Biria Saeid, Malley Phillip P A, Kahan Tara F, Hosein Ian D
Department of Biomedical and Chemical Engineering and ‡Department of Chemistry, Syracuse University, Syracuse, New York 13244, United States.
Department of Biomedical and Chemical Engineering and Department of Chemistry, Syracuse University, Syracuse, New York 13244, United States.
ACS Macro Lett. 2016 Nov 15;5(11):1237-1241. doi: 10.1021/acsmacrolett.6b00659. Epub 2016 Oct 26.
We report a fundamentally new nonlinear dynamic system that couples optical autocatalytic behavior to phase evolution in photoreactive binary polymer blends. Upon exposure to light, the blend undergoes spontaneous patterning into a dense arrangement of microscale polymer filaments. The filaments' growth in turn induces local spinodal decomposition of the blend along their length, thereby regulating the spatially dynamics of phase separation. This leads to the spontaneous organization of a large-scale binary phase morphology dictated by the filament arrangement. This is a new mechanism for polymer blend organization, which couples nonlinear optical dynamics to chemical phase separation dynamics, and offers a new approach to light-directed patterning and organization of polymer and hybrid blends.
我们报道了一种全新的非线性动力学系统,该系统将光自催化行为与光反应性二元聚合物共混物中的相演化相耦合。在光照下,共混物会自发形成微尺度聚合物细丝的密集排列图案。细丝的生长反过来又会沿其长度方向诱导共混物发生局部旋节线分解,从而调节相分离的空间动力学。这导致了由细丝排列决定的大规模二元相形态的自发组织。这是一种聚合物共混物组织的新机制,它将非线性光学动力学与化学相分离动力学相结合,并为聚合物和混合共混物的光控图案化和组织提供了一种新方法。