Meyer Emily E, Lin Qi, Hassenkam Tue, Oroudjev Emin, Israelachvili Jacob N
Department of Physics, University of California, Santa Barbara, CA 93106, USA.
Proc Natl Acad Sci U S A. 2005 May 10;102(19):6839-42. doi: 10.1073/pnas.0502110102. Epub 2005 Apr 29.
We compare the "long-range hydrophobic forces" measured (i) in the "symmetric" system between two mica surfaces that had been rendered hydrophobic by the adsorption of a double-chained cationic surfactant, and (ii) between one such hydrophobic surface and a hydrophilic surface of bare mica ("asymmetric" case). In both cases, the forces were purely attractive, stronger than van der Waals, and of long-range, as previously reported, with those of the asymmetric, hydrophobic-hydrophilic system being even stronger and of longer range. Atomic force microscopy images of these surfaces show that the monolayers transform into patchy bilayers when the surfaces are immersed in water, and that the resulting surfaces contain large micrometer-sized regions of positive charges (bilayer) and negative charges (bare mica) while remaining overall neutral. The natural alignment of oppositely charged domains as two such surfaces approach would result in a long-range electrostatic attraction in water, but the short-range, "truly hydrophobic" interaction is not explained by these results.
我们比较了以下两种情况下测量的“长程疏水力”:(i)在由双链阳离子表面活性剂吸附而变得疏水的两个云母表面之间的“对称”系统中;(ii)在一个这样的疏水表面与裸云母的亲水表面之间(“不对称”情况)。如先前报道,在这两种情况下,力都是纯粹吸引性的,比范德华力更强,且具有长程性,其中不对称的疏水 - 亲水系统的力更强且范围更长。这些表面的原子力显微镜图像显示,当表面浸入水中时,单层会转变为斑状双层,并且所得表面包含大的微米级带正电荷区域(双层)和带负电荷区域(裸云母),而整体仍保持中性。当两个这样的表面靠近时,相反电荷区域的自然排列会在水中产生长程静电吸引力,但这些结果并未解释短程的“真正疏水”相互作用。