Finite Size Scaling for the Glass Transition: the Role of a Static Length Scale
arXiv:1204.6634 · doi:10.1103/PhysRevE.86.061502
Abstract
Over the last decade computer simulations have had an increasing role in shedding light on difficult statistical physical phenomena and in particular on the ubiquitous problem of the glass transition. Here in a wide variety of materials the viscosity of a super-cooled liquid increases by many orders of magnitude upon decreasing the temperature over a modest range. A natural concern in these computer simulation is the very small size of the simulated systems compared to experimental ones, raising the issue of how to assess the thermodynamic limit. Here we offer a theory for the glass transition based on finite size scaling, a method that was found very useful in the context of critical phenomena and other interesting problems. As is known, the construction of such a theory rests crucially on the existence of a growing {\em static} length scale upon decreasing the temperature. We demonstrate that the static length scale that was discovered in Ref. \cite{12KLP} fits the bill extremely well, allowing us to provide a finite size scaling theory for the relaxation time of the glass transition, including predictions for the thermodynamic limit based on simulations in small systems.
6 pages and 6 figures
References in corpus (7)
- Theoretical perspective on the glass transition and amorphous materials
- Supercooled Liquids for Pedestrians
- Growing length and time scales in glass forming liquids
- Growing point-to-set length scale correlates with growing relaxation times in model supercooled liquids
- Finite size effects in the dynamics of glass-forming liquids
- The Adam-Gibbs relation for glass-forming liquids in 2, 3 and 4 dimensions
- Characterizing order in amorphous systems
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