Simple non-fused ring electron acceptors with well-controlled terminal group stacking
Source abstract
Abstract
Producing high-performance and inexpensive non-fullerene acceptors is a great challenge in the field of organic photovoltaics. Herein, three non-fused ring electron acceptors (NFREAs), TT-O-2F, TT-S-2F, and TT-Se-2F, have been designed and can be modularly synthesized with a few high-productivity steps. According to our results, TT-S-2F and TT-Se-2F have planar molecular backbones because of the existence of S⋅⋅⋅O and Se⋅⋅⋅O intramolecular non-covalent interactions, whereas TT-O-2F has a twisted molecular backbone. In particular, TT-S-2F exhibits the largest terminal group overlapping area and exciton diffusion length among these acceptors, which could facilitate charge transport. The devices based on TT-S-2F can generate an excellent power conversion efficiency (PCE) of 15.29%, much higher than TT-O-2F (10.43%) and TT-Se-2F (12.23%), which are also among the highest PCEs based on NFREAs. Our work highlights the importance of well-controlled terminal packing in designing high-performance NFREAs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (49)
Show source-provided references
1. Wide-gap non-fullerene acceptor enabling high-performance organic photovoltaic cells for indoor applications10.1038/s41560-019-0448-5 ↗
2. Non-fullerene acceptors with branched side chains and improved molecular packing to exceed 18% efficiency in organic solar cells10.1038/s41560-021-00820-x ↗
3. Processing Strategies for an organic photovoltaic module with over 10% efficiency10.1016/j.joule.2019.11.006 ↗
4. Recent advances in bulk heterojunction polymer solar cells10.1021/acs.chemrev.5b00098 ↗
5. Recent progress in organic solar cells (Part I material science)10.1007/s11426-021-1180-6 ↗
6. Molecular optimization enables over 13% efficiency in organic solar cells10.1021/jacs.7b02677 ↗
7. Single-junction organic solar cell with over 15% efficiency using fused-ring acceptor with electron-deficient core10.1016/j.joule.2019.01.004 ↗
8. Reduced non-radiative charge recombination enables organic photovoltaic cell approaching 19% efficiency10.1016/j.joule.2021.06.020 ↗
9. Single-junction organic solar cells with 19.17% efficiency enabled by introducing one asymmetric guest acceptor10.1002/adma.202110147 ↗
10. Manipulating the D:A interfacial energetics and intermolecular packing for 19.2% efficiency organic photovoltaics10.1039/D2EE00595F ↗
11. Single-junction organic photovoltaic cell with 19% efficiency10.1002/adma.202102420 ↗
12. A tandem organic photovoltaic cell with 19.6% efficiency enabled by light distribution control
13. Tandem organic solar cell with 20.2% efficiency10.1016/j.joule.2021.12.017 ↗
14. Exploiting noncovalently conformational locking as a design Strategy for high performance fused-ring electron acceptor used in polymer solar cells10.1021/jacs.7b00566 ↗
15. Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells10.1038/s41467-019-11001-6 ↗
16. Simple non-fused electron acceptors for efficient and stable organic solar cells10.1038/s41467-019-10098-z ↗
17. High-performance noncovalently fused-ring electron acceptors for organic solar cells enabled by noncovalent intramolecular interactions and end-group engineering10.1002/anie.202100390 ↗
18. Simple nonfused ring electron acceptors with 3D network packing structure boosting the efficiency of organic solar cells to 15.4410.1002/aenm.202102591 ↗
19. Completely non-fused electron acceptor with 3D-interpenetrated crystalline structure enables efficient and stable organic solar cell10.1038/s41467-021-25394-w ↗
20. Efficient organic solar cell with 16.88% efficiency enabled by refined acceptor crystallization and morphology with improved charge transfer and transport properties
21. Polymerized small molecular acceptor with branched side chains for all polymer solar cells with efficiency over 16.7
22. Chlorination: an effective Strategy for high-performance organic solar cells10.1002/advs.202000509 ↗
23. 17.1 %-Efficient eco-compatible organic solar cells from a dissymmetric 3D network acceptor10.1002/anie.202013053 ↗
24. High-performance fluorinated fused-ring electron acceptor with 3D stacking and exciton/charge transport10.1002/adma.202000645 ↗
25. Small molecule acceptors with a nonfused architecture for high-performance organic photovoltaics10.1021/acs.chemmater.8b04087 ↗
26. Semi-crystalline photovoltaic polymers with efficiency exceeding 9% in a ∼300 nm thick conventional single-cell device10.1039/C4EE01529K ↗
27. Organic and polymeric semiconductors enhanced by noncovalent conformational locks10.1021/acs.chemrev.7b00084 ↗
28. A simple high-performance fully nonfused ring electron acceptor with a planar molecular backbone10.1016/j.cej.2022.136472 ↗
29. Improving the photovoltaic performance by employing alkyl chains perpendicular to the π-conjugated plane of an organic dye in dye-sensitized solar cells10.1039/C9TC01520E ↗
30. n-Channel polymers by design: optimizing the interplay of Solubilizing substituents, crystal packing, and field-effect transistor characteristics in polymeric bithiophene-imide semiconductors10.1021/ja710815a ↗
31. Pyrrole-fused azacoronene family: the influence of replacement with dialkoxybenzenes on the optical and electronic properties in neutral and oxidized states10.1021/ja402371f ↗
32. Selenium-containing organic photovoltaic materials10.1021/acs.accounts.1c00443 ↗
33. Enhancing the photovoltaic performance of ladder-type heteroheptacene-based nonfullerene acceptors by incorporating halogen atoms on their ending groups10.1002/adfm.202010436 ↗
34. Enhancing the photovoltaic performance of nonfullerene acceptors via conjugated rotatable end groups10.1002/aenm.201802131 ↗
35. Enhancing the performance of organic solar cells by hierarchically Supramolecular Self-assembly of fused-ring electron acceptors10.1021/acs.chemmater.8b01319 ↗
36. Crystal engineering in organic photovoltaic acceptors: a 3D network approach
37. Exciton diffusion in organic semiconductors10.1039/C5EE00925A ↗
38. Exciton diffusion in organic photovoltaic cells10.1039/C3EE42444H ↗
39. Over 16% efficiency from thick-film organic solar cells10.1016/j.scib.2020.08.027 ↗
40. Design, application, and morphology study of a new photovoltaic polymer with strong aggregation in solution state10.1021/ma301900h ↗
41. A large-bandgap conjugated polymer for versatile photovoltaic applications with high performance10.1002/adma.201502110 ↗
42. Chlorination enabling a low-cost benzodithiophene-based wide-bandgap donor polymer with an efficiency of over 17
43. A versatile planar building block with C2V Symmetry for high-performance non-halogenated solvent processable polymer donors
44. Assessing the validity of transient photovoltage measurements and analysis for organic solar cells10.1103/PhysRevApplied.10.024038 ↗
45. Experimental determination of the rate law for charge carrier decay in a polythiophene: fullerene solar cell10.1063/1.2891871 ↗
46. High-efficiency organic solar cells with reduced nonradiative voltage loss enabled by a highly emissive narrow bandgap fused ring acceptor
47. A fully non-fused ring acceptor with planar backbone and near-IR absorption for high performance polymer solar cells10.1002/anie.202010856 ↗
48. High-efficiency organic solar cells based on a low-cost fully non-fused electron acceptor
49. Simple nonfused-ring electron acceptors with noncovalently conformational locks for low-cost and high-performance organic solar cells enabled by end-group engineering