Cornucopia of Nanoscale Ordered Phases in Sphere-Forming Tetrablock Terpolymers

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• 作者：Siddharth Chanpuriya ; Kyungtae Kim ; Jingwen Zhang ; Sangwoo Lee ; Akash Arora ; Kevin D. Dorfman ; Kris T. Delaney ; Glenn H. Fredrickson ; Frank S. Bates
• 刊名：ACS Nano
• 出版年：2016
• 出版时间：May 24, 2016
• 年：2016
• 卷：10
• 期：5
• 页码：4961-4972
• 全文大小：704K
• 年卷期：0
• ISSN：1936-086X

文摘

We report the phase behavior of a series of poly(styrene)-b-poly(isoprene)-b-poly(styrene)′-b-poly(ethylene oxide) (SIS′O) tetrablock terpolymers. This study was motivated by self-consistent field theory (SCFT) calculations that anticipate a rich array of sphere-forming morphologies with variations in the molecular symmetry parameter τ = N_S/(N_S + N_S′), where N is the block degree of polymerization and the volume fraction of O is less than about 0.22. Eight SIS′O samples, with τ ranging from 0.21 to 0.73, were synthesized and investigated using small-angle X-ray scattering and transmission electron microscopy, yielding evidence of nine different spherical phases: hexagonal, FCC, HCP, BCC, rhombohedral (tentative), liquid-like packing, dodecagonal quasicrystal, and Frank–Kasper σ and A15 phases. At temperatures close to the order–disorder transition, these tetrablocks behave as pseudo-[SIS′]-O diblocks and form equilibrium morphologies mediated by facile chain exchange between micelles. Transition from equilibrium to nonequilibrium behavior occurs at a temperature (T_erg) several tens of degrees below the order–disorder transition temperature, speculated to be coincident with the loss of ergodicity, as chain exchange is arrested due to increased segregation strength between the core (O) and corona (SIS′) blocks. Nonequilibrium ordered structures form when T < T_erg; these are interpreted using SCFT calculations to elucidate the free energy landscape driving ordering in the S and I block matrix. These experiments demonstrate a profound dependence on phase stability with variations in τ and temperature, providing insights into the formation of ordered phase symmetry in this class of asymmetric multiblock polymers.