Can Low Structural Anisotropy Produce High Optical Anisotropy? Anomalous Giant Optical Birefringent Effect in PIAlI in Focus.

J Am Chem Soc

Functional Crystals Lab, Key Laboratory of Functional Crystals and Laser Technology, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

Published: January 2025

Tetrahedral halides with broad transparency and large second harmonic effects have the potential to serve as mid-infrared wide-bandgap materials with balanced nonlinear-optical (NLO) properties. However, their regular tetrahedral motifs tend to exhibit low optical birefringence (Δ < 0.03) due to limited structural anisotropy, which constrains their practical phase-matched capability. A significant challenge in halide structural chemistry and material exploration is to enhance the Δ of tetrahedral halides while maintaining their balanced properties. The question of whether tetrahedra with low structural anisotropy can produce high optical anisotropy remains unanswered. In this study, in addition to the conventional strategy of enhancing Δ by increasing structural anisotropy, we identify a previously unreported strategy of enhancing Δ by increasing electronic anisotropy. This novel strategy model unprecedentedly enhances the Δ of an existing tetrahedral halide, PIAlI, to a degree not achievable by conventional techniques, with the value reaching up to 0.31@1 μm. The anomalous increase in Δ is achieved by anisotropic charge redistribution resulting from a unique charge transfer effect between the anionic and cationic tetrahedral motifs. First-principles analysis provides further corroboration of the detailed chemical bonding electronic distributions and charge transfer illustrations. It is predicted that analogous AsIAlI and TeIZnI will exhibit a greater propensity for giant Δ (> 0.5@1 μm). This finding will greatly enrich the structural chemistry of -hybridized tetrahedra and provide seminal ideas for the design and modulation of highly birefringent structures.

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Source
http://dx.doi.org/10.1021/jacs.4c14624DOI Listing

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