Intrinsically Chemo- and Thermostable Electron Acceptors for Efficient Organic Solar Cells
Publication in refereed journal

Times Cited
Altmetrics Information

Other information
AbstractThe traditional preparation of non-fullerene acceptors (NFAs) via Knoevenagel condensation reaction (KCR) of aldehyde and active methylene leaves vulnerable and reversible exocyclic vinyl bonds in structures, which undermine the intrinsic chemo- and photostability of NFAs. In this work, we demonstrate a new access to acceptor-donor-acceptor (A-D-A) NFAs via Stille coupling between new electron deficient groups and classic donor core in over 90% yield, wherein the robust carbon-carbon bonds, replacing the exocyclic double bonds from traditional KCR, result in stable A-D-A acceptors, Q1-XF (X representing 0, 2 and 4 fluorine atoms, respectively). Among the three studied examples, Q1-4F exhibits improved optoelectronic and electron transport properties, leading to the best photovoltaic performance with optimal charge kinetics for Q1-4F based OSCs. Overall, this strategy can lead to a new way for developing stable photovoltaic materials.
All Author(s) ListZhang QQ, Li YK, Wang D, Chen Z, Li YH, Li SX, Zhu HM, Lu XH, Chen HZ, Li CZ
Journal nameBulletin of the Chemical Society of Japan
Volume Number94
Issue Number1
Pages183 - 190
LanguagesEnglish-United Kingdom
KeywordsOrganic solar cells, Non-fullerene acceptors, Stability
Web of Science Subject CategoriesChemistry, Multidisciplinary;Chemistry

Last updated on 2021-14-06 at 00:09