Engineering Block Copolymers To Achieve Equal Surface Free Energy and Tunable χN For Directed Self-Assembly Applications

ORAL

Abstract

Directed Self-Assembly (DSA) of block copolymers (BCPs) is a promising technique for creating well-defined nanoscale features. The suitable BCPs for this application demand both blocks have equal surface free energies (SFE), a high enough Flory-Huggins parameter (χ) for moderate phase separation but not so high as to prohibit defect annihilation, and high etch contrast. To date, the BCPs that meet these requirements are still very limited. Here we demonstrate a high throughput approach to create a series of BCPs with full pitch sizes from 8- 15 nm that meet all these requirements. Furthermore, the capability of incorporation of etch resistant elements is shown to enable potential pattern transfer. We believe the work here will broaden the scope for DSA suitable materials and promote the next generation of nanolithography.

*We gratefully acknowledge the support by National Institute of Standards and Technology through the Center for Hierarchical Materials Design. We acknowledge the MRSEC Shared User Facilities (NSF DMR-1420709) and the Pritzker Nanofabrication Facility of the Pritzker School of Molecular Engineering at the University of Chicago (NSF ECCS-1542205).

Presenters

  • Hongbo Feng

    • University of Chicago

Authors

  • Hongbo Feng

    • University of Chicago
  • Moshe Dolejsi

    • University of Chicago
  • Ning Zhu

    • NanJing Tech University
  • Chun Zhou

    • IME, University of Chicago
    • University of Chicago
  • Stuart J Rowan

    • University of Chicago
  • Paul F Nealey

    • University of Chicago
    • IME, University of Chicago
    • Pritzker School of Molecular Engineering, University of Chicago