An asymmetric wide-bandgap acceptor simultaneously enabling highly efficient single-junction and tandem organic solar cells

Jianqiu Wang, Maojie Zhang*, Ji Lin, Zhong Zheng, Lei Zhu, Pengqing Bi, Haiyan Liang, Xia Guo, Jingnan Wu, Yafei Wang, Linfeng Yu, Jiayao Li, Junfang Lv, Xiaoyu Liu, Feng Liu, Jianhui Hou, Yongfang Li

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

88 Citations (Scopus)

Abstract

Ternary and tandem strategies are effective methods for improving the photovoltaic performance of organic solar cells (OSCs). Here an asymmetric wide-bandgap nonfullerene acceptor named AITC is synthesized. AITC with a bandgap of 1.75 eV exhibits a good complementary absorption spectrum with the narrow bandgap acceptor BTP-eC9. AITC also shows good miscibility with BTP-eC9, which facilitates the formation of a stable mixing phase in blends. Moreover, the large dipole moment of AITC reinforces the molecular packing in the blend films of PM6 and BTP-eC9, thereby enhancing the photoconductivity, suppressing charge recombination and reducing nonradiative voltage loss in ternary OSCs. As a result, the ternary OSCs based on PM6:BTP-eC9:AITC achieve an outstanding power conversion efficiency (PCE) of 18.8%. In addition, tandem OSCs using PM6:AITC as a bottom subcell and the PM6:AITC:BTP-eC9 ternary active layer as a top subcell exhibit a remarkable efficiency of 19.4%, which is one of the highest PCEs in the field.

Original languageEnglish
JournalEnergy and Environmental Science
Volume15
Issue number4
Pages (from-to)1585-1593
Number of pages9
ISSN1754-5692
DOIs
Publication statusPublished - 21 Feb 2022
Externally publishedYes

Bibliographical note

Funding Information:
This work was financially supported by the National Natural Science Foundation of China (NSFC) (51973146 and 51773142), the Jiangsu Provincial Natural Science Foundation (grant BK20190099), the Collaborative Innovation Center of Suzhou Nano Science & Technology, and the Priority Academic Program Development of Jiangsu Higher Education Institutions. J. H. would like to acknowledge the National Natural Science Foundation of China (NSFC, 21835006, 51961135103 and 51673201). Z. Z. would like to acknowledge the financial support from NSFC (51703041) and the Beijing National Laboratory for Molecular Sciences (BNLMS) Junior Fellowship.

Publisher Copyright:
© 2022 The Royal Society of Chemistry.

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