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Synthesis of Dysprosium Oxychloride (DyOCl)

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Abstract

Dysprosium oxychloride, DyOCl, was synthesized using a simple hydrolysis method with DyCl3·6H2O. X-ray powder diffraction (XRD) data was used to determine the crystal structure. The DyOCl compound is isostructural to the matlockite (PbFCl) crystal structure and crystallizes in the tetragonal P4/nmm (#129) space group. The crystal structure contains the alternating cationic layers of (DyO)n and anionic layers of nCl along the c-axis. The structural data including unit cell, volume, and density of DyOCl were compared to other rare-earth oxychloride data from the Inorganic Crystal Structure Database (ICSD) and our previous study on TbOCl. Fourier-transform infrared spectroscopy was performed on DyOCl and peaks observed at 543 and 744 cm−1 were attributed to Dy–O and Dy–Cl. Scanning electron microscopy analysis showed irregularly shaped crystals. Hot-stage XRD, thermogravimetry, as well as differential scanning calorimetry coupled to a gas chromatograph and a mass spectrometer (evolved gas analysis) were performed on DyCl3·6H2O to understand the phase transformation to DyOCl (and Dy2O3) as a function of temperature and time at temperature.

Graphic Abstract

DyOCl compound with the tetragonal P4/nmm space group is composed of the alternating layers of (DyO)n and nCl along the c-axis.

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Acknowledgements

The Pacific Northwest National Laboratory is operated by Battelle under Contract Number DE-AC05-76RL01830.

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Correspondence to Saehwa Chong.

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Chong, S., Riley, B.J., Marcial, J. et al. Synthesis of Dysprosium Oxychloride (DyOCl). J Chem Crystallogr 52, 185–193 (2022). https://doi.org/10.1007/s10870-021-00904-2

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  • DOI: https://doi.org/10.1007/s10870-021-00904-2

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