摘要
A mechanochemical activation route has been applied in order to obtain the n = 1–4 and ∞ members of the Sr2[Srn − 1TinO3n + 1] Ruddlesden–Popper series from different (n + 1)SrO:nTiO2 mixtures. The mechanosynthesis of SrTiO3 and Sr2TiO4 was observed during the milling process from the initial stoichiometric mixture, but in the cases of the n = 2–4 members, a subsequent thermal treatment was needed. The synthesis protocol of Sr3Ti2O7 has been greatly improved and this compound can be isolated as a single, crystalline phase after annealing at 800 °C. In the case of Sr4Ti3O10 and Sr5Ti4O13, the formation temperature was also decreased, but members with n = 3 and 4 could not be isolated. Detailed investigations using electron microscopy methods (TEM, HREM and SAED) were carried out in the samples corresponding to n = 2–4. Although a single ordered Sr3Ti2O7 structure is dominant in the sample corresponding to n = 2, a few intergrowths of other Ruddlesden–Popper phases were observed. In the cases of n = 3 and 4, the intergrowths of Ruddlesden–Popper phases are more frequent than in the n = 2 composition and are randomly distributed in the sample. The more frequent occurrence of such stacking faults, with increasing n value, leads to a somewhat disordered layer stacking sequence.