Design narrow band gap small-molecule acceptors with unilateral vinylene π-bridge for high-performance optoelectronic devices

Abstract

Narrow band gap (NBG) small-molecule acceptors (SMAs) are crucial for enhancing the performance of organic solar cells (OSCs) and near-infrared organic photodetectors (NIR OPDs). Two novel SMAs, namely BTP-1V-4F and BTP-1V-4Cl, were developed via a synergistic strategy combining unilateral vinylene π-bridge introduction and terminal halogen atom modulation. The unilateral vinylene π-bridge not only effectively extends the intramolecular conjugated electron cloud distribution, promoting a narrowed bandgap and a redshifted absorption, but also synergistically suppresses molecular disorder in conjunction with the terminal halogen atoms, thereby optimizing the orderly packing. The results revealed that although BTP-1V-4Cl possesses a narrower bandgap and stronger crystallinity, BTP-1V-4F exhibits better compatibility with the donor material and achieves a more ordered and well-proportioned crystalline morphology in the blends. Consequently, BTP-1V-4F devices deliver superior performance. The NBG OSCs achieved a power conversion efficiency (PCE) of 14.2% with the open-circuit voltage of 0.8 V. Meanwhile, the NIR OPDs exhibited a remarkable specific detectivity (D * ) of 3.85×10 13 Jones with an ultralow dark current density (JD) of 5.22×10 -10 A cm -2 and a responsivity of 0.497 A W -1 at 870 nm and -1 V bias. This work demonstrates the promise of the BTP-1V-4X series for semi-transparent cells, tandem cells, and photodetectors.

Supplementary files

Article information

Article type
Paper
Submitted
23 Jan 2026
Accepted
11 Apr 2026
First published
13 Apr 2026

J. Mater. Chem. A, 2026, Accepted Manuscript

Design narrow band gap small-molecule acceptors with unilateral vinylene π-bridge for high-performance optoelectronic devices

S. Li, T. Liu, F. Bi, R. Shao, H. Q. Liu, J. Wang, T. Wang, S. Wen and X. Bao, J. Mater. Chem. A, 2026, Accepted Manuscript , DOI: 10.1039/D6TA00658B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements