激子
有机太阳能电池
接受者
材料科学
原子物理学
光电子学
光伏系统
电荷(物理)
化学物理
化学
物理
凝聚态物理
电气工程
量子力学
工程类
作者
Andrej Classen,Christos L. Chochos,Larry Lüer,Vasilis G. Gregoriou,Jonas Wortmann,Andres Osvet,Karen Forberich,Iain McCulloch,Thomas Heumüller,Christoph J. Brabec
出处
期刊:Nature Energy
[Nature Portfolio]
日期:2020-08-31
卷期号:5 (9): 711-719
被引量:290
标识
DOI:10.1038/s41560-020-00684-7
摘要
Organic solar cells utilize an energy-level offset to generate free charge carriers. Although a very small energy-level offset increases the open-circuit voltage, it remains unclear how exactly charge generation is affected. Here we investigate organic solar cell blends with highest occupied molecular orbital energy-level offsets (∆EHOMO) between the donor and acceptor that range from 0 to 300 meV. We demonstrate that exciton quenching at a negligible ∆EHOMO takes place on timescales that approach the exciton lifetime of the pristine materials, which drastically limits the external quantum efficiency. We quantitatively describe this finding via the Boltzmann stationary-state equilibrium between charge-transfer states and excitons and further reveal a long exciton lifetime to be decisive in maintaining an efficient charge generation at a negligible ∆EHOMO. Moreover, the Boltzmann equilibrium quantitatively describes the major reduction in non-radiative voltage losses at a very small ∆EHOMO. Ultimately, highly luminescent near-infrared emitters with very long exciton lifetimes are suggested to enable highly efficient organic solar cells.
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