Yuexin Zhang, Yipeng Song, Zhiyong Bai, Zhou Yuan, Wei Huang, Ji Qi, Xinwei Zhou, Sangen Zhao, Ling Chen, Kang Min Ok, Junhua Luo
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) ZrPO 4 F ( I ), two-dimensional (2D) Zr(H 2 PO 4 )(HPO 4 )F·3H 2 O ( II ) and (NH 4 ) 4 Zr 4 (HPO 4 ) 2 (PO 4 ) 4 F 4 ( III ), as well as the one-dimensional (1D) Rb 2.9 (NH 4 ) 3.1 Zr 4 (H 2 PO 4 )F 21 ( IV ) and Rb 4.2 (NH 4 ) 3.8 Zr 4 (PO 4 ) 2 F 18 ( 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.