Abstract
Although fragility of glass forming liquids is traditionally related to cooperativity in molecular motion, the connection between those parameters remains unclear. In this paper we present the estimates of cooperativity (heterogeneity) length scale ξ obtained from the boson peak spectra. We demonstrate that ξ agrees well with the dynamic heterogeneity length scale for the structural relaxation estimated by 4-dimensional NMR, justifying the use of ξ. Presented analysis of large number of materials reveals no clear correlation between ξ and fragility. However, there is a strong correlation between the cooperativity volume ξ3 and the activation volume measured at Tg. This observation suggests that only the volume (pressure) dependence of structural relaxation time correlates directly with the cooperativity size. However, the pure thermal (energetic) contribution to the structural relaxation, the so-called isochoric fragility, exhibits no correlation to the heterogeneity length scale ξ, or the amount of structural units in ξ3. The presented results call for a revision of traditional view on the role of cooperativity/heterogeneity in structural relaxation of glass forming systems.
| Original language | English |
|---|---|
| Pages (from-to) | 351-356 |
| Number of pages | 6 |
| Journal | Journal of Non-Crystalline Solids |
| Volume | 357 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 15 2011 |
Funding
We thank Puru Gujrati and Ken Schweizer for many helpful discussions. Akron team acknowledges funding from the NSF , Polymer program ( DMR-0804571 ), APS acknowledges the support from the Division of Materials Sciences and Engineering, DOE Office of Basic Energy Sciences , and VNN acknowledges the financial support from the LDRD Program of ORNL, managed by UT-Battelle, LLC, for DOE, and from the RFBR (grant no. 09-02-01297a ).
Keywords
- Cooperativity
- Fragility
- Glass transition