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Updated: Jun 13, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Self-assembly of all-conjugated poly(3-alkylthiophene) diblock copolymer nanostructures from mixed selective solvents
1The Key Laboratory of Molecular Engineering of Polymers, Ministry of Education, Department of Macromolecular Science, Fudan University, Shanghai 200433, China.
Abstract:
The use of mixed selective solvents provides an effective means to control self-assembly of the all-conjugated diblock copolymer poly(3-butylthiophene)-b-poly(3-hexylthiophene) (P3BHT) into nanostructured morphologies. The solvent and temperature effects on the self-assembly of P3BHT during cooling and subsequent crystallization were explored for the first time. Depending on the poor/good solvent ratio (i.e., anisole/chloroform), P3BHT chains experience different kinetic pathways, yielding nanowires at a low anisole/chloroform ratio (< or =2:1), and nanorings coexisted with some nanowires at a high anisole/chloroform ratio (> or =6:1). The nanowires are formed as a direct consequence of strong interchain pi-pi stacking, while the formation of nanorings is governed by solvophobic interactions between conjugated blocks and the poor solvent anisole to minimize the unfavorable contacts between the P3BT block ( approximately 50 degrees C) and later P3HT (below 35 degrees C) block and anisole.

