Affiliation:
1. School of Materials and Chemical Engineering Zhongyuan University of Technology Zhengzhou 451191 China
2. Henan Institute of Advanced Technology Zhengzhou University Zhengzhou 450003 China
3. CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology Beijing 100190 China
4. National Engineering Research Center for Colloidal Materials School of Chemistry & Chemical Engineering Shandong University Jinan 250100 China
Abstract
AbstractAsymmetric non‐fullerene small molecules acceptor (as‐NF‐SMAs) exhibit greater vitality in photovoltaic materials compared to their symmetric counterparts due to their larger dipole moments and stronger intermolecular interactions, which facilitate exciton dissociation and charge transmission in organic solar cells (OSCs). Here, we introduced a new as‐NF‐SMAs, named IDT‐TNIC, as the third component in ternary organic solar cells (TOSCs). The asymmetric IDT‐TNIC used indacenodithiophene (IDT) as the central core, alkylthio‐thiophene as a unilateral π‐bridge and extended end groups as electron‐withdrawing. Due to the non‐covalent conformational lock (NCL) established between O⋅⋅⋅S and S⋅⋅⋅S, the IDT‐TNIC molecule preserves its coplanar structure effectively. Furthermore, IDT‐TNIC exhibits complementary absorption and excellent compatibility with donor and acceptor materials, as well as optimized ladder energy level arrangement, resulting in a higher and more balanced μh/μe value, more homogeneous and suitable phase separation morphology in TOSCs. Thus, the PCE of the TOSCs reached 17 % when the weight ratio of PM6 : Y6 : IDT‐TNIC was 1 : 1.1 : 0.1, and it is noteworthy that when the device area was increased to 1 cm2, the PCE could still be maintained at over 14 %. Detailed studies and analysis indicate that IDT‐TNIC has great potential as a third component in OSCs and for large‐scale printing in the future.
Funder
Natural Science Foundation of Shandong Province