Eu3+-site occupation in CaTiO3 perovskite material at low temperature

In order to clarify the site occupancy of rare-earth ions in rare-earth doped perovskite materials, the un-doped pure CaTiO3 and Eu3+-doped CaTiO3 samples with a series of Ca/Ti ratio were synthesized via high-temperature solid-state reaction method. X-ray diffraction (XRD) powder patterns confirm t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Current applied physics 2017, 17(1), , pp.24-30
Hauptverfasser: Chi, Fengfeng, Qin, Yanguang, Zhou, Shaoshuai, Wei, Xiantao, Chen, Yonghu, Duan, Changkui, Yin, Min
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In order to clarify the site occupancy of rare-earth ions in rare-earth doped perovskite materials, the un-doped pure CaTiO3 and Eu3+-doped CaTiO3 samples with a series of Ca/Ti ratio were synthesized via high-temperature solid-state reaction method. X-ray diffraction (XRD) powder patterns confirm that the crystal structure keeps invariant at various Ca/Ti ratios. Measurement results of unit-cell parameters and X-ray photoelectron spectroscopy (XPS) indicate that Eu3+ ions enter into the Ca2+ site. The high-resolution photoluminescence spectra of Eu3+ ions at 20 K in all samples did not witness a significant change under the excitation at different wavelength, implying that Eu3+ ions occupy only one type of site. Considering the small spectral splitting range of 5D0 → 7F2 transition and the large intensity ratio of 5D0 → 7F2/5D0 → 7F1, it can be concluded that Eu3+ occupies Ca2+ site with larger coordinate numbers rather than Ti4+ site. •Well-crystallized Eu3+-doped perovskite materials CaTiO3 with a series of Ca/Ti ratio were synthesized.•The luminescence of Eu3+ in all samples does not witness a significant change under different wavelength excitation.•It is more likely for Eu3+ to occupy the Ca2+ site and the occupancy of Eu3+ ions is independent of Ca/Ti ratio.
ISSN:1567-1739
1878-1675
DOI:10.1016/j.cap.2016.10.018