卤化物
钙钛矿(结构)
碱金属
光致发光
碘化物
配位场理论
配体(生物化学)
光谱化学系列
化学
溴化物
阳离子聚合
无机化学
结晶学
材料科学
离子
光电子学
高分子化学
有机化学
生物化学
受体
作者
Jiaqian Zhou,Peiran Xie,Chao Wang,Tieyuan Bian,Jian Chen,Yang Liu,Zhu Guo,Congcong Chen,Xin Pan,Min Luo,Jun Yin,Lingling Mao
标识
DOI:10.1002/anie.202307646
摘要
Double perovskites (DP) have attracted extensive attention due to their rich structures and wide application prospects in the field of optoelectronics. Here, we report 15 new Bi-based double perovskite derived halides with the general formula of A2 BBiX6 (A=organic cationic ligand, B=K or Rb, X=Br or I). These materials are synthesized using organic ligands to coordinate with metal ions with a sp3 oxygen, and diverse structure types have been obtained with distinct dimensionalities and connectivity modes. The optical band gaps of these phases can be tuned by changing the halide, the organic ligand and the alkali metal, varying from 2.0 to 2.9 eV. The bromide phases exhibit increasing photoluminescence (PL) intensity with decreasing temperature, while the PL intensity of iodide phases changes nonmonotonically with temperature. Because the majority of these phases are non-centrosymmetric, second harmonic generation (SHG) responses are also measured for selected non-centrosymmetric materials, showing different particle-size-dependent trends. Our findings give rise to a series of new structural types to the DP family, and provide a powerful synthetic handle for symmetry breaking.
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