2018
DOI: 10.1021/acs.jpcc.8b09336
|View full text |Cite
|
Sign up to set email alerts
|

Introducing Four 1,1-Dicyanomethylene-3-indanone End-Capped Groups as an Alternative Strategy for the Design of Small-Molecular Nonfullerene Acceptors

Abstract: Linear A–D–A or A−π–D−π–A architectures are predominant in the design of promising nonfullerene acceptors (NFAs), which promoted the rapid progress of organic solar cells. However, utilization of four electron-accepting units (A) to construct four-armed NFAs is rarely reported and the relationship of structure–properties–performance is unclear. In this study, we designed and synthesized a novel acceptor (A401) with an (AA)−π–D−π–(AA) configuration, where four 1,1-dicyanomethylene-3-indanone groups were used as… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
34
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
7

Relationship

3
4

Authors

Journals

citations
Cited by 85 publications
(34 citation statements)
references
References 51 publications
0
34
0
Order By: Relevance
“…[ 134 ] These molecules showed lower reorganization energy due to restricted rotation about molecular backbone. [ 135 ] Recently, Yu et al synthesized three nonfused acceptors based on 2,2′‐(2,5‐dialkyloxy‐1,4‐phenylene) dithiophene (PT) core. [ 136 ] With PBDB‐TF, highest PCE of 13.97% was achieved.…”
Section: Probing the Active Layer Morphology With Gisaxs And Giwaxsmentioning
confidence: 99%
“…[ 134 ] These molecules showed lower reorganization energy due to restricted rotation about molecular backbone. [ 135 ] Recently, Yu et al synthesized three nonfused acceptors based on 2,2′‐(2,5‐dialkyloxy‐1,4‐phenylene) dithiophene (PT) core. [ 136 ] With PBDB‐TF, highest PCE of 13.97% was achieved.…”
Section: Probing the Active Layer Morphology With Gisaxs And Giwaxsmentioning
confidence: 99%
“…This helps to attain push-pull arrangement that enables polarization of electronic cloud and enhances the chances of holeelectron separation. [46,47] Large number of donor materials are hard to explore. We have put some restrictions to define chemical space.…”
Section: Designing New Small-molecule Donorsmentioning
confidence: 99%
“…[17] Molecular structure of Chemistry-A European Journal materials controls their performance. [18] It is important to study the materials at molecular level. Graphical representation of frontier molecular orbitals is given in Figure 2.…”
Section: Electronic Propertiesmentioning
confidence: 99%