High-Pressure Structural and Optical Studies of Pure Low-Dimensional Cesium Lead Chlorides CsPb(2)Cl(5) and Cs(4)PbCl(6)

纯低维铯铅氯化物 CsPb(2)Cl(5) 和 Cs(4)PbCl(6) 的高压结构和光学研究

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Abstract

We report high-pressure single-crystal X-ray diffraction, optical absorption, and photoluminescence investigations of all-inorganic perovskite-related materials CsPb(2)Cl(5) and Cs(4)PbCl(6). The crystal structure of CsPb(2)Cl(5), composed of alternate layers of Cs(+) cations and Pb-Cl frameworks, is stable under pressure up to at least 4.2 GPa. Because external stress is mainly absorbed by the Cs(+) layers, the optical absorption edge of the crystal only slightly red-shifts with increasing pressure, which correlates well with a moderate shortening of the Pb-Cl bonds. A quite different response to pressure shows Cs(4)PbCl(6), the crystal built of isolated PbCl(6)(4-) octahedra and Cs(+) cations. During the compression at around 3.4 GPa, the trigonal phase I, space group R3̅c, transforms to the orthorhombic phase II, space group Cmce, which at around 4 GPa transforms into phase III. On decompression, phase II is not restored, but phase III converts through a diffuse phase transition into another high-pressure phase IV, which is stable in a wide pressure range and transforms to the initial phase I only around atmospheric pressure. The red shift of the absorption edge and the profound modification of the absorption spectrum in phase II were ascribed to the deformation of the PbCl(6)(4-) octahedra. The transition to phase III induces a blue shift of the absorption edge, while the transition to phase IV is associated with a large red shift. Photoluminescence was detected in phases I and II with the intensity quenched with increasing pressure.

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