Moroni Marco, Gregori Luca, Coccia Clarissa, Boiocchi Massimo, Morana Marta, Capsoni Doretta, Olivati Andrea, Treglia Antonella, Folpini Giulia, Patrini Maddalena, Goncalves Isabel, Wang Heyong, Milanese Chiara, Petrozza Annamaria, Mosconi Edoardo, De Angelis Filippo, Malavasi Lorenzo
University of Pavia, Department of Chemistry and INSTM, Via Taramelli 16, 27100 Pavia, Italy.
University of Perugia, Department of Chemistry, Biology and Biotechnology, Via Elce di Sotto 8, 06123 Perugia, Italy.
ACS Energy Lett. 2025 May 22;10(6):2906-2912. doi: 10.1021/acsenergylett.5c00576. eCollection 2025 Jun 13.
Chiral metal halides are promising materials for nonlinear optics and spin-selective devices. Typically, chirality is introduced via large chiral organic cations, leading to low-dimensional structures and limitations in charge transport. Here, we design a family of chiral metal halides based on the relatively small ditopic /-3-aminoquinuclidine (3-AQ) cation, forming an (/-3AQ)-PbBr structure closely related to the 3D corner-sharing octahedral network of perovskites. The resulting material exhibits a direct bandgap, isotropic band structure, and fully 3D photoexcitation. Circular dichroism confirms a chiral anisotropy factor consistent with theoretical predictions. Moreover, the material displays a Rashba effect in the conduction band, which is attributed to spin-orbit coupling and the lack of inversion symmetry. Offering rich chemical tunability and efficient 3D charge transport, this new class of chiral semiconductors provides a promising platform for advancing nonlinear optoelectronic and spintronic devices.
手性金属卤化物是用于非线性光学和自旋选择性器件的有前景的材料。通常,手性是通过大的手性有机阳离子引入的,这导致低维结构和电荷传输方面的限制。在此,我们基于相对较小的双齿/ -3-氨基奎宁环(3-AQ)阳离子设计了一族手性金属卤化物,形成了与钙钛矿的3D角共享八面体网络密切相关的(/ -3AQ)-PbBr结构。所得材料表现出直接带隙、各向同性能带结构和完全的3D光激发。圆二色性证实了与理论预测一致的手性各向异性因子。此外,该材料在导带中表现出Rashba效应,这归因于自旋轨道耦合和缺乏反演对称性。这类新型手性半导体具有丰富的化学可调性和高效的3D电荷传输,为推进非线性光电器件和自旋电子器件提供了一个有前景的平台。