Non-fullerene acceptor organic photovoltaics with intrinsic operational lifetimes over 30 years

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作者
Yongxi Li
Xiaheng Huang
Kan Ding
Hafiz K. M. Sheriff
Long Ye
Haoran Liu
Chang-Zhi Li
Harald Ade
Stephen R. Forrest
机构
[1] Material Science and Engineering,Departments of Electrical Engineering
[2] and Physics,Department of Physics and Organic and Carbon Electronics Laboratories (ORaCEL)
[3] University of Michigan,undefined
[4] Applied Physics Program,undefined
[5] University of Michigan,undefined
[6] North Carolina State University,undefined
[7] School of Materials Science and Engineering and Tianjin Key Laboratory of Molecular Optoelectronic Sciences,undefined
[8] Tianjin University,undefined
[9] State Key Laboratory of Silicon Materials,undefined
[10] MOE Key Laboratory of Macromolecular Synthesis and Functionalization,undefined
[11] Department of Polymer Science and Engineering,undefined
[12] Zhejiang University,undefined
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摘要
Organic photovoltaic cells (OPVs) have the potential of becoming a productive renewable energy technology if the requirements of low cost, high efficiency and prolonged lifetime are simultaneously fulfilled. So far, the remaining unfulfilled promise of this technology is its inadequate operational lifetime. Here, we demonstrate that the instability of NFA solar cells arises primarily from chemical changes at organic/inorganic interfaces bounding the bulk heterojunction active region. Encapsulated devices stabilized by additional protective buffer layers as well as the integration of a simple solution processed ultraviolet filtering layer, maintain 94% of their initial efficiency under simulated, 1 sun intensity, AM1.5 G irradiation for 1900 hours at 55 °C. Accelerated aging is also induced by exposure of light illumination intensities up to 27 suns, and operation temperatures as high as 65 °C. An extrapolated intrinsic lifetime of > 5.6 × 104 h is obtained, which is equivalent to 30 years outdoor exposure.
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