ترغب بنشر مسار تعليمي؟ اضغط هنا

Structural Color from Solid-State Polymerization-Induced Phase Separation

258   0   0.0 ( 0 )
 نشر من قبل Alba Sicher
 تاريخ النشر 2021
  مجال البحث فيزياء
والبحث باللغة English
 تأليف Alba Sicher




اسأل ChatGPT حول البحث

Structural colors are produced by wavelength-dependent scattering of light from nanostructures. While living organisms often exploit phase separation to directly assemble structurally colored materials from macromolecules, synthetic structural colors are typically produced in a two-step process involving the sequential synthesis and assembly of building blocks. Phase separation is attractive for its simplicity, but applications are limited due to a lack of robust methods for its control. A central challenge is to arrest phase separation at the desired length scale. Here, we show that solid-state polymerization-induced phase separation can produce stable structures at optical length scales. In this process, a polymeric solid is swollen and softened with a second monomer. During its polymerization, the two polymers become immiscible and phase separate. As free monomer is depleted, the host matrix resolidifies and arrests coarsening. The resulting PS-PMMA composites have a blue or white appearance. We compare these biomimetic nanostructures to those in structurally-colored feather barbs, and demonstrate the flexibility of this approach by producing structural color in filaments and large sheets.

قيم البحث

اقرأ أيضاً

We propose an exactly solvable self-consistent kinetic model of polymerization-induced phase separation (PIPS) via spinodal decomposition. Using modified Cahn-Hilliard and Glotzer-Coniglio theories for early and late stages of spinodal decomposition, we find scaling regimes and compare the obtained results with existing experimental and theoretical information on PIPS kinetics, finding a good qualitative agreement.
Using dissipative particle dynamics (DPD) simulation method, we study the phase separation dynamics in block copolymer (BCP) melt in $d=3$, subjected to external stimuli such as light. An initial homogeneous BCP melt is rapidly quenched to a temperat ure $T < T_c$, where $T_c$ is the critical temperature. We then let the system go through alternate light on and off cycles. An on-cycle breaks the stimuli-sensitive bonds connecting both the blocks A and B in BCP melt, and during the off-cycle, broken bonds reconnect. By simulating the effect of light, we isolate scenarios where phase separation begins with the light off (set 1); the cooperative interactions within the system allow it to undergo microphase separation. When the phase separation starts with the light on (set 2), the system undergoes macrophase separation due to the bond breaking. Here, we report the role of alternate cycles on domain morphology by varying bond-breaking probability for both the sets 1 and 2, respectively. We observe that the scaling functions depend upon the conditions mentioned above that change the time scale of the evolving morphologies in various cycles. However, in all the cases, the average domain size respects the power-law growth: $R(t)sim t^{phi}$ at late times, here $phi$ is the dynamic growth exponent. After a short-lived diffusive growth ($phi sim 1/3$) at early times, $phi$ illustrates a crossover from the viscous hydrodynamic ($phi sim 1$) to the inertial hydrodynamic ($phi sim 2/3$) regimes at late times.
We study the thermodynamics of binary mixtures wherein the volume fraction of the minority component is less than the amount required to form a flat interface. Based on an explicit microscopic mean field theory, we show that the surface tension domin ated equilibrium phase of a polymer mixture forms a single macroscopic droplet. A combination of elastic interactions that renormalize the surface tension, and arrests phase separation for a gel-polymer mixture, stabilize a micro-droplet phase. We compute the droplet size as a function of the interfacial tension, Flory parameter, and elastic moduli of the gel. Our results illustrate the importance of the rheological properties of the solvent in dictating the thermodynamic phase behavior of biopolymers undergoing liquid-liquid phase separation.
We study liquid-vapor phase separation under shear via the Shan-Chen lattice Boltzmann model. Besides the rheological characteristics, we analyze the Kelvin-Helmholtz(K-H) instability resulting from the tangential velocity difference of the fluids on two sides of the interface. We discuss also the growth behavior of droplets. The domains being close to the walls are lamellar-ordered, where the hydrodynamic effects dominate. The patterns in the bulk of the system are nearly isotropic, where the domain growth results mainly from the diffusion mechanism. Both the interfacial tension and the K-H instability make the liquid-bands near the walls tend to rupture. When the shear rate increases, the inequivalence of evaporation in the upstream and coagulation in the downstream of the flow as well as the role of surface tension makes the droplets elongate obliquely. Stronger convection makes easier the transferring of material particles so that droplets become larger.
A disordered material that cannot relax to equilibrium, such as an amorphous or glassy solid, responds to deformation in a way that depends on its past. In experiments we train a 2D athermal amorphous solid with oscillatory shear, and show that a sui table readout protocol reveals the shearing amplitude. When shearing alternates between two amplitudes, signatures of both values are retained only if the smaller one is applied last. We show that these behaviors arise because individual clusters of rearrangements are hysteretic and dissipative, and because different clusters respond differently to shear. These roles for hysteresis and disorder are reminiscent of the return-point memory seen in ferromagnets and many other systems. Accordingly, we show how a simple model of a ferromagnet can reproduce key results of our experiments and of previous simulations. Unlike ferromagnets, amorphous solids disorder is unquenched; they require training to develop this behavior.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا