“…The lower true density of amorphous phase was related to weaker atomic binding and looser atomic configuration; therefore, plastic deformation was easier to occur in amorphous phase, which had been explained via shear banding [34], structural densification [35] and free volume theory [36,37]. As plastic deformation occurred in amorphous phase, the densification of amorphous powders was highly promoted; that was why amorphous powders could be consolidated into dense forms under moderate high pressures of 500 to 1000 MPa and low temperatures no higher than 800°C [38,39]. Besides, as the plastic deformation of amorphous particles could eliminate continuous pores [38], the particle packing was more homogenous in the amorphous bulk than in the green body of nanocrystalline powders; according to Azar [19], the better homogeneity of particle packing could promote the particles rearrangement, and were beneficial to the densification of transition powders.…”