Long-Range Order Self-Assembly of Conjugated Block Copolymers at Inclined Air-Liquid Interfaces.

Here, we report that long-range order, direction-controlled, ultrathin conjugated polymer films can be formed by the self-assembly of conjugated block copolymers (i.e., poly(3-hexylthiophene)--poly(ethylene glycol)) at inclined air-water interfaces.

Air-liquid interfacial self-assembly of conjugated block copolymers into ordered nanowire arrays.

The ability to control the molecular packing and nanoscale morphology of conjugated polymers is important for many of their applications. Here, we report the fabrication of well-ordered nanoarrays of conjugated polymers, based on the self-assembly of conjugated block copolymers at the air-liquid interface. We demonstrate that the self-assembly of poly(3-hexylthiophene)-block-poly(ethylene glycol) (P3HT-b-PEG) at the air-water interface leads to large-area free-standing films of well-aligned P3HT nanowires.

Oxidation-induced photoluminescence of conjugated polymers.

Here, we report an unusual oxidation-induced photoluminescence (PL) turn-on response of a poly(3-alkoxythiophene), poly(3-{2-[2-(2-ethoxyethoxy)ethoxy]ethoxy}thiophene) (PEEEET). PEEEET shows a significantly red-shifted absorption spectrum compared to polyalkylthiophenes and is almost nonfluorescent (quantum yield ≪ 1%) in its pristine state. The introduction of sulfonyl defects along the polymer backbone by the oxidation of PEEEET with meta-chloroperbenzoic acid (m-CPBA) increased the emission quantum yield with the intensity increasing with the degree of oxidation.