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Decoupling of Component Diffusion in a Glass-Forming Zr46.75Ti8.25Cu7.5Ni10Be27.5 Melt Far above the Liquidus Temperature
被引:27
作者:
Basuki, Sri Wahyuni
[1
]
Bartsch, Alexander
[1
]
Yang, Fan
[2
]
Raetzke, Klaus
[1
]
Meyer, Andreas
[2
]
Faupel, Franz
[1
]
机构:
[1] Univ Kiel, Tech Fak, Inst Mat Wissensch, Lehrstuhl Materialverbunde, D-24143 Kiel, Germany
[2] Deutsch Zentrum Luft & Raumfahrt DLR, Inst Mat Phys Weltraum, D-51170 Cologne, Germany
关键词:
BULK METALLIC GLASSES;
SELF-DIFFUSION;
DEPENDENCE;
TRANSITION;
DYNAMICS;
VOLUME;
TIME;
D O I:
10.1103/PhysRevLett.113.165901
中图分类号:
O4 [物理学];
学科分类号:
0702 ;
摘要:
We report Zr-95 and Co-57 radiotracer diffusivities and viscosity data in the equilibrium liquid state of a bulk metallic glass forming Zr46.75Ti8.25Cu7.5Ni10Be27.5 melt (Vitreloy 4) far above the liquidus temperature T-l that are not affected by convection, as evidenced via quasielastic neutron scattering. Zr diffusion is strongly decoupled from diffusion of the smaller components by more than a factor of 4 at T-l, although it obeys the Stokes-Einstein equation. The results suggest that, in the present Zr-based metallic glass forming systems, diffusion and viscous flow start to develop solidlike, i.e., energy-landscape-controlled, features already in the stable liquid state more than 300 K above the mode coupling temperature T-c.
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