Long-range specific ion-ion interactions in hydrogen-bonded liquid films

被引:39
作者
Enami, Shinichi [1 ,2 ,3 ]
Colussi, Agustin J. [4 ]
机构
[1] Kyoto Univ, Hakubi Ctr Adv Res, Kyoto 6068302, Japan
[2] Kyoto Univ, Res Inst Sustainable Humanosphere, Uji, Kyoto 6110011, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[4] CALTECH, Ronald & Maxine Linde Ctr Global Environm Sci, Pasadena, CA 91125 USA
基金
美国国家科学基金会; 日本科学技术振兴机构;
关键词
WATER-METHANOL MIXTURES; AIR/WATER INTERFACE; AQUEOUS INTERFACES; CHARGED DROPLETS; CAPILLARY WAVES; SURFACE; ADSORPTION; MECHANISM; NETWORKS; DYNAMICS;
D O I
10.1063/1.4803652
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Anions populate fluid interfaces specifically. Here, we report experiments showing that on hydrogen-bonded interfaces anions interact specifically over unexpectedly long distances. The composition of binary electrolyte (Na+, X-/Y-) films was investigated as a function of solvent, film thickness, and third ion additions in free-standing films produced by blowing up drops with a high-speed gas. These films soon fragment into charged sub-micrometer droplets carrying excess anions detectable in situ by online electrospray ionization mass spectrometry. We found that (1) the larger anions are enriched in the thinner (nanoscopic air-liquid-air) films produced at higher gas velocities in all (water, methanol, 2-propanol, and acetonitrile) tested solvents, (2) third ions (beginning at sub-mu M levels) specifically perturb X-/Y- ratios in water and methanol but have no effect in acetonitrile or 2-propanol. Thus, among these polar organic liquids (of similar viscosities but much smaller surface tensions and dielectric permittivities than water) only on methanol do anions interact specifically over long, viz.: < r(i) - r(j)>/nm = 150 (c/mu M)(-1/3), distances. Our findings point to the extended hydrogen-bond networks of water and methanol as likely conduits for such interactions. (C) 2013 AIP Publishing LLC.
引用
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页数:6
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