Issue 6, 2023

Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells

Abstract

Two small molecule (SM) donors, named CBTSeHR and CBTSeEHR, have been constructed by introducing selenophenes and chlorine atoms simultaneously into the conventional benzodithiophene–terthiophene–rhodanine architecture. In comparison with the non-chlorinated and thiophene based counterpart, the new SM donors exhibit a red-shifted absorption band, lower highest occupied molecular orbital (HOMO) energy levels, stronger intermolecular packing and higher molecular crystallinity. When combined with non-fullerene molecule FO-2Cl, the optimized all-small-molecule organic solar cells (ASM-OSCs) based on CBTSeEHR give a moderate power conversion efficiency (PCE) of 9.30%. Notably, CBTSeHR based devices achieve an outstanding performance of 12.10% with a high open-circuit voltage (Voc) of 0.881 V, short-circuit current densities (Jsc) of 18.76 mA cm−2 and fill factor (FF) of 0.732, benefiting from the deep HOMO level, good light-harvesting ability and favorable morphology in the active layer. These findings provide an effective strategy to develop the medium band-gap SM donors for high-performance ASM-OSCs.

Graphical abstract: Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells

Supplementary files

Article information

Article type
Paper
Submitted
20 Dec 2022
Accepted
04 Jan 2023
First published
05 Jan 2023

New J. Chem., 2023,47, 2840-2846

Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells

C. Liu, Z. Wu, N. Qiu, C. Li and Y. Lu, New J. Chem., 2023, 47, 2840 DOI: 10.1039/D2NJ06222D

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