Journal of Nanomaterials

Volume 2014 (2014), Article ID 934165, 7 pages

http://dx.doi.org/10.1155/2014/934165

Research Article

Hydrothermal Synthesis, Characterization, and Optical Properties of Ce Doped Bi₂MoO₆ Nanoplates

Anukorn Phuruangrat,¹ Nuengruethai Ekthammathat,² Budsabong Kuntalue,³ Phattranit Dumrongrojthanath,² Somchai Thongtem,4,5 and Titipun Thongtem²

¹Department of Materials Science and Technology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand

²Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand

³Electron Microscopy Research and Service Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand

⁴Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand

⁵Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand

Received 14 December 2013; Accepted 17 March 2014; Published 15 April 2014

Academic Editor: Ajay Soni

Copyright © 2014 Anukorn Phuruangrat 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.

Undoped and Ce doped Bi₂MoO₆ samples were synthesized by hydrothermal reaction at 180°C for 20 h. Phase, morphology, atomic vibration, and optical properties were characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectrophotometry, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and UV-visible spectroscopy. In this research, the products were orthorhombic Bi₂MoO₆ nanoplates with the growth direction along the [0b0], including the asymmetric and symmetric stretching and bending modes of Bi–O and Mo–O. Undoped and Ce doped Bi₂MoO₆ samples show a strong absorption in the UV region.

1. Introduction

Aurivillius family of structurally related oxides with chemical formula of (A = Ca, Sr, Ba, Pb, Bi, Na, K, and B = Ti, Nb, Ta, Mo, W, and Fe) was originally attractive material due to its layered structure and unique properties [1, 2]. The perovskite-type blocks lead to variable layers along the -axis due to the integer with and a typical “mica-like” two-dimensional structure [1]. Bi₂MoO₆ with narrow band gap of 2.9 eV is a typical Aurivillius phase with its structure consisting of perovskite layers between (Bi₂O₂)²⁺ bismuth oxide layers, with a general formula [Bi₂O₂] [] [3, 4]. Bi₂MoO₆ is an interesting material due to its unique physical properties for solar energy conversion, ion conduction, and photocatalysis for water splitting under visible-light irradiation and gas sensors [1, 2]. Various synthetic methods for this material have been reported such as hydrothermal/solvothermal [1, 3, 5], aerosol-spraying [4], coprecipitation [6], thermal evaporation [7], and hard-template method [8]. Recently, rare earth dopants have been excessively applied to modify optical properties of nanomaterials due to their possible transition of 4f electron configuration. Among them, cerium is one of the most interesting dopants due to its different electronic structure between Ce³⁺ (4f¹5d⁰) and Ce⁴⁺ (4f⁰5d⁰), leading to different optical properties. It generates oxygen vacancies and bulk oxygen species, which have relatively high mobility. Thus they are more active for oxidation processes [9, 10].

In this paper, 0–3% Ce doped Bi₂MoO₆ crystallites were successfully synthesized by the hydrothermal process. Phase, morphologies, and optical properties of the undoped and Ce doped Bi₂MoO₆ crystallites were intensively investigated.

2. Experimental Procedures

All the reagents were of analytical grade and used as received without further purification. In a typical experiment, 0.5 mmol Na₂MoO₄2H₂O and 1 mmol Bi(NO₃)₃5H₂O were dissolved in 60 mL deionized water to form solution A under 20 min magnetic stirring at room temperature. Concurrently, 1 and 3% by weight Ce(NO₃)₃6H₂O were dissolved in 40 mL deionized water each to form solution B under 20 min magnetic stirring at room temperature. Then, solution B was slowly added to solution A to form homogeneous solutions with further stirring for 30 min. Each solution of both with and without Ce³⁺ dopants was adjusted the level of acid or alkali until reaching at the pH of 10 using 3 M NaOH, poured into each of stainless steel autoclave with a Teflon liner, and heated at 180°C for 20 h. At the conclusion of the process, the autoclaves were cooled to room temperature. The products were separated centrifugally, washed with deionized water and absolute ethanol several times, and dried at 80°C for 12 h.

The phase of the samples was characterized by X-ray diffraction (XRD) using a Philips X’Pert MPD X-ray diffractometer with CuKα irradiation at λ = 1.5406 Å. The surface morphology was investigated by field emission scanning electron microscope (FE-SEM, JEOL JSM 6335F) and transmission electron microscope (TEM, JEOL, JEM2100) operated at the accelerating voltage of 35 and 200 kV, respectively. Raman and FTIR spectra were recorded on HORIBA JOBIN YVON T64000 Raman spectrometer with 50 mW and 514.5 nm wavelength Ar green laser and BRUKER TENSOR27 Fourier transform inferred (FTIR) spectrometer with KBr as a diluting agent and operated in the ranges of 100–1,000 cm⁻¹ and 400–4,000 cm⁻¹, respectively. X-ray photoelectron spectroscopy (XPS) of the products was carried out via an Axis Ultra DLD, Kratos Analytical Ltd., with a monochromated Al Kα (1486.6 eV) radiation as the excitation source at 15 kV. All obtained spectra were calibrated to a C1s electron peak at 285.1 eV. UV-visible absorption spectra of an ethanol suspension of 0–3% Ce doped Bi₂MoO₆ samples were recorded under a Lambda 25, Perkin Elmer UV-visible spectrophotometer.

3. Results and Discussion

The typical XRD patterns as shown in Figure 1 reveal the phase and purity of the as-obtained 0–3% Ce doped Bi₂MoO₆ samples. All peaks of the undoped and Ce doped Bi₂MoO₆ samples were specified as the single phase orthorhombic Bi₂MoO₆ structure (JCPDS card number 73-2020 [11]). The presence of sharp and intense peaks confirmed the formation of highly crystalline nanomaterials. Furthermore, the absence of any impurity related peaks indicates that Ce³⁺ ions were successfully doped into Bi₂MoO₆ nanostructure. However, the intensity ratio of the (060) peak to the (131) peak of 3% Ce doped Bi₂MoO₆ sample is 1.66, obviously larger than the undoped Bi₂MoO₆ which is equivalent to 0.60 [12]. This important result indicates that the crystal has special anisotropic growth along the [0b0] direction.

Figure 1: XRD patterns of the undoped, 1% Ce doped. and 3% Ce doped Bi₂MoO₆ samples synthesized by hydrothermal reaction at 180°C for 20 h.

The morphology and particle sizes of the Ce doped Bi₂MoO₆ with different contents of Ce ions were investigated by SEM as shown in Figure 2. It can be seen that the samples were comprised of a large number of nanoplates with diameters ranging between 0.1 and 0.3 μm and <100 nm thick. The surfaces of these nanoplates are smooth. Interestingly, when the samples were doped by different Ce concentrations, Ce doped Bi₂MoO₆ are still to be nanoplates. These show that Ce doping concentration had little effect on the shape of the products. Clearly, morphology and particle sizes of the Ce doped Bi₂MoO₆ nanoplates were consistent with pure Bi₂WO₆.

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Figure 2: SEM images of the nanostructured ZnO of (a) undoped Bi₂MoO₆, (b) 1% Ce doped Bi₂MoO₆, and ((c), (d)) 3% Ce doped Bi₂MoO₆.

More information of the structure was obtained by TEM observation as shown in Figure 3. It confirms that the undoped Bi₂MoO₆ nanoplates have an average diameter of about 0.2 μm, in accordance with the SEM analysis. Obviously, some of lighter color parts can be seen, due to the difference in the contrast in TEM, mainly related to the difference in thickness of the samples. Furthermore, the 3% Ce doped Bi₂MoO₆ sample was composed of square nanoplates with ~100 nm thick edge. The selected area electron diffraction (SAED) patterns clearly demonstrate the single crystalline nature of the nanoplates. Interestingly, the SAED patterns taken on the whole single nanoplate show single crystalline patterns with sharp diffraction bright spots, giving the [100] zone axis character of orthorhombic Bi₂MoO₆. Based on the above XRD results, it is reasonable to conclude that the nanoplates preferentially grew along the [010] direction.

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Figure 3: TEM images and SAED patterns of ((a), (b)) undoped Bi₂MoO₆, and ((c), (d)) 3% Ce doped Bi₂MoO₆.

The chemical composition of 3% Ce doped Bi₂MoO₆ nanoplates was investigated by XPS spectroscopy as shown in Figure 4 and was calibrated using C1s peak at 285.1 eV. The Bi4f peaks of the 3% Ce doped Bi₂MoO₆ nanoplates appear at 159.52 eV of 4f7/2 and 164.80 eV of 4f5/2, corresponding to Bi³⁺ [4, 13–15]. Additional weak spin-orbit doublet peaks with binding energy of 157.92 eV for Bi 4f7/2 and 163.40 eV for Bi 4f5/2 are also detected, suggesting that some of bismuth exist as the valence state [16]. Probably, the formal oxidation state could be attributed to the substoichiometric phase within the microsized plates [16]. The production of lower oxidation state results in the presence of oxygen vacancies inside. The Mo3d spectrum showed spin-orbit splitting of the Mo3d levels at 232.84 eV and 236.00 eV, corresponding to the 3d5/2 and 3d3/2 orbitals [4, 13, 17, 18]. The spin-orbit splitting between Mo3d5/2 and Mo3d3/2 signals of Ce doped Bi₂MoO₆ nanoplates was set to 3.16 eV which are consistent with the previous reports [17]. However, single spin-orbit doublets showed peaks with binding energies of 231.3 eV (Mo3d5/2) and 234.6 eV (Mo3d3/2). These peaks are associated with Mo in formal (+6) oxidation state [19, 20]. The binding energy of 530.60 eV was in agreement with the literature value [4]. The O element might come from two kinds of chemical states: crystal lattice oxygen and adsorbed oxygen. The triple peaks of core at 529.30 eV, 530.45 eV, and 531.32 eV are attributed to the presence of Bi–O, Mo–O and Ce–O bonds in 3% Ce doped Bi₂MoO₆ sample [13]. The binding energy of 532.58 eV is due to the adsorbed oxygen. The XPS Ce3d peaks of cerium compounds are well known to be complicated because of hybridization of the Ce4f orbital with ligand orbital and fractional occupancy of the valence 4f orbital. The XPS spectrum of the 3d5/2 cerium level is therefore composed of three structures in the case of CeO₂ and only two structures in the case of Ce₂O₃ or other Ce³⁺ compounds [21]. The peaks at 880.73 eV, 884.34 eV, and 887.57 eV are due to 3d5/2 spin-orbit states, and those peaks at 898.68 eV, 901.94 eV, and 905.11 eV are due to the corresponding 3d3/2 states. The spin-orbit splitting is about 17.6 eV. The highest binding energy peaks located at about 902 eV and 884 eV are the result of a Ce3d⁹4f¹ O2p⁶ of Ce(III) in Ce₂O₃ in final state. The lowest binding energies located at 898.68 eV and 880.74 eV are the result of Ce3d⁹4f² O2p4 [10, 21, 22]. The peaks at 887.57 eV and 905.11 eV are shakedown features resulting from the transfer of one or two electrons from a filled O2p orbital to an empty Ce4f orbital, that is, Ce3d⁹4f² O2p⁴ and Ce3d⁹4f¹ O2p⁵ Ce(IV) in the final states. Therefore, from the above results it is quite clear that there is coexistence of Ce³⁺ and Ce⁴⁺ in this sample [10, 21].

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Figure 4: XPS spectra of the 3% Ce doped Bi₂MoO₆ nanoplates for (a) Bi4f, (b) Mo3d, (c) , and (d) Ce4f.

Bi₂MoO₆ crystal is built up of perovskite-like (MoO₄)²⁻ and fluorite-like (Bi₂O₂)²⁺ layers. Its room temperature and ambient pressure structure is orthorhombic (space group symmetry P2₁ab). A standard group theoretical analysis for the P2₁ab room temperature phase of Bi₂MoO₆ unit cell leads to 108 degrees of freedom at the Brillouin zone center (Γ point). The optical modes are distributed among the irreducible representation of the factor group as 26A₁ + 27A₂ + 26B₁ + 26B₂. Selection rules state that the A₁, B₁, and B₂ are both Raman and IR active whereas the A₂ modes are only Raman active [23–25].

Raman spectra of 0–3% Ce doped Bi₂MoO₆ samples are shown in Figure 5. It is well known that the bands in the 180–500 cm⁻¹ range originated from the bending, wagging, and external modes by directly correlating the Mo–O bonds, and the 700–900 cm⁻¹ region originated from the stretching vibration modes of the MoO₆ octahedrons. Raman peaks at 323, 345, and 400 cm⁻¹ corresponded to the symmetry bending modes. Raman modes near 293 cm⁻¹ seemed to be from the bending vibration. The band at 144 cm⁻¹ was assigned as the lattice modes of Bi³⁺ atoms mainly in the direction normal to the layers. The strong band at 792 cm⁻¹ was assigned to mode of Mo–O stretching vibration of the distorted MoO₆ octahedrons. The shoulder peak at 715 cm⁻¹ was identified to the asymmetric stretching of MoO₆ octahedrons involving the vibration of the equatorial oxygen atoms within the layers. The band at 841 cm⁻¹ was assigned as the symmetric and asymmetric stretching vibrations of the MoO₆ octahedrons, relating to the motion of the apical oxygen atoms normal to the layers. When the Ce was doped into the samples, the strong bands at 792 cm⁻¹ and two shoulder peaks at 715 and 840 cm⁻¹ also slightly shifted to 713, 791, and 838 cm⁻¹, confirming an effective substitution of Bi³⁺ ions by Ce³⁺ ions in the as-prepared nanocrystals, as also revealed by the XRD analysis [23–26].

Figure 5: Raman spectra of undoped, 1% Ce doped, and 3% Ce doped Bi₂MoO₆ samples.

FTIR spectra of the samples (Figure 6) show the band in the 400–900 cm⁻¹ range, corresponding to Bi–O stretching and bending, Mo–O stretching, and Mo–O–Mo bridging stretching modes of Bi₂MoO₆. The bands at 843 and 797 cm⁻¹ were assigned as the asymmetric and symmetric stretching modes of MoO₆ relating to vibrations of apical oxygen atoms, respectively. The 731 cm⁻¹ mode was attributed to the asymmetric stretching vibration of the equatorial oxygen atoms of MoO₆ octahedrons. Those at 603 and 570 cm⁻¹ were specified as the bending vibrations of MoO₆. Weak bands at 409 and 448 cm⁻¹ were attributed to the stretching and bending vibrations of BiO₆ octahedrons [2, 26].

Figure 6: FTIR spectra of undoped, 1% Ce doped, and 3% Ce doped Bi₂MoO₆ samples.

The UV-visible absorption spectra of the undoped and Ce doped Bi₂MoO₆ are shown in Figure 7. They show the strong absorption in the UV and visible-light regions. It should be noted that the maximum absorption was detected at 321 nm for 3% Ce doped Bi₂MoO₆, obviously blue shifted compared to that of Bi₂MoO₆ at 383 nm. For a crystalline semiconductor, the optical absorption near the band edge follows the equation , where , and are the absorption coefficient, photonic frequency, energy gap, and a constant, respectively [2, 3]. For Bi₂MoO₆, the value of is 1 for the direct transition. The plot of versus photon energy of undoped and Ce doped Bi₂WO₆ was estimated from the intercepts of the tangents to the plots which are 1.86 eV for pure Bi₂MoO₆ and 2.04 eV for 3% Ce doped Bi₂MoO₆ which imply the possible application for visible-light photocatalysis.

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Figure 7: (a) UV-visible absorption and (b) versus curves of undoped, 1% Ce doped, and 3% Ce doped Bi₂MoO₆ samples.

4. Conclusions

0–3% Ce doped orthorhombic Bi₂MoO₆ nanoplates were successfully synthesized by the hydrothermal method. The experimental results presented that the as-synthesized products were orthorhombic Bi₂MoO₆ with the growth along the [010] direction. UV-visible absorption spectra show strong absorption due to the intrinsic energy gap transition of Bi₂MoO₆.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

The authors are extremely grateful to the Prince of Songkla University, Hat Yai, Songkhla, Thailand, for providing financial support through contract no. SCI560002S.

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