Abstract
Hydrated rare earth hexaborates H3LnB6O12 (Ln = Sm−Lu) have been synthesized by using molten boric acid as the reaction medium. H3LnB6O12 decomposes at certain temperatures to form anhydrous pentaborates LnB5O9 (Ln = Sm−Er) or orthoborates LnBO3 (Ln = Tm−Lu). The crystal structures of the hexaborates and pentaborates have been determined by single-crystal and powder diffraction techniques. The hydrated hexaborates H3LnB6O12 crystallize in a trigonal structure in the space group R3c, which contain a six-membered ring B6O15 as a fundamental fragment. Anhydrous pentaborates LnB5O9 crystallize in a tetragonal structure that is built up with B4O9 and BO3. LnB5O9 decomposes at higher temperature to metaborates (Ln = Sm−Tb) and orthoborates (Ln = Dy−Er). A phase diagram is presented that shows the stable range of both H3LnB6O12 and LnB5O9. The luminescent property of the europium-doped GdB5O9 was studied.
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