材料科学
有机太阳能电池
光电子学
富勒烯
量子产额
量子效率
异质结
活动层
接受者
辐射传输
光伏系统
开路电压
纳米技术
电压
光学
化学
图层(电子)
物理
薄膜晶体管
有机化学
凝聚态物理
复合材料
荧光
聚合物
生态学
量子力学
生物
作者
Quan Liu,Koen Vandewal
标识
DOI:10.1002/adma.202302452
摘要
Abstract Organic solar cells benefit from non‐fullerene acceptors (NFA) due to their high absorption coefficients, tunable frontier energy levels, and optical gaps, as well as their relatively high luminescence quantum efficiencies as compared to fullerenes. Those merits result in high yields of charge generation at a low or negligible energetic offset at the donor/NFA heterojunction, with efficiencies over 19% achieved for single‐junction devices. Pushing this value significantly over 20% requires an increase in open‐circuit voltage, which is currently still well below the thermodynamic limit. This can only be achieved by reducing non‐radiative recombination, and hereby increasing the electroluminescence quantum efficiency of the photo‐active layer. Here, current understanding of the origin of non‐radiative decay, as well as an accurate quantification of the associated voltage losses are summarized. Promising strategies for suppressing these losses are highlighted, with focus on new material design, optimization of donor–acceptor combination, and blend morphology. This review aims at guiding researchers in their quest to find future solar harvesting donor–acceptor blends, which combine a high yield of exciton dissociation with a high yield of radiative free carrier recombination and low voltage losses, hereby closing the efficiency gap with inorganic and perovskite photovoltaics.
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