Synthesis, structure, and properties of EuScCuS3 and SrScCuS3


Тип публикации: статья из журнала

Год издания: 2021

Идентификатор DOI: 10.1016/j.jssc.2020.121926

Ключевые слова: ab initio calculations, inorganic materials, magnetic measurements, optical spectroscopy, raman spectroscopy, thermochemistry, x-ray diffraction

Аннотация: The crystal structures of the first-synthesized compound EuScCuS3 and previously known SrScCuS3 are refined by Rietveld analysis of X-ray powder diffraction data. The structures are found to belong to orthorhombic crystal system, space group Cmcm, structural type KZrCuS3, with a ​= ​3.83413(3) Å, b ​= ​12.8625(1) Å, c ​= ​9.72654(8Показать полностью) Å (SrScCuS3) and a ​= ​3.83066(8) Å, b ​= ​12.7721(3) Å, c ​= ​9.7297(2) Å (EuScCuS3). The temperatures and enthalpies of incongruent melting are the following: Тm ​= ​1524.5 К, ΔHm ​= ​21.6 ​kJ•mol−1 (SrScCuS3), and Тm ​= ​1531.6 К, ΔHm ​= ​26.1 ​kJ•mol−1 (EuScCuS3). Ab initio calculations of the crystal structure and phonon spectrum of the compounds were performed. The types and wavenumbers of fundamental modes were determined and the involvement of ions participating in the IR and Raman modes was assessed. The experimental IR and Raman spectra were interpreted. EuScCuS3 manifests a ferromagnetic transition at 6.4 ​K. The SrScCuS3 compound is diamagnetic. The optical band gaps were found to be 1.63 ​eV (EuScCuS3) and 2.24 ​eV (SrScCuS3) from the diffuse reflectance spectra. The latter value is in good agreement with that calculated by the DFT method. The narrower band gap of EuScCuS3 is explained by the presence of 4f-5d transition in Eu2+ ion that indicates a possibility to control the band gap of the chalcogenides by the inclusion of Eu. The activation energy of crystal structure defects, being the source of additional absorption in the NIR spectral range, was found to be 0.29 ​eV. © 2021 Elsevier Inc.

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Журнал: Journal of Solid State Chemistry

Выпуск журнала: Vol. 296

Номера страниц: 121926

ISSN журнала: 00224596

Издатель: Academic Press Inc.