Abstract
Hydrogen diffusion processes in nonstoichiometric scandium hydrides have been investigated using transient nuclear-magnetic-resonance methods. Activation energies (EA) were found to be strongly concentration dependent with two processes becoming evident as the hydrogen-to-metal ratio (x) approached 2. The variation of EA with x is interpreted as an effect of non-rigid-band behavior for the electron states. Both relaxation-time analysis and rigid-lattice linewidths suggest appreciable occupation of octahedral sites normally vacant in other dihydrides.