Dai Shuting, Xie Miao, Wang Can, Wang Yuying, Han Bin, Xu Shunqi, Wang Kexin, Zhuravlova Anna, Xu Bin, Chi Lifeng, Tian Wenjing, Samorì Paolo, Liu Zhaoyang
State Key Laboratory of Supramolecular Structure and Materials, Jilin University Changchun 130012 China
ISIS, Université de Strasbourg and CNRS 8 allée Gaspard Monge Strasbourg 67000 France
J Mater Chem C Mater. 2024 Aug 12;12(36):14667-14674. doi: 10.1039/d4tc02010c. eCollection 2024 Sep 19.
Hybrid systems based on graphene and organic molecules are highly appealing for "correcting" the limited optoelectronic properties of 2D materials. However, an in-depth understanding of the correlation between the structure of the molecular sensitizer and the physical properties of the hybrid toward high-performance organic-graphene hybrid photodetectors remains elusive. Herein, an molecular design a peripheral editing approach on the organic molecules is employed to elucidate the structure-property relationship when interfaced with graphene forming hybrid systems. Efficient doping of graphene can be attained by physisorption of tetrathiafulvalene molecules exposing electron-donating peripheral groups, benefiting from a strong coupling yielding efficient charge transfer, ultimately leading to photodetectors with an ultra-high responsivity of 1.1 × 10 A W and a specific detectivity of 6.5 × 10 Jones, thereby outperforming state-of-the-art graphene-based photodetectors. These results offer valuable insights for future optimization of graphene-based photodetectors through molecular functionalization.
基于石墨烯和有机分子的混合系统对于“校正”二维材料有限的光电特性极具吸引力。然而,对于高性能有机-石墨烯混合光电探测器而言,深入理解分子敏化剂的结构与混合体系物理性质之间的关联仍然难以实现。在此,我们采用一种分子设计——对有机分子进行外围编辑的方法,来阐明与石墨烯形成混合体系时的结构-性质关系。通过物理吸附带有供电子外围基团的四硫富瓦烯分子,可以实现石墨烯的有效掺杂,这得益于强耦合作用产生的高效电荷转移,最终得到了响应度高达1.1×10 A/W以及比探测率为6.5×10 Jones的光电探测器,从而超越了目前最先进的基于石墨烯的光电探测器。这些结果为未来通过分子功能化优化基于石墨烯的光电探测器提供了有价值的见解。