The combination of chirality and semiconducting properties has enabled chiral metal-halide semiconductors (MHS) to be promising candidates for spin- and polarization-resolved optoelectronic devices. Although several chiral MHS with rich chemical and structural diversity have been reported lately, the macroscopic origin of chiroptical activity remains elusive. Here, combining spectroscopic measurements and Mueller matrix analysis, we discover that the previously reported "apparent" anisotropy factor measured from circular dichroism (CD) in chiral MHS thin films is not an intrinsic chiroptical property, but rather, arising from an interference between the film's linear birefringence (LB) and linear dichroism (LD). We verify the presence of LB and LD effects in both one-dimensional and zero-dimensional chiral MHS thin films. We establish spectroscopic methods to decouple the genuine CD from other spurious contributions, which allows a quantitative comparison of the intrinsic chiroptical activity across different chiral MHS. The relationship between the structure and the genuine chiroptical activity is then uncovered, which is well described by the chirality-induced spin-orbit coupling in the chiral structures. Our study unveils the macroscopic origin of chiroptical activity of chiral MHS and provides design principles for obtaining high anisotropic factors for future chiral optoelectronic applications.
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http://dx.doi.org/10.1021/jacs.2c10309 | DOI Listing |
Chemistry
December 2024
Nagoya University, Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Furo-cho, Chikusa-ku, 464-8603, Nagoya, JAPAN.
The scalable synthesis of figure-eight π-systems is challenging for the conventional bottom-up approach. We have recently reported that the oxidative inner-bond cleavage of commercially available dibenzo[g,p]chrysene efficiently furnishes a figure-eight π-acceptor, cyclobisbiphenylenecarbonyl (CBBC), in large quantity. Furthermore, its donor-acceptor-type derivative with four N-carbazolyl substituents at the meta-positions of the carbonyl groups exhibited thermally activated delayed fluorescence (TADF) and circularly polarized luminescence (CPL) with a high |gCPL| value of 1.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Nankai University, School of Materials Science and Engineering, CHINA.
Chiral hybrid organic-inorganic metal halides (HOMHs) hold great promise in broad applications ranging from ferroelectrics, spintronics to nonlinear optics, owing to their broken inversion symmetry and tunable chiroptoelectronic properties. Typically, chiral HOMHs are constructed by chiral organic cations and metal anion polyhedra, with the latter regarded as optoelectronic active units. However, the primary design approaches are largely constrained to regulation of general components within structural formula.
View Article and Find Full Text PDFSmall
December 2024
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, 266580, China.
Chiral plasmonic nanomaterials have attracted significant awareness due to their applications in chiral catalysis, biosensing, photonics, and separation. Constructing plasmonic core-shell nanomaterials with geometric chirality and desirable optical chirality is a crucial yet challenging task for extending the range of chiral plasmonic nanomaterials. Here, a two-step method is reported for the synthesis of Gold (Au) branches wrapped silver (Ag) nanocubes (L/DBAg@Au) with strong and tunable circular dichroism (CD) signals under the regulation of L/D-cysteine (L/D-Cys).
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Beijing Institute of Smart Energy, Beijing 102200, China.
Supramolecular chirality has gained immense attention for great potential, in which the rational engineering strategy facilitates unique helical stacking/assembly, high chiroptical behavior, and prime biomedical activity. In this study, we reported a novel chiral organic donor-acceptor cocrystal based on asymmetrical components of benzo()naphtho(1,2-)thiophene (BNT) and 9-oxo-9H-indeno(1,2-)pyrazine-2,3-dicarbonitrile (DCAF) that exhibited red emission using a simple solution approach. During the self-assembly, a kinetically controlled growth of polar solvent or substrate induction led to the chiral packing and helical morphology twisted by the cooperation of electrostatic potential energy and chirality.
View Article and Find Full Text PDFMater Horiz
December 2024
State Key Laboratory for Mechanical Behavior of Materials, Shaanxi International Research Center for Soft Matter, School of Materials Science and Engineering, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
Helicenes exhibit promise as active layer materials for circularly polarized light (CPL) detectors due to their strong chiroptical activity. However, their practical application is limited by the complicated synthesis and loosely solid-state packing. This study introduces a chiral induction strategy towards the synthesis of helicene derivatives, chiral tetrachlorinated diperylene diimides (()-4CldiPDI or ()-4CldiPDI).
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