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Conjugated Polymers Based on Difluorobenzoxadiazole toward Practical Application of Polymer Solar Cells
Author(s) -
Wang Junyi,
Wang Shiliang,
Duan Chunhui,
Colberts Fallon J. M.,
Mai Jiangquan,
Liu Xi,
Jia Xiao'e,
Lu Xinhui,
Janssen René A. J.,
Huang Fei,
Cao Yong
Publication year - 2017
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201702033
Subject(s) - materials science , polymer , polymer solar cell , active layer , acceptor , photovoltaic system , context (archaeology) , nanotechnology , fabrication , photoactive layer , rational design , chemical engineering , layer (electronics) , composite material , thin film transistor , electrical engineering , medicine , paleontology , physics , alternative medicine , engineering , condensed matter physics , pathology , biology
To advance polymer solar cells (PSCs) toward real‐world applications, it is crucial to develop materials that are compatible with a low‐cost large‐scale manufacturing technology. In this context, a practically useful polymer should fulfill several critical requirements: the capability to provide high power conversion efficiencies (PCEs) via low‐cost fabrication using environmentally friendly solvents under mild thermal conditions, resulting in an active layer that is thick enough to minimize defects in large‐area films. Here, the development of new photovoltaic polymers is reported through rational molecular design to meet these requirements. Benzodithiophene (BDT)‐difluorobenzoxadiazole (ffBX)‐2‐decyltetradecyl (DT), a wide‐bandgap polymer based on ffBX and BDT emerges as the first example that fulfills the qualifications. When blended with a low‐cost acceptor (C 60 ‐fullerene derivative), BDT‐ffBX‐DT produces a PCE of 9.4% at active layer thickness over 250 nm. BDT‐ffBX‐DT devices can be fabricated from nonhalogenated solvents at low processing temperature. The success of BDT‐ffBX‐DT originates from its appropriate electronic structure and charge transport characteristics, in combination with a favorable face‐on orientation of the polymer backbone in blends, and the ability to form proper phase separation morphology with a fibrillar bicontinuous interpenetrating network in bulk‐heterojunction films. With these characteristics, BDT‐ffBX‐DT represents a meaningful step toward future everyday applications of polymer solar cells.