富勒烯
有机太阳能电池
异质结
接受者
化学物理
材料科学
偶极子
光伏系统
平面的
电荷(物理)
光电子学
纳米技术
化学
物理
凝聚态物理
计算机科学
计算机图形学(图像)
生态学
生物
复合材料
量子力学
有机化学
聚合物
作者
Xian’e Li,Qilun Zhang,Jianwei Yu,Ye Xu,Rui Zhang,Chuanfei Wang,Huotian Zhang,Simone Fabiano,Xianjie Liu,Jianhui Hou,Feng Gao,Mats Fahlman
标识
DOI:10.1038/s41467-022-29702-w
摘要
Abstract Energy level alignment (ELA) at donor (D) -acceptor (A) heterojunctions is essential for understanding the charge generation and recombination process in organic photovoltaic devices. However, the ELA at the D-A interfaces is largely underdetermined, resulting in debates on the fundamental operating mechanisms of high-efficiency non-fullerene organic solar cells. Here, we systematically investigate ELA and its depth-dependent variation of a range of donor/non-fullerene-acceptor interfaces by fabricating and characterizing D-A quasi bilayers and planar bilayers. In contrast to previous assumptions, we observe significant vacuum level (VL) shifts existing at the D-A interfaces, which are demonstrated to be abrupt, extending over only 1–2 layers at the heterojunctions, and are attributed to interface dipoles induced by D-A electrostatic potential differences. The VL shifts result in reduced interfacial energetic offsets and increased charge transfer (CT) state energies which reconcile the conflicting observations of large energy level offsets inferred from neat films and large CT energies of donor - non-fullerene-acceptor systems.
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