Inverted chemical force microscopy:: following interfacial reactions on the nanometer scale

被引:8
作者
Dordi, B
Pickering, JP
Schönherr, H
Vancso, GJ
机构
[1] Univ Twente, Inst Nanotechnol, MESA, NL-7500 AE Enschede, Netherlands
[2] Univ Twente, Fac Sci & Technol, NL-7500 AE Enschede, Netherlands
关键词
atomic force microscopy; reflection spectroscopy; surface chemical reaction; wetting; gold; biological molecules-nucleic acids; biological molecules-proteins; esters;
D O I
10.1016/j.eurpolymj.2004.01.020
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Atomic force microscopy (AFM) with chemical specificity using chemically modified AFM probes, so-called chemical force microscopy, was applied to study surface chemical reactions on the nanometer scale. To overcome the typical limitations of conventional AFM in following reactions in real-time, i.e. slow data acquisition, as well as thermal and instrumental drifts, we have introduced a new approach, named inverted chemical force microscopy (iCFM). In iCFM the reactants are immobilized on the AFM tip rather than on the substrate. The chemical reactions take place at the surface of the tip and are probed in real-time by force-displacement measurements on an inert octadecanethiol-covered An substrate. The reactions studied were the hydrolysis and aminolysis of 11,11'-dithiobis(N-hydroxysuccinimidylundecanoate) (NHS-C-10). By iCFM intermolecular interactions and hence reaction kinetics can be quantitatively studied on the level of similar to10-100 molecules. In particular, our iCFM data showed that the aminolysis reaction with n-butylamine on SAMs of NHS-C-10 is a spatially heterogeneous reaction. In addition, information about the defect density of reactive SAMs was obtained. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:939 / 947
页数:9
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