Suppression of Impurity Phase in Cesium Halide Perovskites by using Pressure
ORAL
Abstract
Cesium halide perovskites, Cs4PbBr6 are new promising candidates for the applications of wide band gap semiconductors. However, the unavoidable appearance of CsPbBr3, during the growth of the host crystal significantly hinders the optical and electrical properties of the materials. We report the suppression of the CsPbBr3 phase by applying pressure in an order of giga-pascal scale.
The results of XRD revealed that the CsPbBr3 phase disappeared at 2.6 GPa. No PL and band edge peak of CsPbBr3 was observed at 3.0 GPa, which demonstrates the disappearance of the fluorescence from the UV irradiated sample. With further pressure, the XRD data showed a reversible phase transition from rhombohedral to monoclinic of Cs4PbBr6 at 2.6 GPa. The main peaks were stable under pressure up to 20.0 GPa. After releasing the pressure, a very small intensity of PL peak, the band edge, and XRD peaks for CsPbBr3 phase were observed. The Cs4PbBr6 phase was recovered at ambient conditions. It is speculated that CsPbBr3 crystals are sensitive to pressure with the distortion of [PbBr6]-4 network at moderately low pressure (<3.0 GPa), while Cs4PbBr6 crystals are much stable at high pressure (up to 20.0 GPa) due to the isolated octahedral PbBR6–4 ions interspersed Cs+ cations.
The results of XRD revealed that the CsPbBr3 phase disappeared at 2.6 GPa. No PL and band edge peak of CsPbBr3 was observed at 3.0 GPa, which demonstrates the disappearance of the fluorescence from the UV irradiated sample. With further pressure, the XRD data showed a reversible phase transition from rhombohedral to monoclinic of Cs4PbBr6 at 2.6 GPa. The main peaks were stable under pressure up to 20.0 GPa. After releasing the pressure, a very small intensity of PL peak, the band edge, and XRD peaks for CsPbBr3 phase were observed. The Cs4PbBr6 phase was recovered at ambient conditions. It is speculated that CsPbBr3 crystals are sensitive to pressure with the distortion of [PbBr6]-4 network at moderately low pressure (<3.0 GPa), while Cs4PbBr6 crystals are much stable at high pressure (up to 20.0 GPa) due to the isolated octahedral PbBR6–4 ions interspersed Cs+ cations.
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Presenters
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LanAnh Nguyen
Hanyang Univ
Authors
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LanAnh Nguyen
Hanyang Univ
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Duong Minh Nguyen
Hanyang Univ
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Youngjong Kang
Hanyang Univ
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Lin Wang
Beijing High Pressure Science Center, HPSTAR, Center for High Pressure Science & Technology Advanced Research, Shanghai 201203, China
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Jaeyong Kim
Hanyang Univ, Department of Physics and HYU-HPSTAR-CIS High Pressure Research Center, Hanyang University, Seoul, 04763, South Korea