Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101554
PIRA download icon_1.1View/Download Full Text
Title: Multicolor tuning and temperature-triggered anomalous Eu³⁺-related photoemission enhancement via interplay of accelerated energy transfer and release of defect-trapped electrons in the Tb³⁺,Eu³⁺-doped strontium–aluminum chlorites
Authors: Kang, F
Sun, G
Wang, A
Xiao, X
Li, YY
Lu, J
Huang, B 
Issue Date: 24-Oct-2018
Source: ACS applied materials and interfaces, 24 Oct. 2018, v. 10, no. 42, p. 36157-36170
Abstract: So far, a large number of rare earth (RE) and non-RE-doped emission-tunable crystals based on controllable energy transfer have become available, but numerous mechanistic issues, particularly for those that involve temperature-dependent energy transfer between the well-shielded 4f RE ions, lack comprehensive theoretical and experimental investigation, limiting greatly their development and applications in the future. Here, we design and report a type of Tb³⁺,Eu³⁺-doped Sr₃Al₂O₅Cl₂ phosphors capable of multiemissions upon excitation at 376 nm, through using the orthorhombic Sr₃Al₂O₅Cl₂ as the host lattice while the well-shielded 4f Tb³⁺ and Eu³⁺ ions as dual luminescent centers. Our results reveal that the energy transfer from Tb³⁺ to Eu³⁺ ions, happening via an electric dipole-quadrupole (d-q) interaction, can be controlled by the doping ratio of Tb³⁺ and Eu³⁺, leading to the tunable emissions from green (0.3159, 0.5572) to red (0.6579, 0.3046). It is found from time-resolved photoluminescence (PL) spectra that this energy transfer begins at t = 5 μs and gradually ends at t ≥ 200 μs. Moreover, from temperature-dependent PL results, we reveal that the Eu³⁺ emission features an anomalous intensity enhancement at the earlier heating state. With the density functional theory (DFT) calculations, we have screened the possibilities of site preferential substitution problem. By jointly taking into account the X-ray diffraction Rietveld refinement, DFT findings, and PL and thermoluminescence spectra, a mechanistic profile is proposed for illustrating the PL observations. In particular, our discussions reveal that the temperature-triggered Eu³⁺ emission enhancement is due to the interplay of the temperature-induced accelerated energy transfer and defect-trapped electrons that are released upon the thermal stimulation. Unlike most of reported phosphor materials that are always suggested for phosphor-converted white light-emitting diodes, we propose new application possibilities for Tb³⁺,Eu³⁺-doped Sr₃Al₂O₅Cl₂ phosphors, such as anticounterfeiting, temperature-controlled fluorescence sensor, data storage, and security devices.
Keywords: Defect-trapped electrons
Energy transfer
Site preferential substitution
Sr3Al2O5Cl2:Tb3+,Eu3+
Temperature-triggered antiquenching luminescence
Tunable emissions
Publisher: American Chemical Society
Journal: ACS applied materials and interfaces 
ISSN: 1944-8244
EISSN: 1944-8252
DOI: 10.1021/acsami.8b13728
Rights: © 2018 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials & Interfaces, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsami.8b13728.
Appears in Collections:Journal/Magazine Article

Files in This Item:
File Description SizeFormat 
Huang_Multicolor_Tuning_Temperature-Triggered.pdfPre-Published version2.25 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Final Accepted Manuscript
Access
View full-text via PolyU eLinks SFX Query
Show full item record

Page views

72
Citations as of Apr 14, 2025

Downloads

80
Citations as of Apr 14, 2025

SCOPUSTM   
Citations

54
Citations as of Dec 19, 2025

WEB OF SCIENCETM
Citations

50
Citations as of Dec 18, 2025

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.