Journal
PHYSICAL REVIEW B
Volume 68, Issue 13, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.68.134107
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Single crystals of the entire series of A(2)Ti(2)O(7) (A=Sm to Lu, and Y) pyrochlore compounds were irradiated by 1-MeV Kr+ ions at temperatures from 293 to 1073 K, and the microstructure evolution, as a function of increasing radiation fluence, was characterized using in situ transmission electron microscopy (TEM). The critical amorphization temperature, T-c, generally increases from similar to480 to similar to1120 K with increasing A-site cation size (e.g., 0.977 Angstrom for Lu3+ to 1.079 Angstrom for Sm3+). An abnormally high susceptibility to ion beam damage was found for Gd2Ti2O7 (with the highest T-c of similar to1120 K). Factors influencing the response of titanate pyrochlores to ion irradiation-induced amorphization are discussed in terms of cation radius ratio, defect formation, and the tendency to undergo an order-disorder transition to the defect-fluorite structure. The resistance of the pyrochlore structure to ion beam-induced amorphization is not only affected by the relative sizes of the A- and B-site cations, but also the cation electronic configuration and the structural disorder. Pyrochlore compositions that have larger structural deviations from the ideal fluorite structure, as evidenced by the smaller 48f oxygen positional parameter, x, are more sensitive to ion beam-induced amorphization.
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