Understanding Self-Assembly at Interfaces

  • ChemPubSoc Europe Logo
  • Author: Theresa Kueckmann
  • Published Date: 11 July 2015
  • Source / Publisher: Chemistry – An Asian Journal/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
thumbnail image: Understanding Self-Assembly at Interfaces

Nucleation and growth are key processes when it comes to understanding how compounds self-assemble on surfaces. The nucleation–elongation mechanism forming 2D supramolecular assemblies is an important concept to realize unprecedented surface-confined, stimulus-responsive systems. These can be developed into sophisticated dynamic molecular devices, if the growth mechanism during the design of functionalized surfaces is taken into account .


Kenji Matsuda and colleagues, Kyoto University, Japan, demonstrated that growth mechanisms at a liquid/solid interface can be quantitatively investigated. They analysed the concentration dependence of surface coverage using scanning tunneling microscopy (STM) at ambient conditions.


The team developed a nucleation–elongation model for surface-confined self-assembly to investigate the Gibbs free energy in 2D self-assembly. According to the researchers, hydrogen bond strength (involving amide or urea groups) and the number of non-hydrogen atoms in a molecular component (i.e., core size and length of the alkyl side chain) play a primary role in determining the stabilization energy during nucleation and elongation processes.


 

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