Subphthalocyanine-cored star-shaped electron acceptors with perylene diimide wings for non-fullerene solar cells

被引:18
|
作者
Hang, Hao [1 ,2 ]
Zhang, Zijian [1 ,2 ]
Wu, Xiaofu [1 ]
Chen, Yonghong [1 ,2 ]
Li, Hua [1 ,2 ]
Wang, Weijie [1 ,2 ]
Tong, Hui [1 ]
Wang, Lixiang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
OPEN-CIRCUIT VOLTAGE; BULK-HETEROJUNCTION; ORGANIC PHOTOVOLTAICS; BORON SUBPHTHALOCYANINES; EFFICIENT SYNTHESIS; AXIAL SUBSTITUENT; POLYMER ACCEPTOR; PERFORMANCE; DIKETOPYRROLOPYRROLE; DONOR;
D O I
10.1039/c8tc01988f
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Two star-shaped electron acceptors (E-SubPc-PDI and S-SubPc-PDI) based on subphthalocyanine (SubPc) as the core and three perylene diimides (PDIs) as wing groups linked with and without acetylene bridges, respectively, have been synthesized. Compared with conventional SubPc-based acceptors with optical absorption full width at half maximum (FWHM) values of less than 100 nm and optical bandgaps over 2 eV, both E-SubPc-PDI and S-SubPc-PDI possess broader absorption spectra with FWHM values of up to 170 nm and smaller optical bandgaps below 1.9 eV. Due to the different linkages between SubPc and PDIs, they exhibit different molecular geometries, optical properties, energy levels and stacking behaviors. With a more twisted molecular structure, the single bond linked S-SubPc-PDI exhibits reduced intermolecular aggregation and a higher lowest unoccupied molecular orbital (LUMO) level compared to the acetylene bridge-linked E-SubPc-PDI. When blending with a donor polymer PBDB-T, the active layer of PBDB-T:S-SubPc-PDI shows more favorable phase separation and more balanced carrier transport. As a result, solution-processed organic solar cells (OSCs) based on S-SubPc-PDI exhibit a power conversion efficiency (PCE) up to 4.53%, which is much higher than that of E-SubPc-PDI-based devices (1.78%).
引用
收藏
页码:7141 / 7148
页数:8
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