Loading…

Liquid–liquid critical point in supercooled silicon

The full phase diagram of supercooled silicon has not been accessible experimentally, so the critical behaviour is highly debated. Numerical simulations now reveal a liquid–liquid critical end-point at negative pressure. This study further supports the similarity between silicon and water. A novel l...

Full description

Saved in:
Bibliographic Details
Published in:Nature physics 2011-07, Vol.7 (7), p.549-553
Main Authors: Vasisht, Vishwas V., Saw, Shibu, Sastry, Srikanth
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The full phase diagram of supercooled silicon has not been accessible experimentally, so the critical behaviour is highly debated. Numerical simulations now reveal a liquid–liquid critical end-point at negative pressure. This study further supports the similarity between silicon and water. A novel liquid–liquid phase transition has been investigated for a wide variety of pure substances, including water, silica and silicon. From computer simulations using the Stillinger–Weber (SW) classical empirical potential, Sastry and Angell 1 demonstrated a first order liquid–liquid transition in supercooled silicon at zero pressure, supported by subsequent experimental and simulation studies. Whether the line of such first order transitions will terminate at a critical point, expected to lie at negative pressures, is presently a matter of debate 2 . Here we report evidence for a liquid–liquid critical point at negative pressures, from computer simulations using the SW potential. We identify T c ∼1,120±12 K, P c ∼−0.60±0.15 GPa as the critical temperature and pressure. We construct the phase diagram of supercooled silicon, which reveals the interconnection between thermodynamic anomalies and the phase behaviour of the system as suggested in previous works 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 . We also observe a strong relationship between local geometry (quantified by the coordination number) and diffusivity, both of which change dramatically with decreasing temperature and pressure.
ISSN:1745-2473
1745-2481
DOI:10.1038/nphys1993