Ultra-broad near-infrared emission of Bi-doped SiO2 Al2O3 GeO2 optical fibers

Bi-doped SiO 2 –Al 2 O 3 –GeO 2 fiber preforms are prepared by modified chemical vapor deposition (MCVD) and solution doping process. The characteristic spectra of the preforms and fibers are experimentally investigated, and a distinct difference in emission between the two is observed. Under 808-nm excitation, an ultra-broad near-infrared (NIR) emission with full-width at half-maximum (FWHM) of 495 nm is observed in the Bi-doped fiber. This observation, to our knowledge, is the first in this field. The NIR emission consists of two bands, which may be ascribed to the Bi 0 and Bi + species, respectively. This Bi-doped fiber is promising for broadband optical amplification and widely tunable laser.     

Broadband Infrared Luminescence from Bismuth-Doped GeS2--Ga2S3 Chalcogenide Glasses

Near-infrared luminescence is observed from bismuth-doped GeS2-Ga2Sa chalcogenide glasses excited by an 808 nm laser diode. The emission peak with a maximum at about 1260 nm is observed in 80GeS2-2OGa2 Sa：O.fBi glass and it shifts toward the long wavelength with the addition of Bi gradually. The full width of half maximum （FWHM） is about 200 nm. The broadband infrared luminescence of Bi-doped GeS2-Ga2Sa chalcogenide glasses may be predominantly originated from the low valence state of Bi, such as Bi＋. Raman scattering is also conducted to claxify the structure of glasses. These Bi-doped GeS2 Ga2Sa chalcogenide glasses can be applied potentially in novel broadband optical fibre amplifiers and broadly tunable laser in optical communication system.     

Bismuth-doped germanate glass fiber fabricated by the rod-in-tube technique

Bismuth(Bi)-doped laser glasses and fiber devices have aroused wide attentions due to their unique potential to work in the new spectral range of 1 to 1.8 μm traditional laser ions, such as rare earth, cannot reach. Current Bi-doped silica glass fibers have to be made by modified chemical vapor deposition at a temperature higher than2000°C. This unavoidably leads to the tremendous loss of Bi by evaporation, since the temperature is several hundred degrees Celsius higher than the Bi boiling temperature, and, therefore, trace Bi(～50 ppm) resides within the final product of silica fiber. So, the gain of such fiber is usually extremely low. One of the solutions is to make the fibers at a temperature much lower than the boiling temperature of Bi. The challenge for this is to find a lower melting point glass, which can stabilize Bi in the near infrared emission center and, meanwhile, does not lose glass transparency during fiber fabrication. None of previously reported Bi-doped multicomponent glasses can meet the prerequisite. Here, we, after hundreds of trials on optimization over glass components,activator content, melting temperature, etc., find a novel Bi-doped gallogermanate glass, which shows good tolerance to thermal impact and can accommodate a higher content of Bi. Consequently, we successfully manufacture the germanate fiber by a rod-in-tube technique at 850°C. The fiber exhibits similar luminescence to the bulk glass, and it shows saturated absorption at 808 nm rather than 980 nm as the incident power becomes higher than 4 W. Amplified spontaneous emissions are observed upon the pumps of either 980 or 1064 nm from germanate fiber.     

Broadband and High Efficient 1530 nm Emission from Oxyfluoride Glass Ceramics Codoped with Er3＋ and Yb3＋ Ions

The emission at 1530nm and its applications in optical communications are discussed. The efficient width of the emission band △eff, which is up to 91 nm, is larger as compared with silica-based glass, bismuth glass and ZrF4-BaF2-LaFa-AIF3-NaF （ZBLAN） glass doped by Er^3＋ ions. Under the excitation of 785 nm laser, the emission integral intensity of 153Onto increases about five times in the glass ceramics higher than that in the glass. This is explained by the quantum cutting process by two-photon emission with phonon assistance. The results indicate that the glass ceramics are a promising candidate for developing broadband optical amplifiers in wavelength-division multiplexed systems.     

Transparent Ni^2＋-Doped MgO-Al2O3-SiO2 Glass Ceramics with Broadband Infrared Luminescence

We report on transparent Ni^2＋-doped MgO-Al2O3-SiO2 glass ceramics with broadband infrared luminescence. Ni^2＋-doped MgO-Al2O3-SiO2 glass is prepared by using the conventional method. After heat treatment at high temperature, MgAl2O4 crystallites are precipitated, and their average size is about 4.3 nm. No luminescence is detected in the as-prepared glass sample, while broadband infrared luminescence centred at around 1315 nm with full width at half maximum （FWHM） of about 300 nm is observed from the glass ceramics. The observed infrared emission could be attributed to the ^3T2g（^3F）→^3A2g（^3F） transition of octahedral Ni^2＋ ions in the MgAl2O4 crystallites of the transparent glass ceramics. The product of the fluorescence lifetime and the stimulated emission cross section is about 1.6×10^-24 s cm^2.     

Broadband Near-Infrared Emission from Transparent Ni^2＋ -Doped Sodium Aluminosilicate Glass Ceramics

Broadband near-infrared emission from transparent Ni^2＋-doped sodium aluminosilicate glass-ceramics is observed. The broad emission is centred at 1290nm and covers the whole telecommunication wavelength region （1100- 1700hm） with full width at half maximum of about 340hm. The observed infrared emission could be attributed to the 3T2（F） → 3A2（F） transition of octahedral Ni^2＋ ions that occupy high-field sites in nanocrystals. The product of the lifetime and the stimulated emission cross section is 2.15 × 10^-24 cm^2s. It is suggested that Ni^2＋- doped sodium aluminosilicate glass ceramics have potential applications in tunable broadband light sources and broadband amplifiers.     

Dependence of spectroscopic properties on doping content and temperature of bismuth-doped lanthanum aluminosilicate glass

The effects of bismuth doping content and temperature on the absorption property and near-infrared(NIR) luminescence of Bi-doped La2O3-Al2O3-SiO2(LAS) glasses are presented.The emission intensity reaches the maximum when the Bi2O3 content in 3.0Bi-LAS is 1.83%.The emission spectra reach their peaks at 1 190 and 1 117 nm,with full-width at half-maximum(FWHM) values of 330 and 228 nm under 500 and 700-nm excitations,respectively.As the Bi2O3 content increases,the peak wavelengths and FWHMs of emission bands increase,but their lifetimes decrease.The lifetime of 2.0Bi-LAS is 460 μs at 9 K,and is almost temperature independent until 350 K.The NIR emission of Bi in the system has strong resistance to thermal quenching from 9 to 350 K.     

Broadband 1.5-um emission of erbium-doped TeO_2-WO_3-Nb_2O_5 glass for potential WDM amplifier

Erbium-doped glass showing the wider 1.5-um emission band is reported in a novel oxide system TeO2-WO3-Nb2O5 and their thermal stability and optical properties such as absorption, emission spectra, cross-sections and fluorescence lifetime were investigated. Compared with other glass hosts, the gain bandwidth properties of Er3+ in TWN glass is close to that of bismuth glasses, and larger than those of tellurite, germanate, silicate and phosphate glasses. The broad and flat 4I13/2-4I15/2 emission and the large stimulated emission cross-section of Er3+ ions around 1.5um can be used as host material for potential broadband optical amplifier in the wavelength-division-multiplexing (WDM) network system.     

Mixed Former Effect：A Kind of COmposition Adjusting Method of Er—Doped Glass for Broadband Amplification

A compositional adjusting method called the mixed former effect is proposed to improve effectively optical properties such as the emission cross sectionk,the fluorescence full width at half maximum(FWHM)and the lifetime of the 4I13/2 level of Er-doped glass.A kind of Er-0doped bismuth-based glass illustrated high emission cross section (σe^p=0.66-0.90pm^2),large fluorescence FWHM(68-85nm),and relatively long lifetime of the ^4I13/2 level(Tm=1.6-4.3ms) using this method.A comparison of spectroscopic parameters shows that bismuth based glass is much better for broadband amplifiers than other glass hosts.     

Er^3＋-doped phosphor-tellurite glass for broadband short-length Er^3＋-doped fiber amplifier

Er^3＋-doped phosphor-tellurite glass for broadband short-length Er^3＋-doped fiber amplifier （EDFA） is fabricated and characterized. The differential value （AT） of onset crystalline temperature （Tx） and glass transition temperature （Tg） is 206 ℃. The stimulated emission cross section of Er^3＋ is calculated from absorption spectrum by McCumber theory and is 0.87 × 10 ^-20 cm^2 at 1532 nm. A broad 1.5-μm fluorescence spectrum with 54-nm full-width at half maximum （FWHM） is demonstrated. Especially, the maximum phonon energy of undoped phosphor-tellurite glass is 1100 cm^- 1, which restricts the upconversion luminescence. It is possible to pump efficiently at 980 nm. These results indicate Er^3＋-doped phosphor-tellurite glass is suitable for fabricating broadband short-length EDFA.     

Highly efficient,tunable, ultrabroadband NIR photoemission from Bi-doped nitridated germanate glasses toward all-band amplification in optical communication

Bismuth(Bi)-doped near-infared(NIR) glass that can cover the entire optical communication window(850, 1310, and1550 nm) has become the subject of extensive research for developing photonic devices, particularly, tunable fiber lasers and ultrabroadband optical amplifiers. However, the realization of highly efficient NIR luminescence from Bi-doped glass is still full of challenges. Notably, due to the co-existence of multiple Bi NIR centers in the glass, the origin of newly generated Bi NIR emissi...     

Composition Dependence of Spectroscopic Properties of Er^3＋ Doped TeO2-WO3-ZnO Glasses

Er^3 -doped TeO2-WO3-ZnO glasses were prepared and the absorption spectra, emission spectra and fluorescence lifetimes were measured. With more Te02 content in the glasses, the emission full width at half maximum (FWHM) increases while the lifetime of the ^4I13/2 level of Er^3 decreases. The stimulated emission cross-sectionof Er^3 calculated by the McCumber theory is as large as 0.86pm^2. The product of the FWHM and the emissioncross-section σe of Er^3 in TeO2-WO3-ZnO glass is larger than those in other glasses, which indicates that the glasses are promising candidates for Er^3 -doped broadband amplifiers. The Judd-Otfelt parameter Ω6 shows close composition dependence of the 1.5μm emission bandwidth. The more the TeO2 content is, the larger thevalues of Ω6 and FWHM.     

Sr3Bi（PO4）3：Eu^2＋ Luminescence,Concentration Quenching and Crystallographic Sites

A blue emitting phosphor Sr3Bi（PO4）3：Eu2＋ is synthesized luminescent property is investigated. Sr3Bi（PO4 ）3 ：Eu^2＋ can by a high-temperature solid state method, and its create blue emission under the 332 radiation excitation, and the prominent luminescence in blue （423nm） due to the 4fSd^1→4f^7 transition of the Eu^2＋ ion. The crystallographic sites of the Eu^2＋ ion in Sr3Bi（PO4）3 are analyzed, and the 420 and 440 nm emission peaks of the Eu^2＋ ion are assigned to the nine-coordination and eight-coordination, respectively. The emission intensity of Sr3Bi（PO4）3：Eu^2＋ is influenced by the Eu^2＋ doping content, and the concentration quenching effect is observed. The quenching mechanism is the dipole-dipole interaction, and the critical distance of energy transfer is calculated by the concentration quenching method to be approximately 1.72nm.     

Spectroscopic Properties of Yb^3＋-doped Germano-Silicate Glasses

We investigate the absorption, stimulated emission cross section and potential laser parameters of Yb^3 doped gernano-silicate glasses (GSY glass). The emission cross section is evaluated by using the measured absorption spectra and the principle of reciprocity. It is found that Yb^3 in GSY glasses has high stimulated emission cross section of 0.5-0.65pm^2 near 1020nm and exists long measured fluorescence lifetime of 1.20-2.00ms. Compared with other glass hosts, the GSY glass exhibits excellent general spectroscopic properties for Yb^3 -doped double-cladding fibres.     

Broadband Infrared Luminescence of Ni^2＋ in Petalite-Type Transparent Glass Ceramics

Transparent Ni^2＋-doped magnesium aluminosilicate glass ceramics are prepared. The formation of petalite-type crystallites in the glass ceramics is confirmed by x-ray diffraction. Broadband infrared luminescence centred at around 1235nm with full width at half maximum （FWHM） of about 300nm is observed from the Ni^2＋-doped glass ceramics. The observed infrared emission could be attributed to the ^3T2（F） → ^3A2（F） transition of octahedral Ni^2＋ ions in petalite-type crystallites. Theproduct of the fluorescence lifetime and the stimulated emission cross sections is 1.2 ×10-24 cm^2s.     

Cooperative Quantum Cutting of Nano-Crystalline BaF2：Tb^3＋, Yb^3＋ in Oxyfluoride Glass Ceramics

We report on cooperative quantum cutting in Tb^3＋- Yb^3＋ codoped glass ceramics. Precipitation of BaF2 nanocrystals is confirmed by XRD and HRTEM analysis. Near-infrared emission due to transition of Yb^3＋ ions under 485 nm excitation indicates cooperative energy transfer from Tb^3＋ to Yb^3＋. The quantum efficiency of this process reaches 145%. The realization of quantum cutting in glass ceramics may have promising applications in solar cells.     

Investigation of emission properties of Tm3＋：Y2O3 transparent ceramic

A transparent and emitting ceramic of Y 2 O 3 doped with 6% Tm 3+ ions is fabricated by vacuum sintering with ZrO 2 . Absorption, photoluminescence (PL), and PL excitation (PLE) spectra are investigated in a spectral range of 200 to 2 100 nm at various temperatures between 296 and 12 K. Intense emission band appears at 450 to 465 nm in the visible range. Near-infrared emission bands are observed at 1 200 to 1 300 nm and 1 400 to 1 550 nm, with intense peaks at 1 270, 1 450, and 1 523 nm. The luminescence mechanisms and potential applications of the emissions are discussed with the help of Judd-Ofelt theory and PLE spectra.     

Visible Upconversion Emission in Er3＋—Doped GeO2—PbO—PbF2 Glass

The upconversion fluorescence emission of Er3 -doped 60GeO2-2OPbO-2OPbF2 glass was experimentally investigated under the pump of 976-nm laser diode. The results reveal the existence of intense emission bands centred around 524, 545, and 657nm at room temperature. The green emission at 524 and 545nm is due to the 4S3/2 2 Hll/2→ 4I15/2 transition and the red emission of 657nm originates from the 4F9/2-→4I15/2 transition of Er3 . The quadratic dependence of the green and red emissions on excitation power indicates that a two-photonabsorption process occurs under the 976-nm excitation. The excited- state absorption from 4I ll/2 and the cross relaxation between two Er3 ions in the 4I ll/2 state contribute to the green emission. The red emission at 657nm is attributed to the excited-state absorption and cross relaxation processes in the 4I13/2 level as well as the 4S3/2 level nonradiative transition of Er3 .     

Enhancement of upconversion luminescence of YAlO3：Er^3＋ by Gd^3＋ doping

Two series of Yb3+-doped silica glasses (YA and YAP) are fabricated using the sol-gel method, and their spectroscopic properties are investigated. The longest fluorescence lifetime of 0.96 ms is obtained in YAP2 and YAP3 glasses. The emission cross-section (σemi) and σemi ×τ of Yb3+ in the YAP1 glass are 1.00 pm2 and 0.94 pm2·ms, respectively. Co-doping with Al and P decreases the hydroxyl group content in the glasses because of the reduction in non-bridging oxygen content. The lowest OH content in the YAP3 glass is 9.6 ppm.     

Efficient 2.7-μm emission in Er3＋-doped bismuth germanate glass pumped by 980-nm laser diode

An Er 3+-doped lead-free bismuth germanate glass is synthesized. Its 2.7-μm emission property is analyzed, and the efficient 2.7-μm emission from the glass is observed under 980-nm laser diode excitation. The prepared glass possesses high spontaneous transition probability (64.8 s 1 ) and a large calculated emission cross section (6.61×10 21 cm 2 ) corresponding to the 4I11/2→4I13/2 transition. The multiphonon relaxation rate for the excited state 4I11/2 is only 236 s 1 . Therefore, the excellent spectroscopic properties and outstanding thermal stability suggest that this glass is a suitable host for developing solid-state lasers operating in the mid-infrared.