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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.
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