In this article, the plasma surface modification effects on the chemical, mechanical, and biological properties of electrospun poly (ε-caprolactone) (PCL) random nanofiber meshes (NFMs) were investigated by adjusting plasma chemistry, that is, using glow discharges of N(2) +H(2), NH(3) +O(2), and Ar+O(2) gas mixtures. The surface property changes of electrospun PCL NFMs after those plasma treatments were examined by water contact angle measurements and X-ray photoelectron spectroscopy. The experimental results showed that the plasma treatments introduced polar groups onto the surfaces and thus increased the surface hydrophilicity. From tensile test data, plasma treatment had limited effect on the mechanical properties of PCL random NFMs. The biological properties of the plasma-treated PCL NFMs were examined by cell proliferation assays using mouse osteoblast cells (MC3T3-E1). It was found that the plasma-treated PCL NFMs gave a higher proliferation rate and improved cell adhesion properties as compared with the untreated controls.

Self‐assembly is important for creating photonic structures and structural color is typically tunable by varying the size of building blocks, which are themselves obtained after time‐consuming chemical syntheses. The molecular conformation of bottlebrush block copolymers (BBCPs) in solution can be manipulated to create libraries of photonic structures. Amphiphilic BBCPs bearing oxidation‐responsive ferrocene groups on the hydrophilic block are used to fabricate porous particles via evaporation‐induced self‐assembly of water‐in‐oil‐in‐water (W/O/W) double emulsions stabilized by the BBCP surfactant. In situ oxidation of the ferrocene groups by hydrogen peroxide at the W/O interface leads to enhanced hydrophilicity, more hydration, and chain extension of the hydrophilic block. Consequently, larger internal water droplets are spontaneously formed, yielding larger pores within the microparticles. The pore diameter is readily tunable from 144 to 301 nm with a single BBCP, thereby generating full‐spectrum structural colors. This work provides a straightforward method for fabrication of libraries of photonic pigments in an easy and scalable manner.

The stretching‐induced phase transition from tetragonal Form II to hexagonal Form I and the evolution of corresponding crystallite orientation were studied for the butene‐1/ethylene random copolymer with 1.5 mol % ethylene by using a combination of tensile test and in situ wide‐angle X‐ray diffraction. Three orientation pathways were distinguished for II‐I phase transition, including phase transition accomplishing within off‐axis oriented crystallites (Orientation Pathway 1), phase transition with simultaneous formation of highly oriented crystallites (Orientation Pathway 2), and phase transition occurring within the highly oriented crystallites already formed (Orientation Pathway 3). The kinetics of II‐I transition was correlated with the macroscopic mechanical response, which exhibits a strong dependence on orientation. In Orientation Pathway 1, the triggering of phase transition corresponds to the mechanical yielding. More interestingly, the kinetics of transition exhibits the identical dependence on stress. However, in Orientation Pathways 2 and 3, appearance of the highly oriented crystallites substantially alters transition kinetics, which is tentatively associated with the stress bearing by interstack tie chains. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019, 57, 116–126

Photonic pigment particles prepared via self-assembly have been suffering from their poor mechanical performances; i.e., they can easily be damaged and lose structural color under a compression force. This greatly limits their uses as mechanochromic pigments. Here, a nanoscale concentric lamellar structure of alternating glassy-rubbery microdomains is successfully created within photonic microparticles through a confined self-assembly and photo-cross-linking strategy. The glassy domain is composed of polystyrene, and cross-linked bottlebrush polydimethylsiloxane served as the supersoft elastic domain. The obtained photonic structure not only shows large deformation and visible color changes under a loaded compression force but also rapidly recovers to its original state in less than 1 s (∼0.16 s) upon unloading. Continuously loading-unloading micro compression test indicates that no obvious damage can be identified after 250 cycles, indicating the high durability of the pigments against deformation. These pigments with different reflected colors are simply obtained using bottlebrush block copolymer formulations with tunable weight percentages of polymer additives. The mechanical robust photonic pigments may be useful in many important applications.

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