Fu Hongyuan, Zhang Ming, Zhang Youdi, Wang Qingyuan, Xu Zheng'ao, Zhou Qiuju, Li Zhengkai, Bai Yang, Li Yongfang, Zhang Zhi-Guo
State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, 100029, Beijing, China.
College of Chemistry, Key Laboratory of Advanced Green Functional Materials, Changchun Normal University, 130032, Changchun, China.
Angew Chem Int Ed Engl. 2023 Aug 28;62(35):e202306303. doi: 10.1002/anie.202306303. Epub 2023 Jul 3.
The operational stability of polymer solar cells is a critical concern with respect to the thermodynamic relaxation of acceptor-donor-acceptor (A-D-A) or A-DA'D-A structured small-molecule acceptors (SMAs) within their blends with polymer donors. Giant molecule acceptors (GMAs) bearing SMAs as subunits offer a solution to this issue, while their classical synthesis via the Stille coupling suffers from low reaction efficiency and difficulty in obtaining mono-brominated SMA, rendering the approach impractical for their large-scale and low-cost preparation. In this study, we present a simple and cost-effective solution to this challenge through Lewis acid-catalyzed Knoevenagel condensation with boron trifluoride etherate (BF ⋅ OEt ) as catalyst. We demonstrated that the coupling of the monoaldehyde-terminated A-D-CHO unit and the methylene-based A-link-A (or its silyl enol ether counterpart) substrates can be quantitatively achieved within 30 minutes in the presence of acetic anhydride, affording a variety of GMAs connected via the flexible and conjugated linkers. The photophysical properties was fully studied, yielding a high device efficiency of over 18 %. Our findings offer a promising alternative for the modular synthesis of GMAs with high yields, easier work up, and the widespread application of such methodology will undoubtedly accelerate the progress of stable polymer solar cells.
聚合物太阳能电池的运行稳定性是一个至关重要的问题,这涉及到受体-供体-受体(A-D-A)或A-DA'D-A结构的小分子受体(SMA)在与聚合物供体的共混物中的热力学弛豫。以SMA为亚基的巨型分子受体(GMA)为这个问题提供了解决方案,然而,通过Stille偶联进行的经典合成存在反应效率低以及难以获得单溴化SMA的问题,使得该方法对于其大规模和低成本制备不切实际。在本研究中,我们通过以三氟化硼乙醚(BF ⋅ OEt )为催化剂的路易斯酸催化的Knoevenagel缩合反应,提出了一种简单且具有成本效益的应对这一挑战的方法。我们证明,在乙酸酐存在下,单醛封端的A-D-CHO单元与亚甲基连接的A-link-A(或其烯醇硅醚对应物)底物的偶联可在30分钟内定量实现,得到通过柔性共轭连接基连接的多种GMA。对其光物理性质进行了充分研究,器件效率高达18%以上。我们的研究结果为高产率模块化合成GMA提供了一种有前景的替代方法,后处理更简便,这种方法的广泛应用无疑将加速稳定聚合物太阳能电池的发展进程。