Efficient Diketopyrrolopyrrole-Based Small-Molecule Bulk-Heterojunction Solar Cells with Different Electron-Donating End-Groups

被引:14
|
作者
Kim, Yu Jin [1 ]
Back, Jang Yeol [2 ,3 ]
Kim, Seul-Ong [2 ,3 ]
Jeon, Chan-Woo [4 ,5 ]
Park, Chan Eon [1 ]
Kim, Yun-Hi [4 ,5 ]
机构
[1] Pohang Univ Sci & Technol, Dept Chem Engn, POSTECH Organ Elect Lab, Pohang 790784, South Korea
[2] Gyeongsang Natl Univ, Sch Mat Sci & Engn, Jinju 660701, South Korea
[3] Gyeongsang Natl Univ, Res Inst Green Energy Convergence Technol REGET, Jinju 660701, South Korea
[4] Gyeongsang Natl Univ, Dept Chem, Jinju 660701, South Korea
[5] Gyeongsang Natl Univ, Res Inst Nat Sci, Jinju 660701, South Korea
关键词
absorption; alkynes; conjugation; cross-coupling; solar cells; HIGH FILL FACTORS; ORGANIC SEMICONDUCTORS; BENZODITHIOPHENE UNIT; CONJUGATED POLYMERS; SIDE-CHAIN; PERFORMANCE; DESIGN; ENERGY; TRANSISTOR; SEPARATION;
D O I
10.1002/asia.201402223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of small molecules that contained identical pi-spacers (ethyne), a central diketopyrrolopyrrole (DPP) unit, and different aromatic electron-donating end-groups were synthesized and used in organic solar cells (OSCs) to study the effect of electron-donating groups on the device performance. The three compounds, DPP-A-Ph, DPP-A-Na, and DPP-A-An, possessed intense absorption bands that covered a wide range, from 350 to 750 nm, and relatively low HOMO energy levels, from -5.50 to -5.55 eV. DPP-A-An, which contained anthracene end-groups, demonstrated a stronger absorbance and a higher hole mobility than DPP-A-Ph, which contained phenyl groups, and DPP-A-Na, which contained naphthalene units. The power-conversion efficiencies (PCEs) of OSCs based on organic: PC71BM blends (1: 1, w/w) with a processed DIO additive were 3.93% for DPP-A-An, 3.02% for DPP-Na, and 2.26% for DPP-A-Ph. These findings suggest that a DPP core that is functionalized with electron-donating capping groups constitutes a promising new class of solution-processable small molecules for OSC applications.
引用
收藏
页码:2505 / 2513
页数:9
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