化学
双折射
紫外线
各向异性
Crystal(编程语言)
光电子学
带隙
硼
结晶学
透明度(行为)
晶体结构
光学各向异性
切断
GSM演进的增强数据速率
光学材料
反向
光学
作者
Mengru Liu,Huijian Zhao,Xianghao Kong,Ning Ye,Zhanggui Hu,Conggang Li
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-10-14
卷期号:64 (42): 21301-21307
被引量:4
标识
DOI:10.1021/acs.inorgchem.5c04445
摘要
Birefringent crystals are indispensable components in optical functional devices that enable the precise manipulation of light polarization. However, achieving a balance between wide ultraviolet (UV) transparency and significant birefringence poses a formidable challenge due to their inherent inverse correlation. Here, we report a novel rare-earth borate fluoride, K2GdB3O6F2 (KGBOF) that overcomes this intrinsic trade-off via the rational assembly of π-conjugated [B3O6] groups. Expectedly, KGBOF exhibits a large birefringence of 0.12@532 nm, comparable to that of the commercially available α-BaB2O4, exceeding that of most rare-earth borate fluorides. Notably, KGBOF demonstrates a wide band gap of 5.71 eV and a short-wavelength cutoff edge (<200 nm). First-principles calculations and structural analysis attribute the exceptional optical anisotropy to the coplanar alignment of π-conjugated [B3O6] clusters. These results establish KGBOF as a promising short-wave UV birefringent crystal and provide a basis for the exploitation of new birefringent materials in the short-wavelength region.
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