2019
DOI: 10.1002/solr.201900475
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New Conjugated Polymers Based on Dithieno[2,3‐e:3′,2′‐g]Isoindole‐7,9(8H)‐Dione Derivatives for Applications in Nonfullerene Polymer Solar Cells

Abstract: The fast evolution of the narrow bandgap nonfullerene acceptors requires new conjugated wide bandgap polymers for the use of nonfullerene polymer solar cells (PSCs). Herein, two new wide bandgap A1–D1–A2–D1 conjugated polymers with the same dithieno[2,3‐e:3′,2′‐g]isoindole‐7,9(8H)‐dione (DTID) acceptor (A1) and thiophene donor (D1) and different A2 acceptor units, i.e., benzothiadiazole (BT) and fluorinated benzothiadiazole (f‐BT) denoted as P113 and P114, are designed, and the effect of fluorination of the BT… Show more

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Cited by 9 publications
(5 citation statements)
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References 78 publications
(89 reference statements)
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“…In Scheme 1 , the synthesis process to design the copolymers P133 and P135 is shown. The monomers 4,8‐Bis (5‐(2‐ethylhexyl) thiophen‐2‐yl) benzo [1,2‐b:4,5‐b'] thiophene‐2,6 diyl) bis (trilstmethyannane) M1, [ 40 ] 2,5‐dibromo‐8,10‐bis (2‐octyldodecyl) −8 H‐thieno [3′,2′:5.6;2″,3″:7.8] naphtho [2,3‐d] imidazole‐9 (10 H) ‐one M2, [ 41 ] and 2,5‐Dibromo‐8‐(2‐octyldodecyl)−7 H‐dithieno [2,3‐e:3′, 2′‐g] isoindole‐7, 9 (8H)‐dione M3 [ 42 ] were synthesized as reported in the literature. The P133 and P135 were prepared by conventional Stille cross‐coupling polymerization among M1 and M2 , or M3 , respectively, in the presence of a palladium catalyst Pd (Ph 3 P) 4 in boiling toluene for 48 h in a stream of argon.…”
Section: Resultsmentioning
confidence: 99%
“…In Scheme 1 , the synthesis process to design the copolymers P133 and P135 is shown. The monomers 4,8‐Bis (5‐(2‐ethylhexyl) thiophen‐2‐yl) benzo [1,2‐b:4,5‐b'] thiophene‐2,6 diyl) bis (trilstmethyannane) M1, [ 40 ] 2,5‐dibromo‐8,10‐bis (2‐octyldodecyl) −8 H‐thieno [3′,2′:5.6;2″,3″:7.8] naphtho [2,3‐d] imidazole‐9 (10 H) ‐one M2, [ 41 ] and 2,5‐Dibromo‐8‐(2‐octyldodecyl)−7 H‐dithieno [2,3‐e:3′, 2′‐g] isoindole‐7, 9 (8H)‐dione M3 [ 42 ] were synthesized as reported in the literature. The P133 and P135 were prepared by conventional Stille cross‐coupling polymerization among M1 and M2 , or M3 , respectively, in the presence of a palladium catalyst Pd (Ph 3 P) 4 in boiling toluene for 48 h in a stream of argon.…”
Section: Resultsmentioning
confidence: 99%
“…In the last few years, the power conversion efficiency (PCE) of organic solar cells (OSCs) has been triggered mainly due to the development of novel wide-bandgap conjugated polymers and low-bandgap non-fullerene acceptors (NFAs), active layer morphology optimization, device interface engineering and utilization of various novel nanomaterials. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19] Several research groups have reported PCEs of more than 19% in single bulk OSCs. [20][21][22][23][24][25][26] Although high-performance devices have been frequently demonstrated, their PCE and open-circuit voltage (V OC ) still lag behind those of other competing technologies such as Si, GaAs, and perovskite solar cells.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, some versatile non‐fullerene acceptors (NFAs) have been dedicated to the OSC owing to easy tuning absorption profile, frontier electronic energy levels adjustment, and modulating crystallinity, leading to OSCs with PCE approaching 20%. [ 26,33–39 ]…”
Section: Introductionmentioning
confidence: 99%
“…Recently, some versatile non-fullerene acceptors (NFAs) have been dedicated to the OSC owing to easy tuning absorption profile, frontier electronic energy levels adjustment, and modulating crystallinity, leading to OSCs with PCE approaching 20%. [26,[33][34][35][36][37][38][39] This observation motivated us to undertake a comprehensive and systematic review to provide an up-to-date account of the research activities in this rapidly growing research field. Our systematic literature review is exhaustive as we cover a large volume of the most recent and relevant literature, from material processing to device performances and stability.…”
Section: Introductionmentioning
confidence: 99%