光激发
接受者
富勒烯
激发态
有机太阳能电池
重组
材料科学
载流子
光化学
光电子学
化学
分析化学(期刊)
化学物理
吸收(声学)
原子物理学
物理
色谱法
有机化学
聚合物
凝聚态物理
复合材料
基因
生物化学
作者
Rokas Jasiūnas,Huotian Zhang,Jun Yuan,Xuehong Zhou,Deping Qian,Yingping Zou,Andrius Devižis,Juozas Šulskus,Feng Gao,Vidmantas Gulbinas
标识
DOI:10.1021/acs.jpcc.0c05263
摘要
Non-fullerene organic solar cells (NFOSCs) demonstrate record efficiencies exceeding 16%. In comparison with cells with the fullerene-based acceptor, the NFOSCs benefit from a longer wavelength absorption, which leads to a small highest occupied molecular orbital (HOMO) level offset. Here, we use several advanced transient investigation techniques, covering timescale from sub-ps to μs, to address all sequence of processes starting from photoexcitation of donors or acceptors to carrier extraction in several NFOSCs and cells with phenyl-C71-butyric acid methyl ester (PCBM). Though small offsets result in higher open-circuit voltage, we show that at the same time, it limits cell performance because of inefficient hole transfer from excited acceptors to donors and enhanced geminate recombination. We demonstrate that 100 meV HOMO level offset and proper acceptor molecule structures are sufficient for efficient hole transfer (>70%) and for reduction of the geminate recombination losses down to about 20%. Subsequent extraction of unbound charge carriers in all NFOSCs is slightly faster than in cells with PCBM, while non-geminate carrier recombination causing additional losses is slightly slower in the best performing NFOSCs than in cells with PCBM.
科研通智能强力驱动
Strongly Powered by AbleSci AI