Order-disorder transition in the electroactive polymer poly(3-dodecylthiophene)

Electrical conductivity is greatly dependent on the quality and degree of crystallinity in semiconjugated polymers. We have investigated. the order formation in electrically conducting poly(3-alkylthiophenes) by combining the uses of thermal analysis and optical microscopy. Initially, we were able to observe a bimodal endothermic melting point using differential scanning calorimetry(DSC). Then, using a slow cooling cycle from the melt state with immediate reheating, it was shown that the two melting points are separate phenomena and depend on the thermal history. A single melting point was observed when the sample was cooled to 120 degrees C and annealed for 1 h. Optical microscopy was then applied for the same conditions. A thermochromic change was observed immediately. This change has been related to changes in chain conformation as the chain planarity increases with the decrease of thermal energy. With the annealing at 120 degrees C a formation of red dot-like domains could be seen. The formation of these domains was related to the above mentioned single high-temperature melting point. This observation is the first visual observation of the order formation in poly(alkylthiophenes) and also the first evidence of thermochromism taking place by an interchain mechanism such as crystallization. The reason for our observation is the very narrow thermal condition used in the experiments. In further experiments we notice further thermochromic change in the background, indicating a further ordering process that is related to the second endothermic melting point observed in the thermal analysis experiments. Our experiments support the earlier findings of two different ordered phases in poly(alkylthiophenes).