Advances in Materials Science and Engineering
Volume 2017 (2017), Article ID 6790635, 7 pages
https://doi.org/10.1155/2017/6790635

Research Article

Effect of Neodymium Nanoparticles on Elastic Properties of Zinc-Tellurite Glass System

Abdulbaset A. Abdulla Awshah,¹ Halimah Mohamed Kamari,¹ Chan Kar Tim,¹ Nurisya Mohd Shah,¹ S. H. Alazoumi,¹ Umar Saad Aliyu,1,2 and Muhammad Noorazlan Abd Azis¹

¹Physics Department, Faculty of Science, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia
²Department of Physics, Faculty of Science, Bauchi State University, Gadau, Nigeria

Correspondence should be addressed to Halimah Mohamed Kamari; hmk6360@gmail.com

Received 14 February 2017; Revised 20 June 2017; Accepted 9 July 2017; Published 29 August 2017

Academic Editor: Cristina Leonelli

Copyright © 2017 Abdulbaset A. Abdulla Awshah et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The aim of this work is to determine the effect of neodymium nanoparticles concentration on the elastic properties of zinc-tellurite glass. A series of neodymium nanoparticles doped zinc-tellurite glass systems (NdNPsZT) of composition [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs), , , , , and , were synthesized by using conventional melt-quenching method. The amorphous nature of the glass system was confirmed by using XRD analysis. The density of the glass system was determined by Archimedes method. The elastic properties were calculated from the measured density and ultrasonic velocity at 5 MHz frequency. The experimental results showed that the elastic properties rely upon the composition of the glass systems and the impact of neodymium nanoparticles (Nd₂O₃ NPs) within the glass network. The increase in ultrasonic velocities is due to the increase in rigidity and change in structural units of the glass system. The softening temperature and the microhardness increased with the increase in Nd³⁺ ions concentration from 0.1 to 0.2 mol and decreased when the Nd³⁺ ions concentration increased from 0.2 to 0.5 mol. Poisson’s ratio and Debye’s temperature decreased with the increase in the Nd³⁺ ions concentration from 0.1 to 0.2 mol and increased when the Nd³⁺ ions concentration was increased from 0.2 to 0.5 mol.

1. Introduction

Tellurite glasses were found to be interesting glasses due to their unique properties and applications [1, 2]. The glass science and technology have found so much interest in tellurite glasses over the years. This may be due to their low melting points, high refractive indices, high dielectric constants, and good infrared transmission [3, 4]. Tellurite glass doped with nanoparticles system has found great interest, mostly in the study of the effect of nanosize particles on optical behavior [2].

Tellurite glasses have also been employed for the synthesis of metallic nanoparticles (NPs) and for the enlargement of metallic NPs. This is especially in the design of simple and sensitive electrochemical and optical sensors through the integration of NPs into biocatalytic reactions. Development of nanobiotechnology has been rapid with the introduction of biocatalysts on metal nanoparticles (MNPs) [3].

In recent times, neodymium oxide nanoparticles (Nd⁺ NPs) had been in the application of optical and magnetic nanomaterials due to their unique optical properties [5]. Like other lanthanides, Nd has a contracted nature of the 4f orbitals shielded by the 5s and 5p shells that affect their physical properties. Below 10 nm particle size, the quantum properties of neodymium compounds are size dependent and exhibit a secondary morphology that is well defined. Such property of Nd compounds makes them suitable for applications in surface catalytic systems, photonics, and advanced NP-based materials and protective coatings [5, 6].

Neodymium doped tellurite glasses are suitable candidates for the development of optical fibers and optical amplifiers, waveguide lasers, and color display devices [7–9]. The study of the elastic properties of glasses by using the nondestructive ultrasonic technique gives some details about the structure of the studied glasses and can be directly connected to the interatomic potentials of the glasses under probe [10, 11]. The study of the elastic properties is of fundamental importance in studying the nature of interatomic bonding and the mechanical properties of materials [12–14].

However, there is no information on elastic properties of neodymium nanoparticles doped zinc-tellurite glass. Therefore, this research is focused on the determination of the elastic properties of neodymium NPs doped zinc-tellurite glass. This is important as it will help the continued research on both scientific and technological applications of the Nd nanoparticles/compounds.

2. Experimental Section

The glass samples of Nd³⁺ doped zinc-tellurite glass system with chemical formula , , , , , and  mol, were prepared by using a conventional method of melt quenching. High purity raw materials (99.99%, purity grade) of TeO₂ (Puratronic, Alfa Aesar), ZnO (Assay, Alfa Aesar), and Nd₂O₃ nanoparticles (Assay, Alfa Aesar) were used to prepare the glass samples. The oxide components used in preparing the glasses were weighed by using a high accuracy (±0.0001 g) digital weighing machine and mixed together in an alumina crucible. The mixture was put in a furnace for 1 hour at 400°C to allow complete drying of the mixture. After heating, the mixture was transferred to a second furnace at 830°C for 90 minutes for the melting process [2]. Then, the molten sample was immediately poured into a stainless steel mould and annealed at 400°C in an electrical furnace before cooling down to room temperature [14]. All the prepared samples were cut into the required dimension, and the sample thickness (4–6 mm) was measured using a digital Vernier caliper with an accuracy of 0.0001 mm, and the samples were then polished using sandpaper to obtain parallel surfaces on both sides. The excessive glass samples were crushed into a powder form for structural analysis. Structural analysis of the prepared samples was studied using X-ray diffraction (XRD) and the FTIR analysis. The density, ρ, of the glasses was measured using electronic densimeter MD-300S based on Archimedes’ principle and the molar volume, , was calculated. The longitudinal and shear velocities for the samples were measured using the ultrasonic pulse-echo technique by Ritec Ram-5000 Snap System. All ultrasonic measurements were taken at 5 MHz frequency and at room temperature.

2.1. Elastic Modulus

Elastic moduli (longitudinal, shear, bulk, and Young’s) of [(TeO₂)0.70(ZnO)0.30] glasses were calculated from the measured ultrasonic velocities and density using the following standard relations:

 Longitudinal modulus is expressed as

 Shear modulus is expressed as

 Bulk modulus is expressed as

 Young’s modulus is expressed as

 Poisson’s Ratio. Poisson’s ratio gives the description of the sample’s expansion in a direction that is perpendicular to the applied stress [16]. It is expressed mathematically as

 Microhardness is expressed as

where and are ultrasonic longitudinal and shear velocities, respectively, and is the sample density [10, 17, 18].

 Softening temperature is expressed as

where is the molecular weight of the glass, is constantly equal to 507.4 ms−1 K−1/2, and is the number of atoms in the chemical formula [10, 17].

 Debye temperature is expressed as

 Mean ultrasonic velocity is expressed as

where is Plank’s constant, is the Boltzmann constant, is the mean ultrasonic velocity, is Avogadro’s number, and is the molar volume [17, 19].

3. Results and Discussion

The XRD spectra of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) are shown in Figure 1. The XRD pattern of the glass shows a broad hump at 20–35° for values without any distinguishable sharp peaks. Such kind of spectra indicates the characteristics of amorphous structures. There are absent sharp peaks from the XRD spectra which in turn confirms the nonexistence of a crystalline phase. This result is consistent with the previous work of many authors [20, 21].

Figure 1: XRD spectra of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

3.1. Fourier Transform Analysis

The Fourier transform infrared (FTIR) spectrometry is an analysis technique that provides structural studies to explore the basic and functional groups in crystalline and noncrystalline matrices. The result of FTIR shows the characteristics of chemical bonds that exist between elements. Absorption peaks in the spectrum represent the frequencies of vibrations between the bonds of the atom or molecule [8]. Tellurite oxide is characterized by two major structural configuration units: trigonal bipyramid (TeO₄) and trigonal pyramid (TeO₃). Pure TeO₂ is characterized by infrared absorption at around 640 cm⁻¹. The absorption band at 600–700 cm⁻¹ represents the stretching vibration of Te-O bonds in the trigonal bipyramid (TeO₄) and trigonal pyramid (TeO₃). The stretching vibration of TeO₃ group is between 650 and 700 cm⁻¹ while the stretching vibration of TeO₄ is between 600 and 650 cm⁻¹ [22].

Figure 2 shows the FTIR spectra that had been obtained within the region 250–1300 cm⁻¹ of wavenumber. The spectra contain a valley which indicates the type of bonding present. The IR characteristic of the two tellurium oxide structural units is observed in the range of 600–700 cm⁻¹. It was reported that, after glass formation, tellurium oxide is formed in two structural units, namely, trigonal pyramid (TeO₃) and trigonal pyramid (TeO₄). The primary cluster of the band is observed within the range 604.48–614.22 cm⁻¹ that correlates to the symmetrical pyramid, TeO₄ structural unit. This result is in agreement with the previous work done by Hajer et al. (2016) [15].

Figure 2: FTIR spectra of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

The presence of ZnO band does not show in the spectra, indicating that the zinc lattice is completely broken down. The formation of TeO₄ in the glass samples leads to the tight binding of oxygen anions in the glass network. Hence, increasing the TeO₄ concentration leads to a decrease in the amount of nonbridging oxygen, whereas the decrease in the concentration of TeO₄ leads to the increase in the amount of nonbridging oxygen [15, 21].

Using the FTIR spectra, the concentration of TeO₄ in each of the glass samples was calculated. In order to calculate the concentration of TeO₄, the transmission spectra were changed to absorption spectra. The area under the TeO₄ absorption curve then represents the concentration of the TeO₄ in the glass. To calculate the concentration, Origin 6.0 software was used to obtain the area under the absorption curve. The absorption value is calculated and plotted against the wavenumber, and the software can be used to calculate the area under each Gaussian absorption curve for each of the functional groups present. The area, therefore, is considered as the concentration of TeO₄ in the glass. Table 1 and Figure 3 present the variation of TeO₄ concentration against the Nd moles.

Table 1: Assignment of infrared transmission bands of the prepared glass sample with different concentrations of lanthanum neodymium oxide nanoparticles.

Number
0.01
0.02
0.03
0.04
0.05
Assignments

(1)
604.48
605.92
609.08
614.22
612.59
TeO₄ group exists in all tellurite containing glasses [15]

(2)
140.73
130.81
131
136.63
141.51
Area (TeO₄ concentration)

(3)
—
—
—
—
—
ZnO participates in the glass network

Figure 3: TeO₄ concentration of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

In this experiment, it was observed that the concentration of TeO₄ decreased as the concentration of Nd³⁺ ions increased from 0.01 to 0.02 mol, indicating an increasing amount of nonbridging oxygen. On the other hand, as the concentration of Nd³⁺ ions increases from 0.02 to 0.05 mol, the TeO₄ concentration was seen to increase steadily. The TeO₄ concentration increase indicates the closely packed network due to the formation of more bridging oxygen (BO) [23]. This trend is supported by the formation of trigonal pyramidal TeO₃ structural units within the glass system and results in a change of structural units from TeO₃ to TeO₄ with the formation of bridging oxygen [22].

3.2. Density and Molar Volume

The values of density and molar volume of glasses are tabulated in Table 2. Figure 4 shows the variation of density and molar volume. The density of the prepared glasses increased from 5346 kg/m³ to 5580 kg/m³ as the concentration of Nd₂O₃ increased from 0.01 to 0.05 mol%. The increase in density of the prepared glass is due to the substitution of lighter atoms of ZnO with heavier atoms of Nd₂O₃ which in turn increases the overall average molecular weight of the glass [18, 24].

Table 2: Density and molar volume of glasses.

ρ (±40 kg/m³)
( ±0.00722 10⁻⁵ m³/mol)

0.01
5390
2.5628

0.02
5437
2.5775

0.03
5507
2.5811

0.04
5570
2.5879

0.05
5606
2.6070

Figure 4: Density and molar volume of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

The molar volume () is defined as the volume occupied by one mol of a material and has been calculated as

where is the molecular weight of the glass sample and is the density of glass [25].

The molar volume shows increasing values from 25.464 cm³/mol to 26.192 cm³/mol as the concentration of Nd₂O₃ NPs increases from 0.01 to 0.05 mol%.

The increasing in the molar volume with the increase in Nd₂O₃ concentration (Table 2) is attributed to the increase in the amount of nonbridging oxygen (NBO). The neodymium oxide in the glass network acts as a modifier by occupying the interstitial space in the network and creating more NBO in the structure. Thus, the addition of  Nd₂O₃ NPs may eventually result in an extension of the glass network [26]. After , the increase in the molar volume may be due to the substitution of smaller atoms of Te and Zn in the network with larger atoms of Nd. In the present work, it is shown that the molar volume of the glasses increases with an increase in Nd₂O₃ NPs concentration. Hence, the increase in molar volume indicates the increasing of free volume in the glass network. This result is consistent with previous work done by Chimalawong et al. (2010) and Zaid et al. (2012) [26, 27].

3.3. Elastic Properties

The variations of shear and longitudinal ultrasonic velocities of [(TeO₂)0.70(ZnO)0.30]-Nd₂O₃ NPs glasses at room temperature are listed in Table 3 and shown in Figure 5. The measured values of the longitudinal and shear ultrasonic velocities ( and , resp.) for the studied (NdNPsZT) glass system with a variation of Nd₂O₃ content are listed in Table 3. The longitudinal and shear ultrasonic velocities decreased from 3737 to 3045 ms⁻¹ and 1959.3 to 1887.8 ms⁻¹, respectively, as the amount of Nd³⁺ NPs ions increased from 0.01 to 0.02 mol. The decrease in the ultrasonic velocities may be due to the decrease in the connectivity in the glass network caused by the increase in nonbridging oxygen (NBOs) [17].

Table 3: Ultrasonic velocities (longitudinal, shear, Young’s, and bulk modulus) and fractal bond connectivity of glasses.

(m/s)
(m/s)
(GPa)
(GPa)
(GPa)
(GPa)

0.01
3357.464
1931.559
60.7591
20.1097
50.3805
33.9462
2.3695

0.02
3190.886
1931.000
55.3582
20.2733
49.1052
28.3272
2.8627

0.03
3281.337
1933.777
59.295
20.5934
50.8222
31.8369
2.5873

0.04
3310.329
1936.346
61.0376
20.8844
51.7908
33.1918
2.5168

0.05
3364.002
1937.360
63.4404
21.0414
52.6819
35.3852
2.3785

Figure 5: Ultrasonic velocities of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses

However, as more Nd³⁺ ions are introduced into this glass network from 0.02 to 0.05 mol, the ultrasonic velocities increase. This may be due to an increase in the particle compactness as a result of an increase in the amount of bridging oxygen as TeO₄ increases [28].

The elastic moduli (, , , and ) are presented in Table 3 and are shown in Figure 6. It is shown that the elastic moduli decreased with the increase in Nd³⁺ NPs concentrations from 0.01 to 0.02 mol. The elastic moduli of glass are related to the number of bonds per unit volume of the glass samples. The decrease observed in elastic moduli is related to the increase of nonbridging oxygen (NBO) and consequently increased glass network connectivity [29].

Figure 6: Elastic moduli of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

Also, like the ultrasonic velocity, the elastic moduli showed the same trend that is increasing with an increment of Nd³⁺ NPs 0.02 to 0.05 mol content. The increase in the elastic moduli of the prepared glasses can be attributed to the change in the structural unit due to the formation of more TeO₄ which in turn leads to the formation of more bridging oxygen (BO) atoms [18]. This increased the rigidity of the glass and consequently increased the elastic moduli of the glass samples [18, 30].

Figure 7 shows the variation of fractal bond connectivity . This parameter tells about the effective dimensionality of the glass network. From the obtained result, it increased with Nd NPs concentration from 0.01 to 0.02 mol and decreased with Nd NPs concentration from 0.02 to 0.05 mol. The initial increase may be due to the increase in the amount of nonbridging oxygen which in turn decreases glass connectivity. The increase in the value may be associated with the increasing amount of bridging oxygen which causes an increase in the glass network connectivity [31].

Figure 7: Fractal bond connectivity of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

Poisson’s ratio is shown in Table 4, and Figure 8 shows a decrease in Poisson’s ratio from 0.01 to 0.02 mol and increase from 0.02 to 0.05 mol as Nd NPs increase. The initial decrease may be associated with a decrease in the rigidity in the glass network. The increase in the Poisson ratio value recorded beyond 0.02 mol may be attributed to increasing rigidity in the glass network due to increasing connectivity [29].

Table 4: Poisson’s ratio, microhardness, Debye temperature, and softening temperature of glasses.

(GPa)
(k)
(k)

0.01
0.2526
3.3161
255.4863
735.1503

0.02
0.2111
3.9048
254.5954
739.1378

0.03
0.2339
3.6526
256.1572
745.6174

0.04
0.2399
3.6207
257.1575
751.8914

0.05
0.2519
3.4807
257.7215
756.9057

Figure 8: Poisson’s ratio of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

The microhardness is the amount of stress required to remove the free volume of glass [32]. It is associated with the glass rigidity as it increases as the glass gets less rigid and decreases with increasing rigidity. Hence, the trend in Figure 9 shows an initial increase in the value with the increase in Nd ion concentration from 0.01 to 0.02 mol and may be due to decreasing rigidity. The observed decrease in the values of microhardness (H) with Nd ion concentration from 0.02 up to 0.05 can be said to be due to increasing rigidity [29]. The rigidity increase is due to increasing connectivity [33].

Figure 9: Microhardness of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

The variations of Debye and the softening temperatures with Nd₂O₃ concentration are presented in Table 4 and Figure 10. Debye temperature represents the temperature at which almost all the vibration modes in the glass are at excited states. The observed decrease in the value may be due to the increase in the rigidity as a result of the amount of nonbridging oxygen increase and Debye temperature also decreases with a decrease in the ultrasonic velocities. The increase observed from 0.02 to 0.05 mol of Nd NPs ions is attributed to the increasing rigidity and connectivity [34].

Figure 10: Debye and softening temperature of [(TeO₂)0.70(ZnO)0.30](Nd₂O₃ NPs) glasses.

The observed value of the softening temperature as shown in both Table 4 and Figure 10 may be attributed to the increase in the connectivity in the glass and increase in the degree of compactness [29].

4. Conclusion

A series of neodymium nanoparticles doped zinc-tellurite glass systems of composition , , , , , and mol, have been successfully prepared. The structural characteristics of neodymium nanoparticles doped zinc-tellurite glasses were studied thoroughly. XRD patterns showed that the present glasses were amorphous in nature. The density of neodymium nanoparticles doped zinc-tellurite glasses increased as Nd₂O₃ NPs content increased while molar volume showed both decreasing and increasing values. The changes in density and molar volume are due to the high molecular weight of Nd₂O₃ NPs and structural change in the glass network. It is observed that the ultrasonic velocities and elastic moduli decreased from 0.01 to 0.02 molar concentrations of Nd NPs ions and later increased from 0.02 to 0.05 molar concentrations. This decrease and the later increase are due to the increase in the amount of nonbridging oxygen in the beginning and bridging oxygen after 0.02 molar Nd NPs. The increase in the nonbridging oxygen leads to the decrease in rigidity while the increase in bridging oxygen increases its rigidity. The microhardness was found to decrease after 0.02 which can be attributed to the increase in glass rigidity and compactness. The observed variation of Poisson’s ratio, Debye temperature, and softening temperature was attributed to the change in the rigidity and connectivity in the glass system caused by the introduction of high Nd³⁺ NPs ions in the glass network.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

The authors would like to appreciate the financial support from the Ministry of Higher Education of Malaysia and Universiti Putra Malaysia through FRGS (5524817).

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