Nanostar and nanonetwork crystals were prepared from fully conjugated poly(3-(2-ethylhexyl)thiophene)-block-polythiophene (P3EHT-b-PT) via a simple INCP process. The structural conformation of the nanocrystals was investigated in detail, revealing that with an increase in the block length of PT, the morphology of the nanocrystals changed from nanospheres to nanorods, nanostars, and to nanonetworks.
1D nanocaterpillar structures were spontaneously formed during the synthesis of fully conjugated poly(2,5-dihexyloxy-1,4-phenylene)-block-polythiophene due to the strong π-π interactions between the polythiophene blocks. With the elongation of the polythiophene block, nanostructures evolved from nanospheres to nanocaterpillars and their length and height increased with good control.
Tris-(8-hydroxyquinoline)aluminum (Alq3), which is the most widely used material in organic electroluminescent devices, has been synthesized. Alq3 thin films have been deposited on glass and silicon substrates. The influence of light exposure on the optical properties of Alq3 thin films has been studied. It is confirmed that the photoluminescence (PL) of Alq3 thin film originates from its two geometrical isomers, namely, facial and meridional, which result from PL decay analysis (biexponential fit). It is also confirmed that the PL from both the isomers decreases for increasing light exposure time leading to the creation of luminescent quencher in Alq3 thin film.
A unique hierarchical evolution from single-line nanocaterpillars to multi-line nanocaterpillars was demonstrated byin situnanoparticlisation of fully conjugated poly(2,5-dihexyloxy-1,4-phenylene)-block-poly(3-methylthiophene).
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