TY - JOUR
T1 - Liquid nucleation around charged particles in the vapor phase
AU - Kroll, Roni
AU - Tsori, Yoav
N1 - Funding Information:
This work was supported by the Israel Science Foundation (ISF) Grant No. 274/19.
Publisher Copyright:
© 2021 Author(s).
PY - 2021/11/7
Y1 - 2021/11/7
N2 - We theoretically investigate the nucleation of liquid droplets from vapor in the presence of a charged spherical particle. Due to field gradients, sufficiently close to the critical point of the vapor-gas system, the charge destabilizes the vapor phase and initiates a phase transition. The fluid's free energy is described by the van der Waals expression augmented by electrostatic energy and a square-gradient term. We calculate the equilibrium density profile at arbitrary temperatures, particle charges, and vapor densities. In contrast to classical nucleation theory, here, both liquid and vapor phases are different from the bulk phases because they are spatially nonuniform. In addition, the theory applies to both sharp and diffuse interfaces and calculates the surface tension self-consistently. We find the composition profiles and integrate them to get the adsorption near the particle. We find that the adsorption changes discontinuously at a first-order phase transition line. This line becomes a second-order phase transition at high enough temperatures. We describe the transition point numerically and provide approximate analytical expressions for it. Similarly to prewetting, the adsorption diverges at the binodal phase boundary. We construct a phase diagram indicating changes in the binodal, spinodal, and critical temperature. It is shown that the field gradient enlarges the range of temperature and vapor density where liquid can nucleate.
AB - We theoretically investigate the nucleation of liquid droplets from vapor in the presence of a charged spherical particle. Due to field gradients, sufficiently close to the critical point of the vapor-gas system, the charge destabilizes the vapor phase and initiates a phase transition. The fluid's free energy is described by the van der Waals expression augmented by electrostatic energy and a square-gradient term. We calculate the equilibrium density profile at arbitrary temperatures, particle charges, and vapor densities. In contrast to classical nucleation theory, here, both liquid and vapor phases are different from the bulk phases because they are spatially nonuniform. In addition, the theory applies to both sharp and diffuse interfaces and calculates the surface tension self-consistently. We find the composition profiles and integrate them to get the adsorption near the particle. We find that the adsorption changes discontinuously at a first-order phase transition line. This line becomes a second-order phase transition at high enough temperatures. We describe the transition point numerically and provide approximate analytical expressions for it. Similarly to prewetting, the adsorption diverges at the binodal phase boundary. We construct a phase diagram indicating changes in the binodal, spinodal, and critical temperature. It is shown that the field gradient enlarges the range of temperature and vapor density where liquid can nucleate.
UR - http://www.scopus.com/inward/record.url?scp=85118774356&partnerID=8YFLogxK
U2 - 10.1063/5.0067249
DO - 10.1063/5.0067249
M3 - Article
C2 - 34742214
AN - SCOPUS:85118774356
SN - 0021-9606
VL - 155
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 17
M1 - 174101
ER -