Zhang Tianhao, Li Mingyuan, Li Xinyu, Jiang Xiaofan, Tao Yu, Zheng Shixuan, Gu Jiazhen, Zheng Nanlong, Bai Guangsheng, Zhang Meng, Li Chen, Guan Yan, Wang Bingwu, Fu Yongping
Beijing National Laboratory for Molecular Science, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
J Am Chem Soc. 2025 Apr 30;147(17):14856-14868. doi: 10.1021/jacs.5c04810. Epub 2025 Apr 19.
Two-dimensional (2D) organic-inorganic hybrid lead halide perovskites are promising semiconductors for optoelectronics, spintronics, and ferroelectrics due to their versatile structural and physical properties enabled by a variety of organic spacer cations. While previous research has focused on new spacer cations for templating 2D perovskite structures and influencing their properties, the intercalation of functional molecules within the organic layers has been less explored. Here, we demonstrate the intercalation of iodine within the organic sublattice as an effective tool to tune interlayer electronic interactions and stabilize 2D perovskite structures that would otherwise not form. We synthesized and determined the single-crystal structures of seven new iodine-intercalated 2D perovskites with varying spacer cations and inorganic compositions. The intercalated iodine bridges neighboring inorganic layers via halogen bonding with the apical iodides, leading to interlayer vibrational and electronic couplings. The iodine intercalation enhances the lattice rigidity, which decreases phonon-phonon scattering and exciton-phonon coupling. Adjusting the inorganic composition further tunes the electronic band structures, because iodine's frontier orbitals contribute differently to the band edge states, leading to varied band alignments and photoluminescence quenching behaviors. Moreover, a decreased anisotropic emission polarization is observed after iodine intercalation due to the decreased in-plane confinement of the excitons. Our results demonstrate iodine intercalation as a powerful tool for tuning the structural and optoelectronic properties of 2D perovskites.
二维(2D)有机-无机杂化铅卤化物钙钛矿因其多种有机间隔阳离子赋予的多样结构和物理性质,在光电子学、自旋电子学和铁电学领域具有广阔应用前景。尽管此前的研究主要集中在用于构建二维钙钛矿结构并影响其性质的新型间隔阳离子,但对有机层内功能分子的插层研究较少。在此,我们证明碘在有机亚晶格中的插层是一种有效手段,可调节层间电子相互作用并稳定原本无法形成的二维钙钛矿结构。我们合成并确定了七种具有不同间隔阳离子和无机组成的新型碘插层二维钙钛矿的单晶结构。插层的碘通过与顶端碘化物形成卤键连接相邻无机层,导致层间振动和电子耦合。碘插层增强了晶格刚性,降低了声子-声子散射和激子-声子耦合。进一步调整无机组成可调节电子能带结构,因为碘的前沿轨道对能带边缘态的贡献不同,导致能带排列和光致发光猝灭行为各异。此外,由于激子的面内限制减小,碘插层后观察到各向异性发射极化降低。我们的结果表明,碘插层是调节二维钙钛矿结构和光电性质的有力工具。