Probing intermolecular forces and potentials with magnetic feedback chemical force microscopy

被引:46
作者
Ashby, PD [1 ]
Chen, LW [1 ]
Lieber, CM [1 ]
机构
[1] Harvard Univ, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
关键词
D O I
10.1021/ja0020613
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnetic feedback chemical force microscopy (MF-CFM) was used to map the complete force profile between hydroxyl- and carboxyl-terminated self-assembled monolayers (SAMs) in aqueous solution. The snap-to-contact and snap-out instabilities intrinsic to force-displacement measurements made with weak spring constant cantilevers were eliminated by using a cantilever with an attached magnetic particle and a solenoid in a servo loop to balance the tip-sample interactions. The interaction between hydroxyl-terminated surfaces in deionized water was well fit by a van der Waals model to short distances. The Hamaker constant that was determined from experiment, 1.0 x 10(-19) J, is similar to that expected for a gold-gold interaction and shows that the underlying gold support dominates the attractive interaction over a large range of separations. The interaction between a carboxyl-terminated tip and a sample in 0.010 M phosphate buffer at pH 7.0 was fit: with a model that includes both van der Waals and electrostatic terms. The Hamaker constant, 1.2 x 10(-19) J, which is similar to that obtained for hydroxyl-terminated surfaces, confirms that the gold-gold interaction dominates the attractive part of the interaction. In addition, the Debye length, 2.9 nm, surface potential, -1.5 x 10(2) mV, and charge regulation parameter, -0.71, obtained from analysis of the data are consistent with previous work (Vezenov et al. J. Am. Chem. Sec. 1997, 119, 2006-2015. Hu; Bard. Langmuir 1997, 13, 5114-5119). The implications of these results and applications of MF-CFM are discussed.
引用
收藏
页码:9467 / 9472
页数:6
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