共 44 条
Novel identification of ultraviolet/visible Cr6+/Cr3+ optical transitions in borate glasses
被引:93
作者:
Hassan, M. A.
[1
]
Ahmad, F.
[2
]
Abd El-Fattah, Z. M.
[1
,3
]
机构:
[1] Al Azhar Univ, Fac Sci, Dept Phys, Cairo 11884, Egypt
[2] Al Azhar Univ, Fac Sci, Dept Phys, Girls Branch, Cairo 11754, Egypt
[3] Barcelona Inst Sci & Technol, ICFO Inst Genies Foton, Barcelona 08860, Spain
关键词:
Borate glasses;
Chromium hexavalent;
Ligand field theory;
UV-Visible optical devices;
ESR;
FTIR;
ELECTRON-PARAMAGNETIC-RESONANCE;
EXCITED-STATE SPECTROSCOPY;
PHYSICAL-PROPERTIES;
PHOSPHATE-GLASSES;
CHROMIUM IONS;
CR3+ IONS;
BOROPHOSPHATE GLASSES;
ABSORPTION SPECTRA;
EPR;
CERAMICS;
D O I:
10.1016/j.jallcom.2018.03.351
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Chromium oxide-doped borate glasses with composition xP(2)O(5)-(70-x) B2O3- 29.5Li(2)O-0.5 Cr2O3 (x= 0.0, 0.5, 1.0, 1.2, 1.5 and 2.0 mol %) were prepared following the melt quenching technique. A detailed deconvolution process, applied to their optical absorption spectra, revealed distinct optical transitions from Cr6+/Cr3+ in the ultraviolet/visible spectral regimes, which are simultaneously tuned through slight P2O5 additives. This tuability is mainly derived by the ligand field experienced by the optically-active Cr6+/Cr3+ ions. Interestingly, the intensity reduction of Cr6+/Cr3+ transitions with P2O5 contents allowed smooth variations of the glass color and unravel the, otherwise masked, optical band gap of the homogenous glass host. The coexistence of Cr6+ and Cr3+ was, further, confirmed by mapping its oxidation states via electron spin resonance spectroscopy, while structural rearrangements, produced by P2O5, and Cr6+ vibrational signal were inferred from infrared spectroscopy. The rich optical transitions provided by the coexistence of Cr6+ and Cr3+ within the same host and their simultaneous tuability should find applications in multifunctional optical devices operating in the ultraviolet and visible spectral regimes. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:320 / 327
页数:8
相关论文