journal article·2024-07Open access

Experimental Evidence of the Molecular and Macroscopic Origins of Circular Dichroism in Chiral Metal‐Halide Networks

Alexandre Abhervé

Advanced Optical Materials· Volume 12· Issue 19

Abstract

Abstract Clockwise or counter‐clockwise spin coating? In the current hot research topic of chiral metal‐halide semiconductors, several investigations have been undertaken in order to reveal their natural optical activity and have reported dissymmetry factors ( g abs ) for thin films of many hybrid compounds, usually without considering the macroscopic anisotropies inherent to solid‐state samples. Yet, CD in the solid state can be strongly modulated by the co‐existence of linear dichroism (LD) and linear birefringence (LB). Theoretical studies recently revealed the importance of such macroscopic interferences in the CD response of solid‐state samples, often referred as symmetric (sLDLB) and antisymmetric (aLDLB) effects. Based on the newly synthesized one‐dimensional lead‐halide networks of formula ( S/R ‐HP1A)PbBr 3 and ( S/R ‐HP1A)PbI 3 , an experimental method to accurately discriminate between CD, sLDLB and aLDLB in chiral metal‐halide networks is here presented. The main experimental conditions influencing sLDLB and aLDLB amplitude are also highlighted, such as the concentration of the precursor solution and the spin‐coating rotation direction, finally providing a complete experimental guide for the forthcoming chiroptical investigations of such important family of chiral hybrid materials.
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Research context

OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · Molecular spectroscopy and chirality

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratoire MOLTECH‐Anjou UMR 6200 CNRS UNIV Angers 2 Boulevard Lavoisier ANGERS Cedex 49045 France

References (25)

Show source-provided references
1. 10.1039/C7MH00197E10.1039/C7MH00197E ↗
2. 10.1021/acs.jpcc.2c0419210.1021/acs.jpcc.2c04192 ↗
3. 10.1002/adom.20220199610.1002/adom.202201996 ↗
4. 10.1021/acs.nanolett.8b0161610.1021/acs.nanolett.8b01616 ↗
5. 10.1038/s41570-022-00399-110.1038/s41570-022-00399-1 ↗
6. 10.1021/acs.jpclett.9b0371810.1021/acs.jpclett.9b03718 ↗
7. Chen C. · Nat. Commun. · 1927 · 2019 · 10
8. 10.1126/sciadv.abd327410.1126/sciadv.abd3274 ↗
9. 10.1002/cnma.20220021910.1002/cnma.202200219 ↗
10. 10.1002/anie.20070307510.1002/anie.200703075 ↗
11. 10.1039/C7QM00233E10.1039/C7QM00233E ↗
12. 10.1021/jacs.1c0675210.1021/jacs.1c06752 ↗
13. 10.1021/jacs.2c1030910.1021/jacs.2c10309 ↗
14. 10.1021/acsnano.1c0113410.1021/acsnano.1c01134 ↗
15. 10.1038/s41467-022-31017-910.1038/s41467-022-31017-9 ↗
16. 10.1002/adma.20230578410.1002/adma.202305784 ↗
17. 10.1039/B916369G10.1039/B916369G ↗
18. 10.1126/science.106083510.1126/science.1060835 ↗
19. 10.1039/C9NJ02746G10.1039/C9NJ02746G ↗
20. Albano G. · Chem. Nano. Mat. · 2018 · 4 · 1059
21. 10.1002/adma.20160411310.1002/adma.201604113 ↗
22. 10.1016/j.optmat.2023.11410210.1016/j.optmat.2023.114102 ↗
23. 10.1021/acs.analchem.3c0293310.1021/acs.analchem.3c02933 ↗
24. 10.1021/acs.jpclett.0c0258910.1021/acs.jpclett.0c02589 ↗
25. 10.1038/s41467-023-38927-210.1038/s41467-023-38927-2 ↗