Catching Waves: Measuring Self-Assembly in Action

In addition, the researchers say, the results reported in this week’s Proceedings of the National Academy of Science should be important to understanding self-propagating chemical reactions and ordering and self-assembly phenomena in situations involving confinement, such as thin films and the porous internal geometries of many materials, such as rocks and cement.

Systems that are transformed by so-called ‘self-propagating’ or ‘autocatalytic’ wave fronts actually are very common. Diverse molecular processes, and even social processes and population dynamics, often can be described in terms of fundamental ‘entities’ that undergo changes randomly on an individual level, but at large scales exhibit some regular motion or pattern formation as they collectively move from some unstable situation to a relatively stable state. Mathematicians have developed a highly successful basic model for such processes, called mean field theory.

The same basic equations describe, for example, the spread of advantageous genes in an animal population, the growth of brain tumors, wound healing, flame propagation, the spread of contagious epidemics, the spread of Neolithic farming techniques, and chemical reaction fronts and nerve propagation—all phenomena that grow outward on waves of change.

In recent years, simulations and theoretical arguments have suggested that small fluctuations can significantly influence the advance of these wavefronts as they grow. In the simple case of growth of a layer of molecules by self-assembly, this would lead to a progressive roughening of the interface between the ordered and disordered regions. This phenomenon is completely missed in the classical mean field theory, raising important questions about the applicability of these and philosophically similar models to describe propagating fronts under general conditions.

To provide experimental verification of this phenomenon in a real system, the NIST/NCSU team examined the spontaneous assembly of organosilane molecules into a monolayer film on an oxidized silicon surface. If a supply of the carbon-silicon-based molecules is placed along one edge of a treated silicon wafer, under controlled conditions, the organosilane molecules spontaneously organize themselves into a well-ordered layer, creating a carpet-like layer on the silicon that advances from the edge of the wafer at a constant velocity.

The technique involved was developed in the 1990s as a simple way to create substrates with a gradually changing surface-energy gradient, a useful experimental tool for surface scientists. The system lends itself to high-resolution measurement because the process is slow enough to allow highly precise, quantitative measurements of the layer as it advances using a high-resolution synchrotron X-ray technique. The team found wavelike ordering, as expected from classical theory, but with the interface of the growing front broadened in time, as predicted by the recent theoretical modeling, but in contrast with classical theory.

Citation: J.F. Douglas, K. Efimenko, D.A. Fischer, F.R. Phelan and J. Genzer. Propagating waves of self-assembly in organosilane monolayers. Proceedings of the National Academy of Science, 2007 104: 10324-10329.

Source: National Institute of Standards and Technology