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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Sollich, Peter
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (17/17 displayed)
- 2022Delayed elastic contributions to the viscoelastic response of foamscitations
- 2018On the existence of thermodynamically stable rigid solidscitations
- 2017Aging and linear response in the Hébraud–Lequeux model for amorphous rheologycitations
- 2015Non-affine fluctuations and the statistics of defect precursors in the planar honeycomb latticecitations
- 2012Unified study of glass and jamming rheology in soft particle systemscitations
- 2006Simulation estimates of cloud points of polydisperse fluids
- 2006Simulation estimates of cloud points of polydisperse fluidscitations
- 2006Phase behavior of weakly polydisperse sticky hard spheres: Perturbation theory for the Percus-Yevick solution
- 2005Effects of polymer polydispersity on the phase behaviour of colloid-polymer mixturescitations
- 2005Dynamic Heterogeneity in the Glauber-Ising chain
- 2005Liquid-vapour phase behaviour of a polydisperse Lennard-Jones fluidcitations
- 2005Effects of colloid polydispersity on the phase behavior of colloid-polymer mixturescitations
- 2003Fluctuation-dissipation relations in the nonequilibrium critical dynamics of Ising modelscitations
- 2003Equivalence of driven and aging fluctuation-dissipation relations in the trap modelcitations
- 2002Observable dependence of fluctuation-dissipation relations and effective temperaturescitations
- 2001Predicting phase equilibria in polydisperse systemscitations
- 2000Aging and rheology in soft materialscitations
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article
On the existence of thermodynamically stable rigid solids
Abstract
Customarily, crystalline solids are defined to be rigid since they resist changes of shape determined by their boundaries. However, rigid solids cannot exist in the thermodynamic limit where boundaries become irrelevant. Particles in the solid may rearrange to adjust to shape changes eliminating stress without destroying crystalline order. Rigidity is therefore valid only in the metastable state that emerges because these particle rearrangements in response to a deformation, or strain, are associated with slow collective processes. Here, we show that a thermodynamic collective variable may be used to quantify particle rearrangements that occur as a solid is deformed at zero strain rate. Advanced Monte Carlo simulation techniques are then used to obtain the equilibrium free energy as a function of this variable. Our results lead to a unique view on rigidity: While at zero strain a rigid crystal coexists with one that responds to infinitesimal strain by rearranging particles and expelling stress, at finite strain the rigid crystal is metastable, associated with a free energy barrier that decreases with increasing strain. The rigid phase becomes thermodynamically stable when an external field, which penalizes particle rearrangements, is switched on. This produces a line of first-order phase transitions in the field–strain plane that intersects the origin. Failure of a solid once strained beyond its elastic limit is associated with kinetic decay processes of the metastable rigid crystal deformed with a finite strain rate. These processes can be understood in quantitative detail using our computed phase diagram as reference.