TY - JOUR
T1 - Structure formation due to antagonistic salts
AU - Onuki, Akira
AU - Yabunaka, Shunsuke
AU - Araki, Takeaki
AU - Okamoto, Ryuichi
N1 - Funding Information:
This work was supported by KAKENHI (No. 25610122 ) and Grants-in-Aid for Japan Society for Promotion of Science (JSPS) Fellows (Grants Nos. 241799 and 263111 ).
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Antagonistic salts are composed of hydrophilic and hydrophobic ions. In a mixture solvent (water-oil) such ion pairs are preferentially attracted to water or oil, giving rise to a coupling between the charge density and the composition. First, they form a large electric double layer at a water-oil interface, reducing the surface tension and producing mesophases. Here, the cations and anions are loosely bound by the Coulomb attraction across the interface on the scale of the Debye screening length. Second, on solid surfaces, hydrophilic (hydrophobic) ions are trapped in a water-rich (oil-rich) adsorption layer, while those of the other species are expelled from the layer. This yields a solvation mechanism of local charge separation near a solid. In particular, near the solvent criticality, disturbances around solid surfaces can become oscillatory in space. In mesophases, we calculate periodic structures, which resemble those in experiments.
AB - Antagonistic salts are composed of hydrophilic and hydrophobic ions. In a mixture solvent (water-oil) such ion pairs are preferentially attracted to water or oil, giving rise to a coupling between the charge density and the composition. First, they form a large electric double layer at a water-oil interface, reducing the surface tension and producing mesophases. Here, the cations and anions are loosely bound by the Coulomb attraction across the interface on the scale of the Debye screening length. Second, on solid surfaces, hydrophilic (hydrophobic) ions are trapped in a water-rich (oil-rich) adsorption layer, while those of the other species are expelled from the layer. This yields a solvation mechanism of local charge separation near a solid. In particular, near the solvent criticality, disturbances around solid surfaces can become oscillatory in space. In mesophases, we calculate periodic structures, which resemble those in experiments.
KW - Antagonistic salt
KW - Charge inversion
KW - Ion adsorption
KW - Mesophases
KW - Selective solvation
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U2 - 10.1016/j.cocis.2016.02.007
DO - 10.1016/j.cocis.2016.02.007
M3 - Review article
AN - SCOPUS:84961206685
SN - 1359-0294
VL - 22
SP - 59
EP - 64
JO - Current Opinion in Colloid and Interface Science
JF - Current Opinion in Colloid and Interface Science
ER -