Academic Editor:Junyou Yang
School of Mechanical Engineering, Yeungnam University, Gyeongsan 712-749, Republic of Korea
Received 8 April 2015; Revised 21 May 2015; Accepted 27 May 2015; 1 October 2015
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.
1. Introduction
Molybdenum disulfide (MoS2 ) is one of the important transition metal dichalcogenides (TMDs) with indirect band gap (1.23 eV) semiconductor characteristics [1]. Because of their outstanding properties like mechanical-to-electrochemical capabilities, MoS2 is used in wide spectrum of applications in catalytic support materials [2, 3], solar cells [4], batteries [5], solid lubricants [6], and gas sensors [7]. These unique properties have attracted many researchers to design new synthesis approaches for uniform and well-controlled MoS2 nanostructures. Synthesis methods include chemical vapor deposition [8], wetness impregnation method [9], hydrothermal methods [10], and solid state reaction [11]. These techniques have been used to prepare various morphologies of MoS2 , like fullerene-like (IF) structures, nanoflowers, nanorods, nanosheets, nanoplates, and nanospheres.
In a recent report, Wang et al. demonstrated that carbon-decorated MoS2 nanospheres have better cycling performance with good capacity as a Na-iron battery anode [12]. MoS2 is clearly one of the most significantly and broadly used TMDs for transistors due to its favorable band gap compared to graphene. In addition, MoS2 is also a suitable candidate for photocatalytic materials. MoS2 is an indirect narrow-band-gap semiconductor with good stability against photocorrosion in solution [13]. General issues with semiconductor catalysts in the conversion of solar energy to hydrogen are poor charge transport ability, slow kinetics for evolution reactions, poor stability, and the hydrophobic nature of the catalyst [14, 15]. On the other hand, individual MoS2 catalyst has lower charge separation due to its poor crystallinity.
Despite previous efforts, there has been no material system that can simultaneously satisfy all the criteria for cost-effective photoelectrochemical hydrogen production, and new materials with new properties are needed. To overcome these problems, core-shell structures of MoS2 coupled with another material with different activity are promising. Such structures could enable charge separation by gathering electrons and holes. The major parameters for the selection of shell materials are band alignment and small lattice mismatch between the core and shell materials [16]. There are very few studies that have focused on preparing MoS2 nanosphere structures. Wu et al. [17] synthesized MoS2 microspheres (with diameter up to 2 μ m) using a solvothermal method with the addition of SUDEI. Wu et al. [18] prepared MoS2 nanospheres (with average diameter of 100 nm) using HCl as a surfactant. Park et al. [19] synthesized MoS2 nanospheres with high capacity and cycle stability for lithium ion batteries using L-cysteine in a surfactant-assisted solvothermal route.
Common ways to synthesize core-shell structures are decorating the core particles with a surface coating [5] or shell formation using surface modification processes [20]. In this study, we report the influence of Al2 O3 as a shell material on the photocatalytic activity of MoS2 nanosphere core-shell structures under UV light irradiation. We studied the variations of the activity and selectivity in the degradation of rhodamine B (RhB) using Al2 O3 -coated MoS2 nanospheres as a catalyst.
2. Experimental Procedure
A schematic illustration of the methodology for the formation of Al2 O3 -coated MoS2 nanospheres is shown in Figure 1. For the synthesis, 0.3 g of ammonium heptamolybdate tetrahydrate and 0.17 g of L-cysteine were dissolved in 30 mL of deionized water. This solution was stirred vigorously for 1 h at 80°C. The suspension was continuously stirred and refluxed near pH 1. Then, 1.2 mmol of Al(NO3 )3 ·9H2 O and 0.3 mmol of trisodium citrate dehydrate (TSC) were added to the stirred solution and again stirred for 30 min at 80°C. Then, the solution was transferred to a Teflon-lined autoclave and heated at 230°C for 24 h. Finally, the resulting precipitates were collected by centrifugation and then the precipitates were washed three times with acetone and water. The obtained precipitates were dried at 250°C for 6 h and sintering at 450°C for 2 h.
Figure 1: Schematic illustration of the methodology for the formation of Al2 O3 -coated MoS2 nanospheres.
[figure omitted; refer to PDF]
The structural properties of the obtained precipitates were characterized by powder X-ray diffraction (XRD) with a Shimadzu Labx XRD 6100 using Cu-Kα radiation (λ = 0.14056 nm). The scan range was 10-80°, and the scan speed was 3 deg/min. The nanoparticles were analyzed with a transmission electron microscope (TEM, Hitachi H-7000) at 100 kV and a high-resolution TEM (HRTEM, Tecnai G2 F 20 S-Twin TEM) at an accelerating voltage of 210 kV. The optical properties of the nanoparticles were studied using UV-visible spectroscopy (Cary 5000 UV-Vis spectrophotometry). Thermogravimetric (TG) and differential thermal analysis (DTA) were carried out on a SDT Q600 thermogravimetric analyzer under N2 flow at a rate of 30 cm3 /min. The furnace temperature was increased from room temperature to 900°C at a heating rate of 10°C per minute. The purity of the final product was examined by X-ray photoelectron spectroscopy (XPS, Thermo Scientific K-alpha surface analysis instrument).
The photocatalytic experiments were carried out at the natural pH of the RhB organic pollutant solution. The photoreactor has a 150-W mercury lamp with a main emission wavelength of 254 nm as an internal light source, which is surrounded by a quartz vessel. The suspension includes the Al2 O3 -decorated MoS2 nanosphere catalyst and aqueous RhB (100 mL, 10 mg/L), which completely surrounds the light source. Before irradiation, the suspension was stirred in the dark for 30 min to obtain a good dispersion and to ensure adsorption-desorption equilibrium between the organic pollutant molecules and the catalyst. During light irradiation, the samples of the reaction solution were collected at given intervals and examined using an optical spectrophotometer.
3. Results and Discussions
The XRD patterns of MoS2 nanospheres and Al2 O3 -coated MoS2 nanospheres were shown in Figure 2. In case of MoS2 sphere sample exhibits three well-resolved peaks which can be indexed as the 002, 103, and 110 reflections of the 2D hexagonal structure, which is matched with JCPDS number 77-1716. On the other hand, XRD pattern of Al2 O3 -coated MoS2 sample exhibits hexagonal structure, whereas Al2 O3 layer is been crystallized, which is corresponding to JCPDS number 78-2426. The coexisting peaks of Al2 O3 -coated MoS2 nanospheres corresponding to the 012, 110, 006, 024, and 018 crystal plane are ascribed to γ -Al2 O3 phase for the sintered samples at 450°C [21, 22]. The diffraction lines characteristics of MoS2 and Al2 O3 and no other elemental peaks were detected.
Figure 2: XRD pattern of MoS2 nanospheres (curve (a)) and Al2 O3 -coated MoS2 nanospheres (curve (b)).
[figure omitted; refer to PDF]
The morphology of the MoS2 nanospheres and Al2 O3 -coated MoS2 nanospheres was examined using TEM, as shown in Figure 3. MoS2 nanospheres were coated with Al2 O3 using Al(NO3 )3 ·9H2 O as a precursor via a hydrothermal method. For better understanding of the morphology of the composite, we initially tested the MoS2 nanospheres without using Al precursors. The morphology of the MoS2 nanospheres is shown in Figures 3(a) and 3(b). The MoS2 materials reveal typical sphere-like morphology with several nanometers in diameter. On the other hand, the MoS2 spheres obtained using Al precursors retained their spherical morphology with the formation of a uniform layer, forming a core-shell structure (Figures 3(c) and 3(d)). The average thickness of the Al2 O3 layer around the periphery of the MoS2 is about 15 nm.
Figure 3: TEM images of ((a), (b)) MoS2 nanospheres, ((c), (d)) Al2 O3 -coated MoS2 nanospheres.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
(c) [figure omitted; refer to PDF]
(d) [figure omitted; refer to PDF]
Further understanding of the structural and compositional characterizations of Al2 O3 -coated MoS2 nanospheres was obtained using HRTEM. The HRTEM image of an edge portion of a core-shell sphere is shown in Figures 4(a)-4(d). The HRTEM image (Figure 4(a)) confirms that the Al2 O3 colloids are aggregated on the MoS2 nanospheres. The lattice fringes of the core-shell structure with lattice spacings of about 0.213 and 0.316 nm could be attributed to the (103) and (110) planes of 2H-MoS2 , respectively. Figures 4(e)-4(i) show typical energy dispersive X-ray spectrometer (EDX) elemental mappings of the core-shell spheres of various elements in the core-shell structure, along with its TEM image. The Mo, S, Al, or O signals are predominantly distributed in the core and shell regions within the selected area, respectively. Figure 5 shows the EDX mapping of Al2 O3 -coated MoS2 nanospheres. There are no other traces observed.
Figure 4: HR-TEM images ((a)-(e)) of Al2 O3 -coated MoS2 nanospheres, ((f)-(i)) HR-TEM elemental mapping images of Al2 O3 -coated MoS2 nanospheres.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
(c) [figure omitted; refer to PDF]
(d) [figure omitted; refer to PDF]
(e) [figure omitted; refer to PDF]
(f) [figure omitted; refer to PDF]
(g) [figure omitted; refer to PDF]
(h) [figure omitted; refer to PDF]
(i) [figure omitted; refer to PDF]
Figure 5: HR-TEM EDX data of Al2 O3 -coated MoS2 nanospheres.
[figure omitted; refer to PDF]
Thermogravimetric and differential thermal analysis (TG-DTA) was conducted to quantitatively determine the Al2 O3 content present in the Al2 O3 -coated MoS2 nanospheres, as shown in Figure 6. The initial weight loss below 220°C is ascribed to the evaporation of physically absorbed water from the product, whereas the weight loss between 550 and 680°C that occurred with an exothermic peak at 650°C could essentially be attributed to the decomposition and separation of the Al2 O3 layer. The Al2 O3 content was estimated to be approximately 47.25% by weight.
Figure 6: TG-DTA analysis of Al2 O3 -coated MoS2 nanospheres.
[figure omitted; refer to PDF]
The electronic states of the metals and sulfur in the Al2 O3 -coated MoS2 nanospheres were tested using XPS, as shown in Figures 7(a)-7(e). The XPS survey spectra of the Al2 O3 -coated MoS2 nanospheres are shown in Figure 7(a). The Al2p XPS spectra were estimated for the Al2 O3 -coated MoS2 nanospheres to examine the chemical state of Al. The Mo3d, S2P, Al2p, and O1s peaks from the Al2 O3 -coated MoS2 sphere sample (Figures 7(b)-7(e)) show no presence of addition chemical states. The binding energy difference [figure omitted; refer to PDF] between the Al2p and 2s levels is 53.34 eV for the Al2 O3 -coated MoS2 nanospheres. The XPS results strongly indicate that Al species interacted with the MoS2 nanospheres and are preferentially formed in the Al2 O3 -MoS2 composite using Al(NO3 )3 ·9H2 O as a precursor. The Al2p and O1s peaks were centered at 74.45 eV and 532.36 eV, as described elsewhere [23].
Figure 7: XPS data of Al2 O3 -coated MoS2 nanospheres: (a) survey spectrum, (b) Mo 3d, (c) S2p, (d) Al2p, and (e) O1s.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
(c) [figure omitted; refer to PDF]
(d) [figure omitted; refer to PDF]
(e) [figure omitted; refer to PDF]
The S2p spectrum shows a supplementary peak at 164.58 eV coexisting with an O1s peak, which is ascribed to the oxidation of sulfur. The formation of covalent S-O bonding without breakage of the Mo-S bond is likely due to the oxidation state of sulfur. No S-O bond is observed in the S2s spectrum, which suggests that only the top surface of sulfur atoms of MoS2 are oxygen functionalized. This is good evidence that the Al2 O3 formed a bond with MoS2 nanospheres, resulting in the formation of the core-shell structure. The XPS binding energies [figure omitted; refer to PDF] (Mo 2p3/2 - S 2p3/2 ) and [figure omitted; refer to PDF] (Mo 3d5/2 - S 2p3/2 ) of the Al2 O3 -coated MoS2 nanospheres are 70.3 and 67.09 eV, respectively.
The UV-Vis spectrum of the synthesized Al2 O3 -coated MoS2 nanospheres is shown in Figure 8(a). The absorption edge at 275 nm could be attributed to the absorption of Al2 O3 -MoS2 in the UV region. The absorption spectrum shows two absorption edges at 603 and 660 nm. These are attributed to excitonic transitions of the Brillouin region at the [figure omitted; refer to PDF] point, which is consistent with an earlier report [24]. The energy separation between the two absorption peaks (at 603 and 660 nm) is 0.15 eV due to the spin-orbit splitting at the [figure omitted; refer to PDF] point at the surface of the valence band [24]. Moreover, there is weak absorbance in the visible region at a wavelength of 425 nm. The UV-absorption behavior of MoS2 strongly depends on its size due to quantum effects [25]. For example, the absorption edges of MoS2 nanoparticles with average diameters of about 4.5 and 9 nm have edges at 470 and 700 nm, respectively, in the visible light region [26]. In contrast, bulk MoS2 (with a band gap of 1.23 eV) has an absorption peak at around 1040 nm [25]. MoS2 -based composites have diverse absorption edges with respect to their dimensional parameters [26].
Figure 8: (a) UV-Vis light spectra of the Al2 O3 -coated MoS2 nanospheres, (b) Tauc plots of Al2 O3 -coated MoS2 nanospheres.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
The indirect band gap is estimated using the Tauc equation with optical absorption data for near the band edge [24]: [figure omitted; refer to PDF] . The band gaps ( [figure omitted; refer to PDF] ) are determined from extrapolation of a linear fit onto the [figure omitted; refer to PDF] -axis. A plot of [figure omitted; refer to PDF] versus the photon energy [figure omitted; refer to PDF] and the intercept of the tangent to the [figure omitted; refer to PDF] -axis gives the band gap of the Al2 O3 -coated MoS2 nanospheres, as shown in Figure 8(b). The band gap energy of Al2 O3 -coated MoS2 nanospheres was found to be 2.42 eV.
Figure 9 shows the progressive changes of the UV-Vis absorption spectra of RhB solution in the presence of Al2 O3 -coated MoS2 nanosphere catalyst under UV light as a function of time. The strong absorption peak of the RhB solution at 564 nm gradually decreases from dark conditions to 60 min, and the color of the solution turns from pink to colorless at the end of the photodegradation process. Figure 10 shows the photodegradation efficiency of MoS2 nanospheres and Al2 O3 -coated MoS2 nanosphere catalysts under UV light in RhB solution. The results are shown as the relative concentration [figure omitted; refer to PDF] as a function of irradiation time, where [figure omitted; refer to PDF] and [figure omitted; refer to PDF] (mg/L) are the initial and final concentrations of the pollutant solution.
Figure 9: Time-dependent UV-Vis absorbance spectra of Al2 O3 -coated MoS2 nanospheres of the rhodamine B solution samples at different times.
[figure omitted; refer to PDF]
Figure 10: Photodegradation rate of the rhodamine B under UV light and light irradiation time for without catalyst, MoS2 nanospheres, and Al2 O3 -coated MoS2 nanospheres.
[figure omitted; refer to PDF]
A blank experiment was carried out in the absence of photocatalyst for comparison, which showed no obvious change in the RhB concentration within 60 min. The introduction of MoS2 nanospheres and Al2 O3 -coated MoS2 nanosphere catalysts can greatly enhance the photocatalytic activity under UV light. Interestingly, the Al2 O3 -coated MoS2 nanosphere photocatalysts displayed much higher photodegradation performance than the MoS2 nanospheres, and more than 97% of the RhB was degraded within 60 min. The presence of Al2 O3 -coated MoS2 nanospheres plays a key role in the photocatalytic degradation process. The significant enhancement in photoactivity can be ascribed to the favorable van der Waals surfaces of the Al2 O3 -coated MoS2 nanospheres.
Figure 11 shows a kinetic plot of the photocatalytic degradation of RhB over time under UV light irradiation as ln [figure omitted; refer to PDF] . The removal efficiency of the Al2 O3 -coated MoS2 nanospheres was much faster than that of the MoS2 nanosphere catalyst. To understand the photostability and reusability of the photocatalyst, four successive recycling tests of the photocatalysts were done for the degradation of RhB under UV light, as shown in Figure 12. There were no significant changes in photocatalytic activity, which shows the steadiness of the degradation efficiency of RhB solution. This result implies that the Al2 O3 -coated MoS2 nanosphere photocatalysts have high stability during the photocatalytic oxidation of the pollutant molecules and are reusable.
Figure 11: The kinetic plot of Al2 O3 -coated MoS2 nanospheres photocatalytic degradation of rhodamine B under UV light irradiation.
[figure omitted; refer to PDF]
Figure 12: Recycling photocatalytic degradation of rhodamine B in the presence of Al2 O3 -coated MoS2 nanospheres photocatalytic under UV light irradiation.
[figure omitted; refer to PDF]
The catalytic activity increased with the Al2 O3 -coated MoS2 nanospheres. Figure 13 shows the RhB removal efficiency of the Al2 O3 -coated MoS2 photocatalytic nanospheres with 5 mg of catalyst and 50 mL of 10 mgL-1 RhB solution. The pollutant removal efficiency and the adsorption amount at equilibrium (qe) were calculated using the following equation: [figure omitted; refer to PDF] where [figure omitted; refer to PDF] and [figure omitted; refer to PDF] (mg/L) are the initial and final concentrations of the pollutant, respectively, [figure omitted; refer to PDF] is the volume of the pollutant solution, and [figure omitted; refer to PDF] (g) is the mass of the catalyst. The Al2 O3 -coated MoS2 nanospheres exhibit high RhB removal efficiency (95%), in contrast to the (69%) MoS2 nanosphere sample. It is well known that catalytic ability increases with increasing content of the catalyst with respect to processing time and other environmental conditions like temperature and pH. In this work, the degradation rate of the RhB solution also increased with increasing catalyst content due to the small particle size and good dispersibility of the Al2 O3 -coated MoS2 nanoparticles, which facilitate electron migration between the catalyst and pollutant. The Al2 O3 -coated MoS2 nanospheres exhibit high catalytic activity due to the high dispersibility of the Al2 O3 coating around the MoS2 nanospheres, which secured more efficient charge transfer between the MoS2 and Al2 O3 .
Figure 13: RhB removal efficiency of Al2 O3 -coated MoS2 nanospheres photocatalytic, adsorption conditions: 5 mg catalyst, 50 mL 10 mgL-1 RhB solution (conditions: 5 mg of catalyst and 50 mL of 10 mgL-1 RhB solution).
[figure omitted; refer to PDF]
The MoS2 behaves as the photoactive center, which is generating excited photoelectron pairs under UV irradiation, while the Al2 O3 provides better adsorption sites in the vicinity of the MoS2 . The presence of insulating layers of Al2 O3 on the surface of MoS2 nanospheres suppresses the unwanted charge recombination, thus enhancing the photocatalytic activity. The greater photocatalytic activity of Al2 O3 -coated MoS2 nanospheres can be explained as follows. The HRTEM mapping results indicated that the periphery of the MoS2 was covered with Al2 O3 . Under UV light irradiation, both MoS2 and Al2 O3 are photoexcited, and holes and electrons form in the valance band and conduction band. The photogenerated holes and electrons are transferred within the valance and conduction bands of both the MoS2 and Al2 O3 materials. This tendency helps to extend the charge carriers. The excited electrons and holes react with dissolved oxygen in the water or directly oxidize the pollutant molecules to form oxide radicals ( [figure omitted; refer to PDF] ) and hydroxyl radicals (* OH), which are responsible for the degradation of RhB.
A possible mechanism for formation of MoS2 @Al2 O3 core-shell structure is suggested involving MoS2 spheres acting as a template for the formation of the coated nanospheres. Due to hydrothermal reactions between the metal-oxoanions and surfactant, cations form a composite phase at the surfactant/inorganic interfaces. Thus, nucleation domains were formed during the hydrothermal reaction between [figure omitted; refer to PDF] and S2- and formed MoS2 spheres. In this manner, the diameter of the nanospheres is no longer limited by the micelle dimensions. A spherical phase of MoS2 is formed during hydrothermal treatment under the synthetic conditions, in which L-cysteine acts as a sulfur source to stabilize the spherical organization of Mo and S species. The Al species of the precursor solution can absorb to the surface of MoS2 spheres, and layer upon layer is formed by the electrostatic interaction. The TSC could be considered a crucial component for the growth mechanism of Al2 O3 coating because it acts as a capping agent for the formation of the coating surface on the MoS2 nanospheres. The complete synthetic mechanism is expressed in Figure 1.
4. Conclusions
Al2 O3 -coated MoS2 nanospheres were successfully synthesized using a simple hydrothermal method. The Al2 O3 shell materials serve as additional electron sources that can significantly recover the electron conduction in MoS2 , which favors the photodegradation of the pollutant. We revealed the appropriate selection of surfactants that could facilitate the adherence of Al species to the surfaces of the cores. Hydrothermally synthesized Al2 O3 -coated MoS2 nanosphere catalysts show photocatalytic activity higher than that of the MoS2 nanosphere catalyst due to the enhanced crystallites with high metal content, which minimize the poisoning effect of sulfur by the chemisorption process.
Acknowledgments
This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) and funded by the Ministry of Science, ICT, and Future Planning (2014R1A2A2A01007081).
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
[1] H. S. S. Ramakrishna Matte, A. Gomathi, A. K. Manna, D. J. Late, R. Datta, S. K. Pati, C. N. R. Rao, "MoS2 and WS2 analogues of graphene," Angewandte Chemie International Edition , vol. 49, no. 24, pp. 4059-4062, 2010.
[2] Y. Li, H. Wang, L. Xie, Y. Liang, G. Hong, H. Dai, "MoS2 nanoparticles grown on graphene: an advanced catalyst for the hydrogen evolution reaction," Journal of the American Chemical Society , vol. 133, no. 19, pp. 7296-7299, 2011.
[3] J. J. Lee, H. Kim, S. H. Moon, "Preparation of highly loaded, dispersed MoS2 /Al2 O3 catalysts for the deep hydrodesulfurization of dibenzothiophenes," Applied Catalysis B: Environmental , vol. 41, no. 1-2, pp. 171-180, 2003.
[4] D. Song, M. Li, Y. Jiang, Z. Chen, F. Bai, Y. Li, B. Jiang, "Facile fabrication of MoS2 /PEDOT-PSS composites as low-cost and efficient counter electrodes for dye-sensitized solar cells," Journal of Photochemistry and Photobiology A: Chemistry , vol. 279, pp. 47-51, 2014.
[5] C. Zhang, H. B. Wu, Z. Guo, X. W. Lou, "Facile synthesis of carbon-coated MoS2 nanorods with enhanced lithium storage properties," Electrochemistry Communications , vol. 20, pp. 7-10, 2012.
[6] H.-H. Chien, K.-J. Ma, S. V. P. Vattikuti, C.-H. Kuo, C.-B. Huo, C.-L. Chao, "Tribological behaviour of MoS2 /Au coatings," Thin Solid Films , vol. 518, no. 24, pp. 7532-7534, 2010.
[7] M. Donarelli, S. Prezioso, F. Perrozzi, F. Bisti, M. Nardone, L. Giancaterini, C. Cantalini, L. Ottaviano, "Response to NO2 and other gases of resistive chemically exfoliated MoS2 -based gas sensors," Sensors and Actuators B: Chemical , vol. 207, pp. 602-613, 2015.
[8] Y. Shi, Y. Wang, J. I. Wong, A. Y. S. Tan, C.-L. Hsu, L.-J. Li, Y.-C. Lu, H. Y. Yang, "Self-assembly of hierarchical MoSx /CNT nanocomposites (2<x<3): towards high performance anode materials for lithium ion batteries," Scientific Reports , vol. 3, article 2169, 2013.
[9] K. Hagiwara, T. Ebihara, N. Urasato, T. Fujikawa, "Application of 129 Xe NMR to structural analysis of MoS2 crystallites on Mo/Al2 O3 hydrodesulfurization catalyst," Applied Catalysis A: General , vol. 285, no. 1-2, pp. 132-138, 2005.
[10] Y. Feldman, G. L. Frey, M. Homyonfer, V. Lyakhovitskaya, L. Margulis, H. Cohen, G. Hodes, J. L. Hutchison, R. Tenne, "Bulk synthesis of inorganic fullerene-like MS2 (M = Mo, W) from the respective trioxides and the reaction mechanism," Journal of the American Chemical Society , vol. 118, no. 23, pp. 5362-5367, 1996.
[11] W. K. Hsu, B. H. Chang, Y. Q. Zhu, "An alternative route to molybdenum disulfide nanotubes," Journal of the American Chemical Society , vol. 122, no. 41, pp. 10155-10158, 2000.
[12] J. Wang, C. Luo, T. Gao, A. Langrock, A. C. Mignerey, C. Wang, "An advanced MoS2 /carbon anode for high-performance sodium-ion batteries," Small , vol. 11, pp. 473-481, 2015.
[13] R. Coehoorn, C. Haas, J. Dijkstra, C. J. F. Flipse, R. A. De Groot, A. Wold, "Electronic structure of MoSe2 , MoS2 , and WSe2 . I. Band-structure calculations and photoelectron spectroscopy," Physical Review B , vol. 35, no. 12, pp. 6195-6202, 1987.
[14] J. A. Glasscock, P. R. F. Barnes, I. C. Plumb, N. Savvides, "Formation of fractal-like structures driven by carbon nanotubes-based collapsed hollow capsules," The Journal of Physical Chemistry C , vol. 111, pp. 331-337, 2007.
[15] O. Khaselev, J. A. Turner, "A monolithic photovoltaic-photoelectrochemical device for hydrogen production via water splitting," Science , vol. 280, no. 5362, pp. 425-427, 1998.
[16] R. G. Chaudhuri, S. Paria, "Core/shell nanoparticles: classes, properties, synthesis mechanisms, characterization, and applications," Chemical Reviews , vol. 112, no. 4, pp. 2373-2433, 2012.
[17] D. M. Wu, X. D. Zhou, X. Fu, H. Q. Shi, D. B. Wang, Z. S. Hu, "Synthesis and characterization of molybdenum disulfide micro-sized solid spheres," Journal of Materials Science , vol. 41, no. 17, pp. 5682-5686, 2006.
[18] Z. Wu, D. Wang, A. Sun, "Surfactant-assisted fabrication of MoS2 nanospheres," Journal of Materials Science , vol. 45, no. 1, pp. 182-187, 2010.
[19] S.-K. Park, S.-H. Yu, S. Woo, J. Ha, J. Shin, Y.-E. Sung, Y. Piao, "A facile and green strategy for the synthesis of MoS2 nanospheres with excellent Li-ion storage properties," CrystEngComm , vol. 14, no. 24, pp. 8323-8325, 2012.
[20] J. Li, P. Wu, Y. Ye, H. Wang, Y. Zhou, Y. Tang, T. Lu, "Electronic structure of MoSe2 , MoS2 , and WSe2 . I. Band-structure calculations and photoelectron spectroscopy," CrystEngComm , vol. 16, no. 4, pp. 517-521, 2014.
[21] G. Paglia, C. E. Buckley, A. L. Rohl, R. D. Hart, K. Winter, A. J. Studer, B. A. Hunter, J. V. Hanna, "Boehmite derived γ -alumina system. 1. structural evolution with temperature, with the identification and structural determination of a new transition phase, γ [variant prime]-alumina," Chemistry of Materials , vol. 16, no. 2, pp. 220-236, 2004.
[22] M. Trueba, S. P. Trasatti European Journal of Inorganic Chemistry , vol. 2005, no. 17, pp. 3393-3403, 2005.
[23] F. Lan, Z. Lai, R. Yan, Y. Xu, H. Cheng, S. Zhang, J. Chen, Z. Jia, Z. Wang, C. Qi, "Epitaxial growth of single-crystalline monolayer MoS2 by two-step method," ECS Solid State Letters , vol. 4, pp. 19-21, 2015.
[24] R. Coehoorn, C. Haas, R. A. de Groot, "Electronic structure of MoSe2 , MoS2 , and WSe2 . II. The nature of the optical band gaps," Physical Review B: Condensed Matter and Materials Physics , vol. 35, no. 12, pp. 6203-6206, 1987.
[25] K. K. Kam, B. A. Parkinson, "Detailed photocurrent spectroscopy of the semiconducting group VI transition metal dichalcogenides," Journal of Physical Chemistry , vol. 86, no. 4, pp. 463-467, 1982.
[26] T. R. Thurston, J. P. Wilcoxon, "Photooxidation of organic chemicals catalyzed by nanoscale MoS2 ," The Journal of Physical Chemistry B , vol. 103, no. 1, pp. 11-17, 1999.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Copyright © 2015 S. V. Prabhakar Vattikuti and Chan Byon. 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
This paper reports the synthesis of novel monodisperse Al2O3-coated molybdenum disulfide nanospheres (i.e., core-shell structures) using a one-step facile hydrothermal method. XPS analysis confirmed the purity and stable structure of the Al2O3-coated MoS2 nanospheres. A possible growth mechanism of the core-shell structure is also reported, along with their influence on the photodegradation process of rhodamine B (RhB). The Al2O3-coated MoS2 nanospheres demonstrate good photocatalytic activity and chemical stability compared to MoS2 spheres. TG-DTA analysis provided insight into the decomposition process of the precursor solution and the stability of the nanoparticles. The enhanced photocatalytic activity makes the Al2O3-coated MoS2 nanospheres a promising candidate as a photocatalyst that could be used in place of traditional Al2O3/MoS2 photocatalyst for the removal of pollutants from waste water.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer