Chelating Ligand-Mediated Hydrothermal Synthesis of Samarium Orthovanadate with Decavanadate as Vanadium Source

Li, Quanguo; Zuo, Wenli; Li, Feng

doi:https://doi.org/10.1155/2013/127816

The Scientific World Journal

On this page

Abstract Introduction Results and Discussion Conclusions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2013 | Article ID 127816 | https://doi.org/10.1155/2013/127816

Chelating Ligand-Mediated Hydrothermal Synthesis of Samarium Orthovanadate with Decavanadate as Vanadium Source

Quanguo Li,¹Wenli Zuo,¹and Feng Li¹

Academic Editor: E. R. Dockal, B. I. Kharisov

Received28 Apr 2013

Accepted21 Jul 2013

Published28 Aug 2013

Abstract

A new ethylenediaminetetraacetic acid- (EDTA-) mediated hydrothermal route to prepare chrysanthemum-shaped samarium orthovanadate (SmVO₄) nanocrystals with decavanadate (K₆V₁₀O₂₈·9H₂O) as vanadium source has been developed. The present hydrothermal approach is simple and reproducible and employs a relatively mild reaction temperature. The EDTA, pH value, and temperature of the reaction systems play important roles in determining the morphologies and growth process of the SmVO₄ products. The products have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), photoluminescence spectra (PL), and UV-Vis spectroscopy.

1. Introduction

Controllable synthesis of well-defined nanocrystals with uniform size and morphology such as wires, belts, tubes, cubes, and rods has attracted a worldwide interest due to their unique electronic, optical, and magnetic properties associated with the reduced dimensionality and their potential applications in nanotechnology [1–5]. As a consequence, various nanocrystals such as elemental semiconductors, II–VI and III–V semiconductors, metal oxides, metals, and inorganic salts on large scale have been prepared through all sorts of methods including templating direction, catalytic growth, electrochemistry, chemical vapor deposition, and solution-based solvothermal or hydrothermal treatment [6–13]. In the synthesis of nanocrystals, there are two challenges now: (1) the morphology is restricted by the nature of crystals, which makes it difficult to control the morphology of the product; (2) the products always deviate from our research target. In recent reports, a special “capping reagent” has been used in the synthesis of nanocrystals. The “capping reagent” is used for tailoring the crystal growth and may also provide the possibility of breaking the nature of crystals, which may lead to more different morphologies and wider applications [14–16].

In recent years, SmVO₄ nanocrystals have been widely studied as a prospective material because they exhibit unique properties and applications in many fields, such as catalysis [17], gas sensors [18], optical polarizers [19], lithium intercalated electrodes [20], thin film phosphors [21], laser host materials [22], solar cells [23], and unusual magnetic materials [24]. For example, SmVO₄ nanocrystals exhibit high activity and selectivity as catalysts for many organic reactions, such as oxidative dehydrogenation of alkanes, olefins, ethylbenzene, and oxidation of hydrogen sulfide to elemental sulfur [25–35].

To date, most of the syntheses of SmVO₄ nanocrystals adopt solid-state reaction and citrate method [36], which needs harsh conditions. For example, Tojo et al. synthesized SmVO₄ crystals by milling the mixture of single oxides of Sm₂O₃ and V₂O₅ powders at 1000–1100°C [37]. Thus, it is expected to develop a low cost and convenient method for the synthesis of SmVO₄ nanocrystals with well-defined sizes and shapes [38]. For this purpose, the hydrothermal method has been considered as one of the most convenient methods for the controlled synthesis of SmVO₄ nanocrystals [39]. In the preparation of SmVO₄, most syntheses adopted as the vanadium source, so it may be a good strategy for preparing SmVO₄ with a new vanadium precursor [40]. Isopolyanions (e.g., decavanadate) may be a good candidate. In aqueous solutions, isopolyanions have versatile structures, and the structure of isopolyanions can be controlled by controlling the pH value. It means that we can obtain the target structure by adjusting the pH to a certain value, which is important for the preparation of aimed productions in the system of Sm-V-O. To the best of our knowledge, there are no reports on the synthesis of SmVO₄ with novel precursor decavanadate by the hydrothermal method yet.

In this paper, we synthesized chrysanthemum-shaped SmVO₄ nanorods from the reaction of K₆V₁₀O₂₈·9H₂O and SmCl₃·XH₂O precursors in the presence of capping reagent (EDTA) by hydrothermal method. The effects of the capping reagent, solution pH value, and reaction temperature on the shapes of the obtained SmVO₄ nanocrystals have been studied. The possible mechanism for the formation of SmVO₄ nanocrystals with various shapes is also proposed.

2. Experimental Section

2.1. Preparation of Decavanadate

The decavanadate (K₆V₁₀O₂₈·9H₂O) was prepared according to a described procedure [41].

2.2. Preparation of SmVO₄ Products

SmVO₄ products were prepared by hydrothermal method in the presence of capping reagent (EDTA). All reagents were analytical grade pure and used without further purification. In a typical procedure, 0.107 g K₆V₁₀O₂₈·9H₂O and 0.215 g ethylenediaminetetraacetic acid (EDTA) were dissolved into 30 mL distilled water, respectively. Stirring for 30 min, 0.073 g SmCl₃·XH₂O was dissolved into 20 mL distilled water. SmCl₃·XH₂O solution was added into K₆V₁₀O₂₈·9H₂O solution. After stirring for 10 min, EDTA solution was added into the solution, and 20 min later, sodium hydroxide solution (1 mol/L) was added dropwise into the solution to adjust the pH to the designed range (from 4 to 10). The resulting suspension was transferred into a 100 mL Teflon-lined stainless steel autoclave and sealed tightly. Hydrothermal synthesis was carried out at 140~180°C for 48 h in an electric oven without shaking or stirring. After cooling to room temperature naturally, the precipitates were collected, washed with distilled water and absolute ethanol for several times, and then dried in a vacuum oven at about 60°C for 10 h.

2.3. Characterization of SmVO₄ Products

The pH values of the solution were measured by Leici pH Meter of Shanghai Precision and Scientific Instrument Corporation China. The phase purity and crystal structure of the obtained products were examined by X-ray diffraction (XRD) using a MiniFlex2 goniometer, employing a scanning rate of 0.02° s⁻¹ in the 2θ range of 5°–70°. The operation voltage and current were maintained at 30 kV and 15 mA, respectively. The size distribution and morphology of the products were analyzed by scanning electron microscopy (SEM) (JSM-6610LV). The UV-Vis spectra of the as-synthesized SmVO₄ nanocrystals were recorded on a Lambda 25 spectrometer. Fourier transform infrared spectroscopic (FTIR) analysis was carried out in the region of 4000-400 cm⁻¹ by a PerkineElmer spectrometer instrument (pressed KBr disks). Room temperature photoluminescence (PL) spectra were recorded on a Hitachi 850 fluorescence spectrometer with Xe lamp as the excitation source at 25°C.

3. Results and Discussion

3.1. Structural Analysis

The phase identification of all the products was performed by XRD. Figure 1(a) shows the XRD patterns of the products obtained via hydrothermal method with deferent pH values. The products synthesized with pH values of 4, 6, 8, and 10 show similar patterns, which can be indexed as the tetragonal zircon phase of SmVO₄ with lattice contents of Å and Å, and are in good agreement with the standard values for the tetragonal phase SmVO₄ (Fm3hm, JCPDS no. 17-0876) [42]. No XRD peaks correspond to single metal oxides of V₂O₅ [43], and Sm₂O₃ [44] were detected, indicating that the pure SmVO₄ nanocrystals with tetragonal zircon-type structure can be obtained by this method. From Figure 1(a), we observed that the crystallinity of obtained products increased with the increasing of the pH value of the solution, when we kept the reaction temperature at 180°C. Obviously, the pH value of the solution plays an important role in the preparation of pure SmVO₄ by hydrothermal method.

To investigate the effect of temperature on the crystallinity, SmVO₄ was prepared at different reaction temperatures. When the reaction temperature was 140°C, the crystallinity of the as-prepared product was low, and few peaks can be observed. Therefore, a higher temperature may help the formation of the thermodynamically stable, well-crystallized, and uniform products. It is very clear that the crystallinity of the obtained products increases with the increasing of the reaction temperature at pH = 10 (Figure 1(b)). Thus, we conclude that the solution pH value and temperature of the reaction systems play important roles in determining the crystallinity of the SmVO₄ nanocrystals. Moreover, it can also be concluded that the formation of the pure tetragonal SmVO₄ phase results in complete reaction of the 1 : 1 ratio of Sm³⁺ cation and anion monomers in the bulk solution during the synthesis.

To further confirm the formation of the SmVO₄, Fourier transform infrared (FT-IR) spectroscopy was performed (Figure 2). The weak band at 447 cm⁻¹ is due to the antisymmetric deformation, and the strong absorption band at 803 cm⁻¹ corresponds to the vibrational mode that belongs to antisymmetric stretching of VO₄ tetrahedron [45]. It shows that the crystalline phase of SmVO₄ formed in the as-prepared product. The absorption band located at 3430 cm⁻¹ and 1643 cm⁻¹ can be ascribed to the O–H stretching and bending vibrations of free water molecules adsorbed by products from the aqueous solution.

3.2. Morphology Control

The morphology and structure of the as-prepared SmVO₄ nanocrystals were further characterized by SEM. Figure 3 shows the typical SEM images of the SmVO₄ nanocrystals at the reaction temperature of 180°C. When the pH is lower than 4, the obtained products take on a dumbbell-shaped structure (Figure 3(a)). It is noted that the centers of several dumbbells are connected together. When the pH is higher than 8, the obtained products are chrysanthemum shaped with a high density of nanorods (Figure 3(d)). When the pH values are higher than 4 and lower than 8, the chrysanthemum-shaped structure appears with a lower ratio. As shown in Figure 3(b), we can observe that the amount of nanorods is relatively rare. With the increasing of the pH value, the density and aspect ratio of those nanorods are improved (Figures 3(c) and 3(d)). These results indicate that pH value is a key factor in the formation of the chrysanthemum-shaped structure of SmVO₄ nanocrystals.

(a)

(b)

(c)

(d)

(e)

In order to better understand the formation and evolution of SmVO₄ nanostructures with the reaction temperature, reactions at 140°C and 160°C with the pH value of 10 were carried out. The SEM image of the product obtained from hydrothermal reactions at 140°C was shown in Figure 4(a). It is clearly shown that the as-synthesized products are composed of nanorods with inhomogeneous size distribution. When the reaction temperature was increased to 160°C, a large number of nanorods formed (Figure 4(b)). Some of them arranged regularly, and the density is higher than that in Figure 4(a). However, when the reaction temperature was increased to 180°C, the chrysanthemum-shaped structure of nanorods appeared, and the density and aspect ratio were further improved (Figure 4(c)). These results indicate that the reaction temperature has an important effect on the formation of chrysanthemum-shaped SmVO₄ nanocrystals.

(a)

(b)

(c)

3.3. Formation Mechanism

Without EDTA in the reaction system, the tetragonal SmVO₄ precipitates are aggregates of highly nanorods with inhomogeneous size distribution, and those nanorods were arranged inconstantly (Figure 3(e)). When EDTA was introduced into the reaction system, SmVO₄ products with a high aspect ratio and density can be obtained, if the pH value and the reaction temperature are well controlled. These initial products can be mediated by the ligands adsorbed on the surface of crystals, and they will serve as seeds for the growth of highly anisotropic nanostructures in the solution-solid process via the dissolution and crystallization mechanisms [46, 47]. The reason of introducing EDTA is based on its chelating and capping effects, which will influence the growth rate of different facets distinguishingly. Once the EDTA is dissociated from the Sm³⁺ ions, it will bind to the specific surface of the precipitated SmVO₄, which directly affects the facet growth and crystallinity of the nanocrystals [48]. The reason that the pH values influence the morphology of SmVO₄ nanocrystals can be easily understood by taking the following considerations. When the pH value is lower than 4, is stable, and the product is a dumbbell-shaped framework [49]. Since Sm³⁺ exists near the surrounding of anion framework, we suppose that the nucleation happens at the interface. When the framework is broken due to the increasing of the pH value of the reaction system, polyorthovanadate anion turns into ions and forms chrysanthemum-shaped structure. When pH is kept at 10, anion is the main form of orthovanadate, so no dumbbell shapes are observed. When the pH of the reaction system is kept at lower value, the aspect ratio of the chrysanthemum-shaped nanostructure of SmVO₄ is reduced because of the weakened chelation and capping abilities of EDTA. Moreover, the heat treatment temperature also plays important roles in determining the shape of the products. The strong ligand (EDTA) plays two roles. It is not only required to form a stable complex with Sm³⁺ but also acts as a capping reagent binding to the surface of crystals, which directly affects the facet growth and crystallinity of the nanocrystals. Therefore, we can control the aspect ratio and the density of SmVO₄ nanocrystals by adjusting the pH value and the reaction temperature when EDTA is introduced.

3.4. UV-Vis Spectroscopy and Photoluminescence Properties of SmVO₄ Nanocrystals

UV-Vis spectroscopy has been used for characterizing the optical property of the SmVO₄ nanocrystals. Examples for the UV-Vis absorption spectra experiments were prepared by dispersing the as-prepared SmVO₄ nanocrystals in ethanol with sonication bath for 30 min to form clear solutions. Figure 5 gives the UV-Vis absorption spectra of the SmVO₄ nanocrystals obtained at different pH values of 4, 6, 8, and 10. As shown in Figure 5, the absorption peaks of the products at about 250 nm are attributed to the charge transfer from the oxygen ligands to the central vanadium atom inside the groups in the samarium orthovanadate [50].

The room temperature photoluminescence spectrum of the as-synthesized SmVO₄ with the excitation of 288 nm was shown in Figure 6. It shows one strong and broad red emission at 605 nm, which is a characteristic transition from ⁴G_5/2 to ⁶H_7/2 states of Sm (III) [50].

4. Conclusions

In summary, chrysanthemum-shaped SmVO₄ nanorods have been successfully prepared with a novel precursor decavanadate in the presence of EDTA. It was found that the pH value, the reaction temperature, and the introduction of EDTA play key roles in the morphology evolution of the products. In addition, a possible growth mechanism of SmVO₄ with the morphology of chrysanthemum was discussed. Due to the simplicity of this system and the efficient control over the morphology, we suppose that this method may have wide applications in exploring the crystal growth process and provide guidance for the morphology controllable synthesis of other functional inorganic materials.

Acknowledgments

The authors acknowledge the financial support of Scientific Research Fund of Hunan Provincial Education Department, China (11C1205), and Provincial Natural Science Foundation of Hunan, China (13JJ6041).

References

J. T. Hu, T. W. Odom, and C. M. Lieber, “Chemistry and physics in one dimension: synthesis and properties of nanowires and nanotubes,” Accounts of Chemical Research, vol. 32, no. 5, pp. 435–445, 1999.
View at: Publisher Site | Google Scholar
Y. Xia, P. Yang, Y. Sun et al., “One-dimensional nanostructures: synthesis, characterization, and applications,” Advanced Materials, vol. 15, no. 5, pp. 353–389, 2003.
View at: Publisher Site | Google Scholar
Y. Y. Wu, H. Q. Yan, M. Huang, B. Messer, J. H. Song, and P. D. Yang, “Inorganic semiconductor nanowires: rational growth, assembly, and novel properties,” Chemistry, vol. 8, pp. 1260–1268, 2002.
View at: Google Scholar
G. R. Patzke, F. Krumeich, and R. Nesper, “Oxidic nanotubes and nanorods—anisotropic modules for a future nanotechnology,” Angewandte Chemie, vol. 41, no. 14, pp. 2446–2461, 2002.
View at: Google Scholar
D. L. Klein, R. Rotht, A. K. L. Lim, A. P. Alivisatosti, and P. L. McEuen, “A single-electron transistor made from a cadmium selenide nanocrystal,” Nature, vol. 389, no. 6652, pp. 699–701, 1997.
View at: Publisher Site | Google Scholar
H. W. Zhu, C. L. Xu, D. H. Wu, B. Q. Wei, R. Vajtai, and P. M. Ajayan, “Direct synthesis of long single-walled carbon nanotube strands,” Science, vol. 296, no. 5569, pp. 884–886, 2002.
View at: Publisher Site | Google Scholar
Y. Feldman, E. Wasserman, D. J. Srolovitz, and R. Tenne, “High-rate, gas-phase growth of MoS₂ nested inorganic fullerenes and nanotubes,” Science, vol. 267, no. 5195, pp. 222–225, 1995.
View at: Google Scholar
Y. D. Li, X. L. Li, Z. X. Deng et al., “From surfactant-Inorganic mesostructures to tungsten nanowires,” Angewandte Chemie, vol. 41, pp. 333–335, 2002.
View at: Google Scholar
X. Duan, Y. Huang, R. Agarwal, and C. M. Lieber, “Single-nanowire elecctrically driven lasers,” Nature, vol. 421, no. 6920, pp. 241–245, 2003.
View at: Publisher Site | Google Scholar
J. Zhang, L. Sun, J. Yin, H. Su, C. Liao, and C. Yan, “Control of ZnO morphology via a simple solution route,” Chemistry of Materials, vol. 14, no. 10, pp. 4172–4177, 2002.
View at: Publisher Site | Google Scholar
D. F. Zhang, L. D. Sun, J. L. Yin, and C. H. Yan, “Low-temperature fabrication of highly crystalline SnO₂ nanorods,” Advanced Materials, vol. 15, no. 12, pp. 1022–1025, 2003.
View at: Publisher Site | Google Scholar
R. Z. Ma, Y. Bando, and T. Sato, “Controlled synthesis of BN nanotubes, nanobamboos, and nanocables,” Advanced Materials, vol. 14, pp. 366–368, 2002.
View at: Google Scholar
M. Nath and C. N. R. Rao, “Nanotubes of group 4 metal disulfides,” Angewandte Chemie, vol. 41, pp. 3451–3454, 2002.
View at: Google Scholar
Y. D. Yin, Y. Lu, Y. G. Sun, and Y. N. Xia, “Silver nanowires can be directly coated with amorphous silica to generate well-controlled coaxial nanocables of silver/silica,” Nano Letters, vol. 2, pp. 427–430, 2002.
View at: Publisher Site | Google Scholar
X. Peng, L. Manna, W. Yang et al., “Shape control of CdSe nanocrystals,” Nature, vol. 404, no. 6773, pp. 59–61, 2000.
View at: Publisher Site | Google Scholar
L. Manna, E. C. Scher, and A. P. Alivisatos, “Synthesis of soluble and processable rod-, arrow-, teardrop-, and tetrapod-shaped CdSe nanocrystals,” Journal of the American Chemical Society, vol. 122, no. 51, pp. 12700–12706, 2000.
View at: Publisher Site | Google Scholar
C. T. Au and W. D. Zhang, “Oxidative dehydrogenation of propane over rare-earthorthovanadates,” Journal of the Chemical Society, Faraday Transactions, vol. 93, no. 6, pp. 1195–1204, 1997.
View at: Publisher Site | Google Scholar
E. V. Tsipis, M. V. Patrakeev, V. V. Kharton, N. P. Vyshatko, and J. R. Frade, “Ionic and p-type electronic transport in zircon-type Ce_1-xA_xVO_{4 ± δ} (A = Ca, Sr),” Journal of Materials Chemistry, vol. 12, no. 12, pp. 3738–3745, 2002.
View at: Publisher Site | Google Scholar
F. Chen, X. Wang, S. Li et al., “Low-loss optical planar waveguides in YVO₄ produced by silicon ion implantation at low doses,” Journal of Applied Physics, vol. 94, pp. 4708–4710, 2003.
View at: Publisher Site | Google Scholar
G. Picardi, F. Varsano, F. Decker, U. Opara-Krasovec, A. Surca, and B. Orel, “Electrochemical characterization of optically passive CeVO₄ counterelectrodes,” Electrochimica Acta, vol. 44, no. 18, pp. 3157–3164, 1999.
View at: Publisher Site | Google Scholar
M. Yu, J. Lin, and S. B. Wang, “Effects of x and R³⁺ on the luminescent properties of Eu³⁺ in nanocrystalline YV_xP_1-xO₄:Eu³⁺ and RVO₄:Eu³⁺ thin-film phosphors,” Applied Physics A, vol. 80, pp. 353–360, 2005.
View at: Publisher Site | Google Scholar
R. A. Fields, M. Birnbaum, and C. L. Fincher, “Highly efficient Nd:YVO₄ diode-laser end-pumped laser,” Applied Physics Letters, vol. 51, no. 23, pp. 1885–1856, 1987.
View at: Publisher Site | Google Scholar
J. F. Liu, Q. H. Yao, and Y. D. Li, “Effects of downconversion luminescent film in dye-sensitized solar cells,” Applied Physics Letters, vol. 88, pp. 173119–173121, 2006.
View at: Publisher Site | Google Scholar
K. Gaur and H. B. Lal, “Unusual magnetic behaviour of heavy rare earth vanadates at higher temperature,” Journal of Materials Science Letters, vol. 2, no. 12, pp. 744–746, 1983.
View at: Publisher Site | Google Scholar
J. W. Stouwdam, M. Raudsepp, and F. C. J. M. van Veggel, “Colloidal nanoparticles of Ln³⁺ -doped LaVO₄: energy transfer to visible- and near-infrared-emitting lanthanide ions,” Langmuir, vol. 21, no. 15, pp. 7003–7008, 2005.
View at: Publisher Site | Google Scholar
J. Matta, D. Courcot, E. Abi-Aad, and A. Aboukaïs, “Identification of vanadium oxide species and trapped single electrons in interaction with the CeVO₄ phase in vanadium-cerium oxide systems.51V MAS NMR, EPR, Raman, and thermal analysis studies,” Chemistry of Materials, vol. 14, no. 10, pp. 4118–4125, 2002.
View at: Publisher Site | Google Scholar
C. T. Au, W. D. Zhang, and H. L. Wan, “Preparation and characterization of rare earth orthovanadates for propane oxidative dehydrogenation,” Catalysis Letters, vol. 37, no. 3-4, pp. 241–246, 1996.
View at: Publisher Site | Google Scholar
S. Sugunan and N. K. Renuka, “Oxidative dehydrogenation of ethylbenzene over Sm₂O₃-V₂O₅ system,” Bulletin of the Chemical Society of Japan, vol. 75, pp. 463–471, 2002.
View at: Publisher Site | Google Scholar
E. A. Mamedov and V. C. Corberfin, “Oxidative dehydrogenation of lower alkanes on vanadium oxide-based catalysts. The present state of the art and outlooks,” Applied Catalysis A, vol. 127, pp. 1–40, 1995.
View at: Publisher Site | Google Scholar
B. P. Barbero and L. E. Cadus, “Vanadium species: Sm-V-O catalytic system for oxidative dehydrogenation of propane,” Applied Catalysis A, vol. 244, no. 2, pp. 235–249, 2003.
View at: Publisher Site | Google Scholar
K. T. Li and Z. H. Chi, “Selective oxidation of hydrogen sulfide on rare earth orthovanadates and magnesium vanadates,” Applied Catalysis A, vol. 206, pp. 197–203, 2001.
View at: Publisher Site | Google Scholar
B. P. Barbero and L. E. Cadus, “Evaluation and characterization of Sm-V-O catalytic system for propane oxydehydrogenation: Sm₂O₃-impregnated V₂O₅ catalysts,” Applied Catalysis A, vol. 234, pp. 245–258, 2002.
View at: Publisher Site | Google Scholar
I. Lee, R. Morales, M. A. Albiter, and F. Zaera, “Synthesis of heterogeneous catalysts with well shaped platinum particles to control reaction selectivity,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 40, pp. 15241–15246, 2008.
View at: Publisher Site | Google Scholar
F. Tao, M. E. Grass, Y. Zhang et al., “Reaction-driven restructuring of Rh-Pd and Pt-Pd core-shell nanoparticles,” Science, vol. 322, no. 5903, pp. 932–934, 2008.
View at: Publisher Site | Google Scholar
H. Friedrich, P. E. De Jongh, A. J. Verkleij, and K. P. De Jong, “Electron tomography for heterogeneous catalysts and related nanostructured materials,” Chemical Reviews, vol. 109, no. 5, pp. 1613–1629, 2009.
View at: Publisher Site | Google Scholar
P. Courty, H. Ajot, C. Marcilly, and B. Delmon, “Oxydes mixtes ou en solution solide sous forme très divisée obtenus par décomposition thermique de précurseurs amorphes,” Powder Technology, vol. 7, no. 1, pp. 21–38, 1973.
View at: Google Scholar
T. Tojo, Q. Zhang, and F. J. Saito, “Mechanochemical synthesis of rare earth orthovanadates from R₂O₃ (R = rare earth elements) and V₂O₅ powders,” Journal of Alloys and Compounds, vol. 427, pp. 219–222, 2007.
View at: Publisher Site | Google Scholar
J. Liu, W. Chen, X. Liu, K. Zhou, and Y. Li, “Au/LaVO₄ Nanocomposite: preparation, characterization, and catalytic activity for CO oxidation,” Nano Research, vol. 1, pp. 46–55, 2008.
View at: Publisher Site | Google Scholar
S. Mahapatra and A. Ramanan, “Hydrothermal synthesis and structural study of lanthanide orthovanadates, LnVO₄ (Ln = Sm, Gd, Dy and Ho),” Journal of Alloys and Compounds, vol. 395, no. 1-2, pp. 149–153, 2005.
View at: Publisher Site | Google Scholar
T. Nguyen, C. Dinh, D. Nguyen, and T. Do, “A novel approach for monodisperse samarium orthovanadate nanocrystals: controlled synthesis and characterization,” Journal of Physical Chemistry C, vol. 113, no. 43, pp. 18584–18595, 2009.
View at: Publisher Site | Google Scholar
J. N. Xu, G. Y. Yang, H. R. Sun, and T. G. Wang, “Synthesis and crystal structure of K₆V₁₀O₂₈ · 9H₂O,” Chemical Research and Application, vol. 9, pp. 576–581, 1997.
View at: Google Scholar
W. Fana, W. Zhao, L. You et al., “A simple method to synthesize single-crystalline lanthanide orthovanadate nanorods,” Journal of Solid State Chemistry, vol. 177, pp. 4399–4403, 2004.
View at: Publisher Site | Google Scholar
T. Nguyen and T. Do, “Solvo-hydrothermal approach for the shape-selective synthesis of vanadium oxide nanocrystals and their characterization,” Langmuir, vol. 25, no. 9, pp. 5322–5332, 2009.
View at: Publisher Site | Google Scholar
T. Nguyen, D. Mrabet, and T. Do, “Controlled self-assembly of Sm₂O₃ nanoparticles into nanorods: simple and large scale synthesis using bulk Sm₂O₃ powders,” Journal of Physical Chemistry C, vol. 112, no. 39, pp. 15226–15235, 2008.
View at: Publisher Site | Google Scholar
W. Chen, L. Q. Mai, J. F. Peng, Q. Xu, and Q. Y. Zhu, “FTIR study of vanadium oxide nanotubes from lamellar structure,” Journal of Materials Science, vol. 39, no. 7, pp. 2625–2627, 2004.
View at: Google Scholar
B. Gates, Y. Yin, and Y. Xia, “A solution-phase approach to the synthesis of uniform nanowires of crystalline selenium with lateral dimensions in the range of 10–30 nm,” Journal of the American Chemical Society, vol. 122, no. 50, pp. 12582–12583, 2000.
View at: Publisher Site | Google Scholar
J. Lu, Y. Xie, F. Xu, and L. Y. Zhu, “Study of the dissolution behavior of selenium and tellurium in different solvents-a novel route to Se, Te tubular bulk single crystals,” Journal of Materials Chemistry, vol. 12, pp. 2755–2761, 2002.
View at: Publisher Site | Google Scholar
T. N. Thomas, T. A. Land, J. J. DeYoreo, and W. H. Casey, “In situ atomic force microscopy investigation of the {100} face of KH 2PO₄ in the presence of Fe(III), Al(III), and Cr(III),” Langmuir, vol. 20, no. 18, pp. 7643–7652, 2004.
View at: Publisher Site | Google Scholar
N. N. Greenwood and A. A. Earnshaw, Eds., Chemistry of the Elements, Butterworth-Heinemann, Oxford, UK, 2nd edition, 1998.
R. K. Selvan, A. Gedanken, P. Anilkumar, G. Manikandan, and C. Karunakaran, “Synthesis and characterization of rare earth orthovanadate (RVO₄; R = La, Ce, Nd, Sm, Eu & Gd) nanorods/nanocrystals/nanospindles by a facile sonochemical method and their catalytic properties,” Journal of Cluster Science, vol. 20, no. 2, pp. 291–305, 2009.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2013 Quanguo Li 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.

PDF Download Citation

Download other formats

Order printed copies

Views

1597

Downloads

1553

Citations

The Scientific World Journal

Chelating Ligand-Mediated Hydrothermal Synthesis of Samarium Orthovanadate with Decavanadate as Vanadium Source

Abstract

1. Introduction

2. Experimental Section

2.1. Preparation of Decavanadate

2.2. Preparation of SmVO4 Products

2.3. Characterization of SmVO4 Products

3. Results and Discussion

3.1. Structural Analysis

3.2. Morphology Control

3.3. Formation Mechanism

3.4. UV-Vis Spectroscopy and Photoluminescence Properties of SmVO4 Nanocrystals

4. Conclusions

Acknowledgments

References

Copyright

2.2. Preparation of SmVO₄ Products

2.3. Characterization of SmVO₄ Products

3.4. UV-Vis Spectroscopy and Photoluminescence Properties of SmVO₄ Nanocrystals