Defects-assisted piezoelectric response in liquid exfoliated MoS2 nanosheets

MoS2 is an intrinsic piezoelectric material which offers applications such as energy harvesting, sensors, actuators, flexible electronics, energy storage and more. Surprisingly, there are not any suitable, yet economical methods that can produce quality nanosheets of MoS2 in large quantities, hence limiting the possibility of commercialisation of its applications. Here, we demonstrate controlled synthesis of highly crystalline MoS2 nanosheets via liquid phase exfoliation of bulk MoS2, following which we report piezoelectric response from the exfoliated nanosheets. The method of piezo force microscopy (PFM) was employed to explore the piezo response in mono, bi, tri and multilayers of MoS2 nanosheets. The effective piezoelectric coefficient of MoS2 varies from 9.6 pm/V to 25.14 pm/V. We attribute piezoelectric response in MoS2 nanosheets to the defects formed in it during the synthesis procedure. The presence of defects is confirmed by X-ray photoelectron spectroscopy (XPS).

One-Pot Synthesis of Chlorophyll-Assisted Exfoliated MoS2/WS2 Heterostructures via Liquid-Phase Exfoliation Method for Photocatalytic Hydrogen Production

Developing strategies for producing hydrogen economically and in greener ways is still an unaccomplished goal. Photoelectrochemical (PEC) water splitting using photoelectrodes under neutral electrolyte conditions provides possibly one of the greenest routes to produce hydrogen. Here, we demonstrate that chlorophyll extracts can be used as an efficient exfoliant to exfoliate bulk MoS2 and WS2 to form a thin layer of a MoS2/WS2 heterostructure. Thin films of solution-processed MoS2 and WS2 nanosheets display photocurrent densities of −1 and −5 mA/cm2, respectively, and hydrogen evolution under simulated solar irradiation. The exfoliated WS2 is significantly more efficient than the exfoliated MoS2; however, the MoS2/WS2 heterostructure results in a 2500% increase in photocurrent densities compared to the individual constituents and over 12 h of PEC durability under a neutral electrolyte. Surprisingly, in real seawater, the MoS2/WS2 heterostructure exhibits stable hydrogen production after solar illumination for 12 h. The synthesis method showed, for the first time, how the MoS2/WS2 heterostructure can be used to produce hydrogen effectively. Our findings highlight the prospects for this heterostructure, which could be coupled with various processes towards improving PEC efficiency and applications.

MoS2-Cysteine Nanofiltration Membrane for Lead Removal

To overcome the limitations of polymers, such as the trade-off relationship between water permeance and solute rejection, as well as the difficulty of functionalization, research on nanomaterials is being actively conducted. One of the representative nanomaterials is graphene, which has a two-dimensional shape and chemical tunability. Graphene is usually used in the form of graphene oxide in the water treatment field because it has advantages such as high water permeance and functionality on its surface. However, there is a problem in that it lacks physical stability under water-contacted conditions due to the high hydrophilicity. To overcome this problem, MoS2, which has a similar shape to graphene and hydrophobicity, can be a new option. In this study, bulk MoS2 was dispersed in a mixed solvent of acetone/isopropyl alcohol, and MoS2 nanosheet was obtained by applying sonic energy to exfoliate. In addition, Cysteine was functionalized in MoS2 with a mild reaction. When the nanofiltration (NF) performance of the membrane was compared under various conditions, the composite membrane incorporated by Cysteine 10 wt % (vs. MoS2) showed the best NF performances.

Nanotoxicity of 2D Molybdenum Disulfide, MoS2, Nanosheets on Beneficial Soil Bacteria, Bacillus cereus and Pseudomonas aeruginosa

Concerns arising from accidental and occasional releases of novel industrial nanomaterials to the environment and waterbodies are rapidly increasing as the production and utilization levels of nanomaterials increase every day. In particular, two-dimensional nanosheets are one of the most significant emerging classes of nanomaterials used or considered for use in numerous applications and devices. This study deals with the interactions between 2D molybdenum disulfide (MoS2) nanosheets and beneficial soil bacteria. It was found that the log-reduction in the survival of Gram-positive Bacillus cereus was 2.8 (99.83%) and 4.9 (99.9988%) upon exposure to 16.0 mg/mL bulk MoS2 (macroscale) and 2D MoS2 nanosheets (nanoscale), respectively. For the case of Gram-negative Pseudomonas aeruginosa, the log-reduction values in bacterial survival were 1.9 (98.60%) and 5.4 (99.9996%) for the same concentration of bulk MoS2 and MoS2 nanosheets, respectively. Based on these findings, it is important to consider the potential toxicity of MoS2 nanosheets on beneficial soil bacteria responsible for nitrate reduction and nitrogen fixation, soil formation, decomposition of dead and decayed natural materials, and transformation of toxic compounds into nontoxic compounds to adequately assess the environmental impact of 2D nanosheets and nanomaterials.

Electronic Properties and Scanning Tunneling Microscopy Simulation of MoS2 Nanosheets by Using Density Functional Theory

The ab-initio Density Functional Theory (DFT) approach is used to study the electronic properties of bulk and layered MoS2 nanosheets. For the layered structures mono, bi, tri, tetra and penta layered structure is used. The direct to indirect transition of bandgap is observed as the number of layers is increasing. This transition of bandgap is attributed to the van der Waals interlayer interaction between two layers of MoS2 nanosheets. The indirect bandgap in the bulk MoS2 is found to be 0.94 eV, whereas for a single layered nanosheet is found to be direct bandgap with the value of 1.83 eV. To confirm the surface termination and understand the surface morphology of MoS2 the scanning tunneling microscopy (STM) simulation is performed in constant height mode. It is found that the detection of surface atoms via STM depends on the tip atom of the STM. Dhaka Univ. J. Sci. 69(1): 53-57, 2021 (January)

Evidence of ideal excitonic insulator in bulk MoS2 under pressure

Spontaneous condensation of excitons is a long-sought phenomenon analogous to the condensation of Cooper pairs in a superconductor. It is expected to occur in a semiconductor at thermodynamic equilibrium if the binding energy of the excitons—electron (e) and hole (h) pairs interacting by Coulomb force—overcomes the band gap, giving rise to a new phase: the “excitonic insulator” (EI). Transition metal dichalcogenides are excellent candidates for the EI realization because of reduced Coulomb screening, and indeed a structural phase transition was observed in few-layer systems. However, previous work could not disentangle to which extent the origin of the transition was in the formation of bound excitons or in the softening of a phonon. Here we focus on bulk MoS2 and demonstrate theoretically that at high pressure it is prone to the condensation of genuine excitons of finite momentum, whereas the phonon dispersion remains regular. Starting from first-principles many-body perturbation theory, we also predict that the self-consistent electronic charge density of the EI sustains an out-of-plane permanent electric dipole moment with an antiferroelectric texture in the layer plane: At the onset of the EI phase, those optical phonons that share the exciton momentum provide a unique Raman fingerprint for the EI formation. Finally, we identify such fingerprint in a Raman feature that was previously observed experimentally, thus providing direct spectroscopic confirmation of an ideal excitonic insulator phase in bulk MoS2 above 30 GPa.

Glucose-Assisted One-Pot Hydrothermal Synthesis of Hierarchical-Structured MoS2/C Quasi-Hollow Microspheres for High-Performance Lithium Ion Battery

In this work, hierarchical MoS2/C quasi-hollow microspheres are prepared by a one-pot hydrothermal process with the addition of glucose. The glucose is not only inclined to form the roundish sphere in the completion of the synthesis of MoS2, but at the same time the microspheres formed by the glucose can act as the nuclei on which the MoS2 grows. Glucose, acting as a nucleating agent, has the advantages of being low-cost and environmentally friendly, which can simplify the fabrication process. The interiors of the MoS2/C samples are multi-hole and quasi-hollow, which is beneficial for the insertion and extraction of lithium ions. For the first time, we demonstrate that hierarchical-structured MoS2/C quasi-hollow microspheres exhibit an excellent cycling stability and rate capability in lithium ion batteries (LIBs) and are significantly superior to the bulk MoS2. The method presented in this article may provide a simple, clean. and economical strategy for the preparation of MoS2/C microspheres as a feasible and promising anode material for LIBs.

Semiconducting bacterial biofilm based on graphene-MoS2 template and component dependent gating behavior

In this paper, we report for the first time, the synthesis of a semiconducting biofilm. Photosynthetic bacterial biofilm has been used to weave together MoS2 nanosheets into an adherent film grown on interdigitated electrodes. Liquid-phase exfoliation of bulk MoS2 powder was used to obtain MoS2 nanosheets. A synchronous-fluorescence scan revealed the presence of two emission maxima at 682nm and 715nm for the MoS2 suspension. Such maxima with bandgap energy 1.82 and 1.73 eV corresponded to the single and double layer of MoS2. The presence of such single and multi-layered structures was confirmed by Raman spectroscopy, FTIR studies, and electron microscopy. The current-voltage (I-V) studies of such a bio-nano hybrid revealed the emergence of the gated nature of the current flow. This Schottky diode like behavior, reported earlier for Graphene-biofilm junctions, is also observed in this case. Gating voltage depended on the composition of the biofilm. The semiconductor biofilms, when studied using electrochemical impedance spectroscopy, revealed characteristic Nyquist and Bode plots, suggesting special circuit-equivalence for each film. While Mos2 was marked with stability with respect to variations in RMS voltage and bias voltage, the graphene biofilm was unique by the absence of any Warburg element.