接受者
激子
重组
离解(化学)
有机太阳能电池
偏移量(计算机科学)
材料科学
化学物理
载流子
光伏系统
能量转换效率
光电子学
化学
聚合物
物理化学
物理
凝聚态物理
电气工程
复合材料
工程类
程序设计语言
基因
生物化学
计算机科学
作者
Nurlan Tokmoldin,Bowen Sun,Floriana Moruzzi,Acacia Patterson,Obaid Alqahtani,Rong Wang,Brian A. Collins,Iain McCulloch,Larry Lüer,Christoph J. Brabec,Dieter Neher,Safa Shoaee
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-05-11
卷期号:8 (6): 2552-2560
被引量:21
标识
DOI:10.1021/acsenergylett.3c00572
摘要
The energetic offset between the highest occupied molecular orbitals of the donor and acceptor components of organic photovoltaic blends is well-known to affect the device efficiency. It is well-established that a decreasing offset increases the open-circuit voltage but reduces the short-circuit current, which has been explained by insufficient exciton dissociation. However, the impact of the offset on the fill factor and underlying processes is less clear. Here, we study free charge generation and recombination in three different nonfullerene acceptors, Y6, ITIC, and o-IDBTR, blended with the same donor polymer PM6. We demonstrate that a diminishing offset results in field-dependent charge generation related to field-assisted exciton dissociation. On the other hand, reformation of excitons from free charges is identified as an additional channel for charge recombination, which goes along with a substantial rise in the bimolecular recombination coefficient. In combination of these two effects, the fill factor drops considerably with a decreasing energy offset. Using the comparison between PM6:ITIC and PM6:o-IDBTR, we show that bulk properties such as morphology and carrier mobilities can not fully explain the observed difference in performance, highlighting the importance of interfacial kinetics and thermodynamics in controlling the device efficiency, both through generation and recombination of charge carriers.
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