Litcius/Paper detail

Noncovalently Fused-Ring Electron Acceptors with <i>C</i><sub>2<i>v</i></sub> Symmetry for Regulating the Morphology of Organic Solar Cells

Ran Hou, Miao Li, Xueqing Ma, Hao Huang, Hao Lu, Qingqing Jia, Yahui Liu, Xinjun Xu, Hai‐Bei Li, Zhishan Bo

2020ACS Applied Materials & Interfaces61 citationsDOI

Abstract

Four noncovalently fused-ring electron acceptors p-DOC6-2F, o-DOC6-2F, o-DOC8-2F, and o-DOC2C6-2F have been designed and synthesized. p-DOC6-2F and o-DOC6-2F have the same molecular backbone but different molecular shapes and symmetries. p-DOC6-2F has an S-shaped molecular backbone and C2h symmetry, whereas o-DOC6-2F possesses a U-shaped molecular backbone and C2v symmetry. The molecular shape and symmetry can influence the dipole moment, solubility, optical absorption, energy level, molecular packing, and film morphology. Compared with the corresponding p-DOC6-2F, o-DOC6-2F exhibits better solubility, a wider band gap, and a larger dipole moment. When blended with the donor polymer PBDB-T, the C2v symmetric o-DOC6-2F can form an appropriate active layer morphology, whereas the C2h symmetric p-DOC6-2F forms oversized domains. Organic solar cells (OSCs) based on p-DOC6-2F, o-DOC6-2F, o-DOC8-2F, and o-DOC2C6-2F obtained power conversion efficiencies of 9.23, 11.87, 11.23, and 10.80%, respectively. The result reveals that the molecular symmetry can facilely regulate the performance of OSCs.

Topics & Concepts

Organic solar cellMaterials scienceDipoleSymmetry (geometry)SolubilityCrystallographyMolecular orbitalRing (chemistry)Morphology (biology)Polymer solar cellHOMO/LUMOMoleculeEnergy conversion efficiencyPolymerChemistryPhysical chemistryOrganic chemistryOptoelectronicsGeometryBiologyMathematicsComposite materialGeneticsOrganic Electronics and PhotovoltaicsConducting polymers and applicationsPerovskite Materials and Applications
Noncovalently Fused-Ring Electron Acceptors with <i>C</i><sub>2<i>v</i></sub> Symmetry for Regulating the Morphology of Organic Solar Cells | Litcius