化学
戒指(化学)
接受者
电子受体
吸收(声学)
电子
结晶学
有机太阳能电池
电子供体
光化学
聚合物
光学
有机化学
物理
催化作用
凝聚态物理
量子力学
作者
Boyu Jia,Jing Wang,Yao Wu,Mingyu Zhang,Yufeng Jiang,Zheng Tang,Thomas P. Russell,Xiaowei Zhan
摘要
The unidirectional extension of a smaller fused-ring system into a larger one in a single direction will increase the conjugation length, allowing a fine-tuning of electronic properties. Here, we designed and synthesized a unidirectionally extended fused-8-ring-based nonfullerene acceptor, AOIC, and a bidirectionally extended fused-11-ring electron acceptor, IUIC2, and compared these with the parent fused-5-ring electron acceptor, F5IC. They share the same electron-accepting groups and alkylphenyl side chains but have different fused-ring electron-donating units. Core extension from 5 to 11 rings up-shifts the energy levels, red shifts the absorption spectra, and reduces bandgaps. The unidirectionally extended AOIC has the highest mobility (2.1 × 10–3 cm2 V–1 s–1) relative to the parent F5IC (1.0 × 10–3 cm2 V–1 s–1) and the bidirectionally extended IUIC2 (4.7 × 10–4 cm2 V–1 s–1). Upon blending with the donor PTB7-Th, AOIC-based organic photovoltaic cells show an efficiency of 13.7%, much better than that of F5IC-based cells (5.61%) and IUIC2-based cells (4.48%).
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