Abstract
AbstractDeveloping environment‐friendly dual‐emission phosphors of both blue–cyan and deep‐red lights is desirable for the utilized indoor plant lighting research. Notably, the naked 6s and 6p Bi3+ ions are sensitive to the lattice sites, which emit from Ultraviolet (UV) to red lights in various crystal compounds. Meanwhile, the 2E → 4A2g transition of Mn4+ ions promises its deep‐red light emissions, which satisfies the demand for specific wavelength lights for plants growth. Hence, a Bi3+/Mn4+ co‐doped Sr2LaGaO5: Bi3+, Mn4+ (SLGO:Bi3+:Mn4+) phosphor was finally synthesized. The phase, micromorphology and luminescent properties were systematically evaluated. Upon excitation at 350 nm light, dual emissions of both blue–cyan (470 nm) and deep‐red (718 nm) lights were observed. Besides, due to the pronounced photoluminescence (PL) spectral overlap between Bi3+ and Mn4+ ions, a potential energy transfer process from Bi3+ to Mn4+ ions was confirmed. The relative PL intensities between Bi3+ and Mn4+ ions can be tuned just by adjusting the Mn4+ ion concentration. Besides, Li+ co‐doping has been evidenced to improve the deep‐red emissions (718 nm) of SLGO:0.005Mn4+ due to charge compensation and rationally designed lattice distortion, together with the improved thermal stability. Finally, the emissions of SLGO:Bi3+, Mn4+, Li+ phosphor suit properly with the absorption of the four fundamental pigments for plant growth, indicating that the prepared phosphorescent materials may have a prospect in plant light‐emitting diodes lighting.
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.