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Photoluminescence and Fourier Transform Infrared Spectral Studies of Varying Levels of Manganese Doping in Zinc Phosphate Oxide Glasses
Zinc phosphate glasses with varying gradient Mn ion concentrations of x MnO-(57.5- x ) ZnO-2.5Al 2 O 3 -40 P 2 O 5 were prepared by melting annealing. UV/Vis, Fourier transform infrared (FTIR), and photoluminescence (PL) spectrophotometric tests examined the spectra and structural changes of the gla...
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Published in: | Journal of electronic materials 2023-07, Vol.52 (7), p.4551-4557 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Zinc phosphate glasses with varying gradient Mn ion concentrations of
x
MnO-(57.5-
x
) ZnO-2.5Al
2
O
3
-40 P
2
O
5
were prepared by melting annealing. UV/Vis, Fourier transform infrared (FTIR), and photoluminescence (PL) spectrophotometric tests examined the spectra and structural changes of the glassy samples. Electronic spectral graphs exhibit considerable ultraviolet absorption with a distinct band shifting to slightly higher wavelengths with MnO
2
addition and two more bands in glasses with increasing manganese ion content (8–10%). FTIR spectral data show phosphate group vibrational peaks between 400 cm
−1
and 1600 cm
−1
, assuming that Zn-O or P-O-Zn vibrations are shared. The PL spectra subsequently exhibited a wider band in the range 500–750 nm and two-component peaks at greater manganese ion concentrations. As manganese ion concentration increases, divalent manganese ions of the known spin-forbidden absorption type that require high MnO
2
content are identified. All spectral data suggest and validate the lack of trivalent manganese ions, and as the manganese ion concentration increases, divalent manganese ions of known spin-forbidden absorption type with high MnO2 content are detected. The reducing nature of the host zinc phosphate glass favors the reduced valence of manganese ions. |
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ISSN: | 0361-5235 1543-186X |
DOI: | 10.1007/s11664-023-10389-8 |