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A Novel Wide‐Bandgap Polymer with Deep Ionization Potential Enables Exceeding 16% Efficiency in Ternary Nonfullerene Polymer Solar Cells.

Authors :
Zhang, Ying
Liu, Delong
Lau, Tsz‐Ki
Zhan, Lingling
Shen, Dong
Fong, Patrick W. K.
Yan, Cenqi
Zhang, Shaoqing
Lu, Xinhui
Lee, Chun‐Sing
Hou, Jianhui
Chen, Hongzheng
Li, Gang
Source :
Advanced Functional Materials; 7/2/2020, Vol. 30 Issue 27, p1-11, 11p
Publication Year :
2020

Abstract

Ternary strategies have attracted extensive attention due to their potential in improving power conversion efficiencies (PCEs) of single‐junction polymer solar cells (PSCs). In this work, a novel wide bandgap polymer donor (Egopt ≈ 2.0 eV) named PBT(E)BTz with a deep highest occupied molecular orbital (HOMO) level (≈−5.73 eV) is designed and synthesized. PBT(E)BTz is first incorporated as the third component into the classic PBDB‐T‐SF:IT‐4F binary PSC system to fabricate efficient ternary PSCs. A higher PCE of 13.19% is achieved in the ternary PSCs with a 5% addition of PBT(E)BTz over binary PSCs (12.14%). Similarly, addition of PBT(E)BTz improves the PCE for PBDB‐T:IT‐M binary PSCs from 10.50% to 11.06%. The study shows that the improved PCE in ternary PSCs is mainly attributed to the suppressed charge carrier recombination and more balanced charge transport. The generality of PBT(E)BTz as a third component is further evidenced in another efficient binary PSC system—PBDB‐TF:BTP‐4Cl: an optimized PCE of 16.26% is realized in the ternary devices. This work shows that PBT(E)BTz possessing a deep HOMO level as an additional component is an effective ternary PSC construction strategy toward enhancing device performance. Furthermore, the ternary device with 5% PBT(E)BTz displays better thermal and light stability over binary devices. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
30
Issue :
27
Database :
Complementary Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
144356158
Full Text :
https://doi.org/10.1002/adfm.201910466