Abstract
The phosphors Ca3(PO4)2:Tm3+ by co-doping Ce3+ have been synthesized by conventional high-temperature solid-state reaction method. Their spectroscopic properties in the UV-VIS-NIR range have been investigated. The first 5d crystal field level location and stokes shift have been determined from the UV excitation and emission spectra of Ca3(PO4)2:Ce3+. The three-photon NIR quantum-cutting luminescence of Tm3+ assigned to the electronic transitions of 1G4→3H4, 3H4→3F4 and 3F4→3H6 is observed, whether in Ca3(PO4)2:Tm3+ or Ca3(PO4)2:Tm3+,Ce3+. The energy transfer from Ce3+ to Tm3+ takes place with energy-transfer efficiency up to 34.5% for the Ca3(PO4)2:Tm3+,Ce3+. A cross relaxation scheme using the 5d states of Ce3+ and f-f transition of Tm3+ is proposed. The mechanism is revealed from energy level and decay measurements. The results show that the broadband absorption of Ce3+ sensitizer not only extends the spectrum conversion in UV region but also greatly enhances the photoluminescence intensities of the three-photon quantum cutting luminescence of Tm3+ doped Ca3(PO4)2.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
