Crystallization driven boost in fill factor and stability in additive-free organic solar cells

材料科学 结晶度 富勒烯 接受者 有机太阳能电池 退火(玻璃) 聚合物太阳能电池 结晶 化学工程 光活性层 聚合物 能量转换效率 纳米技术 光电子学 有机化学 复合材料 化学 物理 工程类 凝聚态物理
作者
David Garcia Romero,Lorenzo Di Mario,Giuseppe Portale,Maria Antonietta Loi
出处
期刊:Journal of materials chemistry. A, Materials for energy and sustainability [Royal Society of Chemistry]
卷期号:9 (42): 23783-23792 被引量:20
标识
DOI:10.1039/d1ta08232a
摘要

The control of morphology and microstructure during and after the active layer processing of bulk-heterojunction solar cells is critical to obtain elevated fill factors and overall good device performance. With the recent development of non-fullerene acceptors, wide attention has been paid to improve miscibility, solubility and nanoscale separation by laborious molecular design processes and by the use of additives. Nonetheless, several post-processing strategies can equally contribute to obtain an optimum phase separation and even to an enhanced crystallinity, but their effect on performance and device lifetime of polymer/non-fullerene acceptor solar cells is still unclear. Herein, we report a systematic comparison between different post-processing treatments including thermal annealing (TA), vacuum drying (VD) and solvent vapor annealing (SVA) on the TPD-3F polymer and IT-4F non-fullerene acceptor, comparing their effects on device performance as well as on the morphology and optical and electrical properties. The optimized SVA treated devices exhibited power conversion efficiencies close to 14% with a remarkable 76% fill factor and superior short-circuit currents compared to the one of untreated devices. Moreover, SVA demonstrated improvements in device stability both under illumination and under ambient conditions. The induced phase separation and the increased crystallinity of the acceptor molecules, as revealed by GIWAXS measurements, led to increased photogenerated currents, with a more effective exciton dissociation and charge collection. The open-circuit voltage losses in the SVA and TA devices were explained by a bandgap reduction and a higher trap-assisted recombination, respectively. Overall, our study points to the role of post-processing in organic solar cell fabrication, and contributes towards a new generation of efficient and stable additive-free organic solar cells.
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