We
carried out extensive molecular dynamics simulations of seeded
crystallization in a Lennard-Jones liquid in a wide range of supercoolings
under zero external pressure. The number of particles in the critical
crystal nucleus, n
*, the particle transport
coefficient at the liquid/nucleus interface,
, the
crystal pressure, p
s*, the crystal density, ρ
s*, and
the thermodynamic driving force, Δμ = p
s*/ρ
s*, were determined at 11 temperatures.
We used the classical nucleation theory (CNT) to calculate the effective
nucleus/liquid interfacial free energy, γe. The results
of seeded crystallization fit rather well to those of a previous work
on spontaneous crystallization and show that γe monotonically
increases with temperature. Using the physical properties determined
from the computer simulations: p
s*, ρ
s*, n
*,
, Δμ, and the
equilibrium melting temperature, we calculated the steady-state crystal
nucleation rates, J(T). The agreement
with a value determined from spontaneous nucleation was excellent,
demonstrating the validity of the CNT, as opposed to the often-reported
colossal discrepancies between the theoretical and experimental values
of nucleation rates. A key factor to explain this agreement is that
we used correct, directly determined physical parameters. In this
work, n
*(T), Δμ(T), and
obtained from the simulations were used
instead of (fitted) average interfacial energy, calculated Δμ, and other approximations, such as viscosity or
nucleation timelags, for the transport term in the analysis of experimental
nucleation rates.