4.8 Article

Medium band-gap non-fullerene acceptors based on a benzothiophene donor moiety enabling high-performance indoor organic photovoltaics

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 14, Issue 8, Pages 4555-4563

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ee00687h

Keywords

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Funding

  1. National Key Research and Development Program of China - MOST [2019YFA0705900]
  2. Basic and Applied Basic Research Major Program of Guangdong Province [2019B030302007]
  3. Guangdong-Hong Kong-Macao Joint Laboratory of Optoelectronic and Magnetic Functional Materials [2019B121205002]
  4. Shen Zhen Technology and Innovation Commission [JCYJ2017041 3173814007, JCYJ20170818113905024]
  5. Hong Kong Research Grants Council [R6021-18, C6023-19G, 16309218, 16310019, 16303917]
  6. Hong Kong Innovation and Technology Commission [ITC-CNERC14SC01, ITS/471/18]
  7. National Natural Science Foundation of China (NSFC) [91433202]

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This study reported the modification of the Y6 structure by replacing its D unit with benzothiophene, synthesizing two novel NFAs for indoor applications, LBT-DF and LBT-SCl. The use of benzothiophene unit resulted in blue-shifting of absorption spectra and up-shifting of LUMO energy levels of the NFAs, leading to higher V-oc and PCE compared to Y6. Interestingly, these NFAs exhibited a non-planar aromatic structure, which is rarely seen in published NFAs known for achieving high PCE.
Organic photovoltaics (OPVs) are one of the most promising technologies to power indoor electronic devices. However, the limited types and design strategies of medium band-gap acceptor materials hinder the development of indoor OPVs. Currently, the state-of-the-art non-fullerene acceptors (NFAs) are Y6 and its derivatives, which are based on an A-DA ' D-A structure. In this paper, we report the modification of the Y6 structure by replacing Y6's D unit (thieno[3,2-b]thiophene) with benzothiophene, and synthesize two novel NFAs (LBT-DF and LBT-SCl) for indoor applications. The use of the benzothiophene unit reduces the intermolecular charge transfer effect, thus blue-shifting the absorption spectra and up-shifting the LUMO energy levels of the NFAs. As a result, LBT-SCl achieves a higher V-oc and thus PCE (up to 25.1%) than Y6 (22.2%) under indoor conditions. Interestingly, these two NFAs exhibit a non-planar aromatic structure, which is rarely observed in the published NFAs, because a better coplanar molecular configuration is usually considered as the critical factor in realizing high PCE. Different from the above mentioned molecular design concept, we find that non-planar structure acceptors also have great potential in OPVs. Our work provides an effective OPV material design guideline for developing high-performance indoor OPVs and also opens a new direction for the design of NFAs.

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