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[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.
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页码:5648 / 5656
页数:9
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