Rebuilding Peripheral F, Cl, Br Footprints on Acceptors Enables Binary Organic Photovoltaic Efficiency Exceeding 19.7 %

被引:6
作者
Cao, Xiangjian [1 ,2 ,3 ]
Wang, Peiran [1 ,2 ,3 ,5 ]
Jia, Xinyuan [1 ,2 ,3 ]
Zhao, Wenkai [5 ]
Chen, Hongbin [1 ,2 ,3 ]
Xiao, Zheng [1 ,2 ,3 ]
Li, Jiaqi [1 ,2 ,3 ]
Bi, Xingqi [1 ,2 ,3 ]
Yao, Zhaoyang [1 ,2 ,3 ]
Guo, Yaxiao [4 ]
Long, Guankui [5 ]
Li, Chenxi [1 ,2 ,3 ]
Wan, Xiangjian [1 ,2 ,3 ]
Chen, Yongsheng [1 ,2 ,3 ]
机构
[1] Nankai Univ, State Key Lab, Tianjin 300071, Peoples R China
[2] Nankai Univ, Inst Elemento Organ Chem, Frontiers Sci Ctr New Organ Matter, Ctr Nanoscale Sci & Technol, Tianjin 300071, Peoples R China
[3] Nankai Univ, Key Lab Funct Polymer Mat, Renewable Energy Convers & Storage Ctr RECAST, Coll Chem,Inst Polymer Chem, Tianjin 300071, Peoples R China
[4] Tiangong Univ, Sch Chem, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[5] Nankai Univ, Natl Inst Adv Mat, Renewable Energy Convers & Storage Ctr RECAST, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
organic photovoltaic; small molecular acceptor; peripheral halogen permutation; halogenated isomer; molecular packing; SOLAR-CELLS; POLYMER; LOSSES;
D O I
10.1002/anie.202417244
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Given homomorphic fluorine (F), chlorine (Cl) and bromine (Br) atoms are featured with gradually enlarged polarizability/atomic radius but decreased electronegativity, the rational screen of halogen species and locations on small molecular acceptors (SMAs) is quite essential for acquiring desirable molecular packing to boost efficiency of organic solar cells (OSCs). Herein, three isomeric SMAs (CH-F, CH-C and CH-B) are constructed by delicately rebuilding peripheral F, Cl, Br footprints on both central and end units. Such a re-permutation of peripheral halogens could not only maintain the structural symmetry of SMAs to the maximum, but also acquire extra asymmetric benefits of enhanced dipole moment and intramolecular charge transfer, etc. Moreover, central brominating enhances molecular crystallinity of CH-B without introducing undesirable steric hindrance on end groups, thus rendering a better balance between high crystallization and domain size control in PM6:CH-B blend. Further benefitting from the large dielectric constant, small exciton binding energy, optimized molecular packing and great electron transfer integral, CH-B affords the first class binary OSC efficiency of 19.78 %, moreover, the highest efficiency of 18.35 % thus far when increasing active layer thickness to similar to 300 nm. Our successful screening in rebuilding peripheral halogen footprints provides the valuable insight into further rational design of SMAs for record-breaking OSCs.
引用
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页数:11
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