Journal of Nanomaterials

Journal of Nanomaterials / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 852735 |

Jing-Yuan Wu, Meng-Na Lin, Long-De Wang, Tong Zhang, "Photoluminescence of MoS2 Prepared by Effective Grinding-Assisted Sonication Exfoliation", Journal of Nanomaterials, vol. 2014, Article ID 852735, 7 pages, 2014.

Photoluminescence of MoS2 Prepared by Effective Grinding-Assisted Sonication Exfoliation

Academic Editor: Jing Chen
Received28 Feb 2014
Accepted20 Apr 2014
Published19 Jun 2014


Exfoliation of bulk molybdenum disulfide (MoS2) using sonication in appropriate solvent is a promising route to large-scale preparation of few-layered or monolayered crystals. Grinding-assisted sonication exfoliation was used for preparing monolayered MoS2 nanosheets from natural mineral molybdenite. By controlling the sonication time, larger crystallites could be further exfoliated to smaller as well as thinner nanosheets without damaging their structures. The concentration of 1.6 mg mL−1 of final solution could be achieved. Several microscopic techniques like scanning electron microscopy, transmission electron microscopy, and atomic force microscopy were employed to evaluate the exfoliation results. Strong photoluminescence with the peak centered at 440 nm was also observed in the resulting dispersion which included several small lateral-sized (~3 nm) nanostructures.

1. Introduction

The discovery of graphene, which is the thinnest two-dimensional (2D) crystal with characteristics of high optical transparency [1], excellent thermal conductivity [2], and exceptional mechanical strength [3], has opened up prospects for a number of emerging technologies in areas of photonics and optoelectronics [4, 5]. These outstanding properties arising from atomic-layer thickness and high specific surface area have also encouraged the exploration of other kinds of 2D crystals including the transition metal dichalcogenides (TMDCs) [68], transition metal oxides [9], and hexagonal boron nitride (hBN) [10]. In particular, single- and few-layer TMDCs have attracted a recent surge of interest due to their newly found remarkable properties, especially layer-dependent property, which can be applied to the fields of catalysis [11, 12] and optoelectronics [1315], to name a few.

Molybdenum disulfide (MoS2), which belongs to the TMDCs material family, has recently attracted considerable attention owing to its remarkable properties [16, 17] and reliable production of atomically thin 2D sheets from bulk counterpart [1821]. As opposed to graphene, which is zero-bandgap, MoS2 is an indirect bandgap semiconductor when in its bulk form. Besides, as the thickness decreases, it turns to a direct bandgap semiconductor, leading to an enhancement of the photoluminescence because of quantum confinement effects [16]. The unique optical properties make it an ideal candidate for the novel optoelectronic devices including phototransistors [22], light detectors [23], and emitters [24].

Due to the weak interaction between adjacent layers and the strong intralayer interaction, the bulk MoS2 crystal can be exfoliated to mono- or few-layer flakes. The monolayer MoS2 was first prepared by scotch tape based micromechanical exfoliation [2527], which was one of the most common methods. However, the method is not scalable and the size and thickness of exfoliated flakes cannot be controlled. With rapid development of study on the characteristic and application of MoS2, high yield preparation methods are in great demand. The chemical vapor deposition (CVD) method is able to generate large-area continuous MoS2 films with great performance, which holds promise in electronic application [19]. The lithium intercalation method is another useful method for the exfoliation of bulk MoS2 and the process can be well controlled to achieve high throughput [7]. However, the processes of the two above methods are relatively complicated, limiting their applications. The liquid exfoliation has been found to have great potential for the scalable production of 2D-nanosheet-based materials, which has been successfully demonstrated for a range of layered quantities including graphite, TMDs, and hBN [18, 28, 29]. Different from the micromechanical method, liquid exfoliation can give suspensions of few-layer 2D flakes which can be processed into composites and films. It is also easier to transfer the exfoliated products to arbitrary substrates avoiding complex transfer processes. The resulting MoS2 nanosheets suggest applications in electrochemistry field [30] and van der Waals heterostructures devices [31]. Liquid exfoliation can be achieved by direct sonication in various organic or aqueous surfactant solvents, but the concentration was relatively low. To increase the concentration of the resulting MoS2 suspension, some improved methods have been reported, for example, the ethanol/water mix-solvent sonication combined with grinding [32] and high power tip sonication [28].

Herein we report an effective grinding-assisted liquid exfoliation technique to achieve MoS2 nanoflakes of high concentration and then analyze their optical absorption and photoluminescent properties. The solution processable MoS2 suspension shows obvious blue-shifted photoluminescence compared to that of monolayer MoS2 exfoliated by the micromechanically cleavage method. The blue-shifted luminescence is mainly caused by the quantum dots (~3 nm) generated by sonication, promising interesting novel application in biology and medicine.

2. Materials and Methods

The MoS2 starting powder was purchased from Sigma Aldrich (<2 μm particle size) and used as supplied. MoS2 powder (1 g) was added to 0.8 mL of N-methyl-2-pyrrolidone (NMP). After grinding for one hour, the mixture was placed in a vacuum oven for two hours at 60°C to dry. Then it was collected and redispersed into a 10 mL NMP solvent. Grinding for several minutes in this process can help dissolve the oven-dried MoS2 in case of wasting the products. The solution was transferred to a beaker and then probe-sonicated (Ultrasonic Processor KH3200) for 100 minutes at the power of 150 W. After that, we deposited a few drops of resulting solution onto the indium tin oxide (ITO)-covered glass slide at room temperature for one day to make it dry naturally. The ITO covered glass was cleaned using piranha solution to make it hydrophilic, on which the mixture can be distributed more uniformly. Then the glass covered with sample was placed onto a hotplate at 200°C for 3 minutes before being removed and allowed to cool. The morphology of the samples was inspected by scanning electron microscopy (SEM, Quanta 200 FEI).

The solution obtained after sonication was centrifuged for 40 minutes at the speed of 4000 rpm and the supernatant containing 2D MoS2 nanoflakes was collected finally. The supernatant was then prepared for further study of their microstructure characterization and optical properties. It was dropped on thermally oxidized SiO2/Si (90 nm) wafer substrate for Raman spectrum characterization (T64000) with the starting MoS2 powder being measured for comparison. Analysis of the samples by Raman spectroscopy was performed under ambient conditions. The pump radiation was supplied at a wavelength of 632.8 nm with the laser power of 1.3 mW. The suspension was diluted and 5 or 6 globs of them were dropped carefully on lacy carbon-coated Cu grid followed by drying one day to volatilize NMP completely for transmission electron microscope (TEM, JEM-2100) observation. Atomic force microscopy (AFM, Dimension ICON) was also used to analyze the structure and thickness of the MoS2 nanosheets. A sample of the diluted dispersion was placed on the clean thermally oxidized SiO2/Si wafer substrate and evaporated at room temperature overnight. The measurements were performed under ambient laboratory conditions in a trapping mode. To determine the concentration of 2D sheets in the supernatant, assuming that NMP was distributed uniformly in it, 1 mL of solution was taken out from the supernatant to the reagent bottle, and then the mass of 2D nanosheets was weighed by a microbalance after drying in a vacuum oven for one day. By subtracting the mass of the empty bottle, the pure mass of MoS2 nanosheets can be obtained. The process was repeated multiple times and the results were averaged to reduce the error. To further analyze their optical properties, UV-visible spectra were measured by UV-3600. The photoluminescence spectra of MoS2 were obtained by fluorospectrophotometer (RF-5301PC).

3. Results and Discussion

Crystals of MoS2 are composed of vertically stacked, van der Waals bonded S-Mo-S units held together, as shown in Figure 1. Each of the units consists of two hexagonal planes of S atoms and an intermediate plane of Mo atoms coordinated through ionic-covalent interactions with the S atoms [25]. Because of the relatively weak interaction between layers and the strong intralayer interaction, exfoliating MoS2 to few layers using liquid exfoliation technique is possible.

Compared to scotch tape microcleavage method, the liquid exfoliation technique can achieve large-scale preparation. The NMP solvent was chosen because its surface energy matches nanosheets’ well, resulting in the enthalpy of mixing being very small [33]. Meanwhile, the surface tension can help overcome the van der Waals force, which makes the exfoliation easier and more effective. It also can be replaced by other organic solvents such as isopropanol (IPA), dimethylformamide (DMF), and dimethylsulphoxide (DMSO) [18]. The grinding process should be gentle and soft to detach the MoS2 layers from the bulk materials relying on pure shear forces [32]. This function can be achieved by ball milling process as well [29]. Besides, adding NMP as a stabilizing surfactant into commercial MoS2 powder in the process can avoid reassembling of the MoS2 nanosheets [18]. After being dried and redispersed into the NMP solvent, a high power tip sonication was used to further exfoliate MoS2 in liquids. The sonication time needs to be selected appropriately. If the time is too long, it will damage MoS2 nanosheets and affect their properties, while if the time is too short, the large flakes cannot be exfoliated effectively. To investigate the nature of the resulted MoS2, we performed SEM characterization. Figure 2 shows the SEM image of the surface of exfoliated MoS2 nanosheets. By imaging the thin MoS2 films, we observed a disordered array of MoS2 nanoflakes stacked predominately in-plane. They were continuous over length scales greater than a few microns. Because the dispersions were not centrifuged, most of the nanoflakes were still relatively thick. Therefore, the last centrifugation step was employed to remove the larger nanoplatelets and any partially exfoliated crystallites [33]. Finally, the smaller flakes remained in the supernatant while the larger flakes and unsonicated powders existed in the sediment.

To confirm that the observed objects are MoS2 flakes, Raman analysis is necessary. Figure 3 shows the Raman spectra ranging from 40 cm−1 to 1000 cm−1 of MoS2 nanosheets exfoliated and the starting powder. We noted that the peak positions slightly shifted from those expected for crystalline MoS2 as was sometimes observed for powdered samples. There are four first-order Raman active modes in MoS2, in which , , and modes are a result of vibrational modes within the S-Mo-S layer. The little downshift of all the peaks from the reported literatures may be related to the laser-induced heating [34]. It was observed that the and modes of the exfoliated MoS2 nanosheets were centered at 379 cm−1 and 404 cm−1, respectively, which were in the expected wavenumber range. Previous researches have demonstrated that the 2D exfoliated nanosheets have a smaller Raman shift difference between the two modes in comparison with their bulk counterparts because of the influence of neighboring layers on the effective restoring forces on atoms and the increase of dielectric screening of long-range Coulomb interactions [35]. However, it was observed that the Raman shift difference between the two modes of our exfoliated sheets was nearly equivalent to that of the starting powder. It was probably due to the aggregation during the process of deposition/drying on the substrate. In the Raman spectrum of MoS2 powder, we also observed three new bands presented at 279, 817, and 988 cm−1 which did not exist in the exfoliated nanosheets. These bands represent MoO3 vibrational energy states as a result of oxidation by the laser irradiation [34].

Transmission electron microscopy (TEM) is used to further analyze the structures of MoS2 nanoflakes. Examples of exfoliated nanoflakes are shown in Figure 4. It can be seen that when the layers were exfoliated to ultrathin layers, the flakes turned to be transparent to the electron beam. From Figures 4(a)-4(b), it was observed that the edge of the flake tended to be thinner. The tendency was also found in the MoS2 nanoflakes which were prepared by scotch tape micromechanically cleavage method. Meanwhile, increasing grinding and sonication time can further exfoliate the flakes to thin layers. By comparing TEM images of MoS2 nanoflakes in the condition of different grinding and sonication time, we determined that the optimized time of grinding and sonication were one hour and 100 minutes, respectively. In this case, we achieved a continuous ultrathin MoS2 with lateral size reaching several micrometers shown in Figure 4(c). Meanwhile, several MoS2 quantum dots with average size of about 3 nm are shown in Figure 4(d). Figure 4(e) depicts the selected area electron diffraction (SAED) pattern of the sample, which is indexed to the near perfect planar 2H MoS2. We next performed AFM analysis to firmly determine the thickness of the obtained MoS2 sheets. Figure 5 shows the AFM image of MoS2 nanosheets deposited on a flat silicon wafer with a 90 nm oxide layer. A step of ~5 nm (corresponding to 7 monolayer MoS2) with average lateral size of nearly 200 nanometers can be observed. There were some small individual nanosheets with the thickness of 2 nm and the size of several dozens of nanometers. Some thick nanosheets whose thickness reached 20 nm were also observed in the measurement.

The supernatant containing MoS2 dispersions after centrifugation appeared to be blackish green in color, as shown in the inset of Figure 6. It was found that the dispersions remained stable over periods of several weeks. By measuring the weight of 2D nanosheets in 1 mL supernatant, the concentration of the solution was estimated to be 1.6 mg mL−1. The detailed optical properties of the nanoflakes were studied by measuring their UV-visible absorption spectra. The absorption spectrum exhibited two typical peaks at 621 nm and 680 nm, which are ascribed to B and A excitonic peaks, respectively, arising from the energy split from valence band spin-orbital coupling in 2D MoS2 with large lateral dimensions [25]. The centrifugation process removed most of the large 2D flake in the suspension, leading to the relatively weak features of the two peaks. In addition to these two weak peaks, there were two other peaks at 394 nm and 460 nm. It is probably due to the optical absorption of smaller lateral-sized MoS2 nanosheets. The absorption peaks of the nanostuctures exhibit strong blue-shift even to ultraviolet wavelength arising from quantum effect [36].

We measured the excitation spectrum and emission spectrum of the exfoliated MoS2, respectively. It was observed that a strong broad peak was centered at 440 nm in the emission spectrum, as shown in Figure 7. The phenomenon was quite different from what was observed in the monolayer MoS2 exfoliated by scotch tape method. In that case, the strong photoluminescence is attributed to the direct excitonic transition as the monolayer MoS2 turns to a direct bandgap semiconductor. Therefore, its photoluminescence peak is centered at 1.9 eV (652 nm), the bandgap of monolayer MoS2, which was demonstrated by previous calculation and experiment [16]. The difference is probably due to quantum confinement effect across the 2D planes [37]. To explain this more clearly, the size of nanoflakes prepared by scotch tape method is usually microndimensional; however, the sonication process in the liquid exfoliation method not only makes the flakes thinner but also further reduces their lateral size. Therefore, the 2D MoS2 products prepared by liquid exfoliation method were generally small in lateral dimensions, even generating quantum dots of nanometer dimension in the process of exfoliation, which were demonstrated in Figure 4(d). The luminescence properties are mainly decided by the size of particles [38]. Therefore, the characteristic of the peak is ascribed to the strong blue-shift hot photoluminescence from the K point [36, 37].

4. Conclusion

In summary, the grinding-assisted sonication method allows a cheap, easy, and scalable fabrication of MoS2 nanosheets exfoliated from its bulk counterpart. The as-fabricated dispersions consisted of ultrathin-layered 2D MoS2 and remained stable in NMP solvent for several weeks. The AFM image further confirmed that the MoS2 was exfoliated to about 7 monolayers with lateral size of 200 nm. The concentration of the final solution reached 1.6 mg mL−1, which would present an environmentally benign method, possibly for large-scale production with high quality. The lateral size of MoS2 nanosheets was reduced even to nanometer dimension after sonication; as a result, there was a blue-shift of the emission peak compared to the nanosheets prepared by scotch tape micromechanically cleavage method. The photoluminescent property makes the exfoliated product a promising choice to be applied to solar cell and light-emitting device.

Conflict of Interests

The authors declare that they have no conflict of interests.


This work is supported by NSFC under Grant no. 61307066, Doctoral Fund of Ministry of Education of China under Grant nos. 20110092110016 and 20130092120024, Natural Science Foundation of Jiangsu Province under Grant no. BK20130630, the National Basic Research Program of China (973 Program) under Grant no. 2011CB302004, and the Foundation of Key Laboratory of Micro-Inertial Instrument and Advanced Navigation Technology, Ministry of Education, China, under Grant no. 201204.


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