Hydrothermal Synthesis and Characterization of Bi 2 MoO 6 Nanoplates and Their Photocatalytic Activities

1 Department 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 3 Electron 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


Introduction
Photodecomposition of organic compounds and water splitting by semiconducting photocatalysts have attracted the research interest because of the economic situation and environmental ecology for solving energy and pollution problems [1][2][3][4].In the past, the thoroughly conventional studies of TiO 2 displayed its excellent activities and stabilities but the technological application seemed to be limited by some parameters.The most restrictive one is the use of ultraviolet as photonic excitation for the 3.2 eV wide energy gap titania (anatase) [5,6].In addition, the solar radiance onto the Earth's surface of less than 5% can be captured by titania, compared to 43% of the visible light [1][2][3]7].Thus the development of a photocatalyst for visible light has become a very interesting topic in the current research on photocatalysis.
In this work, -Bi 2 MoO 6 nanocrystals were successfully synthesized by a simple hydrothermal method.The assynthesized -Bi 2 MoO 6 nanocrystals showed high photocatalytic activity to decompose RhB under visible light radiation.

Experimental Procedures
In this research, 0.03 mole of sodium molybdate (Na 2 MoO 4 ) and 0.06 mole of bismuth nitrate (Bi(NO 3 ) 3 ) were dissolved in 600 mL deionized water.The 600 mL solution was divided into six solutions with 100 mL each.Then HCl (conc.) or 3 M NaOH was added to them until each was achieved at the pH of 2, 4, 6, 8, 10, and 12 with continuous stirring at room temperature.Subsequently, the solutions were hydrothermally processed at 180 ∘ C for 20 h to form precipitates.In the end, the as-synthesized precipitates were separated by filtration, rinsed with distilled water and ethanol, and dried at 80 ∘ C for 24 h for further characterization.
X-ray powder diffraction (XRD) patterns of the products were recorded on a Japan Rigaku D/MAX-A X-ray diffractometer with graphite monochromator and Cu K  radiation ( = 0.154178 nm) at a scanning rate of 0.02 deg./s ranging from 10 to 60 deg.Raman spectra were recorded on a HORIBA JOBIN YVON T64000 Raman spectrometer at 50 mW and 514.5 nm wavelength Ar green laser and FTIR spectra were recorded on a BRUKER TENSOR 27 Fourier transform infrared (FTIR) spectrometer with KBr as a diluting agent and operated in the range of 400-4,000 cm −1 .SEM images were taken on a Hitachi, X650/EDAX, PV9100 scanning electron microscope operating at 35 kV, and TEM images were taken on a JEM 200CX, JEOL transmission electron microscope at an accelerating voltage of 200 kV.UV-visible absorption was carried out on a Lambda 25 PerkinElmer spectrometer, using a quartz cell.
Photocatalytic activities of the as-synthesized samples were tested by measuring the degradation of rhodamine-B (RhB) in an aqueous solution under a visible radiation of Xe lamp.The 150 mg photocatalyst was suspended in a 150 mL of 10 −5 M RhB aqueous solution, which was magnetically stirred for 30 min in the dark to establish an adsorption-desorption equilibrium of RhB on the surface of the photocatalyst.Then the light was turned on to initiate photocatalysis.The solution was analyzed by a Lambda 25 spectrometer, using 450 W of Xe lamp with wavelength of 553 nm.Decolorization efficiency (%) was calculated using where   is the initial concentration of RhB and  is the concentration of RhB after light irradiation.

Results and Discussion
It is well known that the initial pH values of the precursor solutions play an important role in the formation of Aurivillius oxide Bi 2 MoO 6 structure.Therefore, solutions with different pH values were used for the present synthesis.
The samples synthesized at the pH range from 2 to 12 octahedrons  [22,23].Raman spectra of Bi 2 MoO 6 samples synthesized at the pH 4 and 6 by the hydrothermal method are shown in Figure 2(a).They were classified into three regions: <180 cm −1 , 180-500 cm −1 , and 700-850 cm −1 .The modes below 180 cm −1 could be the translation of molybdenum and bismuth atoms.Vibration peak at 144 cm −1 , specified as the lattice mode of Bi 3+ atoms, was mainly in the direction normal to the layers.It is well known that the peaks in the 180-500 cm −1 range originated from bending modes of the MoO 6 octahedrons coupled with stretching and bending modes of the bismuthoxygen polyhedrons.The intense Raman modes near 290 and 280 cm −1 seemed to be from the E g bending vibrations.
Those at 323, 345, and 398 cm −1 corresponded to the E u symmetric bending.The mode at 712 cm −1 , exhibiting no evident shift or broadness, was specified as the asymmetric stretching vibration (E u mode) of the MoO 6 octahedrons involving the motion of equatorial oxygen atoms joining the MoO 6 octahedrons within the layers.The Raman vibrations at 793 cm −1 (A 1g mode) and 840 cm −1 (A 2u mode) were, respectively, assigned to the symmetric and asymmetric stretching vibrations of the MoO 6 octahedrons involving the motion of apical oxygen atoms, normally directed to the (Bi 2 O 2 ) 2+ layers [3,15,22,24].Figure 2(b) shows the FTIR spectra of Bi 2 MoO 6 samples obtained by hydrothermal reactions at the pH 4 and 6.
The main absorption bands at 400-950 cm −1 are mainly related to Bi-O and Mo-O stretching and Mo-O-Mo bridging stretching modes.The bands at 843 and 797 cm −1 were, respectively, assigned as the asymmetric and symmetric stretching modes of MoO 6 involving vibrations of apical oxygen atoms.The 734 cm −1 mode was attributed to the asymmetric stretching mode of MoO 6 involving vibrations of the equatorial oxygen atoms.Those at 603 and 570 cm −1 corresponded to the bending vibrations of MoO 6 .Furthermore, a small band at 454 cm −1 was attributed to the stretching and bending vibrations of BiO 6 octahedrons [3,24].
Figure 3 shows SEM images of the Bi 2 MoO 6 samples synthesized in the solutions with the pH of 4 and 6 by the hydrothermal method at 180 ∘ C for 24 h.The lowmagnification SEM images of both samples showed that the as-synthesized Bi 2 MoO 6 samples were composed of uniform plate-like structures ranging from 100 nm to 200 nm.The corresponding high-magnification SEM images demonstrated close-up views of the individual disks which clearly revealed the presence of orderly packed square nanoplates with their thickness of about several nanometers and the average length of 200-400 nm.The higher pH value seemed to produce smaller crystallites, which led to higher surface areas.
To reveal morphology of the as-synthesized Bi 2 MoO 6 , the samples were characterized by TEM as shown in Figure 4.The -Bi 2 MoO 6 sample at the pH 4 was composed of square nanoplates with thin edge.But for the pH of 6, they exhibited an explicit one.The selected area electron diffraction (SAED) patterns of individual Bi 2 MoO 6 nanoplates present regular square diffraction spot array, revealing the single-crystalline nanoplates.In the present analysis, both SAED patterns can be indexed as (060), (062), and (002) planes with the [100] direction as zone axis of orthorhombic Bi 2 MoO 6 structure.It should be noted that both diffraction patterns were composed of a number of diffraction spots arranged in systematic arrays.Weak diffraction spots, due to the high-order Laue  zone caused by the combined effects of the lengthened diffraction spots in the direction normal to the nanolayers and the narrow Laue zone along the [002] direction, were also detected in the forbidden sites [4].When the center of the circular arc of Ewald sphere does not coincide with bright spots of the transmitted beam, asymmetrical patterns will be detected.A symmetrical pattern is obtainable for a precise zone axis orientation, at which the center of the arc coincides with the spots of the transmitted beam [25].
It has been reported that orthorhombic Bi 2 MoO 6 is constructed by corner-shared MoO 6 octahedral layers with their edges directing along the [100] and [001] directions and (Bi 2 O 2 ) 2+ layers sandwiched between MoO 6 octahedral layers.Therefore, the direction of the nanolayers stacking is along the [010] direction normal to the [100] and [001] directions of the planes.Based on the experimental results, it can be concluded that under low pH value, there existed higher surface energy on the (100) and (001) planes compared with others.The growth of nanocrystals along the [010] direction was inhibited.The cleavages on surfaces of Bi 2 MoO 6 crystal also provide information for explaining the adsorption of H + cations.The (100), (010), and (001) crystal planes are terminated by the Mo, O, and Bi atoms, respectively.The zigzag orientations of Mo octahedral anions on the (100) faces induce these faces to become unfavorable for the adsorption of H + cations.The amount of O atoms on the (010) planes was much higher than others.H + cations preferred to adsorb on the (010) planes due to the high density of oxygen atoms on these faces.Thus the crystal growth along the [010] direction slowed down, including nanoplates formed [24,26].
Figure 5 displays UV-visible absorption spectra of Bi 2 MoO 6 nanoplates, which have strong photoabsorption properties ranging from ultraviolet to visible light with the wavelength being shorter than 500 nm.The steep shape of the absorption edge corresponded to the intrinsic energy gap transition of Bi 2 MoO 6 ranging from the valence band of the O 2p orbitals to the conduction band derived from the primary Mo 4d orbitals in MoO 6 octahedrons and the secondary Bi 6p orbitals [27,28].Their absorption edge wavelengths were determined to be 435-445 nm which were appropriate for the photocatalysis to accelerate the degradation of organic contaminants under UV-visible range.
To study the photocatalytic activities of the hydrothermally synthesized samples, tetraethylated rhodamine (RhB) with a major absorption band at 553 nm was chosen as a model organic contaminant.A change in the UV-visible spectra of the aqueous RhB solutions during photocatalytic decolorization using the Bi 2 MoO 6 nanoplates at the pH 4 and pH 6 is presented in Figure 6.During 180 min testing, the absorption intensity of RhB at 553 nm was gradually decreased and shifted towards the blue region from 553 nm to 498 nm with the formation of deethylated RhB molecules [15,29,30].The fully N,N,N  ,N  -tetraethylated rhodamine molecules (553 nm) show deethylation step by step to N,N,N  -triethylated rhodamine (539 nm), N,N  -diethylated rhodamine (522 nm), N-ethylated rhodamine (510 nm), and rhodamine (498 nm) [3,13,15]; the remains were degraded through the decomposition of conjugated structure.At the completion of visible irradiation for 180 min, the absorption  intensity of RhB aqueous solution became very weak.The RhB solution could turn into a colorless one by further increase in the length of time to longer than 180 min.It should be noted that the content of RhB was exponentially reduced with the increase in the length of irradiation time [2].Thus the RhB content will reach zero concentration at the irradiation time of infinity, and the decolorization of RhB was complete.
Figure 7 displays the degradation process of RhB in the solutions containing Bi 2 MoO 6 synthesized at the pH of 4 and 6 as a photocatalyst, compared to that without Bi 2 MoO 6 .For the controlled solution, RhB did not degrade both in the dark and in the illuminated condition.In the present research, visible light was essential to the RhB photodegradation.Bi 2 MoO 6 at the pH 6 showed significantly better photocatalytic degradation properties than Bi 2 MoO 6 at the pH 4. The pH of the precursors for the formation of Bi 2 MoO 6 nanoplates was found to strongly affect the photocatalytic efficiency.The photodegradation using Bi 2 MoO 6 at the pH 6 reached 98.66% within 180 min under visible-light irradiation, resulting from the smaller crystallites and larger specific surface areas [31].Compared with P25 TiO 2 , the degradation of RhB under the visible light irradiation was 18% within 120 min [32].Thus Bi 2 MoO 6 was claimed to be a potential photocatalyst under visible light.
Based on the photocatalytic degradation of organic compounds in the solutions containing Bi 2 MoO 6 , a possible mechanism was proposed [9,[33][34][35].At the beginning, the -Bi

Conclusions
The present research was to study the effect of pH on phase, morphologies, and photocatalytic properties of orthorhombic Bi 2 MoO 6 nanoplates synthesized by the hydrothermal method at 180 ∘ C for 20 h.Based on the various characterization techniques, the appropriate condition for the synthesis of orthorhombic Bi 2 MoO 6 nanoplates was at the pH 4 and 6.
The photocatalytic activity of Bi 2 MoO 6 nanoplates at the pH 6 was determined to be the highest at 98.66% degradation of RhB under Xe radiation for 180 min.

Figure 3 :
Figure 3: SEM images at low and high magnifications of Bi 2 MoO 6 synthesized in the solutions with the pH ((a), (b)) 4 and ((c), (d)) 6 by a hydrothermal method.

Figure 5 :
Figure 5: UV-visible absorption of Bi 2 MoO 6 nanoplates synthesized in the solutions with the pH 4 and 6 by a hydrothermal method.

2 Figure 6 :
Figure 6: UV-visible absorption of RhB in the solutions containing Bi 2 MoO 6 nanoplates synthesized at the pH (a) 4 and (b) 6.

Bi 2
MoO 6 pH 4 Bi 2 MoO 6 pH 6 Bi 2 MoO 6 -free Figure 7: Decolorization efficiencies of RhB in the solutions containing Bi 2 MoO 6 nanoplates synthesized at the pH 4 and 6 compared to the catalyst-free solution under Xe light.to the Bi 2 MoO 6 surfaces, which were immediately released into the conduction band of Bi 2 MoO 6 to generate BMO(e cb − ) and further reacted with the surface adsorbed oxygen to generate O 2 • − superoxide radicals.Concurrently, BMO(h vb + ) combined with water molecules and/or hydroxyl ions to form OH• radicals.Then all deethylated intermediates were further degraded by both of the radicals.It should be noted that there was a competition between the deethylation and the decomposition of conjugated structure proceeding on the surfaces of the Bi 2 MoO 6 samples: Bi 2 MoO 6 + hv → BMO (e cb − ) + BMO (h vb + ) (2) BMO (e cb − ) + O 2 → O 2 • − + Bi 2 MoO 6