posted on 2018-02-27, 00:00authored byHans Van Gorp, Peter Walke, Ana M. Bragança, John Greenwood, Oleksandr Ivasenko, Brandon E. Hirsch, Steven De Feyter
A network of self-assembled
polystyrene beads was employed as a
lithographic mask during covalent functionalization reactions on graphitic
surfaces to create nanocorrals for confined molecular self-assembly
studies. The beads were initially assembled into hexagonal arrays
at the air–liquid interface and then transferred to the substrate
surface. Subsequent electrochemical grafting reactions involving aryl
diazonium molecules created covalently bound molecular units that
were localized in the void space between the nanospheres. Removal
of the bead template exposed hexagonally arranged circular nanocorrals
separated by regions of chemisorbed molecules. Small molecule self-assembly
was then investigated inside the resultant nanocorrals using scanning
tunneling microscopy to highlight localized confinement effects. Overall,
this work illustrates the utility of self-assembly principles to transcend
length scale gaps in the development of hierarchically patterned molecular
materials.