4.7 Article

Asymmetric simple unfused acceptor enabling over 12% efficiency organic solar cells

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 412, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128770

Keywords

Simple acceptors; Unfused acceptors; Framework-property relationship; Core engineering; Organic solar cells

Funding

  1. National Natural Science Foundation of China [21875111, 21905137, 51573077, 51861145401]
  2. Jiangsu Province Natural Science Foundation [BK20180496]

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The study explores the use of unfused acceptors, specifically DBT-4F, in organic solar cells, which show strong near-infrared absorption and narrow optical band gaps leading to high efficiency. The blends of DBT-4F with PBDB-T exhibit champion power conversion efficiency due to better miscibility, making it one of the highest values reported for unfused acceptor based binary OSCs.
High photovoltaic performance with cost-effective material synthesis and device fabrication are the prerequisite for commercialization of organic solar cells (OSCs). Herein, we conduct a systematic structure?property correlation study on unfused acceptors adopting different frameworks. Dithieno[3,2-b:2?,3?-d]pyrrole (DTP) based AD1-D-D2-A asymmetric acceptor (DBT-4F) has been screened as a promising acceptor for high-efficient OSCs. Three DTP-based unfused acceptors display strong near-infrared absorption with narrow optical band gap (Egopt < 1.45 eV). Blends of DBT-4F with PBDB-T contribute a champion power conversion efficiency (PCE) of 12.14% due to better miscibility to form homogenous fibrous phase separation. To the best of our knowledge, the PCE is among the highest values for unfused acceptor based binary OSCs in the literature. The excellent performance of DBT-4F is revealed with more efficient photon-harvesting, higher and more balanced charge transport, and less charge recombination in the blends. Our work manifests the great potential of DTP based asymmetric unfused acceptor for developing high-efficient OSCs via rational molecular design.

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