Molybdenum Disulfide Nanosheets Research Articles

Ratio design of bimetallic Pd‐Rh nanoparticles on MoS2 nanosheets: Excellent electrocatalysts for hydrogen evolution reaction

The decrease in noble metal content presents an efficient approach to attain commercial, effective, and durable electrocatalysts for the hydrogen evolution reaction (HER) at a low fabrication cost. Nonetheless, achieving a proper balance between bimetallic loading ratios and HER performance remains challenging. In this study, a simple and environmentally friendly sonochemical method is employed to successfully synthesize bimetallic palladium–rhodium nanoparticles (Pd‐Rh) with varying ratios, confined within molybdenum disulfide (MoS2) nanosheets. Bimetallic Pd‐Rh/MoS2 composite with different ratios of Pd:Rh is synthesized by adjusting the feed ratio of Pd and Rh precursors (1:4, 1:1, and 4:1). The HER electrocatalytic activity of the bimetallic Pd1‐Rh1/MoS2 composite exhibits the lowest overpotential and a superior Tafel slope, closely rivaling the electrocatalytic activity of the commercial 20 wt% Pt/C. Furthermore, the bimetallic Pd1‐Rh1/MoS2 composite exhibits remarkable stability and durability, with almost negligible performance decay after 2000 cycles. These outstanding HER electrocatalytic properties of the bimetallic composite result from a higher number of active sites, a significantly larger electrochemically active surface area, reduced charge‐transfer resistance, and a larger double‐layer capacitance. These factors collectively facilitate faster adsorption and desorption of hydron on the surface of electrocatalyst.

Size and Shape Selective Classification of Nanoparticles

As nanoparticle syntheses on a large scale usually yield products with broad size and shape distributions, the properties of nanoparticle-based products need to be tuned after synthesis by narrowing the size and shape distributions or via the removal of undesired fractions. The development of property-selective classification processes requires a universal framework for the quantitative evaluation of multi-dimensional particle fractionation processes. This framework must be applicable to any property and any particle classification process. We extended the well-known one-dimensional methodology commonly used for describing particle size distributions and fractionation processes to the multi-dimensional case to account for the higher complexity of the property distribution and separation functions. In particular, multi-dimensional lognormal distributions are introduced and applied to diameter and length distributions of gold nanorods. The fractionation of nanorods via centrifugation and by orthogonal centrifugal and electric forces is modeled. Moreover, we demonstrate that analytical ultracentrifugation with a multi-wavelength detector (MWL-AUC) is a fast and very accurate method for the measurement of two-dimensional particle size distributions in suspension. The MWL-AUC method is widely applicable to any class of nanoparticles with size-, shape- or composition-dependent optical properties. In addition, we obtained distributions of the lateral diameter and the number of layers of molybdenum disulfide nanosheets via stepwise centrifugation and spectroscopic evaluation of the size fractions.

Layer-by-layer Assembly of Nanosheets with Matching Size and Shape for More Stable Membrane Structure than Nanosheet-Polymer Assembly.

Layer-by-layer (LbL) assembly of oppositely charged materials has been widely used as an approach to make two-dimensional (2D) nanosheet-based membranes, which often involves 2D nanosheets being alternately deposited with polymer-based polyelectrolytes to obtain an electrostabilized nanosheet-polymer structure. In this study, we hypothesized that using 2D nanosheets with matching physical properties as both polyanions and polycations may result in a more ordered nanostructure with better stability than a nanosheet-polymer structure. To compare the differences between nanosheet-nanosheet vs nanosheet-polymer structures, we assembled negatively charged molybdenum disulfide nanosheets (MoS2) with either positively charged graphene oxide (PrGO) nanosheets or positively charged polymer (PDDA). Using combined measurements by ellipsometer and quartz crystal microbalance with dissipation, we discovered that the swelling of MoS2-PrGO in ionic solutions was 60% lower than that of MoS2-PDDA membranes. Meanwhile, the MoS2-PrGO membrane retained its permeability upon drying, whereas the permeability of MoS2-PDDA decreased by 40% due to the restacking of MoS2. Overall, the MoS2-PrGO membrane demonstrated a better filtration performance. Additionally, our X-ray photoelectron spectroscopy results and analysis on layer density revealed a clearer transition in material composition during the LbL synthesis of MoS2-PrGO membranes, and the X-ray diffraction pattern suggested its resemblance to an ordered, layer-stacked structure. In conclusion, the MoS2-PrGO membrane made with nanosheets with matching size, shape, and charge density exhibited a much more aligned stacking structure, resulting in reduced membrane swelling under high salinity solutions, controlled restacking, and improved separation performance.

Surface modified molybdenum disulfide nanosheets for corrosion resistance improvement on polyurethane coatings

Abstract Organic–inorganic hybrid coating has been applied on metallic corrosion protection effectively. Molybdenum disulfide (MoS2) nanosheets with graphene-like two-dimensional lamellar structure were an anticorrosion inorganic additive, rendering the organic coating better corrosion resistant. However, the aggregation and poor solubility are still current issues that should be addressed. Functionalization MoS2 nanosheets with surface modified by polydopamine (PDA) and silane coupling agent (KH560) were prepared in polyurethane (PU) composite coatings to obtain dense and intact multilayer network structure coatings for corrosion protection. KH560-PDA-MoS2/PU coating with crosslinked polymer network structure has a high impedance modulus, large contact angle, and strong hydrophobicity. The coating meets the national technical standards for salt spray testing and nitric acid (HNO3) titration testing, demonstrating excellent corrosion resistance.

Heterogeneous interfaces in 3D interconnected networks of flower-like 1T/2H Molybdenum disulfide nanosheets and carbon-fibers boosts superior EM wave absorption

With the wide application of electromagnetic waves in national defense, communication, navigation and home appliances, the electromagnetic pollution problem is becoming more and more prominent. Therefore, high-performance, and low-density composite wave-absorbing materials have attracted much attention. In this paper, three-dimensional (3D) network structures of flower-like 1T/2H Molybdenum disulfide nanosheets anchored to carbon fibers (1T/2H MoS2/CNFs) were prepared by electrostatic spinning technique and calcination process. The morphology and electromagnetic wave absorption properties were tuned by changing the content of flower-like MoS2. The optimized 1T/2H MoS2/CNFs composite exhibits superior electromagnetic wave absorption with minimum reflection (RLmin) of −42.26 dB and effective absorption bandwidth (EAB) of 6.56 GHz at 2.5 mm. Multi-facts contribute to the super performance. First, the uniquely designed nanosheet and 3D interconnected networks leads to multiple reflection and scattering of electromagnetic waves, which promotes the attenuation of electromagnetic waves. Second, the propriate content of CNFs and MoS2 with different phase regulates its impedance matching characteristic. Third, Numerous heterogeneous interfaces existed between CNFs and MoS2, 1T and 2H MoS2 phase results in interface polarization. Besides, the 1T/2H MoS2 rich in defects induces defect polarization, improving the dielectric loss. Furthermore, the electromagnetic wave absorption performance was proved via radar reflectance cross section simulation. This work illustrates 1T/2H MoS2/CNFs is a promising material for electromagnetic absorption with wide bandwidth, strong absorption, low density, and high thermal stability.

Tribological performances of MoS2/C60 nanocomposite as lubricating additive in dioctyl sebacate

PurposeThis paper aims to solve the problems molybdenum disulfide (MoS2) nanosheets suffer from inadequate dispersion stability and form a weak lubricating film on the friction surface, which severely limits their application as lubricant additives.Design/methodology/approachMoS2/C60 nanocomposites were prepared by synthesizing molybdenum disulfide (MoS2) nanosheets on the surface of hydrochloric acid-activated fullerenes (C60) by in situ hydrothermal method. The composition, structure and morphology of MoS2/C60 nanocomposites were characterized. Through the high-frequency reciprocating tribology test, its potential as a lubricant additive was evaluated.FindingsMoS2/C60 nanocomposites that were prepared showed good dispersion in dioctyl sebacate (DOS). When 0.5 Wt.% MoS2/C60 was added, the friction reduction performance and wear resistance improved by 54.5% and 62.7%, respectively.Originality/valueMoS2/C60 composite nanoparticles were prepared by in-situ formation of MoS2 nanosheets on the surface of C60 activated by HCl through hydrothermal method and were used as potential lubricating oil additives.Peer reviewThe peer review history for this article is available at: https://publons.com/publon/10.1108/ILT-10-2023-0321/

Core-Shell CoS2@MoS2 with Hollow Heterostructure as an Efficient Electrocatalyst for Boosting Oxygen Evolution Reaction.

It is imperative to develop an efficient catalyst to reduce the energy barrier of electrochemical water decomposition. In this study, a well-designed electrocatalyst featuring a core-shell structure was synthesized with cobalt sulfides as the core and molybdenum disulfide nanosheets as the shell. The core-shell structure can prevent the agglomeration of MoS2, expose more active sites, and facilitate electrolyte ion diffusion. A CoS2/MoS2 heterostructure is formed between CoS2 and MoS2 through the chemical interaction, and the surface chemistry is adjusted. Due to the morphological merits and the formation of the CoS2/MoS2 heterostructure, CoS2@MoS2 exhibits excellent electrocatalytic performance during the oxygen evolution reaction (OER) process in an alkaline electrolyte. To reach the current density of 10 mA cm-2, only 254 mV of overpotential is required for CoS2@MoS2, which is smaller than that of pristine CoS2 and MoS2. Meanwhile, the small Tafel slope (86.9 mV dec-1) and low charge transfer resistance (47 Ω) imply the fast dynamic mechanism of CoS2@MoS2. As further confirmed by cyclic voltammetry curves for 1000 cycles and the CA test for 10 h, CoS2@MoS2 shows exceptional catalytic stability. This work gives a guideline for constructing the core-shell heterostructure as an efficient catalyst for oxygen evolution reaction.

Robust pseudocapacitive Na+ intercalation induced by MoS2 on active Mo2C current collector interface for high areal capacity sodium-ion batteries

Sodium-ion batteries (SIBs) have emerged as compelling alternatives in the realm of electrochemical energy devices, poised to substitute lithium-ion batteries (LIBs). The primary challenge encompasses not only the scarcity of anode materials exhibiting exceptional Na+ storage capacity but also the endeavor to achieve high areal capacity. To address this challenge, a comprehensive strategy is proposed that entails utilizing a highly conductive molybdenum dicarbide (Mo2C) current collector (denoted as CCM) as a supporting scaffold for the bottom-up growth of molybdenum disulfide nanosheets (MoS2, serving as the main active component) (denoted as CCM@MoS2). The CCM improves interfacial bonding with MoS2 nanosheets and offers additional capacity to accommodate the increased Na+ insertion activity. Both theoretical and kinetic analyses reveal that the enhanced Na+ storage properties primarily stem from favorable adsorption energy, reduced diffusion barrier, and intercalation pseudocapacitance due to the strong electronic interfacial interaction between active CCM and MoS2. Hence, the as-prepared optimized CCM@MoS2 electrode exhibits a superior areal capacity of 6.36 mAh cm−2 at 0.4 mA cm−2, excellent rate capability of 1.02 mAh cm−2 at 24 mA cm−2 and long cycle life up to 500 cycles at 4 mA cm−2. Interesting, our as-prepared CCM@MoS2 electrode shows better performance for Na+ storage than Li+ storage at higher current density, affirming the enhanced kinetics in our architecture. This work proposes a rational strategy to enhance the areal capacity and stability of MoS2-based anode for SIBs and beyond.

The production of electrodes for microsupercapacitors based on MoS2-modified reduced graphene aerogels by 3D printing

Micro-supercapacitors (MSCs) are of interest because of their high power density and excellent cycling performance, offering a broad array of potential applications. However, preparing electrodes for the MSCs with an extremely high areal capacitance and energy density remains a challenge. We constructed MSC electrodes with an ultra-high area capacitance and a high energy density, using reduced graphene oxide aerogel (GA) and MoS2 as the active materials, combined with 3D printing and surface modification. Using 3D printing, we obtained electrodes with a stable macrostructure and a GA-crosslinked micropore structure. We also used a solution method to load the surface of the printed electrode with molybdenum disulfide nanosheets, further improving the electrochemical performance. The surface capacitance of the electrode reached 3.99 F cm−2, the power density was 194 W cm−2, and the energy density was 1 997 mWh cm−2, confirming its excellent electrochemical performance and cycling stability. This work provides a simple and efficient method for preparing MSC electrodes with a high areal capacitance and energy density, making them ideal for portable electronic devices.

Interactions of monolayer molybdenum disulfide sheets with metalloid antimony in aquatic environment: Adsorption, transformation, and joint toxicity

The tremendous application potentiality of transitional metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS2) nanosheets, will unavoidably lead to increasing release into the environment, which could influence the fate and toxicity of co-existed contaminants. The present study discovered that 59.8 % of trivalent antimony [Sb(III)] was transformed by MoS2 to pentavalent Sb [Sb(V)] in aqueous solutions under light illumination, which was due to hole oxidation on the nanosheet surfaces. A synergistic toxicity between MoS2 and Sb(III, V) to algae (Chlorella vulgaris) was observed, as demonstrated by the lower median-effect concentrations of MoS2 + Sb(III)/Sb(V) (13.1 and 20.9 mg/L, respectively) than Sb(III)/Sb(V) (38.8 and 92.5 mg/L, respectively) alone. Particularly, MoS2 at noncytotoxic doses notably increased the bioaccumulation of Sb(III, V) in algae, causing aggravated oxidative damage, photosynthetic inhibition, and structural alterations. Metabolomics indicated that oxidative stress and membrane permeabilization were primarily associated with down-regulated amino acids involved in glutathione biosynthesis and unsaturated fatty acids. MoS2 co-exposure remarkably decreased the levels of thiol antidotes (glutathione and phytochelatins) and aggravated the inhibition on energy metabolism and ATP synthesis, compromising the Sb(III, V) detoxification and efflux. Additionally, extracellular P was captured by the nanosheets, also contributing to the uptake of Sb(V). Our findings emphasized the nonignorability of TMDs even at environmental levels in affecting the ecological hazard of metalloids, providing insight into comprehensive safety assessment of TMDs.

Electrodeposition of PdPt Nanoparticles on Edges and S-Vacancies in Exfoliated MoS2 Nanosheets for Enhanced Hydrogen Evolution Activity.

Deposition of metal nanoparticles onto the molybdenum disulfide (MoS2 ) nanosheets is an efficient method to tune the electronic structure of the MoS2 and maximize its catalytic performance towards the hydrogen evolution reaction (HER). Herein, we report the electrodeposition of Pd and Pt nanoparticles onto desulfurized MoS2 nanosheets (MoS2-x ) to achieve an improved HER activity in an acidic electrolyte. The initial MoS2 powder was exfoliated and isolated through centrifugation, followed by electrochemical desulfurization to create defect sites. Subsequently, Pt and Pd nanoparticles were electrodeposited onto the S-vacancies of MoS2-x nanosheets. The resulting PdPt nanoparticles, with a diameter of 3.3 ±1.7 nm, were distributed across the surfaces of the nanosheets. A preferential deposition was evident at the edges of the nanosheets, particularly when Pd was deposited first followed by Pt. Owing to this preferential deposition of Pd and Pt and the synergistic interaction of MoS2-x with Pd and Pt, the prepared catalyst exhibited a low overpotential of 30 mV at 10 mA cm-2 , which is 2.7× lower than the MoS2-x alone. The prepared catalyst exhibited a 1.7× increase in the mass activity at 20 mV overpotential, relative to that of a commercial Pt/C nanocatalyst, showcasing its promising potential as an alternative catalyst.

The dependence of electrocatalytic HER activity of decorated MoS2 with Cu nanoclusters

Molybdenum disulfide is a potential electrocatalytic material for water splitting with excellent stability and durability. Here, the electrocatalytic hydrogen evolution reaction performance of Molybdenum disulfide nanosheets decorated with copper nanoclusters was investigated. The Cu@MoS2–1:10 exhibited remarkable hydrogen evolution reaction activity, with an overpotential as low as 150 mV under acidic conditions. The First-principles calculations further confirmed the superior electrocatalytic performance of Cu@MoS2, with a minimum hydrogen adsorption free energy of -0.10 eV. The improved electrocatalytic activity of Cu@MoS2 arises from the accelerated charge migration at the interface. And the addition of Cu increases the number of active sites on the surface of MoS2. This work could offer insights into the advancement of additional non-precious metals and transition metal dichalcogenides.

Ultrahigh Polarization of Emitted Light by Quenched Emissive Material

AbstractThe emission of highly polarized light by organic light‐emitting diodes (OLEDs) is crucial for various applications; however, achieving such emission requires the use of polarizers, which reduce the device efficiency and durability. In this study, ultrahigh‐polarized light with a polarization ratio (PR) of 407:1 is achieved via the rapid thermal quenching (RTQ) of OLEDs. Poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) films, molybdenum disulfide (MoS2) nanosheets, and tungsten disulfide (WS2) nanosheets are applied as hole transport layers and surface‐alignment layers through surface treatment, including rubbing and/or ion‐beam exposure to align the molecules of the emissive materials, namely, {poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT). Quenching is performed at 240 °C, at which F8BT has a nematic liquid crystal (NLC) phase with high molecular ordering. Upon quenching, the high molecular ordering of the NLC‐phased emissive layer instantaneously froze via RTQ, leading to the emission of highly polarized light. Consequently, the PEDOT:PSS‐, MoS2‐, and WS2‐based OLEDs exhibit ultrahigh PRs of 407:1, 349:1, and 328:1, respectively, for photoluminescence at a 540 nm peak wavelength. In contrast, for electroluminescence, the PEDOT:PSS‐based OLED exhibits a high PR of 395:1. This result is the best reported to date and is comparable to the PRs generated by polarizers, indicating that quenching can be utilized for the development of ultrahigh‐polarized light‐emitting devices.

Probing Polymorphic Stacking Domains in Mechanically Exfoliated Two-Dimensional Nanosheets Using Atomic Force Microscopy and Ultralow-Frequency Raman Spectroscopy.

As one of the key features of two-dimensional (2D) layered materials, stacking order has been found to play an important role in modulating the interlayer interactions of 2D materials, potentially affecting their electronic and other properties as a consequence. In this work, ultralow-frequency (ULF) Raman spectroscopy, electrostatic force microscopy (EFM), and high-resolution atomic force microscopy (HR-AFM) were used to systematically study the effect of stacking order on the interlayer interactions as well as electrostatic screening of few-layer polymorphic molybdenum disulfide (MoS2) and molybdenum diselenide (MoSe2) nanosheets. The stacking order difference was first confirmed by measuring the ULF Raman spectrum of the nanosheets with polymorphic stacking domains. The atomic lattice arrangement revealed using HR-AFM also clearly showed a stacking order difference. In addition, EFM phase imaging clearly presented the distribution of the stacking domains in the mechanically exfoliated nanosheets, which could have arisen from electrostatic screening. The results indicate that EFM in combination with ULF Raman spectroscopy could be a simple, fast, and high-resolution method for probing the distribution of polymorphic stacking domains in 2D transition metal dichalcogenide materials. Our work might be promising for correlating the interlayer interactions of TMDC nanosheets with stacking order, a topic of great interest with regard to modulating their optoelectronic properties.

Morphological and Optical Characterization of Hydrothermally-Synthesized Two-Dimensional MoS2 Nanosheets

Transition metal dichalcogenides (TMDs) are extensively utilized in optoelectronics, sensors, and battery storage due to their versatile properties. Among the TMDs, Molybdenum disulfide (MoS2) nanosheets possess remarkable optical, electronic, and chemical properties. This study employed a cost-effective hydrothermal method to synthesize high-quality 2D MoS2 nanosheets. Different characterization techniques such as XRD, SEM, EDS, FTIR, Raman, UV–vis, and photoluminescence (PL) spectroscopy were utilized to evaluate the structural, morphological, chemical, and optical characteristics of the nanosheets. The XRD analysis revealed that the MoS2 nanosheets have a hexagonal crystal structure, with an average crystallite size of 27.76 nm. Furthermore, SEM images confirmed the formation of thin MoS2 nanosheets, with an estimated thickness ranging from 20–30 nm. The growth mechanism of the formation of MoS2 is discussed in detail. Different functional groups present in the material were analyzed using FTIR spectra. The difference in vibration modes analysed by Raman spectroscopy indicated the presence of layered nanosheets. The optical bandgap (2.20 eV) of the material was determined by analyzing its UV–vis spectroscopy data using the Tauc plot. PL analysis indicates a direct transition between the upper valence and lower conduction bands, suggesting that the nanosheets were synthesized with high quality. These findings have opened new possibilities for the use of MoS2 nanosheets in various applications such as optoelectronics and sensing devices.

Inkjet-printed thin-film transistors using surfactant-based transition-metal dichalcogenide nanocomposites suspended in polymeric semiconductors

Ink formulations containing a suspension of single-crystalline molybdenum disulfide (MoS2) nanosheets suspended in the polymeric semiconductor poly(3-hexylthiophene-2,5-diyl) (P3HT) were inkjet printed for the fabrication of thin-film transistors (TFT). The MoS2 nanosheets were treated with the surfactant trichloro(dodecyl)silane (DDTS) to functionalize the MoS2 surface and created a more stable suspension, reducing the agglomeration of MoS2 suspended in the P3HT solution. This ink formulation was inkjet printed onto the surface of thermal oxide coated, p+-Si wafers to form common-gate TFT device structures. The printed semiconductor formed the active region of a hybrid MoS2 suspension in P3HT of the TFTs. The field-effect mobility for the hybrid-ink TFTs was found to be three times (3×) higher compared to reference devices using pristine P3HT without the suspension. The functionalized MoS2 suspension was also found to form thinner nanosheet suspensions within the P3HT matrix that resulted in approximately 60% higher field-effect mobility compared to hybrid inks without the surfactant. The enhancement of the electrical properties of the TFTs was determined to be due to a structural change in the thin-film semiconductor. The observed current–voltage (I–V) changes were correlated to measurable structural alterations in the semiconductor thin film characterized by x-ray diffraction, atomic force microscopy, and UV–visible absorption spectroscopy.

Influence of Inorganic Anions on the Chemical Stability of Molybdenum Disulfide Nanosheets in the Aqueous Environment.

Chemical stability is closely associated with the transformations and bioavailabilities of engineered nanomaterials and is a key factor that governs broader and long-term application. With the growing utilization of molybdenum disulfide (MoS2) nanosheets in water treatment and purification processes, it is crucial to evaluate the stability of MoS2 nanosheets in aquatic environments. Nonetheless, the effects of anionic species on MoS2 remain largely unexplored. Herein, the stability of chemically exfoliated MoS2 nanosheets (ceMoS2) was assessed in the presence of inorganic anions. The results showed that the chemical stability of ceMoS2 was regulated by the nucleophilicities and the resultant charging effects of the anions in aquatic systems. The anions promote the dissolution of ceMoS2 by triggering a shift in the chemical potential of the ceMoS2 surface as a function of the anion nucleophilicity (i.e., charging effect). Fast charging with HCO3- and HPO42-/H2PO4- was validated by a phase transition from 1T to 2H and the emergence of MoV, and it promoted oxidative dissolution of the ceMoS2. Additionally, under sunlight, ceMoS2 dissolution was accelerated by NO3-. These findings provide insight into the ion-induced fate of ceMoS2 and the durability and risks of MoS2 nanosheets in environmental applications.

Epitaxial growth of rare-earth yttrium on nanosheets to form semicoherent interface in zinc implant

Molybdenum disulfide (MoS2) nanosheet as nano reinforcement exhibits great advantages in zinc (Zn) implant due to its coordinated crystal slip and grain boundary strain effect. Nevertheless, the poor interface bonding restrains the coordination effect of MoS2. In this work, rare earth yttrium (Y) was used to epitaxial grow on the vacancy nucleation sites of MoS2 plane through a gas phase reduction method, and then introduced into Zn to improve their interface bonding. On one hand, rare earth Y could form a semicoherent interface with Zn due to the similar atomic arrangement and small lattice misfit between (101)Y plane (0.272 nm) and (002)Zn plane (0.248 nm). On the other hand, it could be tightly integrated together with sulfur element of MoS2 via covalent bond. As a result, the plastic strain of composites was improved from 6.1 % to 10.45 %. Simultaneously, the fracture energy was also increased to 201 × 103 J/m2, since rare earth Y considerably promoted load transfer efficiency from Zn matrix to MoS2 and thereby significantly activated slip systems. Encouragingly, the mechanical strength of the Zn-based biocomposite simultaneously reached 273.3 ± 10.9 MPa due to load transfer strengthening and grain refinement.

Mechanisms and effects of amphiphilic lamellar nanofluid for enhanced oil recovery in low permeability reservoirs

Amphiphilic nanosheets have attracted more attention for enhanced oil recovery (EOR) owing to their unique properties. Here, the amphiphilic molybdenum disulfide (MoS2) nanosheets (AP-MDN) were prepared by functionalizing octadecyl amine (ODA) molecules onto the molybdenum disulfide nanosheets (MDN) surfaces. The dynamic stability and interfacial tension (IFT) measurements of AP-MDN nanofluid were evaluated. Besides, the mechanisms and effects of AP-MDN nanofluid for EOR were also systematically investigated and studied. Experimental results indicate that the dynamic stability of AP-MDN nanofluid is improved when MDN is successfully functionalized with ODA molecules. The IFT is decreased to 10-1 mN/m and micron-emulsions ranging from 1 µm ∼ 2 µm can be formed. In addition, the contraction rate of oil film exposed in ultra-low concentration AP-MDN nanofluid (50 mg/L) experiences two stages: a steep stage (8.5817 × 10-5 cm/s) and a gentle stage (0.6617 × 10-5 cm/s) owing to the generation of structuring disjoining pressure. Comprehensive mechanisms of AP-MDN nanofluid for EOR are also proposed and revealed. Moreover, oil washing efficiency of AP-MDN nanofluid is as high as 95.7 % when the soaking time is 6 hrs and temperature is 75 ℃. Core flooding experimental results demonstrate that the increase in shut-down time and the injection mode of multiple rounds with small slugs can better promote the interaction between AP-MDN nanofluid and crude oil in porous media. The highest oil recovery contributed by AP-MDN nanofluid is 19.1 %. These results are expected to promise AP-MDN nanofluid as an effective candidate for EOR.

Synergistic interaction between molybdenum disulfide nanosheet and metal organic framework for high performance supercapacitor

Zeolitic imidazolate framework-67 crystals (ZIF-67) anchored molybdenum disulfide nanosheets (MS) have been synthesized via a hydrothermal approach followed by a simple chemical method. The concentration of molybdenum disulfide was varied to investigate its impact on the electrochemical efficiency within the electrode nanocomposite. The shiny spot of this composite is the combination of two desirable properties, the conductive path created by MS, and the structural framework support provided by Zeolitic imidazolate framework-67 intercalated with nickel (Z67.Ni). The framework of Z67.Ni inhibits MS nanosheets from restacking over repeated charge and discharge cycles, which is why this specific nanocomposite was chosen. The superior synergistic impact of Z67.Ni crystals and MS nanosheets was established by the improved electrochemical behavior of Z67.Ni with 70 % weight percent of MS (Z67.Ni/MS7). This combination exhibited a specific capacitance of 308.5 F/ g at 1 A g−1 and a power density (Pd) of 2.78 kW kg−1 along with an exceptional energy density (Ed) of 83.98 W h kg−1. These impressive results highlight the high efficiency of this nanocomposite material for supercapacitor applications.