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Synthesis and Exfoliation of Discotic Zirconium Phosphates to Obtain Colloidal Liquid Crystals
Published on: May 25, 2016
Dimensionality Engineering of Fluorozirconium Phosphates for Deep-UV-Transparent Crystals with Enhanced
Yuexin Zhang1,2,3, Yipeng Song1,4,2, Zhiyong Bai1,2
1State Key Laboratory of Functional Crystals and Devices, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, Fujian, China.
Abstract:
Phosphate crystals have attracted significant interest as platforms for deep-ultraviolet (deep-UV) optical materials, attributable to their rich structural chemistry and tunable optical properties. However, simultaneously achieving strong second-harmonic generation (SHG) and enhanced birefringence in phosphate systems remains a formidable challenge. Herein, through a dimensionality-engineering strategy, we report five deep-UV transparent fluorozirconium phosphate compounds, including the three-dimensional (3D) ZrPO4F (I), two-dimensional (2D) Zr(H2PO4)(HPO4)F·3H2O (II) and (NH4)4Zr4(HPO4)2(PO4)4F4 (III), as well as the one-dimensional (1D) Rb2.9(NH4)3.1Zr4(H2PO4)F21 (IV) and Rb4.2(NH4)3.8Zr4(PO4)2F18 (V). These compounds exhibit clear dimension-dependent optical properties, with reduced dimensionality leading to enhanced SHG responses and larger birefringence. Notably, the fluorine-rich 1D compounds display the strongest SHG efficiency (up to 2.1 × KDP) and the largest birefringence (0.053 @ 550 nm) within the series. Structure-property analyses reveal that decreasing the structural dimensionality promotes increased local distortion of Zr-centered polyhedra and more uniform dipole alignment, thereby amplifying both SHG and birefringence. This work establishes dimensionality engineering of fluorozirconium phosphates as an effective strategy for fine-tuning key optical properties while maintaining deep-UV transparency.
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