Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.
University of Chinese Academy of Sciences , Beijing 100049, China.
J Am Chem Soc. 2016 Nov 16;138(45):15011-15018. doi: 10.1021/jacs.6b09110. Epub 2016 Nov 8.
Low bandgap n-type organic semiconductor (n-OS) ITIC has attracted great attention for the application as an acceptor with medium bandgap p-type conjugated polymer as donor in nonfullerene polymer solar cells (PSCs) because of its attractive photovoltaic performance. Here we report a modification on the molecular structure of ITIC by side-chain isomerization with meta-alkyl-phenyl substitution, m-ITIC, to further improve its photovoltaic performance. In a comparison with its isomeric counterpart ITIC with para-alkyl-phenyl substitution, m-ITIC shows a higher film absorption coefficient, a larger crystalline coherence, and higher electron mobility. These inherent advantages of m-ITIC resulted in a higher power conversion efficiency (PCE) of 11.77% for the nonfullerene PSCs with m-ITIC as acceptor and a medium bandgap polymer J61 as donor, which is significantly improved over that (10.57%) of the corresponding devices with ITIC as acceptor. To the best of our knowledge, the PCE of 11.77% is one of the highest values reported in the literature to date for nonfullerene PSCs. More importantly, the m-ITIC-based device shows less thickness-dependent photovoltaic behavior than ITIC-based devices in the active-layer thickness range of 80-360 nm, which is beneficial for large area device fabrication. These results indicate that m-ITIC is a promising low bandgap n-OS for the application as an acceptor in PSCs, and the side-chain isomerization could be an easy and convenient way to further improve the photovoltaic performance of the donor and acceptor materials for high efficiency PSCs.
具有低带隙的 n 型有机半导体(n-OS) ITIC 因其光电性能吸引了人们的极大关注,可作为受体与具有中等带隙的 p 型共轭聚合物给体应用于非富勒烯聚合物太阳能电池(PSCs)中。在这里,我们通过侧链异构化和间位烷基取代对 ITIC 的分子结构进行了修饰,得到了 m-ITIC,以进一步提高其光伏性能。与具有对位烷基取代的 ITIC 相比,m-ITIC 具有更高的薄膜吸收系数、更大的结晶相干性和更高的电子迁移率。m-ITIC 的这些固有优势使得以 m-ITIC 为受体和具有中等带隙聚合物 J61 为给体的非富勒烯 PSCs 的功率转换效率(PCE)提高到了 11.77%,相比于以 ITIC 为受体的相应器件(10.57%)有了显著的提升。据我们所知,在非富勒烯 PSCs 中,11.77%的 PCE 是目前文献报道的最高值之一。更重要的是,与以 ITIC 为基础的器件相比,在活性层厚度为 80-360nm 的范围内,基于 m-ITIC 的器件的光伏性能对厚度的依赖性更小,这有利于大面积器件的制造。这些结果表明,m-ITIC 是一种很有前途的低带隙 n-OS,可作为受体应用于 PSCs 中,而侧链异构化可能是一种简单方便的方法,可以进一步提高供体和受体材料的光伏性能,以获得高效率的 PSCs。