Over 19 % Efficiency Organic Solar Cells Enabled by Manipulating the Intermolecular Interactions through Side Chain Fluorine Functionalization

被引:88
作者
Hu, Huawei [1 ,2 ]
Liu, Shuai [1 ]
Xu, Jiaoyu [1 ]
Ma, Ruijie [3 ]
Peng, Zhengxing [4 ]
Pena, Top Archie Dela [5 ,8 ]
Cui, Yongjie [1 ]
Liang, Wenting [1 ]
Zhou, Xiaoli [1 ]
Luo, Siwei [6 ]
Yu, Han [6 ]
Li, Mingjie [8 ]
Wu, Jiaying [5 ]
Chen, Shangshang [7 ]
Li, Gang [3 ]
Chen, Yiwang [1 ,2 ]
机构
[1] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Jiangxi Normal Univ, Natl Engn Res Ctr Carbohydrate Synth, Key Lab Fluorine & Silicon Energy Mat & Chem, Minist Educ, 99 Ziyang Ave, Nanchang 330022, Peoples R China
[3] Hong Kong Polytech Univ, Res Inst Smart Energy RISE, Dept Elect & Elect Engn, Guangdong Hong Kong Macao GHM Joint Lab Photon The, Hong Kong 999077, Peoples R China
[4] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[5] Hong Kong Univ Sci & Technol Guangzhou, Adv Mat Thrust, Funct Hub, Guangzhou 511400, Peoples R China
[6] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong 999077, Peoples R China
[7] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210023, Peoples R China
[8] Hong Kong Polytech Univ, Fac Sci, Dept Appl Phys, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
non-fullerene acceptors; fluorine functionalization; intermolecular interactions; solar cells; molecular packing; CONJUGATED POLYMERS; PHASE-SEPARATION; PHOTOVOLTAICS; PERFORMANCE; ACCEPTORS; ENERGY;
D O I
10.1002/anie.202400086
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorine side chain functionalization of non-fullerene acceptors (NFAs) represents an effective strategy for enhancing the performance of organic solar cells (OSCs). However, a knowledge gap persists regarding the relationship between structural changes induced by fluorine functionalization and the resultant impact on device performance. In this work, varying amounts of fluorine atoms were introduced into the outer side chains of Y-series NFAs to construct two acceptors named BTP-F0 and BTP-F5. Theoretical and experimental investigations reveal that side-chain fluorination significantly increase the overall average electrostatic potential (ESP) and charge balance factor, thereby effectively improving the ESP-induced intermolecular electrostatic interaction, and thus precisely tuning the molecular packing and bulk-heterojunction morphology. Therefore, the BTP-F5-based OSC exhibited enhanced crystallinity, domain purity, reduced domain spacing, and optimized phase distribution in the vertical direction. This facilitates exciton diffusion, suppresses charge recombination, and improves charge extraction. Consequently, the promising power conversion efficiency (PCE) of 17.3 % and 19.2 % were achieved in BTP-F5-based binary and ternary devices, respectively, surpassing the PCE of 16.1 % for BTP-F0-based OSCs. This work establishes a structure-performance relationship and demonstrates that fluorine functionalization of the outer side chains of Y-series NFAs is a compelling strategy for achieving ideal phase separation for highly efficient OSCs. The introduction of precisely controlled fluorine atoms into the outer side chains of Y-series non-fullerene acceptors substantially increased the overall average electrostatic potential and charge balance factor. This enhancement improved intermolecular interaction, allowing for precise tuning of molecular packing and bulk-heterojunction morphology. Consequently, BTP-F5-based binary and ternary devices achieved remarkable power conversion efficiencies of 17.3 % and 19.2 %, respectively. image
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页数:10
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