材料科学
聚合物太阳能电池
光电流
有机太阳能电池
异质结
光电子学
活动层
接受者
氧化铟锡
能量转换效率
纳米技术
有机半导体
聚合物
化学工程
图层(电子)
复合材料
凝聚态物理
物理
薄膜晶体管
工程类
作者
Liqiang Huang,Gang Wang,Weihua Zhou,Boyi Fu,Xiaofang Cheng,Lifu Zhang,Zhibo Yuan,Sixing Xiong,Lin Zhang,Yuanpeng Xie,Andong Zhang,Youdi Zhang,Wei Ma,Weiwei Li,Yinhua Zhou,Elsa Reichmanis,Yiwang Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-04-20
卷期号:12 (5): 4440-4452
被引量:98
标识
DOI:10.1021/acsnano.8b00439
摘要
High-efficiency organic solar cells (OSCs) can be produced through optimization of component molecular design, coupled with interfacial engineering and control of active layer morphology. However, vertical stratification of the bulk-heterojunction (BHJ), a spontaneous activity that occurs during the drying process, remains an intricate problem yet to be solved. Routes toward regulating the vertical separation profile and evaluating the effects on the final device should be explored to further enhance the performance of OSCs. Herein, we establish a connection between the material surface energy, absorption, and vertical stratification, which can then be linked to photovoltaic conversion characteristics. Through assessing the performance of temporary, artificial vertically stratified layers created by the sequential casting of the individual components to form a multilayered structure, optimal vertical stratification can be achieved. Adjusting the surface energy offset between the substrate results in donor and acceptor stabilization of that stratified layer. Further, a trade-off between the photocurrent generated in the visible region and the amount of donor or acceptor in close proximity to the electrode was observed. Modification of the substrate surface energy was achieved using self-assembled small molecules (SASM), which, in turn, directly impacted the polymer donor to acceptor ratio at the interface. Using three different donor polymers in conjunction with two alternative acceptors in an inverted organic solar cell architecture, the concentration of polymer donor molecules at the ITO (indium tin oxide)/BHJ interface could be increased relative to the acceptor. Appropriate selection of SASM facilitated a synchronized enhancement in external quantum efficiency and power conversion efficiencies over 10.5%.
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