Impact of Glass Free Volume on Femtosecond Laser-Written Nanograting Formation in Silica Glass.

In this study, we investigate the effects of densification through high pressure and temperature (up to 5 GPa, 1000 °C) in the making of nanogratings in pure silica glass, inscribed with femtosecond laser. The latter were monitored through retardance measurements using polarized optical microscopy, and their internal structure was observed under scanning electron microscopy. We reveal the difficulty in making nanogratings in densified silica glasses. Based on this observation, we propose that free volume may be a key precursor to initiate nanograting formation.

Paramagnetic Point Defect in Fluorine-Doped Silica Glass: The E

Fluorine-doped silica is a key material used in all low-loss and/or radiation-resistant optical fibers. Surprisingly, no fluorine-related radiation-induced point defects have been identified. By using electron paramagnetic resonance, we report the first observation of F-related defects in silica. Their fingerprint is a doublet with 10.5 mT splitting due to hyperfine coupling (hfc) to ^{19}F nuclear spins. An additional 44.4 mT hfc to the ^{29}Si nucleus indicates that this defect belongs to the "E^{'} center" family and has a structure of a fluorine-modified Si dangling bond: 3-coordinated Si atoms with an unpaired electron in an sp^{3} orbital, bonded to a glass network by 2 bridging oxygen atoms and to a F atom.

Single crystal growth, optical absorption and luminescence properties under VUV-UV synchrotron excitation of type III Pr3+:KGd(PO3)4.

Scintillator materials are widely used for a variety of applications such as high energy physics, astrophysics and medical imaging. Since the ideal scintillator does not exist, the search for scintillators with suitable properties for each application is of great interest. Here, Pr3+-doped KGd(PO3)4 bulk single crystals with monoclinic structure (space group: P21) are grown from high temperature solutions and their structural, thermal and optical properties are studied as possible candidates for scintillation material. The change in the unit cell parameters as a function of the Pr3+ level of doping and temperature is studied. Differential thermal analysis reveals that KGd0.942Pr0.058(PO3)4 is stable until 1140 K. The 5d3, 5d2 and 5d1 levels of Pr3+ with respect to the 3H4 ground state are centred at 166, 196 and 218 nm, respectively, in this host. The luminescence of KGd0.990Pr0.010(PO3)4, by exciting these 5d levels, shows intense emissions centred at 256 and 265 nm from the 5d1 to 3F3,4 and 1G4 levels of Pr3+ with a short decay time of 6 ns. The 6P3/2,5/2,7/2 → 8S7/2 transitions of Gd3+ appear after exciting the 5d levels of Pr3+ and the 4 f levels of Gd3+, showing an energy transfer between Pr3+ and Gd3+.

Relaxation study of pre-densified silica glasses under 2.5 MeV electron irradiation.

We examined the "relaxation properties" of pre-densified synthetic fused silica glass under 2.5 MeV electron irradiation. The densification of the glass was either obtained by hot compression (5 GPa-350 °C and 5 GPa-1000 °C) or via a thermal treatment increasing its fictive temperature (Tf = 1050, 1250 and 1400 °C). Under irradiation, the pre-densified silica glasses exhibit a relaxation of their macroscopic density with increasing integrated dose. Density was reduced for hot compressed silica and increased for Tf samples with different relaxation rates but it is remarkable that all sample densities follow a trend towards the same equilibrium value around 2.26 for a dose larger than 10 GGy despite a different final topology. After irradiation of hot compressed silica, the Raman spectra display a significant increment of 4 and almost 3-membered rings whereas they exhibit a glass density reduction; demonstrating that a D2 band increase cannot be considered as an absolute marker of the glass compaction. The correlation between density and D2 intensity remains valid until silica density remains lower than 2.26. In contrast, the FWHM of the main band peaking at 440 cm-1 appears to remain correlated to the silica glass density for all investigated samples.

Single crystal growth, optical absorption and luminescence properties under VUV-UV synchrotron excitation of type III Ce3+:KGd(PO3)4, a promising scintillator material.

Scintillator materials have gained great interest for many applications, among which the medical applications stand out. Nowadays, the research is focused on finding new scintillator materials with properties that suit the needs of each application. In particular, for medical diagnosis a fast and intense response under high-energy radiation excitation is of great importance. Here, type III Ce3+-doped KGd(PO3)4 single crystals with high crystalline quality are grown and optically characterized as a new promising scintillator material. The 4f → 5d electronic transitions of Ce3+ are identified by optical absorption. The optical absorption cross section of Ce3+ for the electronic transition from the 2F5/2 to the 5d1 level is 370 × 10-20 cm2. The luminescence of KGd0.996Ce0.004(PO3)4 crystal by exciting the 5d levels of Ce3+ with VUV-UV synchrotron radiation shows down-shifting properties with strong emissions at 322 and 342 nm from the 5d1 to 2F5/2 and 2F7/2 levels of Ce3+ with a short decay time of ~16 ns, which is very suitable for scintillator applications. Moreover, these intense emissions are also observed when Gd3+ is excited since an energy transfer from Gd3+ to Ce3+ exists.

Origin of Radiation-Induced Darkening in Yb3+/Al3+/P5+-Doped Silica Glasses: Effect of the P/Al Ratio.

Yb3+/Al3+/P5+-co-doped silica glasses with different P/Al ratios were prepared using the sol-gel method combined with high-temperature sintering. The evolution of composition-dependent color centers caused by X-ray irradiation in these glasses was correlated with their structural changes, which are controlled by the P/Al ratio. Nuclear magnetic resonance (NMR) and Raman spectra have been used to characterize the glass network structure, and advanced pulse electron paramagnetic resonance (EPR) has been employed to study the local coordination atomic structures of Yb3+ ions in pristine glasses as a function of the P/Al ratio. Si- (Si-E'), Al- (Al-E', Al-ODC, AlOHC), P- (P1, P2, POHC), and Yb-related (Yb2+) color centers in irradiated glasses have been observed and explained by optical absorption and continuous wave-EPR spectroscopies. The formation mechanisms of these centers, the structural models of glasses, and the relationship between them were proposed. Direct evidence confirms that the formation of Yb2+ ions induced by radiation is highly dependent on the coordination environment of Yb3+ ions in glasses. In addition, the glass network structure significantly affects the generation of oxygen hole color centers (AlOHCs/POHCs) caused by radiation. These results are useful in understanding the microstructural origin and the suppression mechanism of the radiodarkening effect by phosphorus co-doping in Yb3+-doped silica fibers.

Manipulating refractive index, homogeneity and spectroscopy of Yb3+-doped silica-core glass towards high-power large mode area photonic crystal fiber lasers.

Output power scaling of single mode large mode area (LMA) photonic crystal fiber (PCF) amplifiers urgently requires the low refractive index of Yb3+-doped silica glasses whilst maintaining high optical homogeneity. In this paper, we report on a promising alternative Yb3+/Al3+/F-/P5+-co-doped silica core-glass (YAFP), which is prepared by modified sol-gel method developed by our group and highly suitable for fabricating high power LMA PCF amplifiers. By controlling the doping combinations of Al3+/F-/P5+ in Yb3+-doped silica glass,it not only ensures low refractive index (RI) but also maintains the excellent optical homogeneity and spectroscopic properties of Yb3+. The spectroscopic properties of Yb3+ ions have not deteriorated by the co-doping of F- and P5+ in YAFP glass compared with that of Yb3+/Al3+ co-doped silica glass. A large-size (⌀5 mm × 90 mm) YAFP silica-core glass rod with low average RI difference of 2.6 × 10-4 (with respect to pure silica glass), and low radial and axial RI fluctuations of ~2 × 10-4, was prepared. A LMA PCF with 50 µm core diameter was obtained by stack-capillary-draw techniques using YAFP core glass. Its core NA is 0.027. An average amplified power of 97 W peaking at 1030 nm and light-light efficiency of 54% are achieved from a 6.5 m long PCF in the pulse amplification laser experiment. Meanwhile, quasi-single-mode transmission is obtained with laser beam quality factor M2 of 1.4.

Determination of paramagnetic concentrations inside a diamagnetic matrix using solid-state NMR.

The determination of very low doping levels in solid materials is an important issue for many applications. When considering paramagnetic dopants, the NMR relaxation technique appears to be much more accurate than classical techniques such as Vegard's law resulting from X-ray diffraction (XRD) measurements or chemical analysis that cannot provide information on appropriate dopant spatial distributions. In a recent report, the linear variation of 1/T1, i.e. the nuclear relaxation rate, as a function of Nd3+ content has been used to determine doping levels with a good dispersion homogeneity in the monazite LaPO4 matrix down to 0.1 mol%. We here extend this study to more complex compounds doped with Nd3+, such as YPO4, the solid solution Y0.8Sc0.2PO4, Ba5(PO4)3Cl and a phosphate glass. For all considered compounds except Ba5(PO4)3Cl:Nd, 1/T1 is found to be linearly proportional to the nominal Nd concentration, confirming the ability of the method to investigate the dopant concentration and spatial homogeneity. The results obtained for different compounds open up the discussion on the parameters, such as the orbital overlap and the average P-P distances, influencing the nuclear relaxation rate.

Radiation hardening of sol gel-derived silica fiber preforms through fictive temperature reduction.

The impact of fictive temperature (Tf) on the evolution of point defects and optical attenuation in non-doped and Er3+-doped sol-gel silica glasses was studied and compared to Suprasil F300 and Infrasil 301 glasses before and after γ-irradiation. To this aim, sol-gel optical fiber preforms have been fabricated by the densification of erbium salt-soaked nanoporous silica xerogels through the polymeric sol-gel technique. These γ-irradiated fiber preforms have been characterized by FTIR, UV-vis-NIR absorption spectroscopy, electron paramagnetic resonance, and photoluminescence measurements. We showed that a decrease in the glass fictive temperature leads to a decrease in the glass disorder and strained bonds. This mainly results in a lower defect generation rate and thus less radiation-induced attenuation in the UV-vis range. Furthermore, it was found that γ-radiation "hardness" is higher in Er3+-doped sol-gel silica compared to un-doped sol-gel silica and standard synthetic silica glasses. The present work demonstrates an effective strategy to improve the radiation resistance of optical fiber preforms and glasses through glass fictive temperature reduction.

Impact of rare earth element clusters on the excited state lifetime evolution under irradiation in oxide glasses.

Rare earth doped active glasses and fibers can be exposed to ionizing radiations in space and nuclear applications. In this work, we analyze the evolution of (2)F(5/2) excited state lifetime in Yb(3+) ions in irradiated aluminosilicate glasses by electrons and γ rays. It is found that the variation of lifetimes depends on the Yb(3+) clusters content of the glasses for irradiation doses in the 10(2)- 1.5∙10(9) Gy range. In particular, glasses with high clustering show a smaller decrease in lifetime with increasing radiation dose. This behavior is well correlated to the variation in paramagnetic defects concentration determined by electron paramagnetic resonance. This effect is also observed in Yb(3+) doped phosphate and Er(3+) doped aluminosilicate glasses, inferring that clustering plays an important role in irradiation induced quenching.

Interplay between photo- and radiation-induced darkening in ytterbium-doped fibers.

This Letter demonstrates a remarkable interplay between photo- and radiation-induced darkening of ytterbium-doped alumino-silica optical fibers operated in amplifying conditions and harsh environments (as, e.g., in space-based applications). Influences of the pump power, ionizing dose, and dose rate on this interaction are characterized. The pump is capable of accelerating or slowing down the radiation-induced darkening build-up depending on the ionizing dose. The steady-state photo-radio-darkening level is independent of the dose and at least equal to the equilibrium level of pure photo-darkening. This lower limit is notably reached at low dose rates, including those encountered in space. We, therefore, argue that photo-resistant ytterbium-doped fibers will resist against a space mission, whatever the dose.

Evidence of AlOHC responsible for the radiation-induced darkening in Yb doped fiber.

Using a combination of experimental techniques such as optical absorption, Raman scattering, continuous wave and pulse Electron Spin Resonance (ESR), we characterize a set of γ-irradiated Yb(3+) doped silica glass preforms with different contents of phosphorous and aluminum. We demonstrate that when P is introduced in excess compared to Al, nearly no radiodarkening is induced by γ-rays. On the other hand, when Al>P, a large absorption band is induced by radiation. Thermal annealing experiments reveal the correlation between the decrease of the optical absorption band and the decrease of the Al-Oxygen Hole Center (AlOHC) ESR signal, demonstrating the main role of AlOHC defects in the fiber darkening. HYSCORE (HYperfine Sublevel CORElation) pulse-ESR experiments show a high Al-P nuclear spin coupling when P>Al and no coupling when Al>P. This result suggests that both AlOHC and POHC creation is inhibited by Al-O-P linkages. Confronting our data with previous works, we show that the well-known photodarkening process, meaning losses induced by the IR pump, can also be explained in this framework.

Laser-induced periodic alignment of Ag nanoparticles in soda-lime glass.

One-, two- or three-dimensional arrays of closely spaced silver nanoparticles may lead to new optical properties, due to short or long range coupling between their resonant surface plasmons, so that the spatially controlled growth of silver nanoparticles provides an efficient way to tune their optical properties. Towards this way, we present here the periodic pattern of a glass surface with silver nanoparticles by continuous ultraviolet laser exposure. The formation of the 160 nm period pattern is well described by an interference-based model which agrees with the experimental conclusions, mainly obtained by various forms of microscopy. Statistical approach based on the autocorrelation function gives quantitative description about the quality of the order in the periodic structure and about the nanoparticles averaged diameter (80 nm). We also present the optical extinction spectrum of the Laser Induced Periodic Surface Structure (LIPSS)-containing area of the glass, which unusually shows several bands in the visible range. The period of 160 nm of the periodic structure is short enough to allow coupling between nanoparticles, which makes it a possible candidate for plasmon-based optical applications.