串联
重组
结晶
材料科学
光伏系统
接受者
有机太阳能电池
硒化铜铟镓太阳电池
光电子学
能量转换效率
激子
化学物理
纳米技术
分子
混合太阳能电池
无辐射复合
同源重组
跟踪(教育)
太阳能
转化(遗传学)
作者
Xinyue Cui,Guanshui Xie,Guangliu Ran,Yuqiang Liu,Xueqing Ma,Gendi Zhang,Qiumin Kong,Wenkai Zhang,Hongxiang Li,Pei Cheng,Dan Ouyang,Longbin Qiu,Zhishan Bo
标识
DOI:10.1038/s41467-025-64032-7
摘要
Perovskite/organic tandem solar cells are a promising strategy to surpass the efficiency limits of single-junction devices, yet their performance is restricted by recombination losses in the organic subcells. Here, we investigate these losses by tracking film evolution from the very initial stage of organic film formation. We strategically manipulated donor and acceptor ratios to modulate film growth characteristics, while employing in situ techniques to monitor the real-time crystallization dynamics. Our research findings underscore that the variance in donor content within the organic blend exerts a fine-tuning effect on the solution-to-solid transformation process. When the donor content is inadequate, the acceptor molecules tend to aggregate, disrupting molecular packing and lowering crystallinity. These morphological changes hinder exciton dissociation, thereby leading to charge recombination and deteriorating overall device performance. Optimizing film morphology and crystallization reduces recombination losses, enabling perovskite/organic tandem solar cells with a record 26.42% power conversion efficiency. The efficiency of perovskite/organic tandem devices is impeded by recombination losses that occur within the organic subcells. Here, the authors monitor film growth and crystallization dynamics in real-time and mitigate exciton recombination losses, achieving maximum device efficiency of 26.42%.
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