2016
DOI: 10.1016/j.orgel.2016.05.010
|View full text |Cite
|
Sign up to set email alerts
|

An asymmetric small molecule based on thieno[2,3-f]benzofuran for efficient organic solar cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
8
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
6
1

Relationship

2
5

Authors

Journals

citations
Cited by 20 publications
(8 citation statements)
references
References 51 publications
0
8
0
Order By: Relevance
“…However, the wide scale development of organic devices is hampered by the fact that the formers are burdened by a relatively low efficiency, and generally by a lower stability compared to inorganic materials. Hence, an important research activity is constantly developed by many research groups in order to develop new materials to overcome the well-known efficiency and stability issues. …”
Section: Introductionmentioning
confidence: 99%
“…However, the wide scale development of organic devices is hampered by the fact that the formers are burdened by a relatively low efficiency, and generally by a lower stability compared to inorganic materials. Hence, an important research activity is constantly developed by many research groups in order to develop new materials to overcome the well-known efficiency and stability issues. …”
Section: Introductionmentioning
confidence: 99%
“…This compound finds its application in organic solar cells as donor material having wide absorption characteristics. [38] Vincetti and co-workers synthesized benzofuran-2-carboxamides via microwave-assisted one pot protocol, the steps involed are shown in Scheme 6. They improved and standardized metal-free multicomponent microwave synthesis of title compounds by using commercially available raw materials such as 2-hydroxyacetophenones, benzonitrile, and benzaldehyde (48).…”
Section: Synthetic Strategies Of Benzofuran Derivativesmentioning
confidence: 99%
“…Qiu et al designed a small molecule ( SMTBF1 ) by utilizing 2‐ethylhexyloxy‐substituted TBF as the central donor block and ethylrhodanine as terminal ( Figure ). [ 278 ] Owing to the good stacking of TBF unit, SMTBF1 showed good phase separation and proper aggregation size in the blend films gave a very high FF of 0.72 and a promising PCE of 6.32%. In order to systematically investigate the effect of the central BDC derivatives on the photovoltaic performance of small molecules, Fan et al used BDT, TBF ( SMTBF2 ), or BDF as donor core and DPP as acceptor unit to construct three small molecule donors.…”
Section: Benzodichalcogenophene‐based Materials Used In Oscsmentioning
confidence: 99%