Related Experiment Video
Updated: Jan 18, 2026

Low Pressure Vapor-assisted Solution Process for Tunable Band Gap Pinhole-free Methylammonium Lead Halide Perovskite Films
Published on: September 8, 2017
Internally and externally induced chiral hybrid metal halide materials for advanced chiroptoelectronic applications
Puxin Cheng1, Yue Wang1, Peihan Wang1
1School of Materials Science and Engineering, Tianjin Key Laboratory of Metal and Molecular Materials Chemistry, Frontiers Science Center for New Organic Matter, Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin 300350, P. R. China. jialiang.xu@nankai.edu.cn.
Abstract:
Chiral hybrid metal halides (CHMHs) comprise tunable chiral and noncentrosymmetric structures with remarkable optoelectronic characteristics, offering new avenues for synergistically manipulating the optical, electrical, and magnetic physical degrees of freedom. In these systems, chiral structures act not only as functional scaffolds but also as bridges that link microscopic electronic states with macroscopic optoelectronic behaviors. This review follows a progressive framework to systematically present recent advances in the field of CHMHs, spanning synthetic strategies, physical mechanisms, and device implementations. The chemical routes and transfer mechanisms underlying chiral structure formation are elucidated, with an emphasis on the roles of molecular chirality and external potential field. A central focus is placed on the inherent coupling among linear/nonlinear chiroptical effects, ferroelectric/piezoelectric behaviors, and chirality-induced spin selectivity (CISS) effects, with the "chiral structure-Rashba effect-CISS" chain identified as the key to enabling cross-coupling among spin, charge, and photons. The potential of CHMHs in the detection and emission of circularly polarized light and spin light-emitting diodes is also evaluated, underscoring their irreplaceability in multifunctional integration and magnetic-field-free spin manipulation. This review aims to provide a systematic basis for understanding the structure-function relationships in CHMHs while outlining the strategic direction of opto-electro-magnetic coupling through chirality engineering, thereby laying a foundation for future applications in quantum information platforms and low-power spintronic devices.
More Related Videos
Related Concept Videos
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Prochirality
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Radical Halogenation: Stereochemistry
Halogenation to form a new chiral center:
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...

