Synthesis and Characterization of Block Copolymers for Nanolithography Based on Thiol‐Ene “Click” Functionalized Polystyrene‐Block‐Polybutadiene

• Published in: Advanced functional materials 2022-11, Vol.32 (46), p.n/a
• Main Authors: Feng, Hongbo, Dolejsi, Moshe, Zhu, Ning, Griffin, Philip J., Craig, Gordon S. W., Chen, Wen, Rowan, Stuart J., Nealey, Paul F.
• Format: Article
• Language: English
• Subjects: Annealing; Block copolymers; Chemical synthesis; click chemistry; directed self‐assemblies; equal surface energy; Flory–Huggins interaction parameter; Free surfaces; high throughput approaches; Materials science; Morphology; Nanolithography; Polybutadiene; Polystyrene resins; Surface energy; Thiols
• ISSN: 1616-301X; 1616-3028
• DOI: 10.1002/adfm.202206836

In developing block copolymers (BCPs) for nanolithography, the preferred materials and processes are BCPs that can be thermally annealed with a free surface to yield perpendicularly orientated nanodomains with specific feature sizes and morphologies. Thiol‐ene “click” chemistry is used to modify a single parent polystyrene‐block‐poly(1,2‐butadiene) (PS‐b‐PB) to create both cylinder‐ and lamellae‐forming A‐block‐(B‐random‐C) BCPs with different Flory–Huggins parameters (χs) while maintaining an equal surface energy (γ, Δγ = 0) between the blocks, necessary to form perpendicular nanodomains by thermal annealing with a free surface. The use of BCPs with an A‐block‐(B‐random‐C) architecture effectively decouples the covarying properties of χ and Δγ. The effects of the size of the thiol and degree of thiol functionalization (φ) on χ, morphology, and Δγ of the blocks are investigated for four different thiols. Modification of PS‐b‐PB with methyl thioglycolate or 2‐(Boc‐amino)ethanethiol creates BCPs that form cylinders, whereas modification with smaller thiols, mercaptoethanol or 1‐thioglycerol, retains the lamellar morphology of the parent PS‐b‐PB. Cross‐linking of the double bonds in PB at annealing temperatures prevents directed self‐assembly (DSA) of these BCPs, but by adding a radical scavenger, butylated hydroxytoluene, the cross‐linking can be suppressed, enabling DSA. Thiol‐ene “click” chemistry is used to create A‐block‐(B‐random‐C) block copolymers with the ability to impart multiple covarying properties including the Flory–Huggins interaction parameter, equal surface energy of the blocks, and the different morphologies preferred for block copolymer nanolithography.