The energy landscape of glassy dynamics on the amorphous hafnium diboride surface

被引:8
|
作者
Duc Nguyen [1 ,2 ]
Mallek, Justin [1 ]
Cloud, Andrew N. [3 ]
Abelson, John R. [3 ]
Girolami, Gregory S. [1 ,2 ]
Lyding, Joseph [2 ,4 ]
Gruebele, Martin [1 ,2 ,5 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Beckman Inst, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[5] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 141卷 / 20期
基金
美国国家科学基金会;
关键词
MODE-COUPLING THEORY; SUPERCOOLED LIQUIDS; STRUCTURAL GLASSES; TRANSITION; RELAXATION; FILMS; VIEW;
D O I
10.1063/1.4901132
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Direct visualization of the dynamics of structural glasses and amorphous solids on the sub-nanometer scale provides rich information unavailable from bulk or conventional single molecule techniques. We study the surface of hafnium diboride, a conductive ultrahigh temperature ceramic material that can be grown in amorphous films. Our scanning tunneling movies have a second-to-hour dynamic range and single-point current measurements extend that to the millisecond-to-minute time scale. On the a-HfB2 glass surface, two-state hopping of 1-2 nm diameter cooperatively rearranging regions or "clusters" occurs from sub-milliseconds to hours. We characterize individual clusters in detail through high-resolution (<0.5 nm) imaging, scanning tunneling spectroscopy and voltage modulation, ruling out individual atoms, diffusing adsorbates, or pinned charges as the origin of the observed two-state hopping. Smaller clusters are more likely to hop, larger ones are more likely to be immobile. HfB2 has a very high bulk glass transition temperature T-g, and we observe no three-state hopping or sequential two-state hopping previously seen on lower T-g glass surfaces. The electronic density of states of clusters does not change when they hop up or down, allowing us to calibrate an accurate relative z-axis scale. By directly measuring and histogramming single cluster vertical displacements, we can reconstruct the local free energy landscape of individual clusters, complete with activation barrier height, a reaction coordinate in nanometers, and the shape of the free energy landscape basins between which hopping occurs. The experimental images are consistent with the compact shape of alpha-relaxors predicted by random first order transition theory, whereas the rapid hopping rate, even taking less confined motion at the surface into account, is consistent with beta-relaxations. We make a proposal of how "mixed" features can show up in surface dynamics of glasses. (C) 2014 AIP Publishing LLC.
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页数:10
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