Micro- and nanopatterning of functional organic monolayers on oxide-free silicon by laser-induced photothermal desorption

摘要

The photothermal laser patterning of functional organic monolayers, prepared on oxide-free hydrogen-terminated silicon, and subsequent backfi lling of the laser-written lines with a second organic monolayer that differs in its terminal functionality, is described. Since the thermal monolayer decomposition process is highly nonlinear in the applied laser power density, subwavelength patterning of the organic monolayers is feasible. After photothermal laser patterning of hexadecenyl monolayers, the lines freed up by the laser are backfi lled with functional acid fl uoride monolayers. Coupling of cysteamine to the acid fl uoride groups and subsequent attachment of Au nanoparticles allows easy characterization of the functional lines by atomic force microscopy (AFM) and scanning electron microscopy (SEM). Depending on the laser power and writing speed, functional lines with widths between 1.1 μm and 250 nm can be created. In addition, trifl uoroethyl-terminated (TFE) monolayers are also patterned. Subsequently, the decomposed lines are backfi lled with a nonfunctional hexadecenyl monolayer, the TFE stripes are converted into thiol stripes, and then finally covered with Au nanoparticles. By reducing the lateral distance between the laser lines, Au-nanoparticle stripes with widths close to 100 nm are obtained. Finally, in view of the great potential of this type of monolayer in the fi eld of biosensing, the ease of fabricating biofunctional patterns is demonstrated by covalent binding of fl uorescently labeled oligo-DNA to acidfl uoride-backfi lled laser lines, which-as shown by fl uorescence microscopy-is accessible for hybridization.