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Fiber Bragg gratings are key components for optical fiber sensing applications in harsh environments. This paper investigates the structural and chemical characteristics of femtosecond laser photo-inscribed microvoids. These voids are at the base of type III fs-gratings consisting of a periodic array of microvoids inscribed at the core of an optical fiber. Using high-resolution techniques such as quantitative phase microscopy, electron transmission microscopy, and scattering-type scanning near-field IR optical microscopy, we examined the structure of the microvoids and the densified shells around them. We also investigated the high-temperature behavior of the voids, revealing their evolution in size and shape under step isochronal annealing conditions up to 1250 °C.
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An all-glass optical fiber capable of two distinct methods of optical thermometry is described. Specifically, a silica-clad, barium fluorosilicate glass core fiber, when pumped in the infrared, exhibits visibly intense green defect luminescence whose intensity and upper-state lifetime are strong functions of temperature. Intensity-based optical thermometry over the range from 25°C to 130°C is demonstrated, while a lifetime-based temperature sensitivity is shown from 25°C to 100°C. Time-domain measurements yield a relative sensitivity of 2.85% K -1 at 373 K (100°C). A proof-of-concept distributed sensor system using a commercial digital single-lens reflex camera is presented, resulting in a measured maximum relative sensitivity of 1.13% K -1 at 368 K (95°C). The sensing system described herein stands as a new blueprint for defect-based luminescence thermometry that takes advantage of pre-existing and relatively inexpensive optical components, and allows for the use of standard cameras or simply direct human observation.
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Femtosecond (fs) laser irradiation inside transparent materials has drawn considerable interest over the past two decades. More specifically, self-assembled nanogratings, induced by fs laser direct writing (FLDW) inside glass, enable a broad range of potential applications in optics, photonics, or microfluidics. In this work, a comprehensive study of nanogratings formed inside fused silica by FLDW is presented based on high-resolution electron microscopy imaging techniques. These nanoscale investigations reveal that the intrinsic structure of nanogratings is composed of oblate nanopores, shaped into nanoplanes, regularly spaced and oriented perpendicularly to the laser polarization. These nanoporous layers are forced-organized by light, resulting in a pseudo-organized spacing at the sub-wavelength scale, and observed in a wide range of optical glasses. In light of the current state of the art, we discuss the imprinting of nanoporous layers under thermomechanical effects induced by a plasma-mediated nanocavitation process.
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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.
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This publisher's note contains corrections to Appl. Opt.62, 6794 (2023)APOPAI0003-693510.1364/AO.496351.
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The thermal stability of self-assembled porous nanogratings inscribed by an infrared femtosecond (fs) laser in five commercial glasses (BK7, soda lime, 7059, AF32, and Eagle XG) is monitored using step isochronal annealing experiments. Their erasure, ascertained by retardance measurements and attributed to the collapse of nanopores, is well predicted from the Rayleigh-Plesset (R-P) equation. This finding is thus employed to theoretically predict the erasure of nanogratings in the context of any time-temperature process (e.g., thermal annealing, laser irradiation process). For example, in silica glass (Suprasil CG) and using a simplified form of the R-P equation, nanogratings composed of 50 nm will erase within â¼30m i n, â¼1µs, and â¼30n s at temperatures of â¼1250∘ C, 2675°C, and 3100°C, respectively. Such conclusions are expected to provide guidelines to imprint nanogratings in oxide glasses (for instance, in the choice of laser parameters) or to design appropriate thermal annealing protocols for temperature sensing.
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Self-assembled nanogratings, inscribed by femtosecond laser writing in volume, are demonstrated in multicomponent alkali and alkaline earth containing alumino-borosilicate glasses. The laser beam pulse duration, pulse energy, and polarization, were varied to probe the nanogratings existence as a function of laser parameters. Moreover, laser-polarization dependent form birefringence, characteristic of nanogratings, was monitored through retardance measurements using polarized light microscopy. Glass composition was found to drastically impact the formation of nanogratings. For a sodium alumino-borosilicate glass, a maximum retardance of 168â nm (at 800 fs and 1000 nJ) could be measured. The effect of composition is discussed based on SiO2 content, B2O3/Al2O3 ratio, and the Type II processing window is found to decrease as both (Na2O + CaO)/Al2O3 and B2O3/Al2O3 ratios increase. Finally, an interpretation in the ability to form nanogratings from a glass viscosity viewpoint, and its dependency with respect to the temperature, is demonstrated. This work is brought into comparison with previously published data on commercial glasses, which further indicates the strong link between nanogratings formation, glass chemistry, and viscosity.
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Nanogratings (NGs) are self-assembled subwavelength and birefringent nanostructures created by femtosecond laser direct writing (FLDW) in glass, which are of high interest for photonics, sensing, five-dimensional (5D) optical data storage, or microfluidics applications. In this work, NG formation windows were investigated in nine commercial glasses and as a function of glass viscosity and chemical composition. The NG windows were studied in an energy-frequency laser parameter landscape and characterized by polarizing optical microscopy and scanning electron microscopy (SEM). Pure silica glass (Suprasil) exhibits the largest NG window, whereas alkali borosilicate glasses (7059 and BK7) present the smallest one. Moreover, the NG formation windows progressively reduced in the following order: ULE, GeO2, B33, AF32, and Eagle XG. The NG formation window in glasses was found to decrease with the increase of alkali and alkaline earth content and was correlated to the temperature dependence of the viscosity in these glasses. This work provides guidelines to the formation of NGs in commercial oxide glasses by FLDW.
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This paper is dedicated to the lifetime prediction of Type II modifications (i.e., nanogratings) written in silica glass using an infrared femtosecond laser. Herein we report accelerated aging experiments of such nanogratings through the monitoring of their characteristic linear birefringence signature. Based on the master curve formalism, we demonstrate that these laser-induced nanostructures can survive for 200 hours at 1100°C. Under the reported processing conditions and after a dedicated passivation treatment, the estimated lifetime of the birefringent optical elements is beyond 10 years at 800°C with a minor erasure of 7%.
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Femtosecond (fs) laser written fiber Bragg gratings (FBGs) are excellent candidates for ultra-high temperature (>800 ºC) monitoring. More specifically, Type II modifications in silicate glass fibers, characterized by the formation of self-organized birefringent nanostructures, are known to exhibit remarkable thermal stability around 1000 ºC for several hours. However, to date there is no clear understanding on how both laser writing parameters and glass composition impact the overall thermal stability of these fiber-based sensors. In this context, this work investigates thermal stability of Type II modifications in various conventional glass systems (including pure silica glasses with various Cl and OH contents, GeO2-SiO2 binary glasses, TiO2- and B2O3-doped commercial glasses) and with varying laser parameters (writing speed, pulse energy). In order to monitor thermal stability, isochronal annealing experiments (Δtâ 30 min, ΔTâ 50 ºC) up to 1400 ºC were performed on the irradiated samples, along with quantitative retardance measurements. Among the findings to highlight, it was established that ppm levels of Cl and OH can drastically reduce thermal stability (by about 200 ºC in this study). Moreover, GeO2 doping up to 17 mole% only has a limited impact on thermal stability. Finally, the relationships between glass viscosity, dopants/impurities, and thermal stability, are discussed.
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This paper compares anisotropic linear optical properties (linear birefringence, linear dichroism, degree of polarization) and performances (absorption coefficient, thermal stability) of two types of birefringent waveplates fabricated in silica glass by femtosecond laser direct writing. The first type of waveplate is based on birefringence induced by self-organized nanogratings imprinted in the glass. One the other hand, the second design is based on birefringence originating from the stress-field formed around the aforementioned nanogratings. In addition to the provided comparison, the manufacturing of stress-engineered half waveplates in the UV-Visible range, and with mm-size clear aperture and negligible excess losses, is reported. Such results contrast with waveplates made of nanogratings, as the later exhibit significantly higher scattering losses and depolarization effects in the UV-Visible range.
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The molten core method (MCM) is a versatile technique to fabricate a wide variety of optical fiber core compositions ranging from novel glasses to crystalline semiconductors. One common feature of the MCM is an interaction between the molten core and softened glass cladding during the draw process, which often leads to compositional modification between the original preform and the drawn fiber. This causes the final fiber core diameter, core composition, and associated refractive index profile to vary over time and longitudinally along the fiber. Though not always detrimental to performance, these variations must, nonetheless, be anticipated and controlled as they directly impact fiber properties (e.g., numerical aperture, effective area). As an exemplar to better understand the underlying mechanisms, a silica-cladding, YAG-derived yttrium aluminosilicate glass optical fiber was fabricated and its properties (core diameter, silica concentration profile) were monitored as a function of draw time/length. It was found that diffusion-controlled dissolution of silica into the molten core agreed well with the observations. Following this, a set of first order kinetics equations and diffusion equation using Fick's second law was employed as an initial effort to model the evolution of fiber core diameter and compositional profile with time. From these trends, further insights into other compositional systems and control schemes are provided.