CsCl-type intermetallic compounds TiM (M=Co, Fe) were obtained by deoxidizing trigonal ilmenite-type MTiO3 with a reducing agent CaH2 in molten LiCl at 600 °C. X-ray diffraction, nitrogen adsorption, scanning electron microscopy, and transmission electron microscopy with energy-dispersive X-ray, and X-ray photoelectron spectroscopy analyses revealed the formation of nanoscale layered structures, which enhanced specific surface areas (approximately 20 m2 /g) in the intermetallic compounds. In the initial deoxidation stage, Li2 TiO3 -like compounds were observed as an intermediate, suggesting the substitution of M in MTiO3 by Li from the molten LiCl. Compound MTiO3 has a layered structure perpendicular to the c axis of the trigonal structure, suggesting that the layered structures may originate from the crystal structure of the precursors. Formation of the Li2 TiO3 -like intermediate may help maintain the original layered structure during deoxidation and the subsequent alloying at temperatures as low as 600 °C.
Keywords: calcium hydride; ilmenite; intermetallic compounds; layered structures; molten salts.
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