Abstract
Layered HLnTiO4 (Ln=La, Nd) compounds belonging to Ruddlesden–Popper phases were found to form partially hydrated compounds Ln2Ti2O7·xH2O during thermal dehydration as well as defect oxides Ln2□Ti2O7 as final products. Further heating of metastable defect Ln2□Ti2O7 substances leads to the formation of pyrochlore-type oxides Ln2Ti2O7 (p), with subsequent transformation under higher temperatures to stable layered 110-type perovskites Ln2Ti2O7. The occurring structure transformations lead to an increase of photocatalytic activity in the order of HLnTiO4<Ln2Ti2O7·yH2O<Ln2□Ti2O7<Ln2Ti2O7 (p)<Ln2Ti2O7 in the reaction of hydrogen evolution from aqueous isopropanol solution.
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