化学
碱金属
双折射
调制(音乐)
晶体结构
Crystal(编程语言)
金属
结晶学
无机化学
有机化学
光学
计算机科学
美学
物理
哲学
程序设计语言
作者
Chao Wei,Danyang Dou,Bingbing Zhang,Ying Wang
标识
DOI:10.1021/acs.inorgchem.5c02868
摘要
Birefringent materials are a pivotal category of optical functional materials; however, finding a new birefringent material that can operate in the deep-ultraviolet (DUV) region remains elusive. Through structural integration of [B3O6] with [AlO3F] units, fluoroaluminoborates have emerged as a chemically tunable platform for engineering birefringent materials. In this study, we report the first demonstration of cation-size-driven crystal structure evolution and birefringence modulation within fluoroaluminoborate systems. Two polymorphic potassium fluoroaluminoborates, α- and β-KAlB3O6F, were successfully synthesized through a high-temperature melting method. Both phases exhibit remarkable DUV optical performance, achieving wide band gaps coupled with exceptional birefringence (α: 0.093 @ 546 nm, β: 0.110 @ 546 nm). By combining the crystal structure analysis and the first-principles calculation results, we reveal cation-size-dependent alignment of [B3O6]/[AlO3F] groups as the origin of birefringence enhancement. This work establishes an effective strategy for simultaneously optimizing birefringence while maintaining DUV transparency through cation structural engineering.
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