Structural and Optical Properties of BaO Nanoparticles Synthesized by Facile Co-precipitation Method

Manauwar Ali Ansari; Nusrat Jahan

doi:10.2991/mathi.k.210226.001

Previous Article In Issue

Volume 2, Issue 1-2, March 2021, Pages 23 - 28

Structural and Optical Properties of BaO Nanoparticles Synthesized by Facile Co-precipitation Method

Downloads:

2,310

Full-Text Views:

103

Citations (Scopus):

0

Citations (Crossref):

0

Download PDF

Cite This Article

Authors

Manauwar Ali Ansari¹^{, *}, Nusrat Jahan²

¹

Department of Material Science and Engineering, University of Miskolc, Miskolc, Egyetemvaros 3515, Hungary

²

School of Science, JS University, Shikohabad, India

^*

Corresponding author. Email: maansarivce@gmail.com

Corresponding Author

Manauwar Ali Ansari

Article History

Received 7 November 2020
Accepted 24 February 2021
Available Online 3 March 2021

DOI: https://doi.org/10.2991/mathi.k.210226.001
Keywords: Structural property
optical property
barium oxide
co-precipitation
Abstract: This paper presents the synthesis of Barium Oxide Nanoparticles (BaO-NPs) on a large-scale by a simple and cost-effective co-precipitation method. The as-synthesized BaO-NPs were characterized in aspects of their structural, morphological, compositional, and optical properties. X-ray diffraction was done to assess the crystalline property of the nanomaterial and the crystallite size of the BaO-NPs was found to be 15–16 nm. Scanning electron microscopy was used to study the morphology of as-synthesized nanoparticles which confirmed that the prepared materials are flower-shaped nanoparticles. The compositional characteristics of nanoparticles were given by Fourier transform infrared spectroscopy which confirmed that the as-synthesized nanoparticles are pure BaO. A useful optical properties of nanoparticles were also reported via the room temperature UV–Vis and photoluminescence spectroscopy and calculated bandgap of the nanoparticles was found 4.65 eV.
Copyright: © 2021 The Authors. Published by Atlantis Press B.V.
Open Access: This is an open access article distributed under the CC BY-NC 4.0 license (http://creativecommons.org/licenses/by-nc/4.0/).

1. INTRODUCTION

Nanoscience and nanotechnology reveal a significant place in basic to applied material research because of their large number of applications which based on its size and design [1].

Transition metal oxide nanomaterials for example as copper oxide, iron oxide, Barium Oxide (BaO), tin oxide, zinc oxide, titanium oxide, etc. are known as being among the wealthiest nanomaterials family due to its increasing study and flexible applications [1–9], which have size-dependent materials properties compared to their bulk phases, making them widely used in various fields such as sensors, actuators, high-temperature superconductors, capacitors, environmental sciences, biomedical sciences, Li-ion batteries, solar cells, etc. An extensive study has been carried out in this field and published in the literature because of the wide range of applications of this type of material.

Among all the several other metal oxide nanomaterials, BaO is a direct band gap type, group II–VI semiconductor nanomaterial having unique significance due to their wide bandgap (4.4 eV [10]) and hygroscopic characteristics and large applications such as self-cleaning [11], electrical-energy generation [11], sensors and actuators [12–14], Pharmaceutical industry [15], catalysts [1,16]. Apart from this, BaO was seen significantly useful in electron field emission [10], conservation and restoration of cultural heritage such as paper-based artifacts and wall paintings [17,18], diagnostic imaging, orthopedic medicines, and other biomedical applications [19–21].

Hitherto, several BaO Nanoparticles’ (BaO-NPs) preparation routes have been developed to produce nanomaterials with different sizes and shapes such as sol–gel, chemical method, hydrothermal, thermal decomposition, sonochemical, microwave irradiation, and quick-precipitation, etc. [17,18,22,23–28]. Among these preparation methods, the co-precipitation route has gained a lot of popularity in industries due to the facile way of synthesis, low temperature, and energy, cost-effective and inexpensive approach for good yield and large scale production.

The structural and optical properties of semiconductor nanoparticles have increasingly become a topic of great concern. In general, the nanoparticles’ physical properties significantly depend on their microstructure, such as crystal defects, grain boundaries, as well as surface morphology. Therefore, to get a well understanding of the size-dependent physical properties of BaO-NPs, it is essential to acquire knowledge of their microstructure [1,17,18,22,23–28].

This paper presents the facile synthesis and characterization of BaO-NPs prepared through a novel, cost-effective co-precipitation route. The prepared nanoparticles’ structural and optical properties were then analyzed through various characterization techniques such as X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersion X-ray Spectrum (EDS), Fourier Transforms Infrared (FTIR), UV–Vis, and PL. Finally, important results were presented and discussed.

2. MATERIALS AND METHODS

2.1. Materials and Synthesis Process

Barium Nitrate [Ba(NO₃)₂] (Sigma-Aldrich, India, 98%) and Sodium Bicarbonate (NaHCO₃) (Merck, India, 98%) was used as a precursor and as a fuel respectively for the synthesis of BaO-NPs. BaO-NPs were prepared via a facile co-precipitation method. The schematic of the synthesis procedure is shown in Figure 1. In a typical synthesis, 0.5 M of Ba(NO₃)₂ was dissolved in 100 ml de-ionized water (H₂O), which was continuously stirred using a magnetic stirrer for approximately 30 min until the Ba(NO₃)₂ dissolved completely. The pre-prepared NaHCO₃ solution was added drop-wise into the Ba(NO₃)₂ solution, under vigorous stirring. After approximately, 2 h of continuous stirring the reaction white colored mixture forms completely. The produced mixture was kept for 12 h so that all constituent particles are get precipitated. The precipitated material was washed and centrifuged with distilled water and alcohol many times to eliminate the native impurities from the sample. Further, the precipitate was dried and calcined at 400–500°C for 4 h in the air to ensure that Ba(HCO₃)₂ was converted into BaO completely. The whole reactions involve can be given as below:

Ba(NO₃)₂ (aq.) + 2NaHCO₃ (aq.) → Ba(HCO₃)₂ (aq.) + 2NaNO₃ (aq.)

Ba(HCO₃)₂ → BaO + 2CO₂↑ + H₂O ↑ (Calcination)

2.2. Characterization

Structural characterization phase and crystallinity of as-synthesized BaO-NPs was done by using the XRD technique (Rigaku-Miniflex, Japan, X-ray diffractometer) using Cu Kα radiations (λ = 1.5406 Å) in the 2θ range 20–80°. The morphology of as-prepared NPs was observed by FEI (Field Electron and Ion Company) Field Emission (FE)-SEM. FTIR spectroscopy (PerkinElmer, USA) was used in the 400–4000 cm⁻¹ range for the analysis of chemical compositions of the prepared nanoparticles. UV–Vis (PerkinElmer) was used to obtain absorbance spectra of the NPs in the range from 200 to 800 nm at room temperature. PL spectra were recorded by using the Varian Carry Eclipse Fluorescence spectrophotometer (Agilent, California, USA).

3. RESULTS AND DISCUSSION

3.1. Structural and Morphological Properties

3.1.1. X-ray diffraction

Phase and crystallinity of as-synthesized BaO-NPs were done by using the XRD technique with Cu Kα radiations (λ = 1.5406 Å) in the 2θ range 20–60°. XRD spectra of synthesized BaO-NPs is shown in Figure 2. Many well-defined peaks correspond to various planes of BaO as (200), (201), (211), (102), (310) and (212), so on were seen in the observed XRD pattern which is all related and well-matched with the tetragonal phase of BaO-NPs and are in good agreement with the “JCPDS” card No. 26-0178. The observed results are also confirmed with the reported literature [23,26,28]. Sharp and intense peaks indicate the synthesized nanoparticles are highly crystalline in nature. The average crystallite size (D) of the sample is calculated using Debye-Scherrer’s formula [29] which can be given as:

D=Kλβ cosθ (1) [29]

where K is the shape factor (0.90), λ is the wavelength of Cu Kα radiation (λ = 1.5406 Å), β is the full-width at half maximum, and θ is the diffraction angle. The average grain size of BaO-NPs is found to be ~16 nm.

3.1.2. Scanning electron microscopy

The morphology of the synthesized BaO-NPs was assessed by FE-SEM and presented in Figure 3a and 3b. Figure 3a shows a low-resolution (1500) image of prepared BaO-NPs which exhibits a flower-shaped clusters morphology. High-resolution SEM image is presented in Figure 3b shows the synthesized nanomaterials are grown highly crystalline. It can also be seen from the SEM images that some NPs are in nanorods and nanosheets like structures and are joined by accumulation on one above another. The elemental compositional analysis of synthesized NPs was assessed by EDS integrated to SEM. EDS spectra confirmed the chemical purity of synthesized BaO-NPs.

3.1.3. Fourier transform infrared

The chemical composition analysis of prepared BaO-NPs, was done with FTIR in the wavenumber range 4000–400/cm, and obtained results are presented in Figure 4a and 4b. The FTIR spectrum represents a strong absorption band at ~692 cm⁻¹ which corresponds to the Ba–O bond formation. A weak absorption band at ~615 cm⁻¹ also seen due to Ba–O stretching vibration. Two absorption bands observed at ~1754 and ~3456 cm⁻¹ in the FTIR spectra are associated with the O–H stretching and bending vibrations’ modes, respectively. The peak at ~1455 cm⁻¹ is may be due to the barium carbonate formation which is result of absorption of atmospheric CO₂ by BaO-NPs. The peak seen at ~1059 cm⁻¹ is connected with O–O stretching modes of vibration [30]. Two peaks at ~857 and ~2452 cm⁻¹ are associated with the asymmetric vibration modes of NO₃⁻¹ ions and –CO₂ bond vibration, respectively [28,31,32].

The results found are consistent with the previous literature [23,31,32]. No other absorption band associated to any other chemical group has been found in the FTIR spectra that indicate high purity of synthesized BaO-NPs sample.

3.2. Optical Properties

3.2.1. UV–Vis spectroscopy

The optical properties of synthesized BaO-NPs were examined by UV–Vis spectroscopy and the absorbance spectrum taken at room temperature is shown in Figure 5. The measurement procedure followed was given in the literature [31,32].

The highest light absorption was noted at 310 nm, which is known as the characteristic edge or peak of BaO as reported in many literatures [1,23,28]. There is no other absorption peak was detected in the spectra that corroborates the possession of strong optical properties of the synthesized BaO-NPs.

The optical energy bandgap (E_g) of the prepared BaO-NPs was calculated by Tauc’s relation [33,34], which provides the relation between the incident energy of the photon and the absorption coefficient of the semiconductor materials. The Tauc’s equation can be given as:

(αhv)=A(hυ−Eg)n (2)

where A is a constant α is the optical absorption coefficient, hυ is the energy of the photon (where h is plank constant and υ is optical frequency), E_g is the optical band gap energy and n is an exponent its mathematical value relies heavily on the nature of the electronic transition causing the light absorption generally, n is taken equals 2 and 1/2 and for indirect and direct band gap, respectively.

Figure 6 shows the Tauc’s plot for BaO NPs. The calculated optical bandgap energy (E_g) of as-prepared BaO NPs was 4.65 eV. The measured E_g is found very close to the bulk phase BaO and consistent with the previously reported literature [1,23,28]. The bandgap energy of nanophase BaO i.e. 4.65 eV is found higher than that of the bulk phase BaO i.e. 4.4 eV [10]. This enhancement in optical bandgap energy is because of the primarily known quantum size effect of nanophase materials. This theory (quantum size effect) applies only when the particle size is comparable to and in the range of de Broglie wavelength of a charge carrier (i.e. in the nanometer range).

3.2.2. Photoluminescence spectroscopy

Photoluminescence (PL) is the process of spontaneous light emission from the sample material when optically excited. The excitation energy and intensity can be chosen to probe different excitation types, determination of bandgap energy, identification of specific defects for radiative transitions, and impurity levels in the nanomaterial sample. Photoluminescence spectroscopy is a non-destructive analysis technique [6,35–37].

The photoluminescence spectrum of BaO-NPs was collected at the excitation wavelength of 230 nm and shown in Figure 7. The spectrum shows two major emission bands (Blue-violet and red). A total three number of peaks are detected which are as follows: a sharp emission peak at 380 nm, a broad peak at 410–574 nm may be because of the defects in the crystal of BaO, and a peak at 758 nm is may be due to an e–h pair recombination. Optical measurements result of UV–Vis and PL analysis show that the as-synthesized BaO-NPs can be expected as highly useful for optoelectronics and photonic systems and devices.

4. CONCLUSION

Highly crystalline BaO-NPs were successfully synthesized by the facile co-precipitation method and analyzed in detail through various materials analysis techniques. The results of the structural and chemical compositional analysis reveal a pure and highly-crystalline tetragonal phase of BaO-NPs. The average grain size of BaO-NPs is found to be ~16 nm. The FE-SEM morphological analysis of the sample confirmed that the nanoparticles were grown highly crystalline. Also, some NPs are in nanorods and nanosheets like structures and are joined by accumulation on one above another. UV–Vis spectroscopy confirmed a significant optical properties of the sample and the calculated optical bandgap energy (E_g) of BaO-NPs was 4.65 eV which was found very close to the bulk phase BaO. A strong PL emission spectrum in the visible range making the as-synthesized BaO-NPs can be considered to be highly useful in optoelectronics and photonic systems and devices. The followed synthesis method can also be used in the preparation of other transition metal oxide nanomaterials.

CONFLICTS OF INTEREST

The authors declare they have no conflicts of interest.

AUTHORS’ CONTRIBUTION

NJ contributed in conceptualization and in all graphs preparation. MAA carried out the experiment and wrote the original draft.

ACKNOWLEDGMENT

Authors are thankful to the Institute of ceramic and polymer engineering, University of Miskolc, Hungary for laboratories and valuable technical support.

REFERENCES

[1]

R Renukadevi, R Sundaram, and K Kasinathan, Barium oxide nanoparticles with robust catalytic, photocatalytic and humidity sensing properties, J Nanostruct, Vol. 10, 2020, pp. 167-76.

[2]

D Maity and DC Agrawal, Synthesis of iron oxide nanoparticles under oxidizing environment and their stabilization in aqueous and non-aqueous media, J Magn Magn Mater, Vol. 308, 2007, pp. 46-55.

[3]

P Guardia, N Pérez, A Labarta, and X Batlle, Controlled synthesis of iron oxide nanoparticles over a wide size range, Langmuir, Vol. 26, 2010, pp. 5843-7.

[4]

L Wang and M Muhammed, Synthesis of zinc oxide nanoparticles with controlled morphology, J Mater Chem, Vol. 9, 1999, pp. 2871-8.

[5]

M El-Hofy and A Salama, Synthesis and characterization of Ba defective ZnO nano-particle, DJ Fisher (editor), Defect and diffusion forum, Vols. 280–281, Trans Tech Publications Ltd, Switzerland, 2008, pp. 1-8.

[6]

N Mohamed Basith, J Judith Vijaya, L John Kennedy, and M Bououdina, Structural, morphological, optical, and magnetic properties of Ni-doped CuO nanostructures prepared by a rapid microwave combustion method, Mater Sci Semiconduct Process, Vol. 17, 2014, pp. 110-18.

[7]

A Sharma, K Sreenivas, V Gupta, and M Tomar, Room temperature detection of trace level NO2 gas using SnO2 nanoclusters, IEEE, in 2011 IEEE Sensors Applications Symposium (San Antonio, TX, USA, 2011), pp. 145-8.

[8]

YJ Chen, CL Zhu, LJ Wang, and TH Wang, One-pot synthesis of crystalline SnO2 nanoparticles and their low-temperature ethanol sensing characteristics, Sci China Ser G: Phys Mech Astron, Vol. 52, 2009, pp. 1601-5.

[9]

R Sankar, K Rizwana, KS Shivashangari, and V Ravikumar, Ultra-rapid photocatalytic activity of Azadirachta indica engineered colloidal titanium dioxide nanoparticles, Appl Nanosci, Vol. 5, 2015, pp. 731-6.

[10]

Y Cui, J Chen, Y Zhang, X Zhang, W Lei, Y Di, et al., Enhanced performance of thermal-assisted electron field emission based on barium oxide nanowire, Appl Surf Sci, Vol. 396, 2017, pp. 1108-12.

[11]

A Umar and YB Hahn, Metal oxide nanostructures and their application, American Scientific Publishers, Los Angeles, USA, 2010.

[12]

R Renukadevi and R Sundaram, Surfactant – free, facile synthesis of zinc tungstate nanoparticles for photocatalytic, antibacterial and humidity sensing applications, Int J Tech Inn Mod Engg Sci, Vol. 5, 2019, pp. 35-42.

[13]

R Renukadevi and R Sundaram, Synthesis, characterization, humidity sensing, antibacterial, photocatalytic and kinetic studies of novel HgWO4–WO3 nanocomposites, Mater Today Proc, Vol. 8, 2019, pp. 153-61.

[14]

Y Zhang, Y Hou, W Liu, H Zhang, Y Zhang, Z Zhang, et al., A cost-effective relative humidity sensor based on side coupling induction technology, Sensors (Basel), Vol. 17, 2017, pp. 944.

[15]

VR Choudhary, R Jha, and P Jana, Epoxidation of styrene by TBHP to styrene oxide using barium oxide as a highly active/selective and reusable solid catalyst, Green Chem, Vol. 8, 2006, pp. 689-90.

[16]

L Yang, YM Choi, W Qin, H Chen, K Blinn, M Liu, et al., Promotion of water-mediated carbon removal by nanostructured barium oxide/nickel interfaces in solid oxide fuel cells, Nat Commun, Vol. 2, 2011, pp. 357.

[17]

E Cordoncillo, TR Machado, L Ferrazza, and D Juanes, Synthesis and characterization of nanostructured BaO solutions: application in conservation of wall paintings, M Ioannides, D Fritsch, J Leissner, R Davies, F Remondino, and R Caffo (editors), Progress in Cultural Heritage Preservation, Springer, Berlin, Heidelberg, in Euro-Mediterranean Conference, 2012, pp. 801-8.

[18]

KM Saoud, I Ibala, D El Ladki, O Ezzeldeen, and S Saeed, Microwave assisted preparation of calcium hydroxide and barium hydroxide nanoparticles and their application for conservation of cultural heritage, M Ioannides, N Magnenat-Thalmann, E Fink, R Žarnić, AY Yen, and E Quak (editors), Digital Heritage. Progress in Cultural Heritage: Documentation, Preservation, and Protection, Springer, Cham, in Euro-Mediterranean Conference, 2014, pp. 342-52.

[19]

S Alarifi, D Ali, and W Al-Bishri, In vitro apoptotic and DNA damaging potential of nanobarium oxide, Int J Nanomedicine, Vol. 11, 2016, pp. 249-57.

[20]

R Gillani, B Ercan, A Qiao, and TJ Webster, Nanofunctionalized zirconia and barium sulfate particles as bone cement additives, Int J Nanomedicine, Vol. 5, 2010, pp. 1-11.

[21]

M Hiraoka, K Ikeda, and T Sano, The mechanism of barium-induced automaticity in ventricular muscle fibers, Adv Myocardiol, Vol. 1, 1980, pp. 255-66.

[22]

A Zeenath Bazeera and M Irfana Amrin, Synthesis and characterization of barium oxide nanoparticles, IOSR J Appl Phys, Vol. 3, 2017, pp. 76-80.

[23]

N Ahmad, R Wahab, and M Alam, Facile growth of barium oxide nanorods: structural and optical properties, J Nanosci Nanotechnol, Vol. 14, 2014, pp. 5342-6.

[24]

RHP Devamani and M Alagar, Synthesis and characterization of barium hydroxide nanoparticles, Asian Acad Res J Multidisciplinary, Vol. 1, 2014, pp. 60-75.

[25]

AO Mousa, NA Nema, and HH Hasan, Effect of annealing on barium oxide (BaO) thin films prepared by chemical spray pyrolysis (CSP) technique, J Chem Pharm Res, Vol. 8, 2016, pp. 832-40.

[26]

G Suresh and PN Nirmala, Synthesis of barium oxide nanorod by chemical bath deposition, Turk J Phys, Vol. 36, 2012, pp. 392-7.

[27]

SP Prabhavathi, J Punitha, PS Rajam, R Ranjith, G Suresh, N Mala, et al., Simple methods of synthesis of copper oxide, zinc oxide, lead oxide and barium oxide nanoparticles, J Chem Pharm Res, Vol. 6, 2014, pp. 1472-8.

[28]

E Sundharam, AKS Jeevaraj, and C Chinnusamy, Effect of ultrasonication on the synthesis of barium oxide nanoparticles, J Bionanosci, Vol. 11, 2017, pp. 310-14.

[29]

DP Dubal, GS Gund, CD Lokhande, and R Holze, CuO cauliflowers for supercapacitor application: novel potentiodynamic deposition, Mater Res Bull, Vol. 48, 2013, pp. 923-8.

[30]

S Abramowitz and N Acquista, The infrared spectrum of matrix isolated BaO2, J Res Natl Bur Stand A, Vol. 75, 1971, pp. 23-5.

[31]

MS Chauhan, R Kumar, A Umar, S Chauhan, G Kumar, M Faisal, et al., Utilization of ZnO nanocones for the photocatalytic degradation of acridine orange, J Nanosci Nanotechnol, Vol. 11, 2011, pp. 4061-6.

[32]

R Wahab, YS Kim, DS Lee, JM Seo, and HS Shin, Controlled synthesis of zinc oxide nanoneedles and their transformation to microflowers, Sci Adv Mater, Vol. 2, 2010, pp. 35-42.

[33]

Q Xiang, J Yu, W Wang, and M Jaroniec, Nitrogen self-doped nanosized TiO2 sheets with exposed {001} facets for enhanced visible-light photocatalytic activity, Chem Commun (Camb), Vol. 47, 2011, pp. 6906-8.

[34]

W Zhao, X Song, Z Yin, C Fan, G Chen, and S Sun, Self-assembly of ZnO nanosheets into nanoflowers at room temperature, Mater Res Bull, Vol. 43, 2008, pp. 3171-6.

[35]

YC Zhang, JY Tang, GL Wang, M Zhang, and XY Hu, Facile synthesis of submicron Cu2O and CuO crystallites from a solid metallorganic molecular precursor, J Cryst Growth, Vol. 294, 2006, pp. 278-82.

[36]

T Yu, X Zhao, ZX Shen, YH Wu, and WH Su, Investigation of individual CuO nanorods by polarized micro-Raman scattering, J Cryst Growth, Vol. 268, 2004, pp. 590-5.

[37]

S Al-Amri, M Shahnawaze Ansari, S Rafique, M Aldhahri, S Rahimuddin, A Azam, et al., Ni doped CuO nanoparticles: structural and optical characterizations, Curr Nanosci, Vol. 11, 2015, pp. 191-7.

Previous Article In Issue

Cite This Article

ris

TY  - JOUR
AU  - Manauwar Ali Ansari
AU  - Nusrat Jahan
PY  - 2021
DA  - 2021/03/03
TI  - Structural and Optical Properties of BaO Nanoparticles Synthesized by Facile Co-precipitation Method
JO  - Materials Highlights
SP  - 23
EP  - 28
VL  - 2
IS  - 1-2
SN  - 2666-4933
UR  - https://doi.org/10.2991/mathi.k.210226.001
DO  - https://doi.org/10.2991/mathi.k.210226.001
ID  - Ansari2021
ER  -

download

copy

enw

bib

Article Contents

Materials Highlights

1. INTRODUCTION

2. MATERIALS AND METHODS

2.1. Materials and Synthesis Process

2.2. Characterization

3. RESULTS AND DISCUSSION

3.1. Structural and Morphological Properties

3.1.1. X-ray diffraction

3.1.2. Scanning electron microscopy

3.1.3. Fourier transform infrared

3.2. Optical Properties

3.2.1. UV–Vis spectroscopy

3.2.2. Photoluminescence spectroscopy

4. CONCLUSION

CONFLICTS OF INTEREST

AUTHORS’ CONTRIBUTION

ACKNOWLEDGMENT

REFERENCES

Cite This Article