Low Hydroxyl Content Research Articles

A Nd-doped silica glass with high doping concentration, low hydroxyl content, and 900 nm fluorescence emission fabricated by laser additive manufacturing

The 900 nm wavelength laser is effective for atmospheric detection and various other applications.The frequency-doubled 450 nm deep blue laser can be used in maritime military, quantum optics, biomedicine, laser storage, laser display, and deep ultraviolet laser fields, among others. Although Nd3+ is considered the optimal medium for generating 900 nm lasers, competition with the 1060 nm emission wavelength must be addressed. In Nd-doped silica glass, without the introduction of aluminum, the emission intensity of the three-level transition is higher than that of the four-level transition. However, it can cause a concentration quenching between Nd3+, but co-doping with Al can effectively suppress it. As the Al/Nd ratio increases, the emission intensity at 1060 nm increases relative to that at 900 nm. By precisely adjusting the Al/Nd ratio, it is possible to suppress the 1060 nm emission while also inhibiting concentration quenching caused by Nd3+.

Kraft lignin-based polyurethanes: Bulk properties, stability and adhesion to native aluminum surfaces

Lignin as a byproduct from pulp and paper manufacturing has been extensively investigated as raw material for polymer developments. Although, fundamental topics related to the adhesion mechanisms of lignin-based reactive polyurethanes (LPU) still remain unclear. In this work, LPU thin films on native aluminum surface were prepared and characterized. Diluted in THF, employed as the solvent, reactive mixtures of 4,4′-methylene diphenyl isocyanate (4,4′-MDI) and the soluble fraction of three lignins (liquid hydroxypropylated Kraft lignin and two powder Kraft lignins with different pH) were used for LPU thin film deposition via spin coating on aluminum (PVD layer on silicon wafer). The resulting film thickness ranged from 8 nm to several micrometers. The chemical state of the three LPU compositions was assessed in bulk by infrared attenuated total reflectance (IR-ATR) and in the thin films by infrared external reflection absorption spectroscopy (IR-ERAS). Binding energies of 4,4′-methylene diphenyl diisocyanate with aliphatic and aromatic hydroxyl groups were estimated using Density Functional Theory (DFT) simulations. Thus, besides the elucidation of the bulk chemical state of LPUs, the relation to adhesion and stability of LPUs to a native aluminum surface was evaluated. In addition, film topography and homogeneity were monitored by SFM. All lignin types form uniform and homogeneous films. Results revealed a higher consumption of isocyanate groups (NCO) in the formulation with the alkaline Kraft lignin than with the acid one, despite its lower hydroxyl content. A gradient of unreacted NCO was observed in LPU thin films obtained with the powder Kraft lignin types. Residual NCO is also found in thicker films, while the thinnest films did not contain unreacted NCO anymore, indicating the activating effect of the native aluminum surface on LPU formation.

Preparation of high antioxidant nanolignin and its application in cosmetics

Lignin, as a natural polyphenol, displays anti-oxidant activity by trapping and binding free radicals through its free phenolic hydroxyl groups. However, the most accessible form, industrial lignins, generally has low phenolic hydroxyl content, which severely limits their application value and scenarios. Herein, we showed that potassium-glycerate deep eutectic solvent (PG-DES) treatment can be combined with laccase oxidation to afford prepared high antioxidant lignin nanoparticles (HA-LNPs) with notably improved anti-oxidant activities benefiting from both the enhanced phenolic hydroxyl content 170.8 % and reduced average particle size (59.0 nm). At concentrations as low as 60 μg/mL, HA-LNPs showed favorable effects in promoting collagen formation. When HA-LNPs were used as an active ingredient in the anti-aging mask formulation, the reactive oxygen species (ROS) scavenging activity of mask samples containing 0.4 % HA-LNPs reached 37.2 %. The data suggest great promise of HA-LNPs as a natural antioxidant for formulating in anti-aging skin care products.

Multi-site sulfonation of lignin for the synthesis of a high-performance dye dispersant

Sulfonated lignin-based dye dispersants have intensively attracted attention due to their low cost, renewability and abundant sources. However, their utilization is limited by the low content of sulfonic groups and high content of hydroxyl groups in their complex lignin structure, which results in various problems such as high reducing rate of dye, severe staining of the fibers and uneven dyeing. Here, the multi-site sulfonated lignin-based dispersants were prepared with high sulfonic group content (2.20 mmol/g) and low hydroxyl content (2.43 mmol/g). When using it as the dispersant, the dye uptake rate was improved from 69.23 % to 98.55 %, the reducing rate was decreased from 20.82 % to 2.03 %, the K/S value was reduced from 0.69 to 0.02, and the particle sizes in dye system before and after high temperature treatment were stabilized below 0.5 μm. Besides, the dispersion effect was significantly improved because no obvious separation between dye and water was observed even if without the assistance of grinding process. In short, the multi-site sulfonation method proposed in this work could remarkably improve the performances of the lignin-based dye dispersants, which would facilitate the development of the dye dispersion and the high value utilization of lignin.

Exploring chemical reactions to enhance thermal and dispersion stability of kraft and organosolv lignin

Lignin has been overlooked and used as a waste for long due to its complex and partially hydrophobic structure. Many efforts have been carried out to overcome these deficiencies and apply it as a high-value product, which are insufficient to reach the full potential of lignin in various advanced applications, since they require with procedures for the obtaining of more specific and fine-tuned chemical structures. This work focuses on the obtaining of differently structured hydrophilic lignins derived both from Kraft and organosolv isolation processes. The chemical structures of the different lignin types were studied, and the effect of the structural differences in the modification processes and their subsequent properties analyzed, valorizing their potential application for diverse purposes. The carboxymethylation and sulfomethylation reactions were carried out with the aim of enhancing the polarity of the lignin samples, while the methylation reaction aimed to obtain lignins with higher stability. The physicochemical analyses of the samples, carried out by FTIR, GPC, 31P NMR, 13C NMR, and HSQC NMR, verified the effectiveness of the chemical reactions and conditions selected, obtaining lignins with lower hydroxyl content, due to their substitution and insertion of carboxymetyl, sulfomethyl and methyl groups, therefore obtaining more condensed, aromatic and oxygenated aromatic carbon structures. While the methylation reaction was the most efficient in substituting the OH groups, due to its non-selectivity, OL showed higher modification yields than KL. In terms of the thermal and morphological properties, analyzed by DLS and TGA respectively, it was observed that the modified samples showed lower Z potential values, along with higher conductivity, being the sulfomethylated organosolv lignin the one showing the best results, which was also the one with the smallest particle size and polydispersity index. Finally, all the modified samples showed higher T50% values, suggesting a better stability towards degradation.

Spectroscopic properties and numerical analysis of novel erbium doped multi-component tellurite glasses

In this paper, Er3+ doped TeO2-ZnF2-BaF2-KF-Ta2O5 tellurite glasses with low hydroxyl content (∼0.03 × 10−19 cm−3) were investigated employing both glass composition and glass melting process optimization. The Raman spectra and physical properties were characterized to analyze the structure of the glasses. Under the pumping of 980 nm LD laser, intense up-conversion fluorescence at 1.5 and 2.7 μm of samples and their lifetimes were detected and analyzed, and the related transition mechanisms with gradient-varying Er3+ doping concentrations were discussed. The maximum absorption and emission cross section at 2.7 μm was calculated to be 6.4 × 10−21 cm2 and 6.8 × 10−21 cm2, correspondingly, which were higher than those of traditional tellurite glasses. Using the calculated and measured spectroscopic parameters of bulk tellurite glass, a dual-wavelength pumping model was established to verify the feasibility of mid-infrared laser output in similar tellurite glass fiber. Experimental results support the assertion that the Er3+ doped tellurite glasses hold promise as a candidate laser gain medium for mid-infrared fiber laser systems.

The Origin of Anomalous Density Behavior of Silica Glass.

The anomalous density-temperature relationship of vitreous silica with low hydroxyl content is explained by the formation of medium-range ordering structure in the glass transition process. The ordered medium-range structure has the shape of a "nanoflake" and consists of two layers of SiO4 tetrahedra, bonded by O atoms located in the middle of the structure. The nanoflakes interact with their surrounding structures through both covalent chemical bonds and van der Waals bonds. In the formation of the van der Waals bonds, the orientation of SiO4 tetrahedra can change, which results in an increase in distance between the nanoflakes and their surrounding structures. Thus, there is a slight volume enlargement associated with the formation of nanoflakes. Since the nanoflakes' formation starts at a temperature near 1480 °C, and the population of the nanoflakes grows continuously as temperature decreases until about 950 °C, the bulk volume of silica glass increases in the temperature range from about 1480 °C to 950 °C. Therefore, the density anomaly of silica glass can be explained as a byproduct of forming of medium-range ordering structure in the silica glass transition.

Broadband high-gain Tm3+/Ho3+ co-doped germanate glass multimaterial fiber for fiber lasers above 2 µm.

High-gain Tm3+/Ho3+ co-doped optical fibers are urgently desired for high-repetition-rate mode-locked fiber lasers at >2 µm. Here, Tm3+/Ho3+ co-doped germanate glass with low hydroxyl (OH-) content was prepared by the conventional melt-quenching method combined with the reaction atmosphere procedure (RAP) dehydration technique. The doping concentrations of Tm2O3 and Ho2O3 are 2.5 mol.% (7.1 wt.%) and 0.25 mol.% (0.7 wt.%), respectively. Thanks to the high Tm3+ doping (7.1 wt.%) and low energy transfer efficiency (19.8%) between Tm3+ and Ho3+ ions, it enables achieving broadband and high-gain performance in the 2 µm region. Then a silicate-clad Tm3+/Ho3+ co-doped germanate core multimaterial fiber was successfully drawn by using the rod-in-tube method, which has a broadband amplified spontaneous emission (ASE) with a full width at half-maximum (FWHM) of 247.8 nm at 2 µm. What is more, this new fiber has a high gain per unit length of 4.52 dB/cm at 1.95 µm. Finally, an all-fiber-integrated passively mode-locked fiber laser was built by using this broadband high-gain fiber. The mode-locked pulses operate at 2068.05 nm, and the fundamental repetition rate is up to 4.329 GHz. To the best of our knowledge, this is the highest fundamental repetition rate for the all-fiber passively mode-locked fiber laser above 2 µm. These results suggest that the as-drawn multimaterial fibers with broadband high-gain characteristics are promising for high-repetition-rate ultrafast fiber lasers.

Experimental Study on the Wettability of Coal with Different Metamorphism Treated by Surfactants for Coal Dust Control.

Wet dedusting is the main coal dust suppression technique in coal mines, and coal wettability is the main factor affecting dust suppression efficiency. To investigate the main factors affecting the coal wettability and improve it, the coal–water contact angle was used as an index to characterize the coal wettability, and the wettability of six coal samples with different metamorphic degree was studied by analyzing the relationship between the physicochemical properties and the contact angle. To improve the coal wettability, the nonionic surfactant alkyl polyglycoside (APG), anionic surfactant sodium dodecyl benzene sulfonate (SDBS), and polymer surfactant polyacrylamide (PAM) were applied to the coal samples. The results show that SDBS is the most effective surfactant to improve the coal wettability, followed by APG, while the application of PAM would lead to more hydrophobic coal. It is also found that the coal wettability shows a high–low–high trend with the increase in the metamorphic degree. The wettability of long flame coal is the strongest and that of gas coal is the weakest. Moisture is the main hydrophilic factor of coal, while 1,4-dimethylbenzene is the main hydrophobic factor. The main factors affecting the treatment effect of APG, SDBS, and PAM on wettability are the aromatic methylbenzene, hydroxyl, and hydroxyl content of coal, respectively. Therefore, according to the content of hydroxyl in different coals, an SDBS solution can be prepared to improve the coal wettability. For coal with a low hydroxyl content, a higher concentration SDBS solution could be needed.

ZnS enhancing the infrared emission of Er3+ doped oxyfluorosulfide glasses with low hydroxyl content

Different content of ZnS was introduced into Er3+ doped oxyfluorosulfide glasses to explore the effect on the near- and mid-infrared emission properties. The results indicate the addition of a small amount of ZnS can substantially enhance the near- and mid-infrared emission intensity. However, more ZnS (7%) will lead to glass devitrification and decrease the infrared emission intensity greatly. XRD, Raman spectra and DSC tests prove the small amount of ZnS has no obvious effect on the transparency, phonon energy and thermal properties of these glasses. FTIR spectra reveal the addition of ZnS can reduce the content of hydroxyl groups obviously, which is the main reason for the enhancement of infrared emission. Our results show that the proper amount of ZnS is beneficial to reduce hydroxyl content and enhance the near- and mid-infrared emission of these Er3+-doped oxyfluorosulfide glass.

Lignin as a Partial Polyol Replacement in Polyurethane Flexible Foam.

This study was focused on evaluating the suitability of a wide range of lignins, a natural polymer isolated from different plant sources and chemical extractions, in replacing 20 wt.% of petroleum-based polyol in the formulation of PU flexible foams. The main goal was to investigate the effect of unmodified lignin incorporation on the foam’s structural, mechanical, and thermal properties. The hydroxyl contents of the commercial lignins were measured using phosphorus nuclear magnetic resonance (31P NMR) spectroscopy, molar mass distributions with gel permeation chromatography (GPC), and thermal properties with differential scanning calorimetry (DSC) techniques. The results showed that incorporating 20 wt.% lignin increased tensile, compression, tear propagation strengths, thermal stability, and the support factor of the developed PU flexible foams. Additionally, statistical analysis of the results showed that foam properties such as density and compression force deflection were positively correlated with lignin’s total hydroxyl content. Studying correlations between lignin properties and the performance of the developed lignin-based PU foams showed that lignins with low hydroxyl content, high flexibility (low Tg), and high solubility in the co-polyol are better candidates for partially substituting petroleum-based polyols in the formulation of flexible PU foams intended for the automotive applications.

Controlling hydroxyl content of reduced graphene oxide for superior cathode performance of lithium sulfur batteries

Here, the hydroxyl content of reduced graphene oxide (rGO) is controlled by adjusting reduction time with l-ascorbic acid as reduction agent to study the effect on cathode performance of lithium sulfur batteries (LSBs). The results indicate that the hydroxyl content decreases from 35.8% to 17.9% with prolonging reduction time from 6 h to 48 h, and the C/O ratio increases. More importantly, it is demonstrated that the rGO with relatively low hydroxyl content within 36 h of reduction is more beneficial to enhance both the initial capacity and capacity retention as well as rate performance of LSBs, which is ascribed to the higher conductivity, stronger adsorption and relatively few reaction by-products with the decrease of hydroxyl content. However, when the reduction time is further prolonged to 48 h, the cathode performance deteriorates. As a result, rGO-36h/S electrode with the optimum hydroxyl content (19.2%) achieves an initial discharge capacity of 1340.9 mAh g−1, which still maintains 707.8 mAh g−1 over 100 cycles at 0.1C. This work may provide a guide for reducing GO when used as sulfur host material or matrix material of LSBs.

Research progress in surface bonding pretreatment of dental zirconia ceramics

Yttria stabilized tetragonal zirconia polycrystal ceramics is widely used in the field of dentistry because of its excellent mechanical properties and biocompatibility. However, it has low hydroxyl content and does not contain silica. Therefore micro mechanical retention induced by hydrofluoric acid etching on its surface is not applicable. The bonding of zirconia is a difficult problem. Zirconia surface pretreatment is commonly used to improve bonding strength and durability. This review summarizes surface pretreatment of dental zirconia ceramic including air abrasion, laser etching, acid etching, silica coating, non-thermal plasmas treatment, et al. In addition, it presents advantages and disadvantages of each treatment, provides guidance for application and future research directions.

High-value utilization of hydroxymethylated lignin in polyurethane adhesives

Lignin is a good candidate for the polymerization and chemical modification to prepare sustainable chemicals and materials, but a relatively low hydroxyl content becomes an obstacle for the preparation of lignin-based polyurethane (PU) adhesives. In order to improve its reactivity, the acetic acid lignin (AAL) was hydroxymethylated before copolymerized with isocyanate during the preparation of PU adhesives. The hydroxymethylation was carried out in an alkaline formaldehyde solution and it was found that 85 °C is the optimal temperature. On that condition, the free formaldehyde content of the corresponding product HL-6 was as low as 0.32%, while the hydroxymethyl was increased by 189.11% compared with original AAL and reached 2.92 mmol/g. In the polymerization of PU adhesives, the hydroxymethylated lignin with a higher aliphatic hydroxyl content formed a more compact three-dimensional urethane cross-linking network with isocyanate. The mechanical properties and thermal stability of the lignin-based PU adhesive were improved by 15–30 wt% in HL-6, and particularly the tensile strength was increased by 21–41 MPa, which indicated that the hydroxymethylation is an efficient way to enrich the hydroxyl in lignin, and the modified lignin is adequate to partially replace petroleum-based polyols for the preparation of PU adhesives with excellent properties.

Optical properties of Nd3+-doped TeO2-TiO2-ZnO glasses with lower hydroxyl content

This paper describes Nd3+-ions doped multicomponent tellurite glasses TeO2-TiO2-ZnO (TTZ) applicable to advanced optical devices, which were characterized by UV–Vis-NIR absorption, Raman, and photoluminescence (PL) techniques. Not only did we perform experimental characterizations but also theoretically predicted the PL properties of Nd3+-doped TTZ glasses by using the Judd-Ofelt theory. The influence of the residual hydroxyl (OH) groups and types of crucible used in the melt preparation on the structures and optical properties of TTZ glasses was investigated. We found that the use of a Pt crucible increased the network-connecting structures of trigonal bipyramidal TeO4 compared to the case of a Al2O3 crucible. Moreover, reducing the OH groups in TTZ glasses improved the optical properties of Nd3+-doped TTZ glass, and a higher spectral figure of merit of 8.71 × 10−24 s cm2 for Nd3+:4F3/2 → 4I11/2 emission at 1075 nm could be achieved, indicating that Nd3+-doped TTZ glass with lower hydroxyl content is promising for laser or active optical applications.

Tm/Al Co-Doped Silica Glass Prepared by Laser Additive Manufacturing Technology for 2-μm Photonic Crystal Fiber Laser

In this article, we demonstrated the Tm/Al co-doped silica glass fabricated by the laser additive manufacturing technology for the first time. The measurements show that the glass was doped with Tm3+ concentration of 1.64 wt% without any crystallization. The Tm3+ and Al3+ were uniformly distributed, and no additional defects were introduced during the fabrication process. The glass exhibits low hydroxyl content level of 11.56 ppm. Using the prepared silica glass as the core rod, a Tm/Al co-doped photonic crystal fiber (PCF) was fabricated and performed 13.9% slope efficiency with nearly 600 mW output laser power. This novel technology provides an alternative method to fabricate Tm-doped fiber materials with high homogeneity and large core size, promoting the further spread and development of 2 μm fiber lasers.

Extremely low structural hydroxyl contents in upper mantle xenoliths from the Nógrád-Gömör Volcanic Field (northern Pannonian Basin): Geodynamic implications and the role of post-eruptive re-equilibration

The structural hydroxyl content of the nominally anhydrous minerals (olivine and pyroxenes) in the upper mantle is among the important attributes that influence the physical and chemical features of the upper mantle. In this study, we provide detailed Fourier-transform infrared (FTIR) data on 63 petrographically and geochemically well-defined upper mantle xenoliths from the Nógrád-Gömör Volcanic Field (Pannonian Basin, Central Europe). These xenoliths show extremely low average structural hydroxyl contents (~0, 31 and 185 ppm for olivine, orthopyroxene and clinopyroxene, respectively) compared to values reported regionally and worldwide. The studied xenoliths have anomalous types of FTIR spectra and high structural hydroxyl ratios between clinopyroxenes and orthopyroxenes (an average of ~8). Furthermore, there is usually no correlation between the structural hydroxyl content and other physical or chemical properties of the xenoliths. These specific FTIR characteristics suggest that the Nógrád-Gömör upper mantle xenoliths were exposed to significant modification of their structural hydroxyl contents, which may be linked to pre- and post-eruptive processes. Decompression during extension leads to lower ‘water’ activity, which is most likely to have played a key role. However, pre-eruptive mantle metasomatism with an agent having low water activity cannot be excluded either. The post-eruptive cooling can be significant as well, as suggested by the higher structural hydroxyl content in xenoliths hosted in more rapidly cooled volcanic facies (i.e. pyroclastics).Our study reveals how FTIR characteristics may evolve in continental rift settings in young extensional basins. Furthermore, novel applications of our study are the diagnostic features that indicate significant changes in structural hydroxyl properties. This contributes to distinguishing low structural hydroxyl contents linked to the pre-eruptive (i.e., low structural hydroxyl content in pyroxenes, anomalous partitioning and anomalous band characteristic in pyroxenes) or the post-eruptive (completely ‘dry’ olivines) periods.

Development and characterization of polyurethane foams with substitution of polyether polyol with soy-based polyol

Bio-based polyols can replace petroleum-based polyols for producing a wide range of polyurethane (PU) products. Bio-based polyols are derived from renewable resources, however, their utilization is limited due to the complex molecular structure and relatively low primary hydroxyl content. This study aims to substitute the petroleum-based polyols with soy-based polyols for the fabrication of rigid PU foams with comparable or better physical properties required for thermal and structural applications. The effects of blending soy-based polyol, of hydroxyl number 230 mg KOH/g with high functionality soy-based cross-linker were investigated. The fabricated samples were tested for density, compressive strength, tensile strength, thermal resistivity, thermal stability and dimensional stability. The blended foam samples exhibited better thermal resistivity (8% higher), compressive properties (about 512% higher) and tensile strength (287% higher) when compared to control specimens. It was concluded that the polyols blended with soy-based cross-linker in 95:5 ratio by weight resulted in properties better than control samples, and comparable to commercial petroleum-based foams.

Characterization of spectral and intensity changes with measurement geometry in various light guides used in scintillation dosimetry.

To characterize response changes of various light guides used in megavoltage (MV) photon beam scintillation dosimetry as a function of irradiation conditions. Particular emphasis was placed on quantifying the impact of response changes on the Čerenkov light ratio (CLR). Intensity and spectral response measurements as a function of dose, depth, and fiber-beam angle were performed with a commercial scintillation detector stripped of its scintillation material and five different custom-made light guides. The core materials of the light guides investigated consisted of polymethyl methacrylate (PMMA), low- and high-hydroxyl content silica, and polystyrene. Dose levels ranging from 50monitor units (MU) to 1000MU, depths ranging from 1 to 20cm, and fiber-beam angles ranging from 10° to 90° were investigated. All measurements were performed at a photon beam energy of 6MV. The CLR was calculated by taking the ratio of the responses in the blue to green spectral regions. There was no significant change in the CLR measured with the modified commercial scintillation detector as a function of delivered dose. In addition, increases in the CLR as functions of depth and fiber-beam angle were observed where the maximum changes were 4.2% and 3.6%, respectively. The spectrum measurements showed no observable changes in spectral shape with depth except for the low-hydroxyl content silica fiber. Variations in the measured spectral shape with fiber-beam angle were observed for all fibers investigated. The magnitude of the changes in the spectral shape varied with fiber type, where the silica fibers exhibited the largest changes and the plastic fibers exhibited the smallest changes. Increases in the CLR were observed for the silica fibers with depth and for all fibers with fiber-beam angle. The plastic fibers showed no significant change in the CLR as a function of depth. Increases of 3.1% and 9.5% in the CLR were observed for the high- and low-hydroxyl content silica fibers, respectively, over the range of depths investigated. Variations of 2.3%, 6.1%, 5.1% and 11.9% were observed for the PMMA, polystyrene, high-hydroxyl, and low-hydroxyl content silica fiber CLR values as a function of fiber-beam angle, respectively. The insignificant change in the CLR with delivered dose indicates that a single CLR value over the investigated dose range is sufficient for accurate Čerenkov subtraction. Variations in the stem-effect spectrum shape can occur with changes in irradiation geometry. The magnitude of the changes are governed by the fiber construction and the optical properties of the fiber. The observed spectral shape changes can be explained by a combination of variations in optical path length through the fiber and the fiber fluorescent signal contribution to the stem-effect. These spectral shape variations directly influence the calculated CLR values. This work confirms that careful characterization of scintillation detectors is important as changes in the stem-effect spectrum can cause changes in the CLR. If the CLR changes between the reference and measurement conditions, this could result in an incorrect stem-effect subtraction and reduced measurement accuracy.

Highly Er3+ doped fluorotellurite glass for 1.5 µm broadband amplification and 2.7 µm microchip laser applications

The fluorescence properties in IR region of fluorotellurite glass with high Er3+ concentration up to 13 mol% are investigated and optimum concentration of 2.7 µm emission is 11 mol%, followed by a decrease in fluorescence intensity. The thermal characteristic parameter (ΔT = 98 °C) based on DSC curve shows a good thermal stability. The FWHM corresponding to 1.5 µm broadens as Er3+ increases and reaches a maximum of 110 nm (13 mol%) which shows superior bandwidth properties. The high amplifier gain value(σemi × τmea) of 11.87 × 10–21 cm2 ms, along with longer lifetime (1.72 ms), which benefits from the low phonon energy (612 cm−1) and hydroxyl content (0.03 cm−1), indicates the ideal 2.7 µm laser characteristics. Hopefully, the glass studied here may be find potential applications in the fields of fiber amplifier and MIR microchip lasers.