| Literature DB >> 28635174 |
Hyeong Min Jin1, Dae Yong Park2, Seong-Jun Jeong3, Gil Yong Lee1, Ju Young Kim1, Jeong Ho Mun1, Seung Keun Cha1, Joonwon Lim1, Jun Soo Kim1, Kwang Ho Kim4, Keon Jae Lee2, Sang Ouk Kim1.
Abstract
One of the fundamental challenges encountered in successful incorporation of directed self-assembly in sub-10 nm scale practical nanolithography is the process compatibility of block copolymers with a high Flory-Huggins interaction parameter (χ). Herein, reliable, fab-compatible, and ultrafast directed self-assembly of high-χ block copolymers is achieved with intense flash light. The instantaneous heating/quenching process over an extremely high temperature (over 600 °C) by flash light irradiation enables large grain growth of sub-10 nm scale self-assembled nanopatterns without thermal degradation or dewetting in a millisecond time scale. A rapid self-assembly mechanism for a highly ordered morphology is identified based on the kinetics and thermodynamics of the block copolymers with strong segregation. Furthermore, this novel self-assembly mechanism is combined with graphoepitaxy to demonstrate the feasibility of ultrafast directed self-assembly of sub-10 nm nanopatterns over a large area. A chemically modified graphene film is used as a flexible and conformal light-absorbing layer. Subsequently, transparent and mechanically flexible nanolithography with a millisecond photothermal process is achieved leading the way for roll-to-roll processability.Entities:
Keywords: block copolymers; directed self-assembly; flash light; photothermal effects
Year: 2017 PMID: 28635174 DOI: 10.1002/adma.201700595
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849