Direct Visualization of Two-State Dynamics on Metallic Glass Surfaces Well Below Tg

被引:40
作者
Ashtekar, Sumit [1 ]
Scott, Gregory [1 ]
Lyding, Joseph [1 ,2 ]
Gruebele, Martin [1 ,3 ]
机构
[1] Univ Illinois, Beckman Inst Adv Sci & Technol, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
SUPERCOOLED LIQUIDS; LENGTH SCALE; RELAXATION; TEMPERATURE; MODEL;
D O I
10.1021/jz100633d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Direct atomically resolved observation of dynamics deep in the glassy regime has proved elusive for atomic and molecular glasses. Studies below the glass transition temperature T-g are especially rare due to long waiting times required to observe dynamics. Here, we directly visualize surface glass dynamics deep in the glassy regime. We analyze scanning tunneling microscopy movies of the surface of metallic glasses with time resolution as fast as 1 min and extending up to 1000 min. Rearrangements of surface clusters occur almost exclusively by two-state hopping (P3-state approximate to 0.06). All clusters are compact structures with a width of 2-8 atomic spacings along the surface plane. The two-state dynamics is both spatially and temporally heterogeneous. We estimate an average activation free energy of 14 k(B)T for surface clusters.
引用
收藏
页码:1941 / 1945
页数:5
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