The crystallization and melting behavior of poly(3-butylthiophene) (P3BT), poly(3-octylthiophene) (P3OT), and poly(3-dodecylthiophene) (P3DDT) were studied. The equilibrium melting temperatures (T m 0) of these polymers were measured and resulted equal to 321, 230, and 175 °C for P3BT, P3OT, and P3DDT, respectively. The crystallization kinetics was evaluated by the Avrami equation:  it proceeds by heterogeneous nucleation with one-dimensional linear growth (n = 1.1−1.8). The effects of the length of the alkyl side chain and of the undercooling were investigated. Phase I, Phase II, and a nematic mesophase were detected in P3BT and P3DDT. In P3BT, Phase I was differentiable from the mesophase on the basis of wide-angle X-ray scattering (WAXS) patterns. This study gives insight, in particular, on the crystallization and melting behavior of P3BT, a polymer not yet well studied. WAXS, small-angle X-ray scattering (SAXS), and differential scanning calorimetry (DSC) were employed as experimental techniques.

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Herein, we propose convenient routes to produce hybrid-polymers that covalently enclosed, or confined, N-doped carbon quantum dots (CQDs). We focus our attention on polyamide, polyurea-urethane, polyester, and polymethylmetacrylate polymers, some of the most common resources used to create everyday materials. These hybrid materials can be easily prepared and processed to obtain macroscopic objects of different shapes, i.e., fibers, transparent sheets, and bulky forms, where the characteristic luminescence properties of the native N-doped CQDs are preserved. More importantly we explore the potential use of these hybrid composites to achieve photochemical reactions as those of photoreduction of silver ions to silver nanoparticles (under UV-light), the selective photo-oxidation of benzylalcohol to the benzaldehyde (under vis-light), and the photocatalytic generation of H2 (under UV-light).

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