4.8 Article

Symmetry-Induced Ordered Assembly of a Naphthobisthiadiazole-Based Nonfused-Ring Electron Acceptor Enables Efficient Organic Solar Cells

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 46, Pages 52233-52243

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c13304

Keywords

centrosymmetric core; naphthobisthiadiazole; nonfused-ring electron acceptors; nonfullerene acceptors; organic solar cells

Funding

  1. National Research Foundation of Korea (NRF) [2020R1A2C3004477, 2021R1A4A1030944, 2019R1A6A1A11053838]
  2. Ministry of Science and ICT, Korea
  3. National Research Foundation of Korea [2021R1A4A1030944, 2020R1A2C3004477] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study investigates the effects of the structural symmetry of nonfused-ring electron acceptors (NFREAs) on the performance of organic solar cells (OSCs). The results demonstrate that NFREAs with centrosymmetric cores have advantages in terms of electron transport and power conversion efficiency.
Nonfused-ring electron acceptors (NFREAs) have received increasing attention for use in organic solar cells (OSCs) because of their synthetic simplicity and tunable optical spectra. However, their fundamental molecular interactions and the mechanism by which they govern the property-function relations of OSCs remain elusive. Here, to investigate the effects of the structural symmetry of NFREAs, two acceptor-donor-acceptor'-donor-acceptor ( A-D-A'-D-A)-type NFREAs, 2,2'-(((naphtho[1,2-c:5,6-c']bis-[1,2,5]thiadiazole-5,10-diylbis(4,4-bis(2-butyloctyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-6,2-diyl))-bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (NTz-4F) and 2,2'-(((benzo[c][1,2,5]thiadiazole-4,7-diylbis(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-6,2-diyl))bis(methaneylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))- dimalononitrile (BT-4F), are designed and synthesized. They have different A' cores: NTz-4F has a modified centrosymmetric NTz core, whereas BT-4F has a modified axisymmetric BT core. In pristine films, the NTz-4F, which has a centrosymmetric core, shows substantially enhanced intermolecular interaction and microstructural crystalline ordering compared with BT-4F, which has an axisymmetric core. Even in blends with poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b']dithiophene))-alt-(5,5-(1',3'-di-2-thienyl-5',7'-bis(2-ethylhexyl)benzo[1',2'-c:4',5'-c']dithiophene-4,8,-dione))] (PBDB-T), NTz-4F retains its highly crystalline structure, whereas BT-4F loses crystalline packing. These changes in NTz-4F result in increased electron transport and suppressed nonradiative voltage loss, resulting in a power conversion efficiency of 9.14% for PBDB-T:NTz-4F vs 7.18% for PBDBT:BT-4F. This work demonstrates that centrosymmetric-structured cores are promising building blocks for high-performance NFREA-based OSCs.

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