Abstract
A series of Lu2(1-x)Tb2x(WO4)3 (x = 0.00–1.00) white powder materials were prepared by a high-temperature solid-phase method. The crystal structure, microscopic morphology, elemental composition, bandgap energy, photoluminescence properties, and thermal stability of luminescence of the prepared materials were analyzed and studied through room and high temperature X-ray diffraction patterns, field emission scanning electron microscopy images, energy energy-dispersive spectra and X-ray photoelectron spectra, diffuse reflectance spectra, room and high temperature photoluminescence spectra. Under 260 nm excitation, the green emitting Lu2(1-x)Tb2x(WO4)3 samples exhibited an optimum Tb3+ doping concentration at x = 0.30. Calculated results illustrate that the concentration quenching was mainly caused by dipole-dipole interaction. Lu1.98Tb0.02(WO4)3 phosphor exhibited thermally enhanced luminescence at 120 °C, with a maximum luminescence intensity of 254 % of the initial room temperature intensity. Lu1.4Tb0.6(WO4)3 phosphor exhibited thermally enhanced luminescence at 150 °C, with a maximum luminescence intensity of 109 % of the initial room temperature intensity. The mechanism of the thermally enhanced luminescence phenomenon is further discussed to be the adsorbed crystal water and the negative thermal expansion of the material. Thermally enhanced luminescence is of great significance in overcoming luminescent thermal quenching phenomenon, improving the luminescence efficiency, optimizing the material design, and so forth. It has potential applications in high-temperature lighting, display technology, temperature sensing, and optical anti-counterfeiting.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.