Abstract
This work refers to the research results on the ability to form solid solution when synthesizing the manganese-doped zinc alkaline earth silicate luminescent pigment in the form of Zn1,97-xMxMn0,03SiO4 (M is magnesium, calcium, strontium and barium) by the precipitation-impregnation method. The samples were characterized by thermal analysis, X-ray diffraction spectroscopy, luminescence under UV lamp and luminescence spectroscopy at 254 nm excitation wavelength. The results show that when heating the corresponding precipitated precursor at 900 oC for 45 minutes, in general, the ability to form solid solutions decreases when the size difference of alkaline earth metal ions with Zn2+ ions increases. Specifically, Mg2+ ions create single-phase solid solutions with x varying from 0 to 1. Ca2+ ions form solid solutions when x changes from 0 to 0.6. When x = 0.8; in addition to the main phase Zn2SiO4, it also creates Ca2ZnSi2O7 with tetragonal structure. The Ba2+ ions form solid solutions when x varies from 0 to 0.5. When x = 0.6, in addition to Zn2SiO4, there is also BaZn2Si2O7. The Sr2+ ions form a solid solution when x = 0.2. For samples with x ≥ 0.4, in addition to Zn2SiO4, there is also Sr2ZnSi2O7; SrZn2Si2O7/SrO.2ZnO.2SiO2. The single - phase solid solutions all have the rhombo H structure of Zn2SiO4, and all have higher luminescence than the multiphase samples. The sample with the largest x, the sample Zn0,97Mg1,0Mn0,03SiO4 had the highest luminescence, emitting green light corresponding to the wavelength of 525 nm when excited by 254 nm UV light.
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.