Huang Liqiang, Wang Gang, Zhou Weihua, Fu Boyi, Cheng Xiaofang, Zhang Lifu, Yuan Zhibo, Xiong Sixing, Zhang Lin, Xie Yuanpeng, Zhang Andong, Zhang Youdi, Ma Wei, Li Weiwei, Zhou Yinhua, Reichmanis Elsa, Chen Yiwang
College of Chemistry , Nanchang University , 999 Xuefu Avenue , Nanchang 330031 , China.
School of Chemical and Biomolecular Engineering, School of Chemistry and Biochemistry, School of Materials Science and Engineering , Georgia Institute of Technology , Atlanta , Georgia 30332 , United States.
ACS Nano. 2018 May 22;12(5):4440-4452. doi: 10.1021/acsnano.8b00439. Epub 2018 Apr 24.
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%.
高效有机太阳能电池(OSCs)可通过优化组件分子设计、结合界面工程以及控制活性层形态来制备。然而,本体异质结(BHJ)的垂直分层,即在干燥过程中出现的一种自发行为,仍然是一个有待解决的复杂问题。应探索调节垂直分离分布以及评估其对最终器件影响的方法,以进一步提高OSCs的性能。在此,我们建立了材料表面能、吸收与垂直分层之间的联系,进而将其与光伏转换特性联系起来。通过评估由各组分顺序浇铸形成多层结构所产生的临时人工垂直分层的性能,可实现最佳垂直分层。调整衬底之间的表面能偏移会导致该分层的给体和受体稳定。此外,观察到在可见光区域产生的光电流与靠近电极的给体或受体数量之间存在权衡。使用自组装小分子(SASM)实现了衬底表面能的改性,这反过来又直接影响了界面处聚合物给体与受体的比例。在倒置有机太阳能电池结构中使用三种不同的给体聚合物与两种替代受体相结合,相对于受体,ITO(氧化铟锡)/BHJ界面处聚合物给体分子的浓度可以增加。适当选择SASM有助于使外部量子效率和功率转换效率同步提高超过10.5%。