期刊
NEW JOURNAL OF CHEMISTRY
卷 39, 期 8, 页码 6531-6539出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5nj01191d
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Sr2SiO4 is an important inorganic host for lanthanide-doped white-light-emitting diodes. In order to probe the local structure and symmetry around lanthanide ions in Sr2SiO4, detailed experimental and theoretical investigations have been carried out. Samples prepared via sol-gel methods were thoroughly characterized using X-ray diffraction (XRD), extended X-ray absorption fine structure (EXAFS) and photoluminescence (PL) spectroscopy. The local symmetries of SrO9 and SrO10 polyhedra were determined using emission spectroscopy with europium as the probe ion. Despite having the same oxidation state and comparable ionic radii, Sm3+, Dy3+ and Eu3+ behave differently in terms of their site occupation at the Sr sites of SrO9 and SrO10 polyhedra. While Eu replaces Sr in both polyhedra, Sm and Dy reside specifically at the 9-coordinated Sr sites only. Based on density functional theory (DFT) calculations, it has been established that for Dy and Sm, the strong metal-oxygen bonding leads to significant distortion and hence the destabilization of MO10 polyhedra in the host.
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