Search Results (415)

At an ultra-thin 3 nm SnO₂ channel thickness, a record-high effective mobility (µ_eff) of 301 cm²/V·s, field-effect mobility (µ_FE) of 304 cm²/V·s, and a sharp subthreshold swing (SS) of 201 mV/decade are achieved at a high carrier density (N_e) of 5 × 10¹² cm⁻². These excellent transport properties are attributed to ultraviolet (UV) light annealing. The resulting µ_eff is significantly higher than that of Molybdenum Disulfide (MoS₂) and Tungsten Diselenide (WSe₂), and is more than twice that of single-crystalline Si channel transistors at the same quasi-two-dimensional (2D) thickness of 3 nm (equivalent to five monolayers of MoS₂). UV annealing not only enhances µ_eff and µ_FE but also sharpens the SS, which is crucial for low-power operation. This improved SS is attributed to reduced scattering from charged interface traps, as supported by µ_eff-N_e analysis, thereby increasing the transistor’s mobility. The realization of such high-mobility devices at a quasi-2D thickness of only 3 nm is of particular importance for the further downscaling of ultra-thin-body transistors for high-speed computing and monolithic three-dimensional (M3D) integration. Furthermore, the wide bandgap of SnO₂ (3.7 eV) enables operation at relatively high voltages, paving the way for pioneering ternary logic applications. Full article

The irradiation of atomic oxygen (AO) severely restricts the application of polymeric lubricating coatings in low Earth orbit (LEO). Herein, octa- and mono-amino polyhedral oligomeric silsesquioxanes (POSSs) were chemically bonded onto polyimide/molybdenum disulfide (PI/MoS₂) composite coatings with a gradient structure based on Si density. The gradient coatings presented better wear resistance under different loads; notably, the wear rate decreased by 83.5%. Additionally, the effects of AO exposure on the surface morphologies, chemical structure, and tribological properties of the gradient coatings were investigated in detail. The results indicated that the mass loss and wear rates under AO irradiation decreased significantly, which can be attributed to the passivated network-like SiO₂ layer that covered the coating surface after AO irradiation. As a result, the addition of POSS significantly improved the tribological properties and AO resistance. Full article

The stability of nanolubricants is critical for ensuring effective performance under extreme pressure (EP) conditions, where severe boundary lubrication governs friction and wear behaviour. This study examines palm kernel oil (PKO)-based nanolubricants enhanced with carbon graphene (CG), hexagonal boron nitride (hBN), and molybdenum disulfide (MoS₂), with and without oleic acid (OA) as a surfactant. OA incorporation improved CG dispersion stability, reducing agglomerate size by 30.4% (17.61 μm to 12.23 μm) and increasing the viscosity index from ~176 to 188, compared to 152 for the commercial hydrogen engine oil baseline. Under EP conditions, PKO + CG + OA achieved a 51.7% reduction in the coefficient of friction (0.58 to 0.28) and 18.2% improvement in weld load resistance, while wear scar diameter decreased by 13.4%. Surface and elemental analyses indicated the formation of a composite tribofilm containing oxide species, graphene platelets, and carboxylate-derived compounds from OA, consistent with iron–oleate-like chemistry that enhances load-carrying capacity and wear protection. These findings demonstrate the potential of OA-assisted PKO nanolubricants as sustainable, high-performance formulations for extreme pressure boundary lubrication, contributing to the advancement of green tribology. Full article

In this paper, we propose a Bayesian Deep Learning (BDL) framework to model uncertainty and predict the performance of terahertz (THz) biosensors with a graphene and molybdenum disulfide (MoS₂) coating for AML biomarker detection. Although there have been studies on the individual advantage of these 2D materials for biosensing, a comparative analysis taking into account predictive uncertainty is still insufficient. To this end, we have generated a high-fidelity simulation dataset from full-wave EM simulations of DSSRR structures over the 0.1–2.5 THz frequency range. Realistic geometrical and dielectric modifications have been incorporated to mimic bio-sensing conditions. An approach based on a Bayesian Neural Network (BNN) with Monte Carlo dropout was employed for predicting sensitivity, Q-factor, resonance shift, and absorption, along with the estimation of aleatoric, as well as epistemic, uncertainty. Our results demonstrated a trade-off between material types: MoS₂ sensors showed higher sensitivity (3548 GHz/RIU) but with a larger prediction uncertainty range of ±118 GHz/RIU; on the other hand, graphene-based sensors exhibited a better spectral resolution (Q = 48.5) and a more reliable QV prediction range of ±42 GHz/RIU. The uncertainty study further revealed that graphene demonstrated a predominance for aleatoric uncertainty (68%), classifying them as predictable physical characteristics, while MoS₂ presents a higher epistemic one (55%), indicating sensitivity towards underrepresented design cases. We present a material selection algorithm based on utility that balances sensitivity, resolution, and uncertainty, demonstrating that MoS₂ is the best choice for early screening, while graphene is more suitable for high-precision diagnostics. This study offers a scalable and reliable AI framework for quick, uncertainty-aware optimization of THz biosensors, which is directly applicable to clinical diagnostics and 2D-material-based photonic design. Full article

Currently, continuous population growth and unsustainable industrialization have caused ongoing water pollution, with harmful consequences for human health and the environment. Persistent organic pollutants (dyes, active pharmaceutical compounds, pesticides, etc.) are discharged into water from various industrial, agricultural, and domestic activities. Therefore, wastewater treatment through sustainable technologies is imperative, representing a great and real challenge for worldwide research. Photocatalysis, an innovative and green technology, uses advanced oxidation processes in the presence of a photocatalyst, usually a semiconductor with expanded light absorption ability and high conductivity for photogenerated charge carriers. Molybdenum disulfide (MoS₂) is an n-type semiconductor with different morphologies, variable bandgap energies (Eg = 1.1–2.63 eV), and numerous applications. Although pristine MoS₂ exhibits special structural and optoelectronic properties, its photocatalytic activity can be further improved through various strategies, and constructions with the heterojunctions construction with other semiconductors being frequently pursued. This review extensively studies the recent research (the last 4 years) on MoS₂ and MoS₂-based heterojunction (I-type, II-type, Z-scheme, S-scheme) photocatalysts for degrading organic contaminants under simulated and sunlight irradiation in wastewater treatment. Even if in a relatively short time (a few years) valuable studies have been reported on this topic, there are still numerous challenges facing future research. Full article

This study explores the tunable characteristics of optical Tamm states (OTS) in a metal–distributed Bragg reflector (DBR) structure integrated with a monolayer of molybdenum disulfide (MoS₂). Through finite element simulations, we demonstrate that incorporating MoS₂ enhances electromagnetic field localization at the metal–DBR interface, facilitating enhanced exciton–photon interaction. As the number of DBR periods increases, the OTS resonance wavelength undergoes a blue shift and eventually stabilizes, which indicates a wavelength-locking behavior. Under external bias, the locking threshold is lowered, and the resonance wavelength exhibits a nearly linear blue shift of approximately ~1 nm/V. Moreover, absorptance varies non-monotonically with the metal thickness, reaching over 99% at a thickness of 25 nm, due to the combined effects of plasmonic confinement and MoS₂ excitonic enhancement. These findings demonstrate the potential of this structure for application in tunable photonic devices such as optical filters and modulators. Full article

Gold-assisted exfoliation is an effective approach to obtain clean and large-area monolayers of transition metal dichalcogenides, yet the microscopic evolution of interfacial adhesion remains poorly understood. Here, we investigate temperature-controlled exfoliation of MoS₂ between 30 and 170 °C. Based on optical microscopy image analysis, mild heating slightly improves the exfoliation yield, which is associated with the release of interfacial contaminants and trapped gases—these substances enhance the adhesion between gold and molybdenum disulfide (Au-MoS₂). Unexpectedly, as revealed by AFM, SEM-EDS, and Raman analyses, parts of the Au film start to peel off from the underlying Ti adhesion layer at approximately 100 °C. This Au film detachment, resulting from the surprisingly weak Au-Ti adhesion, serves as a unique probe for interfacial strength: it preferentially occurs at the boundaries of MoS₂ flakes, indicating that the reinforcement of the Au-MoS₂ interaction originates at the edges rather than being uniformly distributed. At higher temperatures (>130 °C), Au detachment expands to larger areas, indicating that boundary-localized adhesion progressively extends across the entire interface. Additional STM/STS measurements further confirm that thermal annealing improves local Au-MoS₂ contact by removing interfacial species and enabling surface reconstruction. These findings establish a microscopic picture of temperature-assisted exfoliation, highlighting the dual roles of interfacial contaminant release and boundary effects, and offering guidance for more reproducible fabrication of high-quality 2D monolayers. Full article

This article presents a review of current research on the use of molybdenum disulfide (MoS₂) and its composites as promising materials for energy storage systems and functional coatings. Various MoS₂ morphologies, including nanoflowers, nanoplatelets, and nanorods, are considered, as well as their effects on electrochemical properties and specific capacity. Particular attention is paid to strategies for modifying MoS₂ using carbon nanomaterials (graphene, carbon nanotubes, porous carbon) and conductive polymers, which improve electrical conductivity, structural stability, and durability of electrodes. The important role of chemical vapor deposition (CVD), which allows the formation of uniform coatings with high purity, controlled thickness, and improved performance characteristics, is noted. A comparative analysis of advances in the application of MoS₂ in sodium-ion batteries, supercapacitors, and microwave absorbers is provided. It has been shown that the synergy of MoS₂ with carbon and polymer components, as well as the use of advanced deposition technologies, including CVD, opens new prospects for the development of low-cost, stable, and highly efficient energy storage devices. Full article

The morphology, structure, and composition of CVD-grown molybdenum disulfide (${\mathrm{MoS}}_2$) films were investigated under varying precursor vapor pressures. Increasing sulfur vapor pressure transformed the film morphology from well-defined triangular domains to structures dominated by sulfur-terminated zigzag edges. These morphological changes were accompanied by notable variations in both structural and electrical properties. Non-uniform precursor vapor distribution promoted the formation of intrinsic point defects. To elucidate this behavior, a thermodynamic model was developed to link growth parameters to native defect formation. The analysis considered molybdenum and sulfur vacancies in both neutral and charged states, with equilibrium concentrations determined from the corresponding defect formation reactions. Sulfur vapor pressure emerged as the dominant factor controlling defect concentrations. The model validated experimental observations, with films grown under optimum and sulfur-rich conditions, yielding a carrier concentration of $9.6\times {10}^{11}$ ${\mathrm{cm}}^{-2}$ and $7.5\times {10}^{11}$ ${\mathrm{cm}}^{-2}$, respectively. The major difference in the field-effect transistor (FET) performance of devices fabricated under these two conditions was the degradation of the field-effect mobility and the current switching ratio. The degradation observed is attributed to increased carrier scattering at charged vacancy defect sites. Full article

Polymer-dispersed liquid crystal (PDLC), as an electrically controlled dimming material, has broad application prospects in various fields, including smart glass, display technology, and optical devices. However, traditional PDLC materials still face some challenges in practical applications, such as a high driving voltage and insufficient optical contrast, which limit their further application in high-performance optoelectronic devices. In this study, PDLC composite films exhibiting low-voltage operation (23 V), high contrast ratios (135), and rapid response times (T_R ~1.28 ms, T_D ~48 ms) were developed. This was achieved by modifying the chain length of the crosslinking agent and polymer monomer as well as by incorporating molybdenum disulfide (MoS₂) nanosheets. It shows a good regulation ability in the sunlight range (ΔT_sol = 63.92%, ΔT_lum = 73.97%). Simultaneously, the various chemical bonds inside the film and its special network structure enable it to exhibit a good radiative cooling effect. The indoor sunlight simulation tests showed that the indoor temperature decreased by 5 °C. This study provides valuable ideas for the development and preparation of smart windows with high efficiency and energy savings. Full article

In this study, molybdenum disulfide (MoS₂)-based water nanofluids were prepared and stabilized using two surfactants with opposite charges: the cationic cetyltrimethylammonium bromide (CTAB) and the anionic sodium lauryl sulfate (SLS). Different MoS₂:surfactant ratios (1:1, 1:2, and 1:3) were examined to identify the optimal formulation ensuring stable dispersion. Stability was evaluated through dynamic light scattering (DLS), zeta potential, and UV–Vis spectroscopy analyses. The results showed that the MoS₂:SLS (1:3) nanofluid achieved the highest stability, characterized by a zeta potential of −38 mV and a mean particle size of approximately 290 nm. Thermophysical properties were then investigated for nanoparticle concentrations of 0.05, 0.1, and 0.2 wt%. The 0.1 wt% nanofluid exhibited the best performance, showing a thermal conductivity enhancement of about 49% and an increased specific heat capacity compared with pure water. This improvement is attributed to uniform nanoparticle dispersion and enhanced phonon transport. Overall, the results demonstrate that the anionic SLS surfactant at a 1:3 ratio effectively enhances the stability as well as the thermal performance of MoS₂–water nanofluids, making them promising candidates for thermal management and energy systems applications. Full article

Heavy metal ions (HMIs) threaten ecosystems and human health due to their carcinogenicity, bioaccumulativity, and persistence, demanding highly sensitive, low-cost real-time detection. Electrochemical sensing technology has gained significant attention owing to its rapid response, high sensitivity, and low cost. Molybdenum disulfide (MoS₂), with its layered structure, tunable bandgap, and abundant edge active sites, demonstrates significant potential in the electrochemical detection of heavy metals. This review systematically summarizes the crystal structure characteristics of MoS₂, various preparation strategies, and their mechanisms for regulating electrochemical sensing performance. It particularly explores the cooperative effects of MoS₂ composites with other materials, which effectively enhance the sensitivity, selectivity, and detection limits of electrochemical sensors. Although MoS₂-based materials have made significant progress in theoretical and applied research, practical challenges remain, including fabrication process optimization, interference from complex-matrix ions, slow trace-metal enrichment kinetics, and stability issues in flexible devices. Future work should focus on developing efficient, low-cost synthesis methods, enhancing interference resistance through microfluidic and biomimetic recognition technologies, optimizing composite designs, resolving interfacial reaction dynamics via in situ characterization, and establishing structure–property relationship models using machine learning, ultimately promoting practical applications in environmental monitoring, food safety, and biomedical fields. Full article

The rapid development of industry has led to the discharge of large quantities of organic pollutants into water bodies, posing a significant threat to aquatic safety. It is imperative to develop efficient and environmentally friendly methods for the elimination of organic pollutants. The integration of hydrogel membranes with advanced oxidation processes (AOPs) for water purification has attracted considerable interest due to their high efficiency. However, conventional wet membrane materials stored in aqueous environments are more prone to swelling and leakage of loaded metal species. This limits its application in the degradation of organic pollutants. This study employs a vacuum drying strategy for wet hydrogels, incorporating molybdenum disulfide as a cocatalyst and Co²⁺ cross-linking within the alginate matrix, resulting in a dried MoS₂–cobalt alginate hydrogel membrane (D-MoS₂-CoAlg). The drying process of the D-MoS₂-CoAlg membrane not only significantly enhanced its mechanical strength and anti-swelling capacity but also effectively mitigated the leaching of Co²⁺. Throughout five consecutive cycles, the concentration of leached Co²⁺ remained below 0.032 mg/L. This enables the membrane to achieve a balance between reusability and environmental compatibility. Under the conditions of a drying time of 60 min, a peroxymonosulfate (PMS) dosage of 0.2 mmol/L, and an initial methylisothiazolinone (MIT) concentration of 20 mg/L, the D-MoS₂-CoAlg membrane exhibited exceptional catalytic performance, achieving a degradation rate of MIT as high as 92.14% within 5 min. The D-MoS₂-CoAlg membrane demonstrates high catalytic activity and good stability, showing promising potential for application in the field of organic wastewater treatment. Full article

Hybrid bonding technology has emerged as a critical 3D integration solution for advanced semiconductor packaging, enabling simultaneous bonding of metal interconnects and dielectric materials. However, conventional hybrid bonding processes face significant contamination challenges during O₂ plasma treatment required for OH group formation on SiCN or the other dielectric material surfaces. The aggressive plasma conditions cause Cu sputtering and metal migration, leading to chamber and substrate contamination that accumulates over time and degrades process reliability. In this work, we present a novel approach to address these contamination issues by implementing a molybdenum disulfide (MoS₂) barrier layer formed through plasma-enhanced chemical vapor deposition (PECVD) sulfurization of Mo films. The ultrathin MoS₂ layer acts as an effective barrier preventing Cu sputtering during O₂ plasma processing, thereby eliminating chamber contamination, and it also enables post-bonding electrical connectivity through controlled Cu filament formation via memristive switching mechanisms. When voltage is applied to the Cu-MoS₂-Cu structure after hybrid bonding, Cu ions migrate through the MoS₂ layer to form conductive filaments, establishing reliable electrical connections without compromising the bonding interface integrity. This innovative approach successfully resolves the fundamental contamination problem in hybrid bonding while maintaining excellent electrical performance, offering a pathway toward contamination-free and high-yield hybrid bonding processes for next-generation 3D-integrated devices. Full article

As the scaling of silicon-based CMOS technology approaches its physical limits, two-dimensional (2D) materials have emerged as promising alternatives for future electronic devices. Among them, MoS₂ is a leading candidate due to its fascinating semiconducting nature and compatibility with CMOS processes. However, high contact resistance at the metal–MoS₂ interface remains a major bottleneck, limiting device performance. In this study, we report the fabrication and characterization of graphene–MoS₂ (Gr–MoS₂) lateral heterostructure FETs, where monolayer graphene, synthesized by inductively coupled plasma chemical vapor deposition (ICP-CVD), is directly used as the source and drain. Bilayer MoS₂ is selectively grown along graphene edges via edge-guided CVD, forming a chemically bonded in-plane junction without transfer steps. Electrical measurements reveal that the Gr–MoS₂ FETs exhibit a threefold increase in average field-effect mobility (3.9 vs. 1.1 cm² V⁻¹ s⁻¹) compared to conventional MoS₂ FETs. Y-function analysis shows that the contact resistance is significantly reduced from 85.8 kΩ to 20.5 kΩ at V_G = 40 V. These improvements are attributed to the replacement of the conventional metal–MoS₂ contact with a graphene–metal contact. Our results demonstrate that lateral heterostructure engineering with graphene provides an effective and scalable strategy for high-performance 2D electronics. Full article