Donor–Acceptor–Acceptor's Molecules for Vacuum‐Deposited Organic Photovoltaics with Efficiency Exceeding 9% |
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| Authors: | Xiaozhou Che Chin‐Lung Chung Chou‐Chun Hsu Feng Liu Ken‐Tsung Wong Stephen R Forrest |
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| Institution: | 1. Applied Physics Program, University of Michigan, Ann Arbor, MI, USA;2. Department of Chemistry, National Taiwan University, Taipei, Taiwan;3. Department of Physics and Astronomy and Collaborative Innovation Center of IFSA (CICIFSA), Shanghai Jiaotong University, Shanghai, P. R. China;4. Institute of Atomic and Molecular Science, Academia Sinica, Taipei, Taiwan;5. Department of Physics and Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI, USA |
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| Abstract: | Three vacuum‐deposited donor–acceptor–acceptor (d–a–a') small molecule donors are studied with different side chains attached to an asymmetric heterotetracene donor block for use in high efficiency organic photovoltaics (OPVs). The donor with an isobutyl side chain yields the highest crystal packing density compared to molecules with 2‐ethylhexyl or n‐butyl chains, leading to the largest absorption coefficient and short circuit current in an OPV. It also exhibits a higher fill factor, consistent with its preferred out‐of‐plane molecular π–π stacking arrangement that facilitates charge transport in the direction perpendicular to the substrate. A power conversion efficiency of 9.3 ± 0.5% is achieved under 1 sun intensity, AM 1.5 G simulated solar illumination, which is significantly higher than 7.5 ± 0.4% of the other two molecules. These results indicate that side chain modification of d–a–a' small molecules offers an effective approach to control the crystal packing configuration, thereby improving the device performance. |
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| Keywords: | dipole moment donors solar cells |
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