The theoretical model and the numerical analyses on the Gibbs-free-energy of the association states of amphiphilic molecules in nanoconfined aqueous solutions are presented in detail. We exhibit the continuous change ...The theoretical model and the numerical analyses on the Gibbs-free-energy of the association states of amphiphilic molecules in nanoconfined aqueous solutions are presented in detail. We exhibit the continuous change of the Gibbs-free-energy trend, which plays a critical role in the association states of the system transforming from the dispersion state, through the "reversible state", and finally to the aggregation state in amphiphilic molecule solutions. Furthermore, for the "reversible state", we present the difference in the free-energy barrier heights of the dispersion state and aggregation state, resulting from the competition between the entropy,which makes the solute molecules evenly disperse in the solution and the energy contribution driving the amphiphilic molecules to aggregate into a larger cluster. These findings provide a comprehensive understanding of confinement effects on the solute association processes in aqueous solutions and may further improve the techniques of material fabrication.展开更多
基金Supported by National Science Fund for Outstanding Young Scholars(No.11422542)Key Research Program of the Chinese Academy of Sciences(No.KJZD-EW-M03)+2 种基金Knowledge Innovation Program of Chinese Academy Sciencesthe High Performance Computing Center of Shanghai University(No.ZQ4000)Shanghai Supercomputer Center of China
文摘The theoretical model and the numerical analyses on the Gibbs-free-energy of the association states of amphiphilic molecules in nanoconfined aqueous solutions are presented in detail. We exhibit the continuous change of the Gibbs-free-energy trend, which plays a critical role in the association states of the system transforming from the dispersion state, through the "reversible state", and finally to the aggregation state in amphiphilic molecule solutions. Furthermore, for the "reversible state", we present the difference in the free-energy barrier heights of the dispersion state and aggregation state, resulting from the competition between the entropy,which makes the solute molecules evenly disperse in the solution and the energy contribution driving the amphiphilic molecules to aggregate into a larger cluster. These findings provide a comprehensive understanding of confinement effects on the solute association processes in aqueous solutions and may further improve the techniques of material fabrication.
