Ma Sunihl, Jung Young-Kwang, Ahn Jihoon, Kyhm Jihoon, Tan Jeiwan, Lee Hyungsoo, Jang Gyumin, Lee Chan Uk, Walsh Aron, Moon Jooho
Department of Materials Science and Engineering, Yonsei University, 50 Yonsei-ro Seodaemun-gu, Seoul, 03722, Republic of Korea.
Technology Support Center Korea, Institute of Science and Technology, Seoul, 02792, Republic of Korea.
Nat Commun. 2022 Jun 7;13(1):3259. doi: 10.1038/s41467-022-31017-9.
Chiral perovskites are being extensively studied as a promising candidate for spintronic- and polarization-based optoelectronic devices due to their interesting spin-polarization properties. However, the origin of chiroptical activity in chiral perovskites is still unknown, as the chirality transfer mechanism has been rarely explored. Here, through the nano-confined growth of chiral perovskites (MBAPbIBr), we verified that the asymmetric hydrogen-bonding interaction between chiral molecular spacers and the inorganic framework plays a key role in promoting the chiroptical activity of chiral perovskites. Based on this understanding, we observed remarkable asymmetry behavior (absorption dissymmetry of 2.0 × 10 and anisotropy factor of photoluminescence of 6.4 × 10 for left- and right-handed circularly polarized light) in nanoconfined chiral perovskites even at room temperature. Our findings suggest that electronic interactions between building blocks should be considered when interpreting the chirality transfer phenomena and designing hybrid materials for future spintronic and polarization-based devices.
由于其有趣的自旋极化特性,手性钙钛矿作为自旋电子学和基于极化的光电器件的有前途的候选材料正受到广泛研究。然而,手性钙钛矿中手性光学活性的起源仍然未知,因为手性转移机制很少被探索。在这里,通过手性钙钛矿(MBAPbIBr)的纳米受限生长,我们证实了手性分子间隔物与无机骨架之间的不对称氢键相互作用在促进手性钙钛矿的手性光学活性中起关键作用。基于这一认识,我们观察到即使在室温下,纳米受限手性钙钛矿中也存在显著的不对称行为(左旋和右旋圆偏振光的吸收不对称性为2.0×10,光致发光的各向异性因子为6.4×10)。我们的研究结果表明,在解释手性转移现象和设计用于未来自旋电子学和基于极化的器件的混合材料时,应考虑构建单元之间的电子相互作用。