活动层
极化子
离域电子
有机太阳能电池
激子
材料科学
聚合物太阳能电池
超快激光光谱学
吸收(声学)
化学物理
吸收光谱法
分子物理学
光电子学
能量转换效率
图层(电子)
化学
聚合物
纳米技术
凝聚态物理
光学
物理
电子
有机化学
激光器
薄膜晶体管
量子力学
复合材料
作者
Rong Hu,Liping Zhou,Yurong Liu,Zekai Cai,Guanzhao Wen,Wei Zhang
出处
期刊:Photonics
[Multidisciplinary Digital Publishing Institute]
日期:2023-08-30
卷期号:10 (9): 989-989
被引量:1
标识
DOI:10.3390/photonics10090989
摘要
In this work, we investigated the effects of different acceptors (IT−4F and PC71BM) on the charge dynamics in PM6-based solar cells. The correlation between different acceptors and the performance of organic solar cells was studied by atomic force microscope, steady-state absorption spectrum, transient absorption spectrum, and electrical measurements. Optical absorption exhibited that IT−4F has strong absorption in the near-infrared region for the active layer. Transient absorption measurements showed that different acceptors (IT−4F and PC71BM) had a significant influence on the behaviors of PM6 excitons and charge dynamics. That is, the exciton dissociation rate and delocalized polaron transport in the PM6:IT−4F active layer were significantly faster than that in the PM6:PC71BM active layer. The lifetime of localized polaron in the PM6:PC71BM active layer was longer than that in the PM6:IT−4F active layer. Conversely, the lifetime of delocalized polaron in the PM6:IT−4F active layer was longer than that in the PM6:PC71BM active layer. Electrical measurement analysis indicated that lower bimolecular recombination, higher charge transport, and charge collection ability were shown in the PM6:IT−4F device compared with the PM6:PC71BM device. Therefore, PM6:IT−4F solar cells achieved a higher power conversion efficiency (12.82%) than PM6:PC71BM solar cells (8.78%).
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