卤化物
碘化物
钙钛矿(结构)
结构精修
溴化物
结晶学
带隙
材料科学
化学
晶体结构
无机化学
光电子学
作者
Jiyu Tian,David B. Cordes,Alexandra M. Z. Slawin,Eli Zysman‐Colman,Finlay D. Morrison
出处
期刊:
日期:2021-04-29
被引量:1
标识
DOI:10.26434/chemrxiv.14502372.v1
摘要
Mixed halide azetidinium lead perovskites AzPbBr3-xXx (X = Cl or I) were obtained by mechanosynthesis. With varying halide composition from Cl- to Br- to I-; the chloride and bromide analogs both form in the hexagonal 6H polytype while the iodide adopts the 9R polytype. An intermediate 4H polytype is observed for mixed Br/I compositions. Overall the structure progresses from 6H to 4H to 9R perovskite polytype with varying halide composition. Rietveld refinement of the powder X-ray diffraction patterns revealed a linear variation in unit cell volume as a function of the average radius of the anion, which is not only observed within the solid solution of each polytype (according to Vegard’s law) but extends uniformly across all three polytypes. This is correlated with a progressive (linear) tuning of the bandgap from 3.41 to 2.00 eV. Regardless of halide, the family of azetidinium halide perovskite polytypes are highly stable, with no discernible change in properties over more than 6 months under ambient conditions
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