Topochemically controlled hydrogen reduction of scheelite-related rare-earth metal molybdates
Abstract
Scheelite-related α-Ln2Mo3O12(Ln = La, Pr, Nd, Sm, Gd, Tb, or Dy) oxides are reduced by hydrogen at 780–870 K yielding molybdenum (IV) oxides of formula Ln2Mo3O9. The latter crystallize in a tetragonal scheelite (ABO4) type structure where one third of the A sites and a quarter of the anion sites are vacant: Ln2/3(□cat)1/3MoO3(□an). The reaction Ln2Mo3O12+ 3H2→ Ln2Mo3O9(□an)3+ 3H2O may be regarded as topochemically controlled, since both the parent and the product phases have scheelite-related structures. Infrared spectra and electrical and magnetic properties of these metastable defect scheelite phases are reported.