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Nonlinear response effects in continuum models of the hydration of ions

机译:离子水化连续模型中的非线性响应效应

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The evaluation of the free energy of hydration depends essentially upon a calculation of the difference in polarization energy in a vacuum and in water. This is feasible by electrostatic continuum theory which is lucid and computationally effortless. It is, however, insufficient to apply the frequently used linear response approximation and nonlinear response effects must be integrated with the continuum model. We start from the time-honored Langevin-Debye theory and modify it to even describe polar liquids such as aqueous solvents. The modified Langevin-Debye model is then applied to study the hydration of cations. It is to be noted that reaction-field models are unapplicable to a nonlinear dielectric in an inhomogeneous field. The nonlinear effects are less than 10 kJ/mol or 2% for the monovalent ions. However, for multiply charged ions the effect can be as large as 1000 kJ/mol or 15% and the nonlinear response model reduces the mean error of the calculated hydration free energy by at least 60%, which results in a mean error of only 4% for such ions. The mean error is of the same magnitude as the electrostatic free energy uncertainty.
机译:水合自由能的评估基本上取决于真空和水中极化能差的计算。这通过清晰明了且在计算上不费力的静电连续性理论是可行的。但是,不足以应用经常使用的线性响应近似,并且非线性响应效应必须与连续模型集成。我们从历史悠久的Langevin-Debye理论开始,对其进行修改以甚至描述极性液体,例如水性溶剂。然后将修改后的Langevin-Debye模型应用于研究阳离子的水合作用。要注意的是,反应场模型不适用于非均匀场中的非线性电介质。一价离子的非线性效应小于10 kJ / mol或2%。但是,对于多电荷离子,其影响可能高达1000 kJ / mol或15%,并且非线性响应模型将计算出的水合自由能的平均误差降低了至少60%,这导致平均误差仅为4这些离子的%。平均误差的大小与静电自由能的不确定性相同。

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