Citation
Gw. Yang et al., Phase evolution in Ni-Nb multilayers upon solid-state reaction, J MATER RES, 14(7), 1999, pp. 3027-3036
Abstract
Solid-state amorphization was achieved in the Ni,,Nb,, multilayers upon the
rmal annealing by gradually raising the temperature from 250 to 400 degrees
C and staying at 400 degrees C for 2 h. More interestingly, before complet
e amorphization, a sequential disordering of first Ni and then Nb crystalli
ne lattices was observed for the first time, and it was essentially the phy
sical origin of an asymmetric growth of the amorphous interlayer during sol
id-state reaction reported previously in some binary metal systems. In anot
her two multilayered samples with overall compositions of Ni64Nb36 and Ni70
Nb30, thermal annealing under similar conditions resulted in the formation
of two metastable crystalline phases with face-centered-cubic and hexagonal
-close-packed structures, respectively, although an amorphous phase also ap
peared and coexisted with one of the metastable crystalline phases in the i
ntermediate states. In the ion mixing experiment, such sequential disorderi
ng, as well as formation of metastable phases, was also observed in the res
pective Ni-Nb multilayers upon room-temperature 200-keV xenon ion irradiati
on. Comparatively, however, ion irradiation eventually induced complete amo
rphization in all the multilayers at the respective doses, indicating that
ion-induced disordering frequently predominated in the competition between
amorphization and the growth of a metastable crystalline phase. A Gibbs fre
e energy diagram, including the free energy curves of the newly formed meta
stable crystalline phases, of the Ni-Nb system was calculated based on Mied
ema's model. The constructed free energy diagram can give reasonable explan
ations of the sequential disordering and the thermodynamic possibility of t
he formation of either an amorphous or a metastable crystalline phase, of w
hich the free energy difference was quite small. It follows naturally that
the phase selection, namely, which phase was more favored to be formed even
tually than its competitors, was influenced or even determined by the kinet
ics involved in the respective processes.