New 3,8‐difluoro indoloindole‐based copolymers for organic solar cell

Summary The performance of an array of donor‐acceptor based bulk heterojunction (BHJ) polymer solar cells (PSC) containing indoloindole as a key donor block with varying degrees of fluorinated benzothiadiazole (BT) as an acceptor block is reported. Fluorination of BT can enhance crystallinity and pl...

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Veröffentlicht in:International journal of energy research 2021-04, Vol.45 (5), p.7806-7813
Hauptverfasser: Lee, Gyeong Seok, Shin, Hee Jeong, Shome, Sanchari, Park, Ji‐Hyun, Ko, Seo‐Jin, Choi, Hyosung, Kim, Yun‐Hi
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Sprache:eng
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Zusammenfassung:Summary The performance of an array of donor‐acceptor based bulk heterojunction (BHJ) polymer solar cells (PSC) containing indoloindole as a key donor block with varying degrees of fluorinated benzothiadiazole (BT) as an acceptor block is reported. Fluorination of BT can enhance crystallinity and planarity of the polymer backbone due to intramolecular F‐S interactions. This also leads to deeper highest occupied molecular orbital (HOMO) energy levels leading to high JSC and VOC. The PSC properties of this series of new copolymer donors blended with fullerene acceptors show a homogeneous and uniform fibrous network in the blend film. The most homogeneous film was achieved with monofluorinated BT (PFDHI‐TFT) that resulted in better charge extraction pathway leading to high power conversion efficiency (PCE). The solar cell using PFDHI‐TFT as donor and fullerene acceptor showed PCE of 5.98% with VOC of 0.80 V, JSC of 10.56 mA cm−2, and fill factor (FF) of 0.71, respectively, under AM 1.5G illumination (100 mW cm−2) in the absence of annealing. The performance of an array of donor‐acceptor based bulk heterojunction (BHJ) polymer solar cells (PSC) containing indoloindole as a key donor block with varying degrees of fluorinated benzothiadiazole (BT) as an acceptor block is reported. Fluorination of BT can enhance crystallinity and planarity of the polymer backbone due to intramolecular F‐S interactions.
ISSN:0363-907X
1099-114X
DOI:10.1002/er.6365