TY - JOUR
T1 - Multiple-Asymmetric Molecular Engineering Enables Regioregular Selenium-Substituted Acceptor with High Efficiency and Ultra-low Energy Loss in Binary Organic Solar Cells
AU - Yang, Can
AU - Gao, Yuan
AU - Zhang, Heng
AU - Yao, Ze Fan
AU - Li, Er Long
AU - Guan, Hong Hai
AU - Zhi, Hong Fu
AU - Yuan, Quan
AU - Jee, Min Hun
AU - Woo, Han Young
AU - Min, Jie
AU - Wang, Jin Liang
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Asymmetric molecular engineering is utilized for developing efficient small molecular acceptors (SMAs), whereas adopting multiple asymmetric strategies at the terminals, side chains, and cores of efficient SMAs remains a challenge, and effects on reducing energy loss (Eloss) have been rarely investigation. Herein, four regioregular multiple-asymmetric SMAs (DASe-4F, DASe-4Cl, TASe-2Cl2F, and TASe-2F2Cl) are constructed by delicately manipulating the number and position of F and Cl on end groups. Triple-asymmetric TASe-2F2Cl not only exhibits a unique and most compact 3D network crystal stacking structure but also possesses excellent crystallinity and electron mobility in neat film. Surprisingly, the PM1:TASe-2F2Cl-based binary organic solar cells (OSCs) yield a champion power conversion efficiencies (PCEs) of 19.32%, surpassing the PCE of 18.27%, 17.25%, and 16.30% for DASe-4F, DASe-4Cl, and TASe-2Cl2F-based devices, which attributed to the optimized blend morphology with proper phase separation and more ordered intermolecular stacking and excellent charge transport. Notably, the champion PCE of 19.32% with ultralow nonradiative recombination energy loss (ΔE3) of 0.179 eV marks a record-breaking result for selenium-containing SMAs in binary OSCs. Our innovative multiple-asymmetric molecular engineering of precisely modulating the number and position of fluorinated/chlorinated end groups is an effective strategy for obtaining highly-efficient and minimal ΔE3 of selenium-substituted SMAs-based binary OSCs simultaneously.
AB - Asymmetric molecular engineering is utilized for developing efficient small molecular acceptors (SMAs), whereas adopting multiple asymmetric strategies at the terminals, side chains, and cores of efficient SMAs remains a challenge, and effects on reducing energy loss (Eloss) have been rarely investigation. Herein, four regioregular multiple-asymmetric SMAs (DASe-4F, DASe-4Cl, TASe-2Cl2F, and TASe-2F2Cl) are constructed by delicately manipulating the number and position of F and Cl on end groups. Triple-asymmetric TASe-2F2Cl not only exhibits a unique and most compact 3D network crystal stacking structure but also possesses excellent crystallinity and electron mobility in neat film. Surprisingly, the PM1:TASe-2F2Cl-based binary organic solar cells (OSCs) yield a champion power conversion efficiencies (PCEs) of 19.32%, surpassing the PCE of 18.27%, 17.25%, and 16.30% for DASe-4F, DASe-4Cl, and TASe-2Cl2F-based devices, which attributed to the optimized blend morphology with proper phase separation and more ordered intermolecular stacking and excellent charge transport. Notably, the champion PCE of 19.32% with ultralow nonradiative recombination energy loss (ΔE3) of 0.179 eV marks a record-breaking result for selenium-containing SMAs in binary OSCs. Our innovative multiple-asymmetric molecular engineering of precisely modulating the number and position of fluorinated/chlorinated end groups is an effective strategy for obtaining highly-efficient and minimal ΔE3 of selenium-substituted SMAs-based binary OSCs simultaneously.
KW - End-group engineering
KW - Energy loss
KW - Multiple-asymmetric acceptors
KW - Organic solar cells
KW - Selenium substitution
UR - http://www.scopus.com/inward/record.url?scp=105005991337&partnerID=8YFLogxK
U2 - 10.1002/anie.202506795
DO - 10.1002/anie.202506795
M3 - Article
AN - SCOPUS:105005991337
SN - 1433-7851
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
ER -