Ultrabroad infrared luminescences from Bi-doped alkaline earth metal germanate glasses

2007 ◽  
Vol 22 (6) ◽  
pp. 1574-1578 ◽  
Author(s):  
Jinjun Ren ◽  
Jianrong Qiu ◽  
Botao Wu ◽  
Danping Chen

We report on ultrabroad infrared (IR) luminescences covering the 1000–1700-nm wavelength region, from Bi-doped 75GeO2–20RO–5Al2O3–1Bi2O3(R = Sr, Ca, and Mg) glasses. The full width at half-maximum of the IR luminescences excited at 980 nm increases (315 → 440 → 510 nm) with the change of alkaline earth metal (Mg2+→ Ca2+→ Sr2+). The fluorescence lifetime of the glass samples is 1725, 157, and 264 μs when R is Sr, Ca, and Mg, respectively. These materials may be promising candidates for broad-band fiber amplifiers and tunable laser resources.

2007 ◽  
Vol 280-283 ◽  
pp. 957-962
Author(s):  
Tao Li ◽  
Qin Yuan Zhang ◽  
Zhou Ming Feng ◽  
Yue Hui Liu ◽  
Zai De Deng ◽  
...  

Optical spectroscopic properties of Er3+-doped alkaline-earth metal modified fluoropho sphate glasses have been investigated experimentally for developing broadband fiber and planar amplifiers. The results show a strong correlation between the alkaline-earth metal content and the spectroscopic parameters such as absorption and emission cross sections, full widths at half-maximum and Judd-Ofelt intensity parameters. It is found that strontium ions could have more influences on the Judd-Ofelt intensity parameters and the absorption and emission cross sections than other alkaline-earth metal ions such as Mg2+, Ca2+, Ba2+. The sample containing 23 mol% strontium fluoride exhibits the maximum emission cross section of 7.58 × 10-21 cm2, the broadest full width at half-maximum of 65 nm and the longer lifetime of 8.6 ms among the alkaline-earth metal modified fluorophosphates glasses studied. The Judd-Ofelt intensity parameter W6s, the emission cross sections and the full widths at half-maximum in the Er3+-doped fluorophosphate glasses studied are larger than in the silicate and phosphate glasses.


2019 ◽  
Author(s):  
Nga Phung ◽  
Hans Köbler ◽  
Diego Di Girolamo ◽  
Thi Tuyen Ngo ◽  
Gabrielle Sousa e Silva ◽  
...  

1985 ◽  
Vol 89 (1) ◽  
pp. 175-177 ◽  
Author(s):  
Gerald R. Stevenson ◽  
Laurel E. Schock ◽  
Rosario Concepcion ◽  
Richard A. Peterson

2021 ◽  
Vol 60 (5) ◽  
pp. 2011-2026
Author(s):  
Eng Kein New ◽  
Ta Yeong Wu ◽  
Khai Shing Voon ◽  
Alessandra Procentese ◽  
Katrina Pui Yee Shak ◽  
...  

1998 ◽  
Vol 65 (1) ◽  
pp. 83-86 ◽  
Author(s):  
Yu-Wen Chen ◽  
Hsueh-Ying Chen ◽  
Wen-Fa Lin

Synlett ◽  
2021 ◽  
Author(s):  
Dongxu Yang ◽  
Linqing Wang

AbstractMagnesium (Mg) is a cheap, non-toxic, and recyclable alkaline earth metal that constitutes about 2% weight in the Earth’s crust. The use of magnesium catalysts to forge chiral moieties in molecules is highly attractive. Based on our work in recent years, we describe the current progress in the development of in situ generated magnesium catalysts and their application in asymmetric synthesis. In this perspective, a critically concise classification of in situ generated magnesium catalytic modes, with relevant examples, is presented, and representative mechanisms of each category are discussed. Building on the established diverse strategies, one can foresee that more innovative and structurally creative magnesium catalysts that are generated in situ will be developed to overcome more formidable challenges of catalytic enantioselective reactions.1 Introduction2 Magnesium Catalysts Generated in Situ from Chiral Ligands Containing Dual Reactive Hydrogens3 Magnesium Catalysts Generated in Situ from Monoanionic Chiral Ligands4 Bimetallic and Polymetallic Magnesium Catalysts Assembled in Situ5 Summary and Outlook


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