Self-organized macromolecular materials can provide an alternative pathway to conventional lithography for the fabrication of devices on the nanometer scale. In particular, the self-assembly of the microdomains of diblock copolymers within lithographically-defined templates to create patterns with long range order has attracted considerable attention, with the advantages of cost-effectiveness, large-area coverage, and compatibility with preestablished top-down patterning technologies. Previously, we showed that spherical morphology poly(styrene-b-dimethylsiloxane) (PS-PDMS) block copolymers, which have a large interaction parameter and a high etch-contrast between two blocks, can be templated using an array of nanoscale topographical elements that act as surrogates for the minority domains of the block copolymer ^[1] . Recently, we showed that complex nanoscale patterns can be generated by combining the self-assembly of block-copolymer thin films with minimal top-down templating. A sparse array of nanoscale HSQ posts was used to accurately dictate the assembly of a cylindrical PS-PDMS diblock copolymer into a wide assortment of complex, unsymmetrical features, as shown in Figure 1 ^[2] . To extend the feature sizes to the sub-10-nm range, we demonstrated the formation of highly ordered grating patterns with a line width of 8 nm and period of 17 nm from a self-assembled PS-PDMS diblock copolymer and fabricated sub-10-nm-wide tungsten nanowires from the self-assembled patterns using a reactive ion etching process, as shown in Figure 2.

1. I. Bita, J. K. W. Yang, Y. S. Jung, C. A. Ross, E. L. Thomas, and K. K. Berggren, “Graphoepitaxy of self-assembled block copolymers on two-dimensional periodic patterned templates,” Science, vol. 321, pp. 939-943, 2008.
2. J. K. W. Yang, Y. S. Jung, J.-B. Chang, C. A. Ross, and K. K. Berggren, “Complex self-assembled patterns using sparse commensurate templates with locally varying motifs,” Nature Nanotechnology, vol. 5, pp. 256-260, 2010.