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Article

Influence of Oxide Glass Modifiers on the Structural and Spectroscopic Properties of Phosphate Glasses for Visible and Near-Infrared Photonic Applications

by
Marta Kuwik
*,
Joanna Pisarska
* and
Wojciech A. Pisarski
Institute of Chemistry, University of Silesia, Szkolna 9, 40007 Katowice, Poland
*
Authors to whom correspondence should be addressed.
Materials 2020, 13(21), 4746; https://doi.org/10.3390/ma13214746
Submission received: 15 September 2020 / Revised: 9 October 2020 / Accepted: 21 October 2020 / Published: 23 October 2020
(This article belongs to the Special Issue Rare Earth Doped Glasses/Ceramics: Synthesis, Structure, Properties, and Optical Applications)
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Abstract

The effect of oxide modifiers on multiple properties (structural and spectroscopic) of phosphate glasses with molar composition 60P2O5-(10−x)Ga2O3-30MO-xEu2O3 and 60P2O5-(10−y)Ga2O3-30MO-yEr2O3 (where M = Ca, Sr, Ba; x = 0, 0.5; y = 0, 1) were systematically examined and discussed. The local structure of systems was evidenced by the infrared (IR-ATR) and Raman spectroscopic techniques. The spectroscopic behaviors of the studied glass systems were determined based on analysis of recorded spectra (excitation and emission) as well as luminescence decay curves. Intense red and near-infrared emissions (1.5 μm) were observed for samples doped with Eu3+ and Er3+ ions, respectively. It was found that the value of fluorescence intensity ratio R/O related to 5D0→7F2 (red) and 5D0→7F1 (orange) transition of Eu3+ ions depends on the oxide modifiers MO in the glass host. However, no clear influence of glass modifiers on the luminescence linewidth (FWHM) was observed for phosphate systems doped with Er3+ ions. Moreover, the 5D0 and 4I13/2 luminescence lifetimes of Eu3+ and Er3+ ions increase with the increasing ionic radius of M2+ (M = Ca, Sr, Ba) in the host matrix. The obtained results suggest the applicability of the phosphate glasses with oxide modifiers as potential red and near-infrared photoluminescent materials in photonic devices.

1. Introduction

Over the past years, inorganic glass systems have been paid attention due to their interesting properties and possible applications as fibers and optical broadband amplifiers, lasers, optical temperature sensors and generators of white light [1,2,3,4,5]. The composition of the glass host matrices influences significantly the structural, electrical, optical and physical properties of glass systems [6,7,8,9,10].
Particularly noteworthy are the glass modifiers such as alkaline earth metal oxides (MO = MgO, CaO, SrO, BaO) that strongly influence the properties of glass systems [11,12,13,14]. Previously published results indicate that the depolymerization of the glass network due to the incorporation of alkaline earth oxides into the glass matrix promotes the formation of non-bridging oxygen (NBO) groups [15]. Moreover, Pavić et al. [16] stated that modifiers like MgO, CaO as well as BaO influence some properties (electrical, dielectric and spectroscopic) of Fe2O3 doped into phosphate glasses. The effect of oxide modifiers on the luminescence properties and decay measurements of Ln3+ ion-doped inorganic glass matrices has been the subject of numerous studies. Ratnakaram et al. [17] reported the role of glass modifiers in the luminescence spectra and kinetics of Eu3+-doped lithium fluoroborate systems. The optical properties of Er3+-doped alkaline-earth borotellurite glasses were studied by Swapna et al. [18]. Also, the effect of MgO, CaO, SrO and BaO on white luminescence of borate systems doped with Dy3+ ions has been proven [19]. According to the results obtained for glasses, the addition of modifier oxides into the glass host can provide important advantages. For instance, the lithium antimonate and antimony borate glasses with calcium oxide exhibit better lasing action in comparison to samples with other studied glass modifiers. This is related to the larger value of the branching ratio (β) for CaO modifier glasses [20]. Moreover, comparatively low non-radiative losses for CaO mixed systems are found to be the reason for the high luminescence efficiency of these glasses [21]. Similar results were confirmed for P2O5-Pb3O4-ZnO-CaO systems doped with dysprosium ions [22]. On the other hand, Nd3+-doped lithium fluoroborate glass with MgO shows a higher stimulated emission cross-section than systems with CaO, PbO or CdO [23].
Among the different inorganic glass systems, phosphate glasses have been studied for numerous industrial applications [24,25] and for broad optical applications in the range of visible luminescence [26,27,28,29,30] and infrared luminescence [31,32,33,34,35]. These glass materials containing rare earth ions such as Nd3+, Yb3+, Er3+ can be successfully used for high-power laser systems, optical amplifiers and optical sensors due to their excellent luminescent properties [36,37,38,39,40,41,42]. Special attention has been paid to phosphate glasses containing erbium ions [43,44,45,46]. The thermal, structural and luminescence properties of Er3+-doped phosphate glasses modified by Al2O3, TiO2 and ZnO have been examined [47]. Ga2O3 also belongs to the components playing an important role as an intermediate metal oxide, with is able to serve both as a glass-former and a glass-modifier in inorganic glasses [48]. In general, Ga2O3-based glasses possess quite good IR transparency and can be attractive glass-hosts for wideband transparent windows, achromatic lenses or luminescent materials emitting visible light or near-infrared radiation [49]. In particular, the glass thermal stability and some spectroscopic parameters of rare earth ions are improved significantly in the presence of Ga2O3. The experimental results for Er3+-doped borobismuth glasses clearly suggest that these thermal and spectroscopic parameters are optimal at Ga2O3 = 8 mol% [50], when gallium oxide plays the role as a glass-network-modifier.
It is well known that glasses based on P2O5 are attractive optical materials due to their exceptional characteristics like a high transparency in a wide spectral region, low melting point and low refractive index [51,52]. Furthermore, phosphate systems doped with higher concentrations of rare earths or transition metal ions are amorphous, in contrast to other oxide glasses [53]. The relatively large phonon energy and hygroscopic properties of P2O5 contribute to the lower intensity of luminescence for Ln3+ ions in phosphate glasses. For that reason, the applications of phosphate systems in the development of photonic devices may be limited [54]. However, the incorporation of modifier oxides into the phosphate glasses could improve the spectroscopic properties of systems based on P2O5. To the best of our knowledge, the structural and luminescence properties of P2O5-Ga2O3 glasses with alkaline earth metal oxides (MO) are not frequently examined. Therefore, it is interesting to thoroughly research the multiple properties (structural and spectroscopic) of phosphate glass systems with oxide modifiers as potential photoluminescent materials in photonic devices.
In this paper, we present results for phosphate glasses with oxide glass modifiers MO (where MO = CaO, SrO, BaO). The local structure of systems was evidenced by the infrared and Raman spectroscopic techniques. It was presented that the recorded bands due to the stretching modes of the P–O bonds depend on the type of oxide modifier used. The conversion of phosphate tetrahedral structural units Qn and the depolymerization of the glass network occur when glass modifiers are changed. Moreover, the spectroscopic properties of optical active dopants (Eu3+ and Er3+) were determined based on analysis of registered luminescence spectra and luminescence decay curves. Their properties were compared from the point of view of the alkaline earth oxides in the glass host matrix. It was found that the intensity of the red and orange emissions of glasses doped with Eu3+ ions depends on the oxide modifier, whereas no clear influence of glass modifiers on the luminescence linewidth for 1.5 μm emission was observed for systems doped with Er3+ ions. The 5D0 and 4I13/2 luminescence lifetimes of Eu3+ and Er3+ ions increase with the increasing ionic radius of M2+ (M = Ca, Sr, Ba) in the glass host matrix. Based on that result, important for future applications, we can choose systems with good optical behaviors, which are potential red and near-infrared photoluminescent materials in photonic devices.

2. Materials and Methods

Phosphate glass systems singly doped with Eu3+ and Er3+ ions with the molar composition 60P2O5-(10−x)Ga2O3-30MO-xEu2O3 and 60P2O5-(10−y)Ga2O3-30MO-yEr2O3 (where M = Ca, Sr, Ba; x = 0, 0.5; y = 0, 1) were synthesized by conventional melt-quenching method using oxide components of high purity (99.99%, Aldrich Chemical Co., St. Louis, MO, USA). In the first step, the appropriate amounts of metal oxides were mixed/ground in an agate ball mill. Because of the hygroscopic properties of the glass network former P2O5, the glass samples were fabricated in a glow box under a protective atmosphere of dried argon. The samples were melted in a corundum crucible at 1100 °C for 30 min in an electrical furnace. In order to eliminate internal mechanical stresses, each sample was quenched and annealed below the glass transition temperature (Tg). Next, the obtained systems were slowly cooled to room temperature. Transparent glasses were shaped and polished to meet the requirements for optical measurements. The prepared samples were around 10 mm × 10 mm dimension and 2 mm in thickness.
IR spectroscopy and Raman spectroscopy were used to examine the local structure of studied glasses undoped with rare earth ions. The infrared spectra were performed using the ATR technique. Spectral measurements were performed on a NicoletTM iSTM 50 FT-IR spectrometer (Thermo Scientific, Waltham, MA, USA) equipped with a diamond attenuated total reflectance (ATR) module. The infrared spectra were recorded in the spectral range of 1400–400 cm−1 with a resolution of 4 cm−1. The Raman spectra were obtained using a Thermo Scientific™ DXR™2xi Raman imaging microscope (Thermo Scientific, Waltham, MA, USA). The data were collected using a 455 nm laser and the power on samples was a 5 mW. The Raman spectra were registered with a resolution of 2 cm−1.
Optical measurements were carried out on a Photon Technology International (PTI) Quanta-Master 40 (QM40) UV/VIS Steady State Spectrofluorometer (Photon Technology International, Birmingham, NJ, USA) coupled with tunable pulsed optical parametric oscillator (OPO), pumped by a third harmonic of a Nd:YAG laser (Opotek Opolette 355 LD, OPOTEK, Carlsband, CA, USA). The laser system was equipped with a double 200 mm monochromator, xenon lamp as a light source, a multimode UVVIS PMT (R928) (PTI Model 914) detector and Hamamatsu H10330B-75 (Hammatasu, Bridgewater, NJ, USA) detector controlled by a computer. Excitation and emission spectra were registered with a resolution 0.5 nm. Luminescence decay curves were recorded and stored by a PTI ASOC-10 (USB-2500) oscilloscope. All structural and optical measurements were carried out at room temperature.

3. Results and Discussion

3.1. Structural Properties of Phosphate Glasses

In agreement with the literature, phosphate glass matrices can be described by four different structures Qn. The first is a three dimensional cross-linked network of Q3 tetrahedra. The second is a polymer-like metaphosphate chain of Q2 structural units. There are also glasses based on Q1 and Q0 tetrahedra, which represent pyrophosphate and orthophosphate anions, respectively [55]. Infrared and Raman spectroscopy reveal important information regarding the modification in structural units Qn with a change in the glass composition. According to Moustafa and El-Egili the stretching vibrations (asymmetric and symmetric) characteristic of phosphate lattices are active in the infrared as well as Raman spectra [56]. Most studies devoted to the Raman spectra of glass systems based on P2O5 suggest that intense bands are related to the symmetric stretches, whereas the infrared spectra intense bands correspond to asymmetric stretches.
Figure 1, Figure 2 and Figure 3 show the near-infrared spectra registered for phosphate systems with glass modifiers in 400–1400 cm−1 spectral region. In order to better understand the effect of oxide modifiers MO (calcium oxide, strontium oxide and barium oxide) addition on the phosphate glass structure, the deconvolution of the infrared spectra of all samples was carried out. As reported in the literature, the band (I) located at about 499/488/452 cm−1 is due to harmonics of bending vibrations of O=P–O linkages [57]. It is important to note that the areas of this band increase in comparison to other IR bands when oxide modifiers MO change in direction CaO < SrO < BaO. The next band centered at 640/639/588 cm−1 is attributed to the P–O–P bending vibration and stretching of P–O–P mode [58]. Moreover, the IR band (II) is characteristic of the stretching vibration of M–O–P bonds [59]. On the other hand, the previous results for PbO-Ga2O3-P2O5 glass [60] and Ga2O3-P2O5 glass systems [61] suggest that in this frequency region the IR band corresponding to vibrations localized on GaO4 tetrahedra can be observed at about 610 cm−1 and 640 cm−1, respectively. It was stated that the band located in the 708–722 cm−1 frequency region corresponds to the symmetric stretching of P–O–P linkages in between Q1 and Q2 units [58], whereas the infrared band near at ~780 cm−1 is due to the symmetric stretching mode of P–O–P bonds [62]. An increase in the intensity of the band (III) at the expense of band (IV) could be associated with the conversion of Q2 to Q1 units that is occurring with a change of oxide modifiers in the glass host.
It is clearly seen from Figure 1, Figure 2 and Figure 3 that broad and unresolved infrared bands are located in the 800–1350 cm−1 frequency region. Furthermore, the analysis of this frequency region indicates the effect of calcium oxide, strontium oxide and barium oxide on the structure of phosphate systems. The bands due to asymmetric stretching vibrations of bridging oxygen atoms in P–O–P bonds [63] and asymmetric stretching vibrations of the P–O–P linkage of Q1 and Q2 tetrahedra with non-bridging oxygen are located at about 900 cm−1 [64]. The decrease in the relative area of the band for a sample with BaO as oxide modifier may be associated with the formation of the P–O–Ba bonds at the expense of the rest of the P–O–P linkages. Moreover, the P–O–P asymmetric stretching band (V) shifts to lower frequencies with a change of oxide modifier MO in direction CaO < SrO < BaO as a result of depolymerization of the glass network [65].
The bands in the 949–1009 cm−1 and 1079–1097 cm−1 frequency regions are related to asymmetric stretching vibrations of PO43− structural group and symmetric stretching vibrations of PO43− tetrahedral (PO− ionic group) [66] or PO32− symmetric stretching vibrations in Q1 structure, respectively [67]. The presence of these bands (VI, VII) suggests the ionic character of all samples [57]. The relative areas of these bands are bigger for the glass system with BaO than with CaO or SrO. Therefore, an increase in the quantity of non-bridging oxygen ions due to depolymerization of the glass network can be observed primarily for BaO as oxide modifier. Furthermore, the intensity of band (VIII) at about 1161–1182 cm−1 attributed to the asymmetric stretching of PO2− in the Q2 structure [67] significantly decreases when oxide modifiers MO change in direction CaO < SrO < BaO. The obtained results indicate that when glass modifiers are changed in glass host the conversion of Q2 to Q1 units occurs. The IR band near 1250 cm−1 appears due to overlapping of the asymmetric stretching vibration of P–O bond with the asymmetric stretching vibration of PO2− mode in Q2 units. This band (IX) may be evidence of the stretching mode of P=O double bonds in the phosphate structural units [68]. On the contrary, the band (X) at about 1300 cm−1 is associated with the harmonic of the doubly bonded oxygen vibration (P=O) [58]. Table 1 presents the infrared bands observed for studied phosphate glasses.
The Raman spectra of studied phosphate systems with glass modifiers were registered in the 150–1450 cm−1 spectral region. Also for Raman spectra, it was necessary to deconvolute the spectra for better understanding the influence of calcium oxide, strontium oxide and barium oxide addition on the glass structure (Figure 4, Figure 5 and Figure 6). The observed bands were assigned based on literature data [55,58,61,68,69,70,71,72]. Generally, all spectra can be divided into two main broad and unresolved vibration band groups located in the 200–800 cm−1 and 850–1400 cm−1 frequency regions. Furthermore, bands above 1300 cm−1 corresponding to the Q3 units are not registered for analyzed glass systems. Therefore, it can be concluded that there are no Q3 units in the structure of the studied phosphate glasses [55]. The bands near at ~350 cm−1 and ~400 cm−1 confirmed the presence of gallium oxide in the obtained glass composition because systems containing tetrahedrally coordinated Ga atoms give intense low-frequency Raman bands assignable to bending modes of mixed Ga–O–M bridges [61]. The first one (band (I)) can be attributed to the GaO6 vibrational groups [61].
The second one (band (II)) probably correspond to symmetric bending vibrations of Ga–O–P linkages [61,69] or bending vibrations of PO4 units [68]. The band (III) at about 520 cm−1 corresponds to bending vibrations of P2O74− groups [58]. Moreover, the band (IV) centered at 625/626/607 cm−1 is assigned to the symmetric stretching vibrations of P–O– terminal bonds [70]. It is important to note that the intensity of the band at about 400 cm−1 increases, whereas the intensity of bands located at 350, 520, 625 cm−1 decreases when oxide modifiers MO change in direction CaO < SrO < BaO. The intense Raman bands at around 710 cm−1 (V) and 758 cm−1 (VI) are attributed to the symmetric stretching vibrations of P–O–P bonds in Q2 metaphosphate units and the symmetric stretching vibrations of P–O–P associated with Q1 tetrahedral units, respectively [70]. Additionally, the band at 710 cm−1 is more intense than the band near at 758 cm−1. Therefore, it can be stated that in the structures of the studied phosphate systems with oxide modifiers CaO, SrO and BaO, phosphorus tetrahedra are linked into chains and rings, and presumably Q2 units prevail [71].
Based on the analysis of the Raman spectra in the 850–1400 cm−1 frequency regions it can be assumed that conversion structural units occurs (Q1 to Q2). The band (VII) located at around 1096/1104/1117 cm−1 determines the formation of Q1 phosphate tetrahedra [55]. On the other hand, the bands (VIII, IX) corresponding to the symmetric stretching mode of O–P–O non-bridging oxygens, indicating the formation of metaphosphate structural units (Q2), were registered in the 1135–1176 cm−1 frequency regions [70,72]. The relative areas and intensities of these bands (VII–IX) significantly depend on the type of oxide glass modifiers MO (M = Ca, Sr, Ba). For the glass system with BaO, the intensity and area of band attributed to symmetric stretching vibrations of P–O bonds in pyrophosphate units (Q1) are lower than other obtained glasses. However, the most intense bands due to the formation of Q2 phosphate tetrahedral are observed for phosphate glass with BaO as oxide modifier. For that reason, it could be concluded that the conversion of pyrophosphate tetrahedra (Q1) to metaphosphate (Q2) tetrahedras occurs when oxide modifiers MO change in direction CaO < SrO < BaO. The last two weak Raman bands may correspond to the symmetric stretching of P–O bonds [69] or asymmetric stretching vibrations of PO2− groups in Q2 units [70,71] Its assignment due to the symmetric stretch of P=O terminal oxygens is also taken into consideration [71]. Table 2 presents all registered bands in the Raman spectra for studied phosphate glasses.

3.2. Spectroscopic Properties of Phosphate Glasses

Figure 7 shows the excitation spectra of Eu3+-doped phosphate systems with oxide modifiers MO. These spectra were monitored at λem = 611 nm.
The recorded excitation bands originating with the transition from the 7F0 and 7F1 states to higher-lying states are narrow and well resolved. Independently on the kind of MO, the among registered bands the most intense bands correspond to 7F0→5L6 (395 nm) and 7F0→5D2 (465 nm) transitions. Therefore, the Eu3+ ions that present in the glass host could be excited from the 7F0 ground state through UV or visible radiation into one of the higher-lying levels.
Figure 8 presents the emission spectra of Eu3+ ions in investigated phosphate glasses. For all samples, spectra were registered under excitation λexc = 395 nm. Because of the small energy gaps between 5L6, 5D3, 5D2, 5D1 states, the excitation energy was transferred non-radiatively to the 5D0 level. On the other hand, the energy gaps between the 5D0 and 7FJ (where J = 0, 1, 2, 3, 4) levels are quite large. Consequently, the visible luminescence due to 5D0→7FJ transitions of Eu3+ ions are possible. The intense emission bands located at 577, 591, 611, 651 and 700 nm are assigned to the 5D0→7F0, 5D0→7F1, 5D0→7F2, 5D0→7F3 and 5D0→7F4 transitions, respectively. Moreover, there are additional weak bands in the range 520-560 nm (inset for Figure 8). These visible luminescence bands correspond to the 5D1→7F0, 5D1→7F1 and 5D1→7F2 transitions of Eu3+ ions. The emission spectra were normalized to the 5D0→7F1 transitions (590 nm) in order to better comparison. It was stated that the intensity of band due to 5D0→7F2 depends significantly on the oxide modifiers. It is generally known that the 5D0→7F1 is a magnetic dipole (MD) transition which is independent of local symmetry [73]. However, 5D0→7F2 is strongly influenced by the environment of europium ions and this electric dipole (ED) transition is said to be a hypersensitive transition [74]. For that reason, the ratio of the 5D0→7F2 to 5D0→7F1 transitions informs us about local asymmetry around the Eu3+ ions in the glass host. The ratio of integrated emission intensity of these transitions is defined as the red-to-orange fluorescence intensity ratio R/O [75]. It was found that the value of R/O depends on the modifiers (calcium oxide, strontium oxide and barium oxide) in studied phosphate glass systems. The value of the fluorescence intensity ratio decreases in direction CaO < SrO < BaO. The value of R/O factor is the smallest for glass with BaO (3.09), whereas for the system with CaO (3.77) is the highest. For that reason, the local asymmetry around the europium ions and the covalent character of Eu–O bond in phosphate glasses increase in the same direction.
Next, luminescence decays from the upper 5D0 excited level of europium ions in the studied systems were performed. Figure 9 shows the decay curves for phosphate glasses with modifiers CaO, SrO and BaO. Based on decays, the luminescence lifetime for 5D0 state of Eu3+ was calculated. It is noteworthy that the obtained results for phosphate glasses indicate the influence of modifier MO on the value of lifetime. However, its value is reduced from 2.20 ± 0.0013 ms for glass with BaO to 2.06 ± 0.0013 ms for the sample with CaO. In contrast to the fluorescence intensity ratio R/O, the 5D0 lifetime of europium ions increases in direction CaO < SrO < BaO. The similar trend was obtained for europium ions in tellurophosphate glasses and lithium borate glasses [76,77]. According to Jha et al. [66] the highest lifetime value of the 5D0 state of Eu3+ for glass with BaO as oxide modifier may suggest a lesser cross-relaxation effect between rare earth ions due to the greater depolymerization of phosphate network, resulting from an increase in the non-bridging oxygen (NBO) group. This effect is in good agreement with our analysis of near-infrared spectra (Figure 1, Figure 2 and Figure 3) which confirm that the poly-phosphate structure dominated by metaphosphate (Q2) and pyrophosphate (Q1) units and maximum depolymerization was observed for glass with barium oxide network modifier. Moreover, it was stated that the value of luminescence lifetime for phosphate glass systems doped with Eu3+ ions increases with an increasing ionic radius and atomic weight of oxide modifiers (CaO < SrO < BaO). On the contrary, Hermann et al. [78] investigated silicate systems with different network modifier oxides MO (CaO, SrO, BaO) and shown that 5D0 luminescence lifetime of europium ions increases with an increasing atomic weight of MO.
Phosphate glasses doped with erbium ions were investigated in order to analyze influence of oxide glass modifiers MO (M = Ca, Sr, Ba) on the spectroscopic properties of systems for near-infrared photonic applications. The excitation spectra were monitored at λem = 1535 nm. This wavelength is related to the most typical near-infrared emission for Er3+ ions. The observed bands originating to transitions from 4I15/2 ground state to the higher-lying excited states of erbium ions are shown in Figure 10. Based on the recorded spectra it was found that independently on the kind of oxide modifier used, the erbium ions could be excited through UV, visible or near-infrared radiation. In the wavelength range of 300–700 nm the intense bands due to 4I15/2→4F7/2 (488 nm), 4I15/2→2H11/2 (523 nm), 4I15/2→4F9/2 (652 nm) transitions of Er3+ ions were registered.
Additionally, weak bands corresponding to excitation erbium ions from 4I15/2 ground state to the higher-lying states (4K15/2, 4G7/2, 4G11/2, 4G9/2, 4H9/2, 4F5/2, 4F3/2, 4S13/2) were observed. It is worth noting that recording of excitation bands in the near-infrared spectral range (800 and 980 nm) indicates that studied glass systems doped with Er3+ ions could be also directly pumped by commercially available laser diodes (LD; inset of Figure 10). Taking this into consideration, the emission spectra were registered under direct excitation by 488 nm (4F7/2 state) and 980 nm (4I11/2 state). Regardless of the excitation wavelength, the near-infrared emission spectra consist of a broad luminescence band at about 1.5 μm corresponding to 4I13/2→4I15/2 laser transition of Er3+ ions (Figure 11). It is important to note that potential applications of glass materials for optoelectronic devices require an in-depth analysis of two important parameters. The first is the luminescence linewidth for 4I13/2→4I15/2 transition of Er3+ ions. This spectroscopic parameter is described as the full width at half maximum (FWHM) and it is practically independent of the presence of calcium oxide, strontium oxide or barium oxide in phosphate glass host. The differences between values of FWHM for samples containing metal oxides are comparably small (Table 3.). Moreover, it was stated that the luminescence linewidth values obtained for near-infrared laser transition of erbium ions in studied phosphate glasses are similar to other glass systems based on P2O5 [79,80].
Lastly, luminescence decay curves for 4I13/2 state of erbium ions in studied systems were recorded at λexc = 980 nm and λem = 1535 nm and based on them, the luminescence lifetimes were found out. Independently of glass modifiers (CaO, SrO or BaO), registered decay profiles are nearly exponential (Figure 12). The value of the luminescence lifetime for 4I13/2 state of Er3+ ions is higher for glass with BaO (τm = 920 ± 0.71 μs) than for sample with SrO. However, the phosphate system with CaO as glass oxide modifiers is characterized by the lowest luminescence lifetime (τm = 640 ± 0.66 μs). Therefore, the value of luminescence lifetime for 4I13/2 state of Er3+ ions in studied phosphate systems increased in the direction CaO < SrO < BaO. It is interesting to see that the value of luminescence lifetime for phosphate glass systems doped with Er3+ ions increases with an increasing ionic radius of oxide modifiers MO. On the other hand, based on the results obtained for germanate glasses Wang et al. [81] showed that the radiative lifetime of erbium ions at the 4I13/2 level is decreased, when the radius of alkaline earth ion increases.
Considering the above results that obtained phosphate systems with CaO, SrO and BaO are promising materials for visible and near-infrared photonic applications. Table 4 and Table 5 present a comparison of spectroscopic parameters in various glass hosts doped with europium and erbium ions, respectively.
If we compare the spectroscopic properties determined for systems doped with Eu3+ ions, it can be stated that due to the highest value of luminescence lifetime for 5D0 state, the glass with BaO is a good candidate for red-emitting materials, that may find potential use in photonic devices. According to previous studies, our phosphate system is characterized by longer luminesce lifetime than lead-free borate and germanate glasses [82,83]. The value of lifetime for 5D0 state of Eu3+ ions in phosphate glass is close to the value evaluated for borate (1.81 ms) and silicate (2.17) systems with BaO as oxide modifier [77,78].
Moreover, the luminescence lifetime for glass with BaO is significantly longer than the value of the lifetime for the 5D0 state for heavy metal oxide systems doped with Eu3+ ions [86,87,88,89]. Also, the results obtained for glasses containing with Er3+ ions indicate that among our studied samples the glasses with BaO are the best materials, that may be applied as near-infrared broadband amplifiers. It is well known that there are two important factors in the success of glasses as optical amplifiers. The first is the high value of full width in half maximum (FWHM) while the second is relatively long luminescence lifetime of erbium ions. In comparison to other oxide phosphate glasses [79,80] the FWHM evaluated for the studied system is wider (44 nm). On the other hand, the value of this spectroscopic parameters is significantly lower than those of borate [83] and silicate glasses [90]. In case of luminescence decays from 4I13/2 state of Er3+ ions it can be concluded that the lifetime value in studied phosphate glass is comparable to results obtained for phosphate [80] and silicate systems [90]. However, numerous studies have shown that the values of lifetimes are dependent critically on the glass composition and it is possible to synthesize the more efficiently-emitted materials [79,83,91].

4. Conclusions

In summary, the influence of oxide modifiers on multiple properties (structural and spectroscopic) of phosphate systems singly doped with rare earth ions (Eu3+ and Er3+) was studied. Based on near-infrared (IR-ATR) and Raman spectroscopy it has been proven that a change of modifier (CaO, SrO and BaO) in the glass host cause an increase in the number of Q1 and Q2 tetrahedra with non-bridging oxygens due to the depolymerization of the phosphate network. Independently on the kind of oxide modifier used intense red (611 nm) and near-infrared emissions (1.5 μm) were observed for glasses doped with Eu3+ and Er3+ ions, respectively. It was demonstrated that glass modifiers greatly effect on the spectroscopic parameters of rare earth ions in the studied systems. Firstly, the value of fluorescence intensity ratio R/O for europium ions indicates a high degree of covalence between Eu3+ and O2–, and the local asymmetry around the europium ions in the glass host. Moreover, the value of R/O parameter decreases, whereas the 5D0 lifetime of europium ions increases in direction CaO < SrO < BaO. The effect of glass modifiers on luminescence linewidth for 1.5 μm emission (FWHM) was not clearly observed. The luminescence lifetime for 4I13/2 state of erbium ions change in towards with increasing of the radius of alkaline earth ion CaO < SrO < BaO. Our results suggest the applicability of the phosphate glasses with oxide modifiers as potential red and near-infrared photoluminescent materials in photonic devices. Especially, the systems with BaO show good luminescence properties and we can conclude that these rare earth-doped phosphate glasses are promising materials for visible and near-infrared photonic applications.

Author Contributions

Conceptualization, M.K., J.P, and W.A.P.; investigation, M.K.; data curation, M.K.; formal analysis, W.A.P.; writing—original draft preparation, M.K.; writing—review and editing, J.P.; visualization, M.K.; supervision, W.A.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Liao, X.; Jiang, X.; Yang, Q.; Wang, L.; Chen, D. Spectral Properties of Er3+/Tm3+ Co-Doped ZBLAN Glasses and Fibers. Materials 2017, 10, 486. [Google Scholar] [CrossRef] [PubMed]
  2. Zhang, M.; Wen, H.; Pan, X.; Yu, J.; Shao, H.; Ai, F.; Yu, H.; Tang, M.; Gai, L. Study on Upconversion and Thermal Properties of Tm3+/Yb3+ Co-Doped La2O3-Nb2O5-Ta2O5 Glasses. Materials 2018, 11, 1352. [Google Scholar] [CrossRef] [PubMed]
  3. Ragin, T.; Baranowska, A.; Kochanowicz, M.; Zmojda, J.; Miluski, P.; Dorosz, D. Study of Mid-Infrared Emission and Structural Properties of Heavy Metal Oxide Glass and Optical Fibre Co-Doped with Ho3+/Yb3+ Ions. Materials 2019, 12, 1238. [Google Scholar] [CrossRef] [PubMed]
  4. Ye, Y.; Wang, S.; An, H. White-light emission and chromaticity characterization of Dy3+ doped fluoride glass for standard white light source. J. Non Cryst. Solids 2019, 526, 119697. [Google Scholar] [CrossRef]
  5. Li, B.; Li, D.; Pun, E.Y.B.; Lin, H. Dy3+ doped tellurium-borate glass phosphors for laser-driven white illumination. J. Lumin. 2019, 206, 70–78. [Google Scholar] [CrossRef]
  6. Balaji Rao, R.; Gerhardt, R.A. Effect of alkaline earth modifier ion on the optical, magnetic and electrical properties of lithium nickel borate glasses. Mater. Chem. Phys. 2008, 112, 186–197. [Google Scholar] [CrossRef]
  7. Pavić, L.; Fazinić, S.; Ertap, H.; Karabulut, M.; Moguš-Milanković, A.; Šantić, A. Polaronic Conductivity in Iron Phosphate Glasses Containing B2O3. Materials 2020, 13, 2505. [Google Scholar] [CrossRef]
  8. Balakrishna, A.; Rajesh, D.; Ratnakaram, Y.C. Spectroscopic analysis of Ho3+ transitions in different modifier oxide based lithium-fluoro-borate glasses. Physica B 2014, 450, 58–66. [Google Scholar] [CrossRef]
  9. Naga Raju, G.; Venkateswara Rao, P.; Ravi Kumar, V.; Chandrakala, C.; Ashok, J. Study on the influence of TiO2 on the characteristics of multi component modifier oxide based B2O3 glass system. J. Non Cryst. Solids 2018, 498, 309–314. [Google Scholar] [CrossRef]
  10. Prasad, R.N.A.; Siva, B.V.; Neeraja, K.; Krishna Mohan, N.; Rojas, J.I. Influence of modifier oxides on spectroscopic features of Nd2O3 doped PbO-Ro2O3–WO3–B2O3 glasses (with Ro2O3 = Sb2O3, Al2O3, and Bi2O3). J. Lumin. 2020, 223, 117171. [Google Scholar] [CrossRef]
  11. Liu, C.; Zhuang, Y.; Han, J.; Ruan, J.; Liu, C.; Zhao, X. Multi-band near-infrared emission in low concentration bismuth doped alkaline earth alumino-boro-germanate glass. Ceram. Int. 2020, 46, 15544–15553. [Google Scholar] [CrossRef]
  12. Reddy, K.S.R.K.; Swapna, K.; Mahamuda, S.; Venkateswarlu, M.; Rao, A.S.; Vijaya Prakash, G. Investigation on structural and luminescence features of Dy3+ ions doped alkaline-earth boro tellurite glasses for optoelectronic devices. Opt. Mater. 2018, 85, 200–210. [Google Scholar] [CrossRef]
  13. Griebenow, K.; Bragatto, C.B.; Kamitsos, E.I.; Wondraczek, L. Mixed-modifier effect in alkaline earth metaphosphate glasses. J. Non Cryst. Solids 2018, 481, 447–456. [Google Scholar] [CrossRef]
  14. Kaky, K.M.; Lakshminarayana, G.; Baki, S.O.; Taufiq-Yap, Y.H.; Kityk, I.V.; Mahdi, M.A. Structural, thermal, and optical analysis of zinc boro-aluminosilicate glasses containing different alkali and alkaline modifier ions. J. Non Cryst. Solids 2017, 456, 55–63. [Google Scholar] [CrossRef]
  15. Leśniak, M.; Szal, R.; Starzyk, B.; Gajek, M.; Kochanowicz, K.; Żmojda, J.; Miluski, P.; Dorosz, J.; Sitarz, M.; Dorosz, D. Influence of barium oxide on glass-forming ability and glass stability of the tellurite-phosphate oxide glasses. J. Therm. Anal. Calorim. 2019, 138, 4295–4302. [Google Scholar] [CrossRef]
  16. Pavić, L.; Moguš-Milanković, A.; Raghava Rao, P.; Šantić, A.; Ravi Kumar, V.; Veeraiah, N. Effect of alkali-earth modifier ion on electrical, dielectric and spectroscopic properties of Fe2O3 doped Na2SO4-MO-P2O5 glass system. J. Alloys Compd. 2014, 604, 352–362. [Google Scholar] [CrossRef]
  17. Ratnakaram, Y.C.; Balakrishna, A.; Rajesh, D. Effect of modifier oxides on absorption and emission properties of Eu3+ doped different lithium fluoroborate glass matrices. Physica B 2012, 407, 4303–4307. [Google Scholar] [CrossRef]
  18. Reddy, K.S.R.K.; Swapna, K.; Venkateswarlu, M.; Mahamuda, S.; Rao, A.S. Thermal, Up-Conversion and Near-Infrared Luminescence studies of Erbium ions doped Alkaline-Earth Boro Tellurite glasses. Solid State Sci. 2019, 97, 106016. [Google Scholar] [CrossRef]
  19. Luewarasirikul, N.; Kaewkhao, J. The effect of alkaline earth on luminescence properties of A-Na-B glasses (A = Mg, Ca, Sr and Ba) doped with Dy2O3. Mater. Today Proc. 2018, 5, 15098–15103. [Google Scholar] [CrossRef]
  20. Sudhakar, K.S.V.; Srinivasa Reddy, M.; Srinivasa Rao, L.; Veeraiah, N. Influence of modifier oxide on spectroscopic and thermoluminescence characteristics of Sm3+ ion in antimony borate glass system. J. Lumin. 2008, 128, 1791–1798. [Google Scholar] [CrossRef]
  21. Ashirvadam, A.; Ravi Kumar, V.; Naga Raju, G. Influence of modifier oxide on emission features of Sm3+ ion in lithium antimonate glasses. Mater. Today Proc. 2018, 5, 26191–26198. [Google Scholar] [CrossRef]
  22. Ravi Kumar, V.; Giridhar, G.; Veeraiah, N. Influence of modifier oxide on emission features of Dy3+ ion in Pb3O4-ZnO-P2O5 glasses. Opt. Mater. 2016, 60, 594–600. [Google Scholar] [CrossRef]
  23. Balakrishna, A.; Rajesh, D.; Ratnakaram, Y.C. Structural and optical properties of Nd3+ in lithium fluoro-borate glass with relevant modifier oxides. Opt. Mater. 2013, 35, 2670–2676. [Google Scholar] [CrossRef]
  24. Petit, L. Radiation effects on phosphate glasses: Review. Int. J. Appl. Glass Sci. 2020, 11, 511–521. [Google Scholar] [CrossRef]
  25. Ojha, N.; Tuomisto, M.; Lastusaari, M.; Petit, L. Phosphate glasses with blue persistent luminescence prepared using the direct doping method. Opt. Mater. 2019, 87, 151–156. [Google Scholar] [CrossRef]
  26. Boetti, N.G.; Scarpignato, G.C.; Lousteau, J.; Pugliese, D.; Bastard, L.; Broquin, J.-E.; Milanese, D. High concentration Yb-Er co-doped phosphate glass for optical fiber amplification. J. Opt. 2015, 17, 065705. [Google Scholar] [CrossRef]
  27. Stępień, R.; Franczyk, M.; Pysz, D.; Kujawa, I.; Klimczak, M.; Buczyński, R. Ytterbium-Phosphate Glass for Microstructured Fiber Laser. Materials 2014, 7, 4723–4738. [Google Scholar] [CrossRef]
  28. Filho, J.C.; Messias, D.N.; Pilla, V.; Silva, A.C.; Dantas, N.O.; Andrade, A.A. Temperature-dependence on the lifetime of Nd3+-doped phosphate glass. J. Lumin. 2020, 219, 116901. [Google Scholar] [CrossRef]
  29. Damodaraiah, S.; Reddy Prasad, V.; Ratnakaram, Y.C. Structural and luminescence properties of Sm3+-doped bismuth phosphate glass for orange-red photonic applications. Luminescence 2018, 33, 594–603. [Google Scholar] [CrossRef] [PubMed]
  30. Félix-Quintero, H.; Mejía-Uriarte, E.V.; Falcony, C.; Acosta, D.; Hernández A, J.; Flores J, C.; Camarillo G, E.; Murrieta S, H. Tunable white light emission through energy transfer processes between silver species in Ag-doped zinc phosphate glass. J. Lumin. 2020, 222, 117122. [Google Scholar] [CrossRef]
  31. Marcondes, L.M.; Santagneli, S.H.; Manzani, D.; Cassanjes, F.C.; Batista, G.; Mendoza, V.G.; da Cunha, C.R.; Poirier, G.Y.; Nalin, M. High tantalum oxide content in Eu3+-doped phosphate glass and glass-ceramics for photonic applications. J. Alloys Compd. 2020, 842, 155853. [Google Scholar] [CrossRef]
  32. Dousti, M.R.; Poirier, G.Y.; de Camargo, A.S.S. Tungsten sodium phosphate glasses doped with trivalent rare earth ions (Eu3+, Tb3+, Nd3+ and Er3+) for visible and near-infrared applications. J. Non Cryst. Solids 2020, 530, 119838. [Google Scholar] [CrossRef]
  33. Zhuang, Y.; Mingming, L.; Li, J.; Tang, J.; Cao, W.; Wu, Z. Optical properties of Er3+/Yb3+ co-doped phosphate glass system for NIR lasers and fiber amplifiers. Ceram. Int. 2018, 44, 22467–22472. [Google Scholar] [CrossRef]
  34. Kummara, V.K.; Neelima, G.; Ravi, N.; Nallabala, N.K.R.; Reddy, H.S.K.; Dwaraka Viswanath, C.S.; Lenine, D.; Surekha, G.; Padma Suvarna, R.; Yuvaraj, C.; et al. Near infrared broadband and visible upconversion emissions of erbium ions in oxyfluoride glasses for optical amplifier applications. Opt. Laser Technol. 2020, 127, 106167. [Google Scholar] [CrossRef]
  35. Morassuti, C.Y.; Nunes, L.A.O.; Lima, S.M.; Andrade, L.H.C. Eu3+-doped alumino-phosphate glass for ratiometric thermometer based on the excited state absorption. J. Lumin. 2018, 193, 39–43. [Google Scholar] [CrossRef]
  36. Xiao, Y.B.; Ji, Y.; Liu, J.L.; Wang, W.C. Nd3+-doped mixed-anion fluoro-sulfo-phosphate glass for 1.06 μm solid-state laser. J. Non Cryst. Solids 2019, 522, 119586. [Google Scholar] [CrossRef]
  37. Boetti, N.G.; Pugliese, D.; Ceci-Ginistrelli, E.; Lousteau, J.; Janner, D.; Milanese, D. Highly Doped Phosphate Glass Fibers for Compact Lasers and Amplifiers: A Review. Appl. Sci. 2017, 7, 1295. [Google Scholar] [CrossRef]
  38. Santos, C.C.; Guedes, I.; Loong, C.-K.; Boatner, L.A.; Moura, A.L.; de Araujo, M.T.; Jacinto, C.; Vermelho, M.V.D. Spectroscopic properties of Er3+-doped lead phosphate glasses for photonic application. J. Phys. D Appl. Phys. 2010, 43, 025102. [Google Scholar] [CrossRef]
  39. Chen, Y.; Chen, G.; Liu, X.; Xu, J.; Zhou, X.; Yang, T.; Yuan, C.; Zhou, C. Upconversion luminescence, optical thermometric properties and energy transfer in Yb3+/Tm3+ co-doped phosphate glass. Opt. Mater. 2018, 81, 78–83. [Google Scholar] [CrossRef]
  40. Aryal, P.; Kim, H.J.; Khan, A.; Saha, S.; Kang, S.J.; Kothan, S.; Yamsuk, Y.; Kaewkhao, J. Development of Eu3+-doped phosphate glass for red luminescent solid-state optical devices. J. Lumin. 2020, 227, 117564. [Google Scholar] [CrossRef]
  41. Huerta, E.F.; Meza-Rocha, A.N.; Lozada-Morales, R.; Speghini, A.; Bordignon, S.; Caldiño, U. White, yellow and reddish-orange light generation in lithium-aluminum-zinc phosphate glasses co-doped with Dy3+/Tb3+ and tri-doped with Dy3+/Tb3+/Eu3+. J. Lumin. 2020, 219, 116882. [Google Scholar] [CrossRef]
  42. Huerta, E.F.; Soriano-Romero, O.; Meza-Rocha, A.N.; Bordignon, S.; Speghini, A.; Caldiño, U. Lithium-aluminum-zinc phosphate glasses activated with Sm3+, Sm3+/Eu3+ and Sm3+/Tb3+ for reddish-orange and white light generation. J. Alloys Compd. 2020, 846, 156332. [Google Scholar] [CrossRef]
  43. Yan, Y.; Faber, A.J.; de Waal, H. Luminescence quenching by OH groups in highly Er-doped phosphate glasses. J. Non Cryst. Solids 1995, 181, 283–290. [Google Scholar] [CrossRef]
  44. Yan, Y.C.; Faber, A.J.; de Waal, H.; Kik, P.G.; Polman, A. Erbium-doped phosphate glass waveguide on silicon with 4.1 dB/cm gain at 1.535 μm. Appl. Phys. Lett. 1997, 71, 2922–2924. [Google Scholar] [CrossRef]
  45. Lopez-Iscoa, P.; Salminen, T.; Hakkarainen, T.; Petit, L.; Janner, D.; Boetti, N.G.; Lastusaari, M.; Pugliese, D.; Paturi, P.; Milanese, D. Effect of partial crystallization on the structural and luminescence properties of Er3+-doped phosphate glasses. Materials 2017, 10, 473. [Google Scholar] [CrossRef]
  46. Lopez-Iscoa, P.; Ojha, N.; Aryal, U.; Pugliese, D.; Boetti, N.G.; Milanese, D.; Petit, L. Spectroscopic properties of Er3+-doped particles-containing phosphate glasses fabricated using the direct doping method. Materials 2019, 12, 129. [Google Scholar] [CrossRef]
  47. Lopez-Iscoa, P.; Petit, L.; Massera, J.; Janner, D.; Boetti, N.G.; Pugliese, D.; Fiorilli, S.; Novara, C.; Giorgis, F.; Milanese, D. Effect of the addition of Al2O3, TiO2 and ZnO on the thermal, structural and luminescence properties of Er3+-doped phosphate glasses. J. Non Cryst. Solids 2017, 460, 161–168. [Google Scholar] [CrossRef]
  48. Ren, J.; Eckert, H. Intermediate role of gallium in oxidic glasses: Solid state NMR structural studies of the Ga2O3-NaPO3 system. J. Phys. Chem. 2014, 118, 15386–15403. [Google Scholar] [CrossRef]
  49. Yoshimoto, K.; Masuno, A.; Ueda, M.; Inoue, H.; Yamamoto, H.; Kawashima, T. Low phonon energies and wideband optical windows of La2O3-Ga2O3 glasses prepared using an aerodynamic levitation techniques. Sci. Rep. 2017, 7, 45600. [Google Scholar] [CrossRef]
  50. Ling, Z.; Ya-Xun, Z.; Shi-Xun, D.; Tie-Feng, X.; Qiu-Hua, N.; Xiang, S. Effect of Ga2O3 on the spectroscopic properties of erbium-doped boro-bismuth glasses. Spectrochim. Acta A 2007, 68, 548–553. [Google Scholar] [CrossRef]
  51. Venkatramu, V.; Vijaya, R.; León-Luis, S.F.; Babu, P.; Jayasankar, C.K.; Lavín, V.; Dhareshwar, L.J. Optical properties of Yb3+-doped phosphate laser glasses. J. Alloys Compd. 2011, 509, 5084–5089. [Google Scholar] [CrossRef]
  52. Jha, K.; Vishwakarma, A.K.; Jayasimhadri, M.; Haranath, D. Multicolor and white light emitting Tb3+/Sm3+ co-doped zinc phosphate barium titanate glasses via energy transfer for optoelectronic device applications. J. Alloys Compd. 2017, 719, 116–124. [Google Scholar] [CrossRef]
  53. Pisarska, J.; Sołtys, M.; Żur, L.; Pisarski, W.A.; Jayasankar, C.K. Excitation and luminescence of rare earth-doped lead phosphate glasses. Appl. Phys. B 2014, 116, 837–845. [Google Scholar] [CrossRef]
  54. Terra, I.A.A.; de Camargo, A.S.S.; Nunes, L.A.D.O.; Carvalho, R.A.; Li, M.S. Evaluation of the OH- influence on visible and near-infrared quantum efficiencies of Tm3+ and Yb3+ codoped sodium aluminophoshate glasses. J. Appl. Phys. 2006, 100, 123103. [Google Scholar] [CrossRef]
  55. Stoch, P.; Stoch, A.; Ciecinska, M.; Krakowiak, I.; Sitarz, M. Structure of phosphate and iron-phosphate glasses by DFT calculations and FTIR/Raman spectroscopy. J. Non Cryst. Solids 2016, 450, 48–60. [Google Scholar] [CrossRef]
  56. Moustafa, Y.M.; El-Egili, K. Infrared spectra of sodium phosphate glasses. J. Non Cryst. Solids 1998, 240, 144–153. [Google Scholar] [CrossRef]
  57. Pascuta, P.; Borodi, G.; Jumate, N.; Vida-Simiti, I.; Viorel, D.; Culea, E. The structural role of manganese ions in some zinc phosphate glasses and glass ceramics. J. Alloys Compd. 2010, 504, 479–483. [Google Scholar] [CrossRef]
  58. Jha, P.K.; Pandey, O.P.; Singh, K. FTIR spectral analysis and mechanical properties of sodium phosphate glass-ceramics. J. Mol. Struct. 2015, 1083, 278–285. [Google Scholar] [CrossRef]
  59. Lai, Y.; Liang, X.; Yang, S.; Liu, P.; Zeng, Y.; Hu, C. Raman and FTIR spectra of CeO2 and Gd2O3 in iron phosphate glasses. J. Alloys Compd. 2014, 617, 597–601. [Google Scholar] [CrossRef]
  60. Little Flower, G.; Srinivasa Reddy, M.; Sahaya Baskaran, G.; Veeraiah, N. The structural influence of chromium ions in lead gallium phosphate glasses by means of spectroscopic studies. Opt. Mater. 2007, 30, 357–363. [Google Scholar] [CrossRef]
  61. Ilieva, D.; Jivov, B.; Bogachev, G.; Petkov, C.; Penkov, I.; Dimitriev, Y. Infrared and Raman spectra of Ga2O3-P2O5 glasses. J. Non Cryst. Solids 2011, 283, 195–202. [Google Scholar] [CrossRef]
  62. Vedeanu, N.; Magdas, D.A.; Stefan, R. Structural modifications induced by addition of copper oxide to lead-phosphate glasses. J. Non Cryst. Solids 2012, 358, 3170–3174. [Google Scholar] [CrossRef]
  63. Reza Dousti, M.; Amjad, R.J. Spectroscopic properties of Tb3+-doped lead zinc phosphate glass for green solid state laser. J. Non Cryst. Solids 2015, 420, 21–25. [Google Scholar] [CrossRef]
  64. Lakshmikantha, R.; Rajaramakrishna, R.; Anavekar, R.V.; Ayachit, N.H. Characterization and structural studies of lithium doped lead zinc phosphate glass system. Mater. Chem. Phys. 2012, 133, 249–252. [Google Scholar] [CrossRef]
  65. Liu, H.S.; Chin, T.S.; Yung, S.W. FTIR and XPS studies of low-melting PbO-ZnO-P2O5 glasses. Mater. Chem. Phys. 1997, 50, 1–10. [Google Scholar] [CrossRef]
  66. Magdas, D.A.; Cozar, O.; Chis, V.; Ardelean, I.; Vedeanu, N. The structural dual role of Fe2O3 in some lead-phosphate glasses. Vib. Spectrosc. 2008, 48, 251–254. [Google Scholar] [CrossRef]
  67. Qian, B.; Liang, X.; Wang, C.; Yang, S. Structure and properties of calcium iron phosphate glasses. J. Nucl. Mater. 2013, 443, 140–144. [Google Scholar] [CrossRef]
  68. Suneel Kumar, A.; Narendrudu, T.; Suresh, S.; Sambasiva Rao, M.V.; Chinna Ram, G.; Krishna Rao, D. Role of titanium ions on the physical and structural properties of calcium zinc bismuth phosphate glass ceramics. J. Non Cryst. Solids 2016, 434, 62–70. [Google Scholar] [CrossRef]
  69. Yadav, A.K.; Singh, P. A review of the structures of oxide glasses by Raman spectroscopy. RSC Adv. 2015, 5, 67583–67609. [Google Scholar] [CrossRef]
  70. Wang, C.; Liang, X.; Li, H.; Yu, H.; Li, Z.; Yang, S. Structure and properties of gadolinium loaded calcium phosphate glasses. J. Nucl. Mater. 2014, 453, 220–224. [Google Scholar] [CrossRef]
  71. Kuczek, J.; Jeleń, P.; Stoch, P.; Błachowski, A.; Wacławska, I.; Szumera, M. Raman and Mössbauer studies of iron phosphate-silicate glasses. J. Mol. Struct. 2018, 1170, 82–89. [Google Scholar] [CrossRef]
  72. Ivascu, C.; Timar Gabor, A.; Cozar, O.; Daraban, L.; Ardelean, I. FT-IR, Raman and thermoluminescence investigation of P2O5–BaO–Li2O glass system. J. Mol. Struct. 2011, 993, 249–253. [Google Scholar] [CrossRef]
  73. Deopa, N.; Sumandeep, K.; Prasad, A.; Joshi, B.; Rao, A.S. Spectral studies of Eu3+ doped lithium lead alumino borate glasses for visible photonic applications. Opt. Laser Technol. 2018, 108, 434–440. [Google Scholar] [CrossRef]
  74. Żmojda, J.; Kochanowicz, M.; Miluski, P.; Golonko, P.; Baranowska, A.; Ragiń, T.; Dorosz, J.; Kuwik, M.; Pisarski, W.; Pisarska, J.; et al. Luminescent Studies on Germanate Glasses Doped with Europium Ions for Photonic Applications. Materials 2020, 13, 2817. [Google Scholar] [CrossRef] [PubMed]
  75. Pawlik, N.; Szpikowska-Sroka, B.; Sołtys, M.; Pisarski, W.A. Optical properties of silica sol-gel materials singly- and doubly-doped with Eu3+ and Gd3+ ions. J. Rare Earths 2016, 34, 786–795. [Google Scholar] [CrossRef]
  76. Jha, K.; Jayasimhadri, X.; Haranath, D.; Jang, K. Influence of modifier oxides on spectroscopic properties of Eu3+ doped oxy-fluoro tellurophosphate glasses for visible photonic applications. J. Alloys Compd. 2019, 789, 622–629. [Google Scholar] [CrossRef]
  77. Kirdsiri, K.; Rajaramakrishna, R.; Damdee, B.; Kim, H.J.; Nuntawong, N.; Horphathum, M.; Kaewkhao, J. Influence of alkaline earth oxides on Eu3+ doped lithium borate glasses for photonic, laser and radiation detection material applications. Solid State Sci. 2019, 89, 57–66. [Google Scholar] [CrossRef]
  78. Herrmann, A.; Kuhn, S.; Tiegel, M.; Rüssel, C. Fluorescence properties of Eu3+-doped alumino silicate glasses. Opt. Mater. 2014, 37, 293–297. [Google Scholar] [CrossRef]
  79. Pugliese, D.; Boetii, N.G.; Lousteau, J.; Ceci-Genistrelli, E.; Bertone, E.; Geobaldo, F.; Milanese, D. Concentration quenching in an Er-doped phosphate glass for compact optical lasers and amplifiers. J. Alloys Compd. 2016, 657, 678–683. [Google Scholar] [CrossRef]
  80. Rivera-López, F.; Babu, P.; Jyothi, L.; Rodríguez-Mendoza, U.R.; Martín, I.R.; Jayasankar, C.K.; Lavín, V. Er3+–Yb3+ codoped phosphate glasses used for an efficient 1.5 μm broadband gain medium. Opt. Mater. 2012, 34, 1235–1240. [Google Scholar] [CrossRef]
  81. Wang, R.; Zhou, D.; Zhao, Z.; Yang, Z.; Song, Z.; Zhu, K.; Xu, Y.; Qiu, J. Effect of optical basicity on broadband infrared fluorescence in erbium-doped germanate glasses. J. Alloys Compd. 2012, 513, 339–342. [Google Scholar] [CrossRef]
  82. Janek, J.; Sołtys, M.; Żur, L.; Pietrasik, E.; Pisarska, J.; Pisarski, W.A. Luminescence investigations of rare earth doped lead-free borate glasses modified by MO (M = Ca, Sr, Ba). Mater. Chem. Phys. 2016, 180, 237–243. [Google Scholar] [CrossRef]
  83. Zur, L.; Janek, J.; Pietrasik, E.; Sołtys, M.; Pisarska, J.; Pisarski, W.A. Influence of MO/MF2 modifiers (M = Ca, Sr, Ba) on spectroscopic properties of Eu3+ ions in germanate and borate glasses. Opt. Mater. 2016, 61, 59–63. [Google Scholar] [CrossRef]
  84. Cherbib, M.A.; Kapoor, S.; Bockowski, M.; Smedskjaer, M.M.; Wondraczek, L. Luminescence behavior of Eu3+ in hot-compressed silicate glasses. J. Non Cryst. Solids X 2019, 4, 100041. [Google Scholar] [CrossRef]
  85. Stambouli, W.; Elhouichet, H.; Gelloz, B.; Férid, M. Optical and spectroscopic properties of Eu-doped tellurite glasses and glass ceramics. J. Lumin. 2013, 138, 201–208. [Google Scholar] [CrossRef]
  86. Pisarski, W.A.; Żur, L.; Goryczka, T.; Sołtys, M.; Pisarska, J. Structure and spectroscopy of rare earth—Doped lead phosphate glasses. J. Alloys Compd. 2014, 587, 90–98. [Google Scholar] [CrossRef]
  87. Żur, L.; Janek, J.; Sołtys, M.; Pisarska, J.; Pisarski, W.A. Spectroscopic properties of Eu3+, Dy3+ and Tb3+ ions in lead silicate glasses obtained by the conventional high-temperature melt-quenching technique. Phys. Scr. 2013, 2013, 014035. [Google Scholar] [CrossRef]
  88. Ramesh, P.; Hegde, V.; Pramod, A.G.; Eraiah, B.; Agarkov, D.A.; Eliseeve, G.M.; Pandey, M.K.; Annapurna, K.; Jagannath, G.; Kokila, M.K. Compositional dependence of red photoluminescence of Eu3+ ions in lead and bismuth containing borate glasses. Solid State Sci. 2020, 107, 106360. [Google Scholar] [CrossRef]
  89. Gökçe, M. Development of Eu3+ doped bismuth germanate glasses for red laser applications. J. Non Cryst. Solids 2019, 505, 272–278. [Google Scholar] [CrossRef]
  90. Wei, T.; Chen, F.; Tian, Y.; Xu, S. Broadband 1.53 μm emission property in Er3+ doped germa-silicate glass for potential optical amplifier. Opt. Commun. 2014, 315, 199–203. [Google Scholar] [CrossRef]
  91. Yu, C.; He, D.; Wang, G.; Zhang, J.; Hu, L. Influence of cationic field strength of modifiers on the 1.53 μm spectroscopic properties of Er3+-doped tellurite glasses. J. Non Cryst. Solids 2009, 355, 2250–2253. [Google Scholar] [CrossRef]
  92. Sołtys, M.; Żur, L.; Pisarska, J.; Goryczka, T.; Pisarski, W.A. Selective oxide modifiers M2O3 (M = Al, Ga) as crystallizing agents in Er3+-doped lead phosphate glass host. Ceram. Int. 2015, 41, 4334–4339. [Google Scholar] [CrossRef]
Materials 13 04746 g001
Figure 1. Deconvoluted near-infrared spectra of phosphate glass with CaO as oxide glass modifier.
Figure 1. Deconvoluted near-infrared spectra of phosphate glass with CaO as oxide glass modifier.
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Figure 2. Deconvoluted near-infrared spectra of phosphate glass with SrO as oxide glass modifier.
Figure 2. Deconvoluted near-infrared spectra of phosphate glass with SrO as oxide glass modifier.
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Figure 3. Deconvoluted near-infrared spectra of phosphate glass with BaO as oxide glass modifier.
Figure 3. Deconvoluted near-infrared spectra of phosphate glass with BaO as oxide glass modifier.
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Figure 4. Deconvoluted Raman spectra of phosphate glass with CaO as oxide glass modifier.
Figure 4. Deconvoluted Raman spectra of phosphate glass with CaO as oxide glass modifier.
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Figure 5. Deconvoluted Raman spectra of phosphate glass with SrO as oxide glass modifier.
Figure 5. Deconvoluted Raman spectra of phosphate glass with SrO as oxide glass modifier.
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Figure 6. Deconvoluted Raman spectra of phosphate glass with BaO as oxide glass modifier.
Figure 6. Deconvoluted Raman spectra of phosphate glass with BaO as oxide glass modifier.
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Figure 7. Excitation spectra for Eu3+-doped phosphate glasses with oxide glass modifiers MO.
Figure 7. Excitation spectra for Eu3+-doped phosphate glasses with oxide glass modifiers MO.
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Figure 8. Luminescence spectra for Eu3+-doped phosphate glasses with oxide glass modifiers MO.
Figure 8. Luminescence spectra for Eu3+-doped phosphate glasses with oxide glass modifiers MO.
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Materials 13 04746 g009
Figure 9. Luminescence decay curves for 5D0 state of Eu3+ ions in phosphate glass with oxide glass modifiers MO.
Figure 9. Luminescence decay curves for 5D0 state of Eu3+ ions in phosphate glass with oxide glass modifiers MO.
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Materials 13 04746 g010
Figure 10. Excitation spectra for Er3+-doped phosphate glasses with oxide glass modifiers MO.
Figure 10. Excitation spectra for Er3+-doped phosphate glasses with oxide glass modifiers MO.
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Materials 13 04746 g011
Figure 11. Luminescence spectra for Er3+-doped phosphate glasses with oxide glass modifiers MO.
Figure 11. Luminescence spectra for Er3+-doped phosphate glasses with oxide glass modifiers MO.
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Materials 13 04746 g012
Figure 12. Luminescence decay curves for 4I13/2 state of Er3+ ions in phosphate glasses with oxide glass modifiers MO.
Figure 12. Luminescence decay curves for 4I13/2 state of Er3+ ions in phosphate glasses with oxide glass modifiers MO.
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Table 1. Band positions and their assignments.
Table 1. Band positions and their assignments.
BandFrequency (cm−1)Band AssignmentReferences
(I)499/488/452 cm−1harmonics of bending vibrations of O=P–O linkages[57]
(II)640/639/588 cm−1stretching vibrations the M–O–P bonds
stretching vibrations of P–O–P mode
bending vibrations of O–P–O modes		[58,59]
(III)708/725/722 cm−1symmetric stretching vibrations of P–O–P linkages in between Q1 and Q2[58]
(IV)772/772/784 cm−1symmetric stretching mode of P–O–P bonds[62]
(V)910/891/877 cm−1asymmetric stretching vibrations
of bridging oxygen atoms in P–O–P bonds
asymmetric stretching vibrations of the P–O–P linkage of Q1 and Q2 tetrahedra with non-bridging oxygen		[63,64]
(VI)1006/1009/949 cm−1asymmetric stretching vibrations of
PO43− structural group		[66]
(VII)1086/1087/1079 cm−1symmetric stretching vibrations of PO43− tetrahedral (PO− ionic group)
symmetric stretching vibrations of PO32− in the Q1 tetrahedra		[66,67]
(VIII)1173/1182/1161 cm−1asymmetric stretching vibrations of PO2− in the Q2 tetrahedra[67]
(IX)1255/1258/1240 cm−1P=O stretching vibration of PO2− groups[68]
(X)1304/1301/1303 cm−1harmonic of the doubly bonded oxygen vibration[58]
Table 2. Band positions and their assignments.
Table 2. Band positions and their assignments.
BandFrequency (cm−1)Band AssignmentReferences
(I)350/342/312 cm−1GaO6 vibrational groups[69]
(II)413/392/381 cm−1Ga-O-P linkages bending vibrations of PO4 units[68,69]
(III)535/538/530 cm−1bending vibrations of P2O74− groups[58]
(IV)625/626/607 cm−1symmetric stretching vibrations of P–O– terminal bonds[70]
(V)710/708/695 cm−1symmetric stretching vibrations of P–O–P bonds in Q2 metaphosphate tetrahedra[70]
(VI)758/757/738 cm−1symmetric stretching vibrations of P–O–P bonds associated with Q1 tetrahedra[55,70]
(VII)1096/1104/1117 cm−1
(VIII)1147/1135/1148 cm−1symmetric stretching modes of non-bridging atoms on Q2 tetrahedra[72]
(IX)1165/1156/1176 cm−1
(X)1248/1251/1260 cm−1symmetric stretching of P–O bonds[69]
(XI)1297/1284/1312 cm−1stretching vibrations of non-bridging bonds PO2− of Q2 metaphosphate tetrahedra
P=O stretching of terminal oxygen		[71]
Table 3. Spectroscopic parameters for Ln+-doped phosphate glasses.
Table 3. Spectroscopic parameters for Ln+-doped phosphate glasses.
Ln3+Spectroscopic ParameterOxide Glass Modifier
CaOSrOBaO
Eu3+λmax 5D0→7F1 (nm)590.5590.5591.0
λmax 5D0→7F2 (nm)611.0610.5611.0
R/O3.773.293.09
τm (ms)2.06 ± 0.00132.15 ± 0.00152.20 ± 0.0013
Er3+λmax 4I13/2→4I15/2 (nm)154015401539
FWHM (nm)444344
τm (μs)640 ± 0.66888 ± 0.65920 ± 0.71
Table 4. Comparison of luminescence lifetime for 5D0 state (Eu3+) of inorganic glasses.
Table 4. Comparison of luminescence lifetime for 5D0 state (Eu3+) of inorganic glasses.
Glass Compositionτm for 5D0 State of Eu3+ (ms)References
P2O5-Ga2O3-BaO-Eu2O32.20 ± 0.0013present work
B2O3-Ga2O3-BaO-Eu2O31.60[82]
GeO2-Ga2O3-BaO-Eu2O31.22[83]
Li2O-BaO-B2O3-Eu2O31.81[77]
SiO2-Al2O3-BaO-Eu2O32.17[78]
SiO2-MgO-CaO-Na2O-K2O-Eu2O32.55[84]
TeO2-La2O3-TiO2-Eu2O30.82[85]
PbO-P2O5-Ga2O3-Eu2O32.02[86]
PbO-SiO2-Ga2O3-Eu2O31.27[87]
La2O3-Bi2O3-B2O3-Eu2O31.01[88]
La2O3-PbO-B2O3-Eu2O31.29[88]
Bi2O3-GeO2-Eu2O31.03[89]
Table 5. Comparison of parameters FWHM for band at 1.5 μm (Er3+), luminescence lifetime for 4I13/2 state (Er3+) of inorganic glasses.
Table 5. Comparison of parameters FWHM for band at 1.5 μm (Er3+), luminescence lifetime for 4I13/2 state (Er3+) of inorganic glasses.
Glass CompositionFWHM (nm)τm for 4I13/2 State of Er3+ (ms)References
P2O5-Ga2O3-BaO-Er2O3440.92 ± 0.0071present work
B2O3-Ga2O3-BaO-Er2O3980.42[82]
GeO2-Ga2O3-BaO-Er2O3505.35[83]
P2O5-Li2O-Al2O3-BaO-MgO-Gd2O3-Er2O3307.01[79]
P2O5-K2O-BaO-Al2O3-Yb2O3-Er2O3370.78[80]
SiO2-GeO2-CaO-BaO-Nb2O-Li2O-Er2O3770.78[90]
TeO2-ZnO-BaO-Er2O3464.70[91]
PbO-P2O5-Ga2O3-Er2O3522.50[92]
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Kuwik, M.; Pisarska, J.; Pisarski, W.A. Influence of Oxide Glass Modifiers on the Structural and Spectroscopic Properties of Phosphate Glasses for Visible and Near-Infrared Photonic Applications. Materials 2020, 13, 4746. https://doi.org/10.3390/ma13214746

AMA Style

Kuwik M, Pisarska J, Pisarski WA. Influence of Oxide Glass Modifiers on the Structural and Spectroscopic Properties of Phosphate Glasses for Visible and Near-Infrared Photonic Applications. Materials. 2020; 13(21):4746. https://doi.org/10.3390/ma13214746

Chicago/Turabian Style

Kuwik, Marta, Joanna Pisarska, and Wojciech A. Pisarski. 2020. "Influence of Oxide Glass Modifiers on the Structural and Spectroscopic Properties of Phosphate Glasses for Visible and Near-Infrared Photonic Applications" Materials 13, no. 21: 4746. https://doi.org/10.3390/ma13214746

APA Style

Kuwik, M., Pisarska, J., & Pisarski, W. A. (2020). Influence of Oxide Glass Modifiers on the Structural and Spectroscopic Properties of Phosphate Glasses for Visible and Near-Infrared Photonic Applications. Materials, 13(21), 4746. https://doi.org/10.3390/ma13214746

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