A New Family of Photoluminescent Polymers with Dual Chromophores.

A new family of photoluminescent polymers with dual chromophores is prepared in this study by using poly(maleic anhydride-alt-vinyl acetate), acetone, and metal hydroxide. These polymers, which contain both bulky carboxylic ester groups and metal carboxylate groups, are found to be dual-emission photoluminescent, with a blue luminescence excitation-dependent group and a red luminescence excitation-independent group. These photoluminescence polymers with a nonconjugated structure and dual chromophores also show characteristics of aggregation-induced emission (AIE). The luminous intensities of the AIE fibers prepared using the polymers are found to increase after stretching, in contrast to traditional photoluminescent fibers with the aggregation-caused quenching property. The study also finds that the stretched fibers can emit the three primary colors when irradiated by ultraviolet, blue, and green light.

Water-Soluble Polymers with Strong Photoluminescence through an Eco-Friendly and Low-Cost Route.

Photoluminescence (PL) of nonconjugated polymers brings a favorable opportunity for low-cost and nontoxic luminescent materials, while most of them still exhibit relatively weak emission. Strong PL from poly[(maleic anhydride)-alt-(vinyl acetate)] (PMV) from low-cost monomer has been found in organic solvents, yet the necessity of noxious solvents would hinder its practical applications. Herein, through a novel, eco-friendly, and one-step route, PMV-derived PL polymers can be fabricated with the highest quantum yield of 87% among water-soluble nonconjugated PL polymers ever reported. These PMV-derived polymers emit strong blue emission in both solutions and solids, and can be transformed into red-emission agents easily. These PL polymers exhibit application potentials in light-conversion agricultural films. It is assumed that this work not only puts forward a convenient preparation routine for nonconjugated polymers with high PL, but also provides an industrial application possibility for them.

Biomolecule-doped PEDOT with three-dimensional nanostructures as efficient catalyst for oxygen reduction reaction.

Metal macro-cyclic compounds have drawn considerable attention as alternative catalysts for oxygen reduction reaction. However, the continuous pyrolysis process usually needed for improving the performance of these compounds require an elevated temperature and complicated procedures, thus leading to an unpredictable transformation of the chemical structures and limiting their applications. Herein, we develop a new insight to fabricating hemin-doped poly (3,4-ethylenedioxythiophene) (PEDOT) with controllable three-dimensional nanostructures via a one-step, tri-phase, self-assembled polymerization routine. We demonstrate that the hemin-induced synergistic effect results in a very high 4-electron oxygen reduction activity, a better stability, and free from methanol crossover effects even in a neutral phosphate buffer solution (PBS).