Light-Induced Nanowetting: Erasable and Rewritable Polymer Nanoarrays via Solid-to-Liquid Transitions.

Template wetting methods have been widely applied in the preparation of one-dimensional (1D) polymer nanomaterials. The pattern control using the template wetting methods, however, still remains a great challenge, mainly due to the nonselectivity of the polymers toward the environmental triggering. In this work, we present a facile light-induced nanowetting (LIN) method to fabricate patterned nanoarrays using anodic aluminum oxide (AAO) templates. Photoresponsive azobenzene-containing polymers (azopolymers) that exhibit light-induced reversible solid-to-liquid transitions are used. Upon exposure to ultraviolet lights, the azopolymer chains can wet the nanopores of the AAO templates in a liquid state via capillary force. The azopolymer chains are then solidified by illuminating them with visible lights, resulting in the formation of azopolymer nanoarrays. Notably, using designed photomasks, the patterns of the nanoarrays can be ingeniously controlled with the characteristic of erasable and rewritable nanostructures.

Reproducible and Bendable SERS Substrates with Tailored Wettability Using Block Copolymers and Anodic Aluminum Oxide Templates.

Surface properties are essential for substrates exhibiting high sensitivity in surface-enhanced Raman scattering (SERS) applications. In this work, novel SERS hybrid substrates using polystyrene-block-poly(methyl methacrylate) and anodic aluminum oxide templates is presented. The hybrid substrates not only possess hierarchical porous nanostructures but also exhibit superhydrophilic surface properties with the water contact angle ≈0°. Such surfaces play an important role in providing uniform enhanced intensities over large areas (relative standard deviation ≈10%); moreover, these substrates are found to be highly sensitive (limit of detection ≈10-12 m for rhodamine 6G (R6G)). The results show that the hybrid SERS substrates can achieve the simultaneous detection of multicomponent mixtures of different target molecules, such as R6G, crystal violet, and methylene blue. Furthermore, the bending experiments show that about 70% of the SERS intensities are maintained after bending from ≈30° to 150°.

Laser-Assisted Nanowetting: Selective Fabrication of Polymer/Gold Nanorod Arrays Using Anodic Aluminum Oxide Templates.

1D polymer nanomaterials have attracted significant interest in recent years because of their unique properties and promising applications in various fields. It is, however, still a challenge to fabricate polymer nanoarrays with desired sizes and controlled morphologies. Here, an unprecedented approach, the laser-assisted nanowetting (LAN) method, to selectively fabricate polymer nanoarrays is presented. Polystyrene (PS) is blended with gold nanorods (AuNRs), which are used to absorb the energy from the laser. After the blend films are brought in contact with AAO templates, the AuNRs at regions shone by the laser beams absorb the energy and heat the surrounding polymer chains, resulting in the formation of PS/AuNRs arrays in selected areas. This work paves a new research direction for developing template-based polymer nanomaterials.

Cascade and Effective Syntheses of Functionalized Tellurophenes.

A one-pot and transition-metal-catalyst-free synthetic strategy to construct functionalized tellurophenes has been developed. Substituted 1,1-dibromo-1-en-3-ynes are smoothly converted to tellurophenes with telluride salts in high yield via a series of cascade reactions through reductive debromination, hydrotelluration, nucleophilic cyclization, and aromatization. Close inspection of the results clearly showed that the reactivity of in situ prepared telluride salts are significantly influenced by the polarity of the solvent system and the electronic nature of the substituent on the enyne substrate. This method reports the first direct synthesis of 3-aryltellurophenes in high yields at room temperature. This novel reaction strategy is also found to be a promising synthetic method for multisubstituted tellurophenes and selenophenes.