuclear Complexes Beyond the Spin-Hamiltonian Formalism 117 1-268 Bohrer D, see Schetinger MRC (2003) 104 99-138 Bonnet S, see Baranoff E (2007) 123 41-78... [Pg.219]

The oxide Ba2In205 is another well-studied phase that adopts the brownmillerite structure. This material disorders above 930°C to a perovskite-type structure containing oxygen vacancies. Both the Sr-Fe and Ba-In oxides are of interest for electrochemical applications in fuel cells and similar devices (Section 6.10). [Pg.190]

The disordered structure can be stabilized to room temperature by inclusion of substitutional impurities on the In sites. Thus the oxide formed when Ga is substituted for In, Ba2(ln1 xGaJt-)205+s to form Galn defects has a disordered cubic perovskite structure even at room temperature for values of x between 0.25 and 0.5, and the similar Ba2iln1 vCox)205+3 with Coin defects has a disordered cubic perovskite structure at room temperature when x lies between 0.2 and 0.8. The defects present in the In sites hinder oxygen ordering during the timescale over which the samples cool from the... [Pg.279]

Classical relaxors [22,23] are perovskite soUd solutions like PbMgi/3Nb2/303 (PMN), which exhibit both site and charge disorder resulting in random fields in addition to random bonds. In contrast to dipolar glasses where the elementary dipole moments exist on the atomic scale, the relaxor state is characterized by the presence of polar clusters of nanometric size. The dynamical properties of relaxor ferroelectrics are determined by the presence of these polar nanoclusters [24]. PMN remains cubic to the lowest temperatures measured. One expects that the disorder -type dynamics found in the cubic phase of BaTiOs, characterized by two timescales, is somehow translated into the... [Pg.61]


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See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.6 , Pg.10 ]




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Ordering and Anti-Site (AS) Disorder in Double Perovskites

Relaxor ferroelectrics disordered complex perovskites

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