[Sn3OF]PO4vs. [Sn3F3]PO4: enhancing birefringence by breaking the R3 symmetry and realigning lone pairs

被引:4
|
作者
Hu, Yuhan [1 ,2 ]
Xu, Xi [1 ]
Wang, Ruixi [2 ]
Han, Jingyun [1 ]
Zhang, Shunsong [1 ]
Zhan, Shuhui [1 ]
Guo, Jingyu [1 ,2 ]
Wu, Li-Ming [1 ,2 ]
Chen, Ling [1 ,2 ]
机构
[1] Beijing Normal Univ, Ctr Adv Mat Res, Zhuhai 519087, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China
来源
INORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 17期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
DESIGN;
D O I
10.1039/d4qi01203h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Tin(II)-containing phosphates are promising candidates for designing and studying materials with enhanced birefringence. Herein, we present a novel compound [Sn3OF]PO4 that exhibits significant birefringence (Delta n(obv.) = 0.117 at 546 nm), a five-fold improvement compared to that of the related compound [Sn3F3]PO4 discovered nearly 40 years ago. The remarkable enhancement in birefringence is primarily attributed to the anisotropic [SnO3F](5-) structure building unit. By simple regulation of the F/O ratio, the undesirable R3 symmetry in [Sn3F3]PO4 is disrupted. This regulation also realigns the lone pairs, resulting in substantial optical anisotropy.
引用
收藏
页码:5648 / 5656
页数:9
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