Abstract

CaMg2(SO4)3 host and CaMg2(SO4)3:Dy3+ phosphor (where Dy3+ = 0.05, 0.1,0.2, 0.5 and 1 mol%) were synthesized via solid state synthesis method at 700 °C. Phase formation of the compound was confirmed by obtaining its X-ray diffraction (XRD) pattern and the surface morphology was analyzed with the scanning electron microscopy (SEM) technique. Photoluminescence (PL) excitation and emission spectra of CaMg2(SO4)3:Dy3+ phosphor shows characteristic emission and excitation peaks of Dy3+ ions, which confirms the doping of Dy3+ ions in the host. Material was irradiated with γ-rays and C6+ ion beam. Thermoluminescence (TL) glow curve of irradiated material was recorded at the heating rate of 5 °C s−1. A single TL peak is obtained after γ-rays irradiation for CaMg2(SO4)3 host at 158 °C and two TL peaks were seen for CaMg2(SO4)3:Dy3+ at 129 °C and 355 °C. With increase in Dy3+ concentration, TL intensity is increased but the nature of TL glow curve remained same. Material was quenched from 400 °C and its TL was recorded by irradiating it with γ-rays and C6+ ion beam (75 MeV). TL intensity of quenched CaMg2(SO4)3:Dy3+ compound enhanced significantly as compared to annealed CaMg2(SO4)3:Dy3+ compound. Electron paramagnetic resonance (EPR) study was carried out on irradiated (γ-ray and C6+ beam) CaMg2(SO4)3:Dy3+ compound to analyse radicles formed in the irradiation process and possible mechanism of TL. Correlated study of TL, PL and EPR is done.

Full Text
Paper version not known

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 call

Disclaimer: 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.