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Over 13% Efficient Organic Solar Cells Based on Low-Cost Pentacyclic A-DA D-A-Type Nonfullerene Acceptor

Song, Jiage (författare)
Cent South Univ, Peoples R China
Cai, Fangfang (författare)
Cent South Univ, Peoples R China
Zhu, Can (författare)
Cent South Univ, Peoples R China; Chinese Acad Sci, Peoples R China
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Chen, Honggang (författare)
Cent South Univ, Peoples R China; Chinese Acad Sci, Peoples R China
Wei, Qingya (författare)
Cent South Univ, Peoples R China
Li, Dongxu (författare)
Cent South Univ, Peoples R China
Zhang, Chujun (författare)
Hong Kong Baptist Univ, Peoples R China; Hong Kong Baptist Univ, Peoples R China
Zhang, Rui (författare)
Linköpings universitet,Elektroniska och fotoniska material,Tekniska fakulteten
Yuan, Jun (författare)
Cent South Univ, Peoples R China
Peng, Hongjian (författare)
Cent South Univ, Peoples R China
So, Shu Kong (författare)
Hong Kong Baptist Univ, Peoples R China; Hong Kong Baptist Univ, Peoples R China
Zou, Yingping (författare)
Cent South Univ, Peoples R China
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 (creator_code:org_t)
2021-06-23
2021
Engelska.
Ingår i: Solar RRL. - : Wiley-Blackwell. - 2367-198X. ; 5:8
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Recent studies have almost focused on finding active layer materials with extended pi-conjugation structures for high-performance organic solar cells (OSCs). However, with the extension of conjugate length, the synthesis difficulty and cost of materials will increase. Achieving high efficiency while reducing material costs is a prerequisite for the commercialization of OSCs. Herein, two low-cost A-DA D-A-type (where A and D represent an electron-withdrawing unit and an electron-donating unit, respectively) nonfullerene acceptors (Y25,Y26) are synthesized with pentacyclic fused backbone as the DA D electron-deficient core and 5,6-difluoro-3-(dicyandiamethyl) indigo as the end groups. Compared with classical Y series acceptors with heptacyclic backbone, although Y25 and Y26 own the reduced conjugated length, they still show moderate performance (11.65% and 13.34%), and the cost of synthesis is significantly reduced. Therefore, we provide a new molecular design idea for commercially efficient nonfullerene OSCs acceptors. We also find that adding alkyl chains to the beta site of thiophenes is beneficial to obtaining the reduced energetic disorder, dominant molecular stacking, and desirable morphology, which can facilitate charge carrier transport and prompt higher short-circuit current density (J(sc)) as well as fill factor.

Ämnesord

NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)

Nyckelord

charge transport; energetic disorder; nonfullerene acceptors; side chains

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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  • Solar RRL (Sök värdpublikationen i LIBRIS)

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