ISEL - Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de Lisboa, Rua Conselheiro Emídio Navarro 1, P-1959-007 Lisbon, Portugal and Centro de Física Teórica e Computacional, Faculdade de Ciências da Universidade de Lisboa Campo Grande, Edifício C8, P-1749-016 Lisbon, Portugal.
Dipartimento di Fisica and CNR-ISC, Università di Roma La Sapienza, Piazzale Moro 5, I-00185 Rome, Italy.
J Chem Phys. 2019 Nov 7;151(17):174903. doi: 10.1063/1.5124008.
The well-known and widely used Wertheim thermodynamic perturbation theory (TPT) of associating fluids averages over the orientational dependence of the bonding interactions. For this reason, density functional theories based on the otherwise very successful TPT have been unable to describe the structure of patchy particle fluids at hard walls, when the coupling of positional and orientational degrees of freedom becomes important at low temperatures [N. Gnan et al., J. Chem. Phys. 137, 084704 (2012)]. As a first attempt at remedying this, we propose to introduce into the theory an additional, nonbonding, anisotropic interparticle potential that enforces end-to-end alignment of two-patch particles. Within the simplest mean-field approximation, this additional potential does not change the thermodynamics of the bulk system and hence preserves its phase diagram but has the qualitatively correct effect on the order parameter and density profiles at a hard wall, as determined from computer simulation.
广为人知且应用广泛的缔合流体的 Wertheim 热力学摄动理论(TPT)对键相互作用的方向依赖性进行了平均处理。出于这个原因,基于 otherwise very successful TPT 的密度泛函理论一直无法描述在硬壁处的斑粒子流体的结构,当位置和方向自由度的耦合在低温下变得重要时 [N. Gnan 等人,J. Chem. Phys. 137, 084704 (2012)]。作为对此问题的首次尝试,我们建议在理论中引入额外的、非键合的各向异性粒子间相互作用势能,以强制两斑粒子的端到端对齐。在最简单的平均场近似下,这个额外的势能不会改变体相系统的热力学,因此保留了其相图,但对硬壁处的序参量和密度分布有定性上正确的影响,这是通过计算机模拟确定的。