College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University, Beijing, China.
J Phys Chem B. 2011 Nov 3;115(43):12456-65. doi: 10.1021/jp207652h. Epub 2011 Oct 11.
The higher tendency for anions to accumulate at the salt aqueous solution/air interface than that of cations has been observed experimentally and theoretically, suggesting that the size and polarizability of the ions play essential roles in this effect. Here, we investigate the influence of the nonsymmetrical positive-vs-negative charge distribution in water molecules to the hydration and surface/bulk partition of the solvated positively and negatively charged particles by using molecular dynamics simulations with hypothetical ions to validate our theoretical models. The results indicate that positive and negative charges (called cations and anions, respectively, although they may not really exist in experiments) with all other properties identical are hydrated differently and that the anions are more likely to populate at the surface. The simulation on a combination series of cations and anions in aqueous solution shows significant variations on water dynamics, likely due to the specific cooperativity between oppositely charged ions.
实验和理论都观察到阴离子在盐水溶液/空气界面处比阳离子更倾向于聚集,这表明离子的大小和极化率在这一效应中起着重要作用。在这里,我们通过使用分子动力学模拟带有假想离子的方法来研究水分子中正负电荷分布不对称性对溶剂化正、负离子水合作用和表面/体相分配的影响,以验证我们的理论模型。结果表明,尽管在实验中可能不存在真正的阳离子和阴离子,但具有相同其他性质的正电荷和负电荷(分别称为阳离子和阴离子)的水合作用不同,并且阴离子更有可能出现在表面。在水溶液中一系列阳离子和阴离子的模拟表明,水动力学有显著变化,这可能是由于相反电荷离子之间的特殊协同作用所致。