Feng Wanying, Chen Tianqi, Li Yulu, Duan Tainan, Jiang Xue, Zhong Cheng, Zhang Yunxin, Yu Jifa, Lu Guanghao, Wan Xiangjian, Kan Bin, Chen Yongsheng
School of Materials Science and Engineering, National Institute for Advanced Materials, Nankai University, 300350, Tianjin, China.
State Key Laboratory and Institute of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials, Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry, Nankai University, 300071, Tianjin, China.
Angew Chem Int Ed Engl. 2024 Feb 26;63(9):e202316698. doi: 10.1002/anie.202316698. Epub 2024 Jan 17.
Morphological control of all-polymer blends is quintessential yet challenging in fabricating high-performance organic solar cells. Recently, solid additives (SAs) have been approved to be capable in tuning the morphology of polymer: small-molecule blends improving the performance and stability of devices. Herein, three perhalogenated thiophenes, which are 3,4-dibromo-2,5-diiodothiophene (SA-T1), 2,5-dibromo-3,4-diiodothiophene (SA-T2), and 2,3-dibromo-4,5-diiodothiophene (SA-T3), were adopted as SAs to optimize the performance of all-polymer organic solar cells (APSCs). For the blend of PM6 and PY-IT, benefitting from the intermolecular interactions between perhalogenated thiophenes and polymers, the molecular packing properties could be finely regulated after introducing these SAs. In situ UV/Vis measurement revealed that these SAs could assist morphological character evolution in the all-polymer blend, leading to their optimal morphologies. Compared to the as-cast device of PM6 : PY-IT, all SA-treated binary devices displayed enhanced power conversion efficiencies of 17.4-18.3 % with obviously elevated short-circuit current densities and fill factors. To our knowledge, the PCE of 18.3 % for SA-T1-treated binary ranks the highest among all binary APSCs to date. Meanwhile, the universality of SA-T1 in other all-polymer blends is demonstrated with unanimously improved device performance. This work provide a new pathway in realizing high-performance APSCs.
在制造高性能有机太阳能电池时,全聚合物共混物的形态控制至关重要但颇具挑战。最近,固态添加剂(SAs)已被证实能够调节聚合物:小分子共混物的形态,从而提高器件的性能和稳定性。在此,采用了三种全卤代噻吩,即3,4 - 二溴 - 2,5 - 二碘噻吩(SA - T1)、2,5 - 二溴 - 3,4 - 二碘噻吩(SA - T2)和2,3 - 二溴 - 4,5 - 二碘噻吩(SA - T3)作为固态添加剂来优化全聚合物有机太阳能电池(APSCs)的性能。对于PM6和PY - IT的共混物,得益于全卤代噻吩与聚合物之间的分子间相互作用,引入这些固态添加剂后,分子堆积性质能够得到精细调控。原位紫外/可见光谱测量表明,这些固态添加剂能够促进全聚合物共混物中形态特征的演变,使其达到最佳形态。与PM6 : PY - IT的铸膜器件相比,所有经固态添加剂处理的二元器件的功率转换效率均提高至17.4 - 18.3 %,短路电流密度和填充因子也明显提高。据我们所知,经SA - T1处理的二元器件的18.3 %的功率转换效率在迄今为止所有二元全聚合物有机太阳能电池中排名最高。同时,SA - T1在其他全聚合物共混物中的通用性也通过器件性能的一致提升得到了证明。这项工作为实现高性能全聚合物有机太阳能电池提供了一条新途径。