Related Experiment Video
Updated: Sep 24, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
[2,2'-Bithiophene]-4,4'-dicarboxamide: a novel building block for semiconducting polymers
Xiaocheng Zhou1, Zhifang Zhang1, Arthur D Hendsbee1
1Department of Chemical Engineering/Waterloo Institute for Nanotechnology (WIN), University of Waterloo 200 University Ave West Waterloo ON N2L 3G1 Canada yuning.li@uwaterloo.ca.
Abstract:
A novel electron deficient building block [2,2'-bithiophene]-4,4'-dicarboxamide (BTDCA) was designed to lower the highest occupied molecular orbital (HOMO) energy level of polythiophenes in order to achieve a higher open circuit voltage (V oc) and thus a higher power conversion efficiency in polymer solar cells (PSCs). BTDCA dibromo monomers were conveniently synthesized in four steps, and were used to prepare three thiophene-based D-A polymers, P(BTDCA66-BT) (66BT), P(BTDCA44-BT) (44BT) and P(BTDCA44-TT) (44TT). All the polymers exhibited unipolar hole transport properties, exhibiting mobilities in the range of ∼10-4 to 10-2 cm2 V-1 s-1 with the highest hole mobility of up to 1.43 × 10-2 cm2 V-1 s-1 achieved for 44BT in bottom-gate bottom-contact organic thin film transistors (OTFTs). In PSCs, these polymers achieved high V oc's of 0.81-0.87 V when PCBM or ITIC was used as acceptor. When 44TT was used as donor and ITIC was used as acceptor, a power conversion efficiency (PCE) of up to 4.5% was obtained, a significant improvement when compared with the poly(3-hexylthiophene) (P3HT):ITIC devices, which showed the highest PCE of merely 0.92%.
More Related Videos
06:55Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
08:51Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
Anionic Chain-Growth Polymerization: Mechanism
Anionic Chain-Growth Polymerization: Overview
Characteristics and Nomenclature of Homopolymers
Characteristics and Nomenclature of Copolymers
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction