Straus Daniel B, Guo Shu, Cava Robert J
Department of Chemistry , Princeton University , Princeton , New Jersey 08544 , United States.
J Am Chem Soc. 2019 Jul 24;141(29):11435-11439. doi: 10.1021/jacs.9b06055. Epub 2019 Jul 11.
We use a solid-state method to synthesize single crystals of perovskite-phase cesium lead iodide (γ-CsPbI) that are kinetically stable at room temperature. Single crystal X-ray diffraction characterization shows the compound is orthorhombic with the GdFeO structure at room temperature. Unlike conventional semiconductors, the optical absorption and joint density-of-states of bulk γ-CsPbI is greatest near the band edge and decreases beyond the for at least 1.9 eV. Bulk γ-CsPbI does not show an excitonic resonance and has an optical band gap of 1.63(3) eV, ∼90 meV smaller than has been reported in thin films; these and other differences indicate that previously measured thin film γ-CsPbI shows signatures of quantum confinement. By flowing gases during powder X-ray diffraction measurements, we confirm that γ-CsPbI is stable to oxygen but rapidly and catalytically converts to non-perovskite δ-CsPbI in the presence of moisture. Our results provide vital parameters for theoretical and experimental investigations into perovskite-phase CsPbI that will the guide the design and synthesis of atmospherically stable inorganic halide perovskites.
我们采用固态法合成了在室温下动力学稳定的钙钛矿相碘化铯铅(γ-CsPbI)单晶。单晶X射线衍射表征表明,该化合物在室温下为正交晶系,具有GdFeO结构。与传统半导体不同,块状γ-CsPbI的光吸收和联合态密度在带边附近最大,在至少1.9 eV以上则减小。块状γ-CsPbI不显示激子共振,光学带隙为1.63(3) eV,比薄膜中报道的值小约90 meV;这些差异及其他差异表明,先前测量的薄膜γ-CsPbI显示出量子限域的特征。通过在粉末X射线衍射测量过程中通入气体,我们证实γ-CsPbI对氧气稳定,但在有水分存在时会迅速催化转化为非钙钛矿相的δ-CsPbI。我们的结果为钙钛矿相CsPbI的理论和实验研究提供了重要参数,将指导大气稳定的无机卤化物钙钛矿的设计和合成。