甲脒
碘化物
四方晶系
结晶学
钙钛矿(结构)
负热膨胀
热膨胀
同步加速器
光致发光
相(物质)
相变
化学
材料科学
无机化学
晶体结构
凝聚态物理
光学
有机化学
冶金
物理
光电子学
作者
Douglas H. Fabini,Constantinos C. Stoumpos,Geneva Laurita,Andreas Kaltzoglou,Athanassios G. Kontos,Polycarpos Falaras,Mercouri G. Kanatzidis,Ram Seshadri
标识
DOI:10.1002/ange.201609538
摘要
Abstract The structure of the hybrid perovskite HC(NH 2 ) 2 PbI 3 (formamidinium lead iodide) reflects competing interactions associated with molecular motion, hydrogen bonding tendencies, thermally activated soft octahedral rotations, and the propensity for the Pb 2+ lone pair to express its stereochemistry. High‐resolution synchrotron X‐ray powder diffraction reveals a continuous transition from the cubic α‐phase (Pm m, #221) to a tetragonal β‐phase (P4/mbm, #127) at around 285 K, followed by a first‐order transition to a tetragonal γ‐phase (retaining P4/mbm, #127) at 140 K. An unusual reentrant pseudosymmetry in the β‐to‐γ phase transition is seen that is also reflected in the photoluminescence. Around room temperature, the coefficient of volumetric thermal expansion is among the largest for any extended crystalline solid.
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