The discovery of two-dimensional materials became possible due to the mechanical cleavage technique. Despite its simplicity, the as-cleaved materials demonstrated surprising macro-continuity, high crystalline quality and extraordinary mechanical and electrical properties that triggered global research interest. Here such cleavage processes and associated mechanical behaviours are investigated by a direct in situ transmission electron microscopy probing technique, using atomically thin molybdenum disulphide layers as a model material. Our technique demonstrates layer number selective cleavage, from a monolayer to double layer and up to 23 atomic layers. In situ observations combined with molecular dynamics simulations reveal unique layer-dependent bending behaviours, from spontaneous rippling (<5 atomic layers) to homogeneous curving (~ 10 layers) and finally to kinking (20 or more layers), depending on the competition of strain energy and interfacial energy.
Mechanical cleavage technique, also known as the Scotch-tape method, has resulted in the discovery of two-dimensional (2D) crystals. It is a rather crude procedure, but, surprisingly, the produced samples demonstrated excellent quality and performance1,2,3,4,5,6,7. The simplicity of the Scotch tape method has initiated a booming research on graphene and other 2D materials. A rich family of such materials has been discovered, such as boron nitride (BN), molybdenum disulphide (MoS2), niobium diselenide (NbSe2) and Bi2Sr2CaCu2Ox (ref. 7). However, the atomic processes of the micromechanical cleavage are still poorly understood. How will the atomically thin films behave during the cleavage and under the large bending conditions? Will they bend as a whole plate or will the interlayer sliding occur? Will they lose structural stability under severe bending deformation? These concerns call for a direct investigation into the initial stage of the mechanical cleavage process.
One particularly promising application for the 2D crystals is flexible electronics, because of their strong in-plane bonding and high flexibility8,9,10,11,12,13. MoS2 atomic layers are competitive candidates with suitable electronic structures14,15,16. Bulk MoS2 is a layered semiconductor with an indirect band gap of ~1.29 eV. However, recently it has been demonstrated that MoS2 monolayers have direct band gaps of ~1.8 eV with a strong photoluminescence14,15. In addition, the MoS2-based field effect transistors have shown outstanding performances with high ON/OFF ratios6. Moreover, high-performance MoS2 thin-film transistors and gas sensors have been fabricated on flexible substrates10,11,12,13. It is important to study the 2D-MoS2 mechanical properties for their reliable applications in flexible electronic devices. Bertolazzi et al.5 reported fracture strength as high as 23 GPa at an effective strain of 11%, indicating that the 2D-MoS2 could be almost defect free. The elastic properties were studied by Castellanos-Gomez et al.16 who reported extraordinary high Young’s modulus E=0.33±0.07 TPa for the freely suspended 5–25 layers thick MoS2 nanosheets. However, despite the above-mentioned notable progress, there have been no reports regarding the mechanical behaviour of the MoS2 atomic layers under bending and folding conditions, although this ultimately determines the mechanical reliability of the flexible electronic devices made of such 2D semiconductors.
In this work, we design an in situ transmission electron microscopy (TEM) probing technique17,18,19,20 to investigate the initial stages of the 2D crystal cleavage, which is defined here as the ‘nanomechanical cleavage’, using MoS2 atomic layers as a model material. By precisely manipulating an ultra-sharp metal probe to contact the pre-existing crystalline steps of the MoS2 single crystals, atomically thin flakes are delicately peeled off, selectively ranging from a single, double to more than 20 atomic layers. The mechanical behaviours of the MoS2 atomic layers during cleavage, bending and folding processes are investigated in situ. It is found that the mechanical behaviours are strongly dependent on the number of layers. Combination of in situ TEM and molecular dynamic (MD) simulations allows us to thoroughly investigate a transformation of bending behaviour from homogeneous curving to kinking.
Growth and structure of MoS2 atomic layers
MoS2 crystals for the in situ TEM nanomechanical cleavage experiments were grown by using a CVD method21. As shown in the scanning electron microscopy (SEM) image of Fig. 1a, triangular crystals were uniformly distributed on a SiO2/Si substrate over a large area. Most of them are made of monolayers; however, the by-products having multiple layers were chosen as the target material for our in situ experiments. A plane view of a MoS2 crystal is demonstrated in a high-angle annular dark-field (HAADF) scanning transmission electron microscope (STEM) image (Fig. 1b), revealing a clean surface. Atomic steps are observed at the crystal edges, which are flat and open, rather than rolled up. A high-resolution STEM image is demonstrated in Fig. 1c, where the contrast is proportional to the square of the atomic number. Both molybdenum and sulphur atoms’ positions can individually be resolved to form hexagonal patterns with the Mo-Mo and Mo-S distances of ~3.1 Å and ~1.8 Å, respectively.
Nanomechanical cleavage experimental configurations
To perform the in situ TEM probing and nanomechanical cleavage experiments, the MoS2 crystals were loaded in edge-on orientation, as shown in the schematic (Fig. 1d) and corresponding TEM image (Fig. 1e). A typical sample was about 32 nm in thickness and 380 nm in length. An ultra-sharp tungsten tip was manipulated by a piezoelectric motor to approach and contact a MoS2 single crystal. As shown in the HRTEM image (Fig. 1f), there are pre-existing atomic steps at the crystal surface; therefore, the tungsten probe with a tip diameter as small as ~10 nm could be manipulated to contact the crystalline edges with a selected number of layers. By using this method, a layer-number-selective cleavage of the MoS2 atomic layers was realized. Single-, double-, triple- and multilayers with a thickness of up to 23 atomic layers were successfully cleaved.
Nanomechanical cleavage of monolayer MoS2
The nanomechanical cleavage process of a monolayer MoS2 is presented in Fig. 2a–d and Supplementary Movie 1. Initially, there was a single-layer edge protruding from the MoS2 crystal, which therefore made it possible to contact only the outermost single layer (Fig. 2a). After the contact, the probe was moved at an inclined angle, as marked by the black arrow, causing the single layer to attach to the probe and to be peeled off, and to bridge the nanoprobe and the ‘mother’ crystal (Fig. 2b). It is noted that the peeled-off MoS2 monolayer was naturally curved, consistent with the previous theoretical and experimental works on the intrinsic rippling of 2D crystals22,23,24. By moving the probe away, the MoS2 monolayer flake could be stretched and ultimately separated from the mother crystal (Fig. 2b,c). The insets in Fig. 2b,c demonstrate the snapshots of the corresponding MD simulations, where the profiles of simulated MoS2 layer agree well with the HRTEM images. The simulations confirmed that the smoothly curved profile in Fig. 2b is within elastic regime. When the flake was detached, the edge was perpendicularly attached to the surface atomic step (Fig. 2c). HRTEM image of the MoS2 monolayer taken before its separation is shown in Fig. 2d. MoS2 (100) stacking order could be clearly resolved, indicating the high crystallinity. The inset of Fig. 2d demonstrates the triple-layer atomic structure, with a molybdenum atomic layer sandwiched by two sulphur atomic layers. The free-standing monolayer tends to fold up, as demonstrated using dots at the periphery lines. This also coincides with the formation of spontaneously curved edge when the monolayer was detached from the crystal (Supplementary Movie 1). The spontaneous folding suggests the importance of van der Waals forces for the mechanical behaviour of 2D crystals. Interestingly enough, after initial isolation from the mother crystal, the MoS2 monolayer could be readily restacked onto the surface of the crystal, as presented in Fig. 2e–h and Supplementary Movie 2. First, a point contact was established between the MoS2 monolayer and the crystal surface (Fig. 2e). Second, by pushing the probe, the monolayer was easily bent and formed a plane contact with the surface (Fig. 2f), indicating the re-establishment of crystalline stacking due to the van der Waals interactions. After that, by moving the probe parallel to the crystal surface, the MoS2 monolayer could smoothly slip along the surface, as indicated by a change in distance between the contact point and the crystal edge that reduced from 25.5 to 8.3 nm. Finally, by pushing the probe towards the crystal, the cleaved MoS2 monolayer was almost completely restacked onto the surface. As shown by the inset profile along the arrow in Fig. 2h, the distance between the MoS2 monolayer and the crystal surface became ~0.65 nm, exactly the same as the interlayer distance of the initial crystal. Therefore, the nanomechanical cleavage was reversible, and no structural defects were introduced to the monolayer MoS2. This reversibility can explain the high quality and carrier mobility in the mechanically exfoliated 2D samples, such as graphene and MoS2 atomically thin films1,6.
Nanomechanical cleavage of double and triple layers of MoS2
By selecting the MoS2 edges with a different number of protruding atomic layers, double and triple layers of MoS2 were successfully cleaved from the MoS2 crystal, as demonstrated in Supplementary Figs 1,2 and Supplementary Movies 3,4. A double-layer MoS2 as long as 155 nm was cleaved, as illustrated in Supplementary Fig. 1 and Supplementary Movie 3. It was worth noting that at the beginning of the cleavage process, observations suggested six layers rather than two (Supplementary Fig. 1a). This is because of the mechanical contact with the probe, which led to the edge bending, rolling and crumpling. Under stretching, the crumpled MoS2 sheet became flat, and a double layer lattice became apparent (Supplementary Fig. 1d). Similar process and ability to recover from severe deformations were demonstrated for a triple-layer MoS2 (Supplementary Fig. 2). The extraordinary ability to restore deformed structures demonstrates the high flexibility of the MoS2 atomic layers, which is crucial for their applications in flexible electronics. The minimum bending radius for the inner layer of double and triple MoS2 was about 3.0 nm and 3.1 nm, respectively. A common feature during bending was spontaneous rippling (Supplementary Figs 1c and 2d), which was attributed to thermal fluctuations22,23,24.
Nanomechanical cleavage of 5- and 11-layer MoS2
In our experiments, it was found that the mechanical behaviours of the MoS2 atomic layers had been closely dependent on the number of layers (thickness) of the flakes. In the following section, the mechanical behaviour of comparatively thick MoS2 stacks is discussed. The number of layers ranges from 5 to 11 in the corresponding experiments. In contrast to the relaxed ripples and folded-up configurations in the mono-, double- and triple-layer MoS2, such flakes were more rigid, as demonstrated by the straight profile during the bending process (Fig. 3, Supplementary Fig. 3, and Supplementary Movies 5,6). This change is plausible, because a thicker membrane with a larger bending stiffness will have smaller displacements due to thermal fluctuations according to the relation <h2>∝ TL2/k, where L is the size of the sample and k is the bending rigidity25,26. It is worth noting that, for the 5-layer MoS2, when the flake was released from the probe, it kept the bent configuration and was attached to the surface of the ‘mother crystal’, again indicating the importance of van der Waals forces for the stability and mechanical behaviours of the ultrathin crystals.
Figure 3 and Supplementary Movie 6 present the detailed forward and reverse processes of the nanomechanical cleavage of an 11-layer MoS2. The original structure of the crystal is the same as that in Fig. 1f, in which the atomic steps are almost vertical to the MoS2 (002) lattice fringes. After the initial contact and a small degree of bending, the angle became ~84° and then ~79°, indicating the interlayer sliding rather than bending as a whole plate (Fig. 3a,b). On further bending and cleaving, the angle between the edge and the MoS2 (002) planes remained unchanged (Fig. 3c–g), indicating that the contact with the probe prohibits the interlayer sliding. In the meantime, strain contrast was observed at the transition portion between the bent and straight areas in Fig. 3c–g. Note that even with 11 atomic layers the MoS2 sheet demonstrated high flexibility. It was bent with a radius of curvature of ~4.5 and~1.3 nm for the middle and inner layers, respectively. After release from the probe, the cleaved MoS2 thin flake recovered to the original configuration except for the contact area. A plastic deformation was recorded close to the contact area with the angle between the edge and the MoS2 (002) planes ~44°. Thus, the nanomechanical cleavage is largely reversible except for the contact area with the probe, and the layer damage is due to the point contact and stress concentration. MD simulations were performed for the 11-layer MoS2 with the geometrical parameter inputs matching the experimental data (Supplementary Movie 7). The edge atoms of the layers were fixed to reflect the adhesion between the tip and the sample during the cleavage process, except for the initial and final contact stages, where the MoS2 layers became free of the probe. After that the fixed edge atoms were moved step by step, following the experimental direction. As in the previous case, a good agreement between simulated and experimental images was reached. Because of the constriction on the probe, the MoS2 layers could not slide freely under bending, and delamination of the layers was observed, as marked in the inset of Fig. 3b, consistent with a previous theoretical work on the bending-induced delamination of van der Waals solids27. Under further bending, the delamination vanished due to the redistribution of the stresses in Fig. 3c,d. There were two areas with concentrated strain: one is the contact area with the probe and the other is the bent area. At the site close to the probe, all the layers are under tensile stress due to the adhesion and stretching of the probe, as indicated by the blue colour. In contrast, the site of the bent area demonstrates tensile and compressive stresses on the outer and inner surfaces, respectively. This result is consistent with the in situ observations that during the contact and cleavage process the interlayer sliding could not occur freely due to the constriction of the MoS2-probe interface. Therefore, while the free standing MoS2 atomic crystals can easily slide during bending, the actual deformation process also depends on the boundary conditions.
Nanomechanical cleavage and kinking of 23-layer MoS2
We further investigated the bending process of a 23-layer MoS2 flake (Fig. 4 and Supplementary Movie 8). It was thick enough to directly measure the forces during the cleavage process; therefore, the experiments were performed using an in situ atomic force microscopy (AFM)-TEM holder. In contrast to the smoothly bent configurations for the thinner stacks, the 23-layer MoS2 formed discrete kinks during bending, as marked by the white arrows. Accordingly, abrupt force drops were recorded, as presented in Fig. 4h. Interestingly, the kinks appeared periodically, at the bending angles of around multiples of 20°, such as 23.2°, 39.2°, 19.6° and 39.0°, as marked in Fig. 4. It is noticed that even with the kink appearance, the whole process is largely reversible. After the separation from the AFM probe, delamination was observed only at the contact, due to the stress concentration at the contact (Fig. 4g). A simplified model of the MoS2 film was adopted to simulate the process (Supplementary Movie 9). At the initial state the film and the probe were brought together at a distance of chemical bond (<2.5 Å), and part of the film layers was left unbounded in accordance with the experimental conditions (Fig. 4a). Tangential movement of the probe led to sample cleavage. After the initial contact, the crystal transformed from the free unloaded to the compressed state, as indicated by the colour change from white to red. After that the compressed layers were elastically buckled, and the deformation was then concentrated at the buckled area. With further contact and tangential movement of the AFM probe, the layers were markedly bent and kinking took place. The geometry difference in a simulated model and experimental structure does not allow us to directly compare the calculated and in situ TEM recorded data. However, the theoretical model does capture the main experimental characteristics. The experimental force–time curve can be compared with calculated energy-simulation steps. In both plots, the observed and simulated spontaneous kink formations are represented by pronounced peaks.
Obviously, the bending behaviours of the MoS2 atomic layers during cleavage are closely related to the number of layers, as summarized in Supplementary Table 1. For the bulk layered materials such as MoS2, one common deformation mechanism is the formation of kinks28,29. It is noted that, for the thin 2D MoS2 layers (11 layers), they bend with the absence of kinking, even when the layers are bent to ultimately small radii (1.3~3.0 nm). The force balance of such bent MoS2 monolayer has been analysed. The equilibrium shape is determined by the balance between the forces applied by the nanoprobe and the non-covalent dispersion forces in the vicinity of the contact—same forces that constitute the surface energy. If these van der Waals forces depend on the interlayer distance y as f(y), then the specific surface energy γ can be written as . Near its minimum (x=y=0 and dy/dx=0) at the contact point the bent layer shape can be described by the next quadratic term y=x2/2R, with R being the radius of curvature. Because of this curvature, there is a torque D(1/R), where D=27 eV Å2 atom−1 is the bending stiffness of MoS2 monolayer30. In equilibrium, this torque must be balanced by the opposite moment produced by the distributed van der Waals forces near the contact point at x0, so we have D(1/R)=∫xf (x2/2R)dx=R∫f (y)dy=R·2γ, and therefore, γ=D/2R2. In macroscopic studies, the same relationship can be derived by energy analysis31, but the force approach here permits straightforward generalization for the monolayers investigation. The fitting and calculation of the curvature radius near the contact point are presented in Supplementary Fig. 4. Moreover, the radius of curvature was calculated to be ~1.5 nm. Accordingly, the specific surface energy of MoS2 monolayer is calculated to be ~0.06 eV atom−1 or ~0.11 N m−1. Determination of the surface energy is fundamentally important for various processes, such as catalysis and lubrication. Previously, the specific surface energy of MoS2 has mainly been investigated by theoretical calculations. In early publications, comparatively high values such as 0.26 and 0.28 N m−1 were reported32,33. However, the specific surface energy of MoS2 was derived from liquid exfoliation processes34,35 to be ~0.07 N m−1. Recently, a more accurate random-phase approximation (RPA) method was adopted for the calculations of the binding energy of the van der Waals bonding in layered compounds34. Interlayer binding energies for a large number of layered compounds, including MoS2, were calculated to be around 20 meV Å−2 (~0.32 N m−1), with the specific surface energy being half of that value (~0.16 N m−1)34. Thus, our directly measured value is reasonably consistent with the most accurate RPA calculations currently available.
For the multi-layer MoS2 flakes, an important issue is whether the layers slide or the sample will bend as a plate. Shen et al.26 reported that sliding would dominate the bending for graphene nanoribbons, due to the low interlayer shear modulus. However, Koskinen27 and Nikiforov et al.35 found that when the edge of graphene nanoribbons was fixed, kinks and delamination became the major deformation mechanism. In our experiments, it was found that, while the free standing MoS2 crystals are easy to slide, the interlayer sliding could be restricted by the interaction with the probes. The easy sliding could be understood by the low shear strength, which has been reported to be only around 0.1 GPa (refs 36, 37, 38). With a given maximum shear stress (τmax), the threshold bending angle for sliding can be calculated simply by applying the strength theory of materials39 as , where L is the length, E is the Young’s modulus, N is the layer number and d is the interlayer distance. Therefore, the threshold angle is proportional to the square of length and inversely proportional to the square of layer number, as demonstrated in Supplementary Fig. 5. For example, for an MoS2 sheet with a length of 10 nm and five layers in thickness, the threshold angle would be as small as ~0.7°, which can explain the easy sliding during bending. It is also seen that when the length of the 2D crystal becomes larger it is more difficult to slide, which can explain why buckling rather than interlayer sliding became the major mechanism for bending the long BN and graphene nanoribbons with a length around 1 μm (ref. 35). Because of easy interlayer sliding, the atomic layers bend mostly independently, which is the reason for the minimum radius (corresponding to the maximum bending) to be non-related to the number of layers before the kinking mechanism comes into effect. The regarded 2D crystals might be bent to a radius as small as ~1.3 nm, showing that they are mechanically reliable candidates for future flexible electronic devices.
For the 23-layer MoS2, we observed the appearance of kinking during bending, which is close to the deformation of the bulk crystals28,29. These kinks are different from the buckling and delamination phenomena discussed in the previous reports, where only the inner layers were buckled due to the compressive stress27,35. The formation of kinks could be understood by the competition between bending strain energy and commensurability effects in interfacial energy on interlayer sliding. The strain energy of a bent plate can be calculated using the following formula: , where M is the bending moment, I is the moment of inertia, b is the width, θ is the bending slope, N is the layer number and L is the length. When interlayer sliding occurs, the bending energy is N times that of one atomic layer and can be expressed as , which is proportional to N rather than to N3. Meanwhile, because of the interlayer sliding, the interfaces between the atomic layers become incommensurate and the increased interfacial energy can be calculated as , where γint=0.11 N m−1 is the interfacial energy constant, L is the length of the sliding interface and c is the lattice constant along the sliding direction. It is reasonable to assume that the interfacial energy is a periodic function of the interlayer sliding distance40,41. Figure 5 demonstrates the calculated energy for double-, and 20-layer MoS2, where bending strain energy of the plate-bending model is pictured purple, and the combination of bending strain energy and interfacial energy related to the bending-sliding model is pictured green. For the double-layer MoS2, the interfacial energy dominates and it tends to bend without sliding (Fig. 5a). In constrast, for the 20 layer-MoS2, the bending strain energy becomes dominating, and it tends to bend with interlayer sliding (Fig. 5b). Figure 5c presents the detailed feature of the energy involved in the bending-sliding model for the 20-layer MoS2. Clearly, the interfacial energy is a periodic function of the bending slope. Therefore, for the thick MoS2 flakes, during the sliding, when the interlayer sliding distance equals to the lattice constant or any other periodic distance along the sliding direction, the interfacial energy will show local minima. When the energy ‘valleys’ are met, abrupt force drop can be expected, which reflects the formation of kinks. It is noted that the period is around 0.36 rad (~20.6°), which is well consistent with our experimental observations.
In conclusion, we developed an in situ TEM probing technique for direct investigation of the nanomechanical cleavage of 2D crystals. MoS2 atomic layers were successfully cleaved from a single crystal with the layer number predetermined by the precise manipulation with an ultra-sharp probe. It was demonstrated that such cleavage is highly reversible. In addition, combining the in situ experiments with the MD simulations, the thickness-dependent mechanical behaviours were revealed. The featuring bending kinetics transformed from homogeneous curving and rippling (<5 atomic layers) to interlayer sliding (~10 layers) and to kinking (~20 or more atomic layers).
Growth and characterization
The MoS2 atomic layers were synthesized on a SiO2/Si substrate by a vapour phase growth at 850 °C, using MoO3 nanoribbons and pure sulphur as the precursors and reactants, respectively21. The crystalline structures of the MoS2 atomic layers were characterized by TEM/STEM. The TEM samples were prepared by transferring the grown samples onto the TEM grids by direct contacting, so that the samples were free of contamination. The high-resolution TEM/STEM characterization was carried out on a FEI Titan3 (Cube) microscope, equipped with a monochromator and Cs-correctors for probe-forming and imaging at an accelerating voltage of 300 kV in a HAADF imaging mode.
In situ TEM probing experiments
The in situ TEM probing experiments were mainly conducted using a scanning tunnelling microscope (STM)-TEM platform (‘Nanofactory Instruments AB’) in a HRTEM (JEM-3100FEF) with an accelerating voltage of 300 kV equipped with an OMEGA-type energy filter. Ultra-sharp tungsten probes (~10 nm tip diameter) were produced by electrochemical etching. MoS2 single crystals were loaded on the edge of a gold wire with an edge-on orientation, and the tungsten tip movements were controlled by a piezoelectric motor to approach and selectively contact the atomic edge steps. After that, the tungsten tip was moved backwards to start the nanomechanical cleavage of the MoS2 atomic layers. Bending deformation was then initiated by pushing the tungsten tip towards and along the edge of the MoS2 crystal. The in situ force measurements were carried out by using AFM-TEM holder (‘Nanofactory Instruments AB’). The whole process was video recorded in real time by a charge-coupled device (CCD) camera.
MD simulations were performed using the reactive empirical bond-order and Lennard-Jones potentials implemented into the Large-scale Atomic/Molecular Massively Parallel Simulator (LAMMPS) simulation package42. The Mo-S potential was parameterized to match density functional theory calculations of Mo, S and Mo-S structures43. The parameterization was successfully applied in the investigation of the mechanical properties of crystalline MoS2 by the indentation method44 and in the studies of behaviour of MoS2 multilayered nanotubes in extreme pressure conditions45. This technique is perfect to describe structural and mechanical properties of the Mo-S systems consisting of a large number of atoms (>104). The MoS2 systems were modelled as clusters with a length of ~40 nm (for mono- and 11- layer structures containing 1,400 and 13,300 atoms, respectively) and ~100 nm (for a 23-layer structure containing 19,500 atoms). In the case of mono- and 11-layer samples, the atoms on the end of the upper layers were fixed imitating the tip and moved along the direction corresponding to the experiment with a displacement step equal to 0.1 Å. In the case of 23-layer sample, for the imitation of the adhesion between the bottom edge of AFM tip and the sample, the MoS2 monolayer of finite length was fixed and moved directly to the sample along the direction corresponding to the experiments with a displacement step equal to 0.1 Å.
How to cite this article: Tang, D.-M. et al. Nanomechanical cleavage of molybdenum disulphide atomic layers. Nat. Commun. 5:3631 doi: 10.1038/ncomms4631 (2014).
D.-M.T. and D.G. thank Professor Kazutomo Suenaga, Drs Ryousuke Senga, Ovidiu Cretu, Masanori Mitome and Naoyuki Kawamoto for technical help, and Dr Ilia Nikiforov and Professor Traian Dumitrica for helpful discussions. D.G.K. and P.B.S are grateful to Dr Douglas E. Spearot for the fruitful discussions. We acknowledge support from JSPS KAKENHI Grant Number 25820336, International Center for Young Scientists (ICYS), World Premier International (WPI) Center for Materials Nanoarchitectonics (MANA) of the National Institute for Materials Science (NIMS), and Ministry of Education and Science of the Russian Federation (Agreement No. 11.G34.31.0061) through the Mega-Grant Program for the leading scientists (D.G.). We are also grateful to the ‘Chebishev’ and ‘Lomonosov’ supercomputers of Moscow State University and the Joint Supercomputer Center of the Russian Academy of Sciences for the possibility of using a cluster computer for quantum-chemical calculations. P.B.S. acknowledges the support by ‘FAEMCAR’ (FP7-PEOPLE-2012-IRSES) and the EU-ERC INTIF 226639. D.G.K. acknowledges the support from the Russian Ministry of Education and Science (No. 948 from 21 of November 2012). S.N., P.M.A. and J.L. acknowledge the support of Welch Foundation Grant C-1716, the NSF Grant ECCS-1327093 and the U.S. Army Research Office MURI Grant W911NF-11-1-0362. P.K. acknowledges the Academy of Finland for funding.
In situ TEM video of nanomechanical cleavage of a MoS2 monolayer (Fig. 2a-d).
In situ TEM video of a MoS2 monolayer sliding on the MoS2 crystal surface (Fig. 2e-h).
In situ TEM video of nanomechanical cleavage of a double-layer MoS2 (Supplementary Fig. 2).
In situ TEM video of nanomechanical cleavage of a triple-layer MoS2 (Supplementary Fig. 3).
In situ TEM video of nanomechanical cleavage of a 5-layer MoS2 (Supplementary Fig. 4).
In situ TEM video of nanomechanical cleavage of an 11-layer MoS2 (Fig. 3).
MD simulation of an 11-layer MoS2 cleavage in comparison with in situ TEM observations (Fig. 3).
In situ TEM video of nanomechanical cleavage of a 23-layer MoS2 (Fig. 4).
MD simulation of 23-layer MoS2 cleavage in comparison with in situ TEM observations (Fig. 4).
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