Ion-specific effects in aqueous solution, known as the Hofmeister effect, are prevalent in diverse systems ranging from pure ionic to complex protein solutions. The objective of this paper is to explicitly demonstrate how complex ion-ion and ion-water interactions manifest themselves in the Hofmeister effect based on a series of recent experimental observations. These effects are not considered in the classical descriptions of ion effects, such as the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, and therefore they fail to describe the origin of the phenomenological Hofmeister effect. However, given that models considering the basic forces of electrostatic and van der Waals interactions can offer rationalization for the core experimental observations, a universal interaction model stands a chance of being developed. In this perspective, we separately derive the contribution from ion-ion electrostatic interactions and ion-water interactions from second harmonic generation (SHG) data at the air-ion solution interface, which yields an estimate of the ion-water interactions in solution. The Hofmeister ion effect observed for biological solutes in solution should be similarly influenced by contributions from ion-ion and ion-water interactions, where the same ion-water interaction parameters derived from SHG data at the air-ion solution interface could be applicable. A key experimental data set available from solution systems to probe ion-water interactions is the modulation of water diffusion dynamics near ions in a bulk ion solution, as well as near biological liposome surfaces. This is obtained from Overhauser dynamic nuclear polarization (ODNP), a nuclear magnetic resonance (NMR) relaxometry technique. The surface water diffusivity is influenced by the contribution from ion-water interactions, both from localized surface charges and adsorbed ions, although the relative contribution of the former is larger on liposome surfaces. In this perspective, ion-water interaction energy values derived from experimental data for various ions are compared with theoretical values in the literature. Ultimately, quantifying ion-induced changes in the surface energy for the purpose of developing valid theoretical models for ion-water interactions will be critical to rationalizing the Hofmeister effect.
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http://dx.doi.org/10.1039/c4cp05992a | DOI Listing |
ACS Nano
January 2025
Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Solar water evaporation (SWE) has emerged as an appealing method for water and salt recovery from hypersaline wastewater. However, different ions usually transfer and accumulate uncontrollably during ion-water separation, making salt fractionalization impractical for conventional SWE, and the resulting mixed salts are hard to use and still require significant costs for disposal. To achieve salt fractionalization and reutilization, achieving ion-water and ion-ion separation simultaneously are crucial in advancing SWE toward sustainability.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
School of Physical Science and Technology, ShanghaiTech University, 393 Middle Huaxia Road, Shanghai 201210, China.
Hydration in Mg solutions is critical in the chemical and biological industries. Researchers have identified a rigid first hydration shell, but the effects of ion-water and hydrogen bonding (HB) interactions beyond the first shell of Mg, especially when ion pairs form at high concentrations, remain controversial. On the basis of density functional theory, machine learning molecular dynamics was performed to study the second shell of Mg in MgCl solutions at various concentrations.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Dpto. Química Física I, Fac. Ciencias Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain.
The Madrid-2019 force field was recently developed to perform simulations of electrolytes in water. The model was specifically parameterized for TIP4P/2005 water and uses scaled charges for the ions. In this work, we test the compatibility of the Madrid-2019 force field with another water model: TIP4P/Ice.
View Article and Find Full Text PDFJ Chem Phys
December 2024
State Key Laboratory of Multiphase Flow in Power Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, China.
Comprehending the flow dynamics of ionic solutions within nanoconfined spaces is imperative for diverse applications encompassing desalination, nanofiltration, energy storage, and electrochemical devices. When the confinement space is further reduced to 1 nm (Ångstrom scale), monolayer ionic solutions will emerge. In this regime, ions not only have the ability to influence water properties such as viscosity but also primarily modify the interactions and corresponding slip length (or friction coefficient) between the solution and wall.
View Article and Find Full Text PDFChem Sci
December 2024
Department of Chemistry & Biochemistry, The Ohio State University 151 W. Woodruff Ave. Columbus Ohio 43210 USA
The many-body expansion is a fragment-based approach to large-scale quantum chemistry that partitions a single monolithic calculation into manageable subsystems. This technique is increasingly being used as a basis for fitting classical force fields to electronic structure data, especially for water and aqueous ions, and for machine learning. Here, we show that the many-body expansion based on semilocal density functional theory affords wild oscillations and runaway error accumulation for ion-water interactions, typified by F(HO) with ≳ 15.
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