Colloidal assembly has emerged as an effective avenue for achieving polarized light emission. Here, we showcase the efficacy and versatility of the magnetic colloidal assembly in enabling both linearly and circularly polarized luminescence. Colloidal europium-doped NaYF nanorods with surface-bound FeO nanoparticles are magnetically assembled into linear or chiral superstructures using corresponding fields created in permanent magnets. In a uniform magnetic field generated by opposing poles, the assemblies exhibit photoluminescence with intensity tunable in response to the magnetic field direction, which is higher when the nanorods are perpendicular to light propagation than when they are parallel. The obtained superstructures display strong linearly polarized luminescence when the nanorods are aligned vertically, exhibiting a high degree of polarization up to 0.61. In a quadrupole chiral field generated by permanent magnets, the assemblies emit left-handed or right-handed polarized light depending on the position of the sample placement, attaining a -factor of 0.04. Furthermore, the superstructures immobilized in a hydrogel film are found to retain their chirality, exhibiting opposite chiroptical responses depending on the sample orientation. The magnetic colloidal assembly approach facilitates the convenient and efficient generation of polarized light emissions from nonmagnetic luminescent materials, thus creating opportunities for tailoring light behavior in developing innovative optoelectronic devices.
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http://dx.doi.org/10.1021/acsnano.3c12344 | DOI Listing |
J Am Chem Soc
January 2025
RIKEN Center for Emergent Matter Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Some one-dimensional (1D) crystals containing a screw dislocation along their longer axis exhibit a helical twist due to lattice strain. These chiral structures have been thoroughly investigated by using transmission electron microscopy. However, whether two-dimensional (2D) crystals with a spiral surface pattern, presumably containing a screw dislocation, are structurally chiral remains unclear because their internal structures are not visible.
View Article and Find Full Text PDFMater Horiz
January 2025
Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Circularly polarized luminescence (CPL) materials have developed rapidly in recent years due to their wide application prospects in fields like 3D displays and anti-counterfeiting. Utilizing energy transfer processes to transfer chirality has been proven as an efficient way to obtain CPL materials. However, the physics behind energy-transfer induced CPL is still not clear.
View Article and Find Full Text PDFChirality
January 2025
Department of Applied Molecular Chemistry, College of Industrial Technology, Nihon University, Narashino, Japan.
The synthesis, structure, and circularly polarized luminescence (CPL) properties of axially chiral boron difluoride complexes are described. A series of optically pure bis (boron difluoride) complexes were prepared in 5 steps from commercially available (S)- or (R)-BINOL as starting materials. The complexes were found to exhibit similar yellow photoluminescence in solution, regardless of the type of substituents on the nitrogen atoms.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
January 2025
State Key Laboratory of Green Pesticide, Central China Normal University, Wuhan 430079, PR China. Electronic address:
The construction of helical structures through self-assembly and the exploration of their formation mechanisms not only amplify chiroptical properties but also provide profound insights into the structures and functions of natural helices. In this study, we developed a chiral Au(I) system based on BINAP and alkynyl ligands. The modification of the length or number of alkyl chains at the terminal positions of the alkynyl ligands significantly impacted the self-assembly behavior of the complexes.
View Article and Find Full Text PDFChemistry
January 2025
Natinal Institute of Adavanced Industrial Science and Technology, Interdisciplinary Research Center for Catalytic Chemistry, Higashi 1-1-1, 305-8565, Tsukuba, JAPAN.
Unprecedented (2E,4E,6Z,8Z)-nona-2,4,6,8-tetraenoate derivatives highly substituted by aryl groups have been synthesized by the reaction of rhodium complexes having aryl-substituted hexa-1,3,5-trienyl ligands with acrylates. These compounds have potential axial chirality, and their enantiomers are isolable by the chiral HPLC technique. Although the racemization barrier of isolated enantiomers was not high, it was found that a cyclic dimer synthesized by head-to-tail transesterification of a modified analog has quite a stable axial chirality even at a high temperature.
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