The solubility and mode of incorporation for BaO in BaTiO 3 were studied by X‐ray powder diffraction, scanning and transmission electron microscopy, electron probe microanalysis, and equilibrium electrical conductivity measurements. The presence of barium orthotitanate, Ba 2 TiO 4 , as a second phase for samples containing >0.1 mol% excess BaO was confirmed by direct microscopic examination. There was no evidence to support the incorporation of excess BaO into BaTiO 3 by a Ruddlesden‐Popper type of superlattice ordering mechanism. Measurement of the equilibrium electrical conductivity showed no detectable shift in the conductivity profile resulting from excess BaO, thus setting an upper limit of 100 ppm for the solubility of BaO in BaTiO 3 .
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Hu et al. (1985) studied this question.
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