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The stereocomplexation of poly(methyl methacrylate) (PMMA) is a unique supramolecular assembling system that has been demonstrated to be valuable in many applications. The crystallization behaviors of stereocomplex PMMA (sc-PMMA) under nanoconfinement, however, have yet to be fully understood. In this work, we fabricate sc-PMMA nanorods using anodic aluminum oxide (AAO) templates with various pore sizes to gain a fundamental understanding of sc-PMMA in confined states. A scanning electron microscope (SEM), a differential scanning calorimeter (DSC), and an X-ray diffractometer (XRD) are used to examine their morphologies, crystallization kinetics, and crystal characteristics. We discover that the crystallization kinetics of sc-PMMA inside the nanopores is significantly different from the bulk state. Also, the preferred orientation of sc-PMMA crystallites is mainly governed by the degree of spatial confinement and the polymer molecular weight. This work provides a deeper understanding of sc-PMMA under nanoconfinement and presents opportunities for the applications of supramolecular nanostructures in miniaturized devices.

Monitoring undesired pH deviations in the surroundings is one of the most pervasive issues for environment and industry, and developing efficient, economical, portable, and reusable membranes for p...

Untethered small actuators have drawn tremendous interest owing to their reversibility, flexibility, and widespread applications in various fields. For polymer actuators, however, it is still challenging to achieve programmable structural changes under different stimuli caused by the intractability and single-stimulus responses of most polymer materials. Herein, multi-stimuli-responsive polymer actuators that can respond to light and solvent via structural changes are developed. The actuators are based on bilayer films of polydimethylsiloxane (PDMS) and azobenzene chromophore (AAZO)-crosslinked poly(diallyldimethylammonium chloride) (PDAC). Upon UV light irradiation, the AAZO undergoes trans-cis-trans photoisomerization, causing the bending of the bilayer films. When the UV light is off, a shape recovery toward an opposite direction occurs spontaneously. The reversible deformation can be repeated at least 20 cycles. Upon solvent vapor annealing, one of the bilayer films can be selectively swollen, causing the bending of the bilayer films with the directions controlled by the solvent vapors. The effects of different parameters, such as the weight ratios of AAZO and film thicknesses, on the bending angles and curvatures of the polymer films are also analyzed. The results demonstrate that multi-stimuli-responsive actuators with fast responses and high reproducibility can be fulfilled.

Recently, anodic aluminum oxide (AAO) membranes with ordered and monodispersed nanopores have attracted significant attention because the pore sizes and lengths of the AAO membranes can be systematically controlled by changing the anodization parameters. Asymmetries of geometry, wettability, charge, and polarity in nanoporous AAO membranes are now highly desired for applications such as drug delivery, membrane filtration, and catalysis. Although the asymmetries in AAO membranes have been widely studied, AAO membranes whose nanopores simultaneously possess more than two asymmetric properties still need to be developed. In this work, we present a simple method to fabricate asymmetric AAO membranes by combining the post-treatments with the three-step anodization method. The asymmetries of the AAO membranes simultaneously possessing larger nanopores with higher hydrophobicity and smaller nanopores with lower hydrophobicity are characterized by scanning electron microscopy, water contact angle measurements, an...

Hierarchical structures are commonly observed in nature and possess unique properties. The fabrication of hierarchical structures with well-controlled sizes in different length scales, however, is still a great challenge. To further understand the morphologies and properties of the hierarchical structures, here we present a novel strategy to prepare hierarchical polymer structures by combining the modified breath figure method and the template method. Poly(methyl methacrylate) (PMMA) honeycomb films with regular micropores are first prepared using the modified breath figure method by dipping PMMA films into mixtures of chloroform and methanol. The polymer chains on the honeycomb films are then annealed and wetted into the nanopores of anodic aluminum oxide templates via capillary forces, resulting in the formation of hierarchical polymer structures. The morphologies of the polymer structures, which can be controlled by the molecular weights of the polymers and the concentrations of the polymer solutions, are characterized by scanning electron microscopy. The surface wettabilities of the polymer structures are also examined by water contact angle measurements, and the hierarchical structures are observed to be more hydrophobic than the flat films and honeycomb films. This work not only provides a feasible approach to fabricate hierarchical polymer structures with controlled sizes but also gives a better understanding of the relationship between surface morphologies and properties.

Ordered arrays of polymer nanostructures have been widely investigated because of their promising applications such as solar-cell devices, sensors, and supercapacitors. It remains a great challenge, however, to manipulate the shapes of individual nanostructures in arrays for tailoring specific properties. In this study, an effective strategy to prepare anisotropic polymer nanopillar arrays via photo-fluidization is presented. Azobenzene-containing polymers (azopolymers) are first infiltrated into the nanopores of ordered anodic aluminum oxide (AAO) templates. After the removal of the AAO templates using weak bases, azopolymer nanopillar arrays can be prepared. Upon exposure of linearly polarized lights, azobenzene groups in the azopolymers undergo trans-cis-trans photoisomerization, causing mass migration and elongation of the nanopillar along with the polarization directions. As a result, anisotropic nanopillar arrays can be fabricated, of which the deformation degrees are controlled by the illumination times. Furthermore, patterned nanopillar arrays can also be constructed with designed photomasks. This work presents a practical and versatile strategy to fabricate arrays of anisotropic nanostructures for future technical applications.