Electrostatic Interaction between Ionic Polymer Grafted Surfaces Studied by Atomic Force Microscopy

1997 ◽  
Vol 188 (2) ◽  
pp. 431-438 ◽  
Author(s):  
Junfeng Zhang ◽  
Emiko Uchida ◽  
Yoshikimi Uyama ◽  
Yoshito Ikada
2011 ◽  
Vol 6 (7-8) ◽  
pp. 510-515 ◽  
Author(s):  
O. A. Konovalova ◽  
N. V. Kalacheva ◽  
F. V. Shirshikov ◽  
M. Kh. Salakhov

2012 ◽  
Vol 3 ◽  
pp. 221-229 ◽  
Author(s):  
Antoine Hinaut ◽  
Adeline Pujol ◽  
Florian Chaumeton ◽  
David Martrou ◽  
André Gourdon ◽  
...  

The adsorption on KBr(001) of a specially designed molecule, consisting of a flat aromatic triphenylene core equipped with six flexible propyl chains ending with polar cyano groups, is investigated by using atomic force microscopy in the noncontact mode (NC-AFM) coupled to Kelvin probe force microscopy (KPFM) in ultrahigh vacuum at room temperature. Two types of monolayers are identified, one in which the molecules lie flat on the surface (MLh) and another in which they stand approximately upright (MLv). The Kelvin voltage on these two structures is negatively shifted relative to that of the clean KBr surface, revealing the presence of surface dipoles with a component pointing along the normal to the surface. These findings are interpreted with the help of numerical simulations. It is shown that the surface–molecule interaction is dominated by the electrostatic interaction of the cyano groups with the K+ ions of the substrate. The molecule is strongly adsorbed in the MLh structure with an adsorption energy of 1.8 eV. In the MLv layer, the molecules form π-stacked rows aligned along the polar directions of the KBr surface. In these rows, the molecules are less strongly bound to the substrate, but the structure is stabilized by the strong intermolecular interaction due to π-stacking.


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