2016
DOI: 10.1016/j.dyepig.2016.07.007
|View full text |Cite
|
Sign up to set email alerts
|

Diketopyrrolopyrrole-based oligomers accessed via sequential C H activated coupling for fullerene-free organic photovoltaics

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
18
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 52 publications
(18 citation statements)
references
References 70 publications
0
18
0
Order By: Relevance
“…In addition, it was worth noting that the high V oc value about 1.20 V was the highest result among all the DPP‐based nonfullerene small molecule acceptors to date according to the best knowledge of us. Later, a new nonfullerene small molecule acceptor D10 which was similar to the D2 acceptor was developed by Chen group . However, when blended with the P3HT donor, the PCE performance was only 2.43% of D10 compared to that 5.10% of D2, which was owing to the much lower J sc and FF values.…”
Section: Nonfullerene Small Molecule Acceptorsmentioning
confidence: 99%
See 1 more Smart Citation
“…In addition, it was worth noting that the high V oc value about 1.20 V was the highest result among all the DPP‐based nonfullerene small molecule acceptors to date according to the best knowledge of us. Later, a new nonfullerene small molecule acceptor D10 which was similar to the D2 acceptor was developed by Chen group . However, when blended with the P3HT donor, the PCE performance was only 2.43% of D10 compared to that 5.10% of D2, which was owing to the much lower J sc and FF values.…”
Section: Nonfullerene Small Molecule Acceptorsmentioning
confidence: 99%
“…Owing to the broad and planar structure, high photochemical stability, easy synthesis, and modification, as well as high charge transport ability, common small molecules such as perylene diimides (PDI), naphthalene diimides (NDI), phthalimide (PhI), diketopyrrolopyrrole (DPP), and so on, are widely employed as the electron deficient materials. The strong electron‐withdrawing property of imides also makes them excellent candidates for functionalizing aromatic rings to create building blocks for electron‐deficient photoactive materials.…”
Section: Nonfullerene Small Molecule Acceptorsmentioning
confidence: 99%
“…Recently Chen et al . reported two acceptors DPP38 and DPP39 based on DPP moiety attached with biphenyl and tetraphenyl ethylene moiety by direct arylation of mono‐phenyl capped DPP using tetrakis(4‐bromophenyl)ethene (TBPE) and tetrabromo‐biphenyl (TBBP) as arylating reagents . Tetraphenylethene (TPE) is well known building block used in the field of aggregation induced emission (AIE) and for making 3D non‐fullerene acceptor.…”
Section: Non‐fullerene Acceptors Containing Four Dpp/ Btd/pdi Unitsmentioning
confidence: 99%
“…Liu and co-workers reported a similar molecule, 36 , which had an additional phenyl ring attached to each DPP arm [ 45 ]. The molecule was synthesized using sequential direct C-H arylation with a high overall yield.…”
Section: Organic Photovoltaicsmentioning
confidence: 99%