Journal
PHYSICAL REVIEW LETTERS
Volume 126, Issue 18, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.126.188002
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Funding
- Schmidt Science Fellowship
- Rhodes Trust
- U.S. Department of Energy, Office of Basic Energy Sciences, through the Chemical Sciences Division (CSD) of Lawrence Berkeley National Laboratory (LBNL) [DE-AC02-05CH11231]
- NVIDIA Corporation
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For three-dimensional active Brownian particles, it has been found that metastable states of motility-induced phase separation (MIPS) coexistence decay over long times through an ordering transition called active crystallization. At activity levels just above the MIPS critical point, the liquid-gas binodal is superseded by the crystal-fluid coexistence curve, with solid, liquid, and gas all coexisting at the triple point. Nucleating an active crystal from a disordered fluid requires rare fluctuations exhibiting close-packed density of the solid phase.
Motility-induced phase separation (MIPS), the phenomenon in which purely repulsive active particles undergo a liquid-gas phase separation, is among the simplest and most widely studied examples of a nonequilibrium phase transition. Here, we show that states of MIPS coexistence are in fact only metastable for three-dimensional active Brownian particles over a very broad range of conditions, decaying at long times through an ordering transition we call active crystallization. At an activity just above the MIPS critical point, the liquid-gas binodal is superseded by the crystal-fluid coexistence curve, with solid, liquid, and gas all coexisting at the triple point where the two curves intersect. Nucleating an active crystal from a disordered fluid, however, requires a rare fluctuation that exhibits the nearly close-packed density of the solid phase. The corresponding barrier to crystallization is surmountable on a feasible timescale only at high activity, and only at fluid densities near maximal packing. The glassiness expected for such dense liquids at equilibrium is strongly mitigated by active forces, so that the lifetime of liquid-gas coexistence declines steadily with increasing activity, manifesting in simulations as a facile spontaneous crystallization at extremely high activity.
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