Related Experiment Video
Updated: Dec 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
"Double-Acceptor-Type" Random Conjugated Terpolymer Donors for Additive-Free Non-Fullerene Organic Solar Cells
Youdi Zhang1,2, Yiming Shao1, Zhouyin Wei3
1College of Chemistry, Nanchang University, 999 Xuefu Avenue, Nanchang 330031, China.
Abstract:
Random conjugated terpolymers (RCTs) not only promote great comprehension and realization for the state-of-the-art highly effective non-fullerene organic solar cells (OSCs) but also offer a simple and practical synthetic strategy. However, the photovoltaic properties of RCTs yet lagged behind that of the donor-acceptor (D-A) alternating copolymer, especially in additive-free devices. Hence, we developed two feasible "double-acceptor-type" random conjugated terpolymers, PBDB-TAZ20 and PBDB-TAZ40. The additive-free OSCs based on PBDB-TAZ20:ITIC and PBDB-TAZ40:ITIC exhibit decent efficiencies of 12.34 and 11.27%, respectively, which both surpass the PBDB-T:ITIC-based device. For RCTs, the reasonably weakened crystallinity and the reduced phase separation degree are demonstrated to help in improving charge transport, reducing bimolecular recombination, and thus enhancing the photovoltaic performance of additive-free OSCs. The results imply that adding a third moiety into the D-A polymer donors provides a simple but efficient synthetic approach for high-performance OSCs.
More Related Videos
06:49In situ Grazing Incidence Small Angle X-ray Scattering on Roll-To-Roll Coating of Organic Solar Cells with Laboratory X-ray Instrumentation
Published on: March 2, 2021
07:32Printing Fabrication of Bulk Heterojunction Solar Cells and In Situ Morphology Characterization
Published on: January 29, 2017
Related Concept Videos
Anionic Chain-Growth Polymerization: Overview
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
P-N junction
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction