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Updated: Sep 24, 2025

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Wide Bandgap Polymer Donor with Acrylate Side Chains for Non-Fullerene Acceptor-Based Organic Solar Cells
Yi Yuan1, Pankaj Kumar1, Jenner H L Ngai1
1Department of Chemical Engineering and Waterloo Institute of Nanotechnology (WIN), University of Waterloo, 200 University Ave West, Waterloo, ON, N2L 3G1, Canada.
Abstract:
Organic semiconductors inherently have a low dielectric constant and hence high exciton binding energy, which is largely responsible for the rather low power conversion efficiency of organic solar cells as well as the requirements to achieve delicate bulk-heterojunction nanophase separation in the active layer. In this study, methyl acrylate as a weakly electron-withdrawing side chain for the electron rich thiophene to prepare a new building block, methyl thiophene-3-acrylate (TA), with increased polarity is used. A wide bandgap polymer PBDT-TA synthesized using TA and a benzodithiophene (BDT) monomer shows increased dielectric constant and reduced exciton binding energy compared to the analogous polymer PBDT-TC, which is made of BDT and methyl thiophene-3-carboxylate (TC). An organic solar cell device based on PBDT-TA:ITIC also achieves a higher power conversion efficiency of 10.47% than that of the PBDT-TC:ITIC based solar cell (9.68%). This work demonstrates the effectiveness of using acrylate side chains to increase the dielectric constant, reduce the exciton binding energy, and enhance the solar cell efficiency of polymer semiconductors.
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