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Title: Stress-induced amorphization at moving crack tips in NiTi

Journal Article · · Applied Physics Letters
DOI:https://doi.org/10.1063/1.121904· OSTI ID:639049
; ;  [1]; ; ;  [2];  [3]
  1. Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States)
  2. Department of Materials Engineering, Hokkaido University, Sapporo (Japan)
  3. Department of Nuclear Engineering, University of Illinois, Urbana, Illinois 61801 (United States)

{ital In situ} fracture studies have been carried out on thin films of the NiTi intermetallic compound under plane stress, tensile loading conditions in the high-voltage electron microscope. Local stress-induced amorphization of regions directly in front of moving crack tips has been observed. The upper cutoff temperature, T{sub C{endash}A}{sup max}, for the stress-induced crystalline-to-amorphous transformation was found to be 600 K, identical to that for heavy ion-induced amorphization of NiTi and for ion-beam mixing-induced amorphization of Ni and Ti multilayer specimens. 600 K is also both the lower cutoff temperature, T{sub A{endash}C}{sup min}, for radiation-induced crystallization of initially-unrelaxed amorphous NiTi and the lowest isothermal annealing temperature, T{sub X}{sup min}, at which stress-induced amorphous NiTi crystallizes. Since T{sub X}{sup min} should be T{sub K}, the ideal glass transition temperature, the discovery that T{sub C{endash}A}{sup max}=T{sub A{endash}C}{sup min}=T{sub X}{sup min}=T{sub K} implies that disorder-driven crystalline-to-amorphous transformations result in the formation of the ideal glass, i.e., the glassy state that has the same entropy as that of the defect-free crystal. As the glassy state with the lowest free energy, its formation can be understood as the most energetically-favored, kinetically-constrained response of crystalline alloys driven far from equilibrium. {copyright} {ital 1998 American Institute of Physics.}

OSTI ID:
639049
Journal Information:
Applied Physics Letters, Vol. 73, Issue 4; Other Information: PBD: Jul 1998
Country of Publication:
United States
Language:
English