Search Results (392)

Point-of-care (POC) diagnostic technologies have become essential for the real-time monitoring and management of chronic wounds, where maintaining a moist environment and controlling pH levels are critical for effective healing. In this study, a flexible pH sensor based on a graphene/molybdenum disulfide (graphene/MoS₂) composite interdigitated electrode (IDE) structure was fabricated using pulsed laser ablation. The pH sensor, with an active area of 30 mm × 30 mm, exhibited good adhesion to the polyethylene terephthalate (PET) substrate and maintained structural integrity under repeated bending cycles. Precise ablation was achieved under optimized conditions of 4.35 J/cm² laser fluence, a repetition rate of 300 kHz, and a scanning speed of 500 mm/s, enabling the formation of defect-free IDE arrays without substrate damage. The influence of laser processing parameters on the surface morphology, electrical conductivity, and wettability of the composite thin films was systematically characterized. The fabricated pH sensor exhibited high sensitivity (~4.7% change in current per pH unit) across the pH 2–10 range, rapid response within ~5.2 s, and excellent mechanical stability under 100 bending cycles with negligible performance degradation. Moreover, the sensor retained > 95% of its stable sensitivity after 7 days of ambient storage. Furthermore, the pH response behavior was evaluated for electrode structures with different pitches, demonstrating that structural design parameters critically impact sensing performance. These results offer valuable insights into the scalable fabrication of flexible, wearable pH sensors, with promising applications in wound monitoring and personalized healthcare systems. Full article

The urgent demand for sustainable energy solutions in the face of climate change and resource depletion has catalyzed a global shift toward cleaner energy production and more efficient storage technologies. Lithium-ion batteries (LIBs), as the cornerstone of modern portable electronics, electric vehicles, and grid-scale storage systems, are continually evolving to meet the growing performance requirements. In this dynamic context, two-dimensional (2D) materials have emerged as highly promising candidates for use in electrodes due to their layered structure, tunable electronic properties, and high theoretical capacity. Among 2D materials, molybdenum disulfide (MoS₂) has gained increasing attention as a promising low-dimensional candidate for LIB anode applications. This review provides a comprehensive yet concise overview of recent advances in the application of MoS₂ in LIB electrodes, with particular attention to its unique electrochemical behavior at the nanoscale. We critically examine the interplay between structural features, charge-storage mechanisms, and performance metrics—chiefly the specific capacity, rate capability, and cycling stability. Furthermore, we discuss current challenges, primarily poor intrinsic conductivity and volume fluctuations, and highlight innovative strategies aimed at overcoming these limitations, such as through nanostructuring, composite formation, and surface engineering. By shedding light on the opportunities and hurdles in this rapidly progressing field, this work offers a forward-looking perspective on the role of MoS₂ in the next generation of high-performance LIBs. Full article

Molybdenum disulfide is more attractive and valuable at the molecular level due to its unique structure and exceptional properties. Here, new-type MoS₂-ring chains are constructed and theoretically investigated for relevant electronic properties influenced by the length of the chain and the bias. Different from traditional wires, our findings demonstrate that the conductance of such a new-type chain presents unusually non-exponential decay with the length of the chain, with a particularly anomalous length of seven rings, which shows stronger equilibrium conductance than a shorter four-ring chain. Multi-peaks of electron transmission and delocalized electronic states contribute such uniqueness. Mo atoms play a vital role in electron transport. Essentially, a narrower “HOMO-LUMO” (the two closest energy levels to the Fermi level of MoS₂-ring chain) gap compensates for the lower device density of states of new-type molybdenum disulfide-ring chains. The usual electronic structure of a seven-ring chain is derived from its slightly arched structure and mainly originates from interference, which is the resonance occurring between the electrodes. Noticeably, the bias could greatly enhance conductance, which could reach 1000 times more than the equilibrium conductance. At a certain bias, the conductance of a seven-ring chain even exceeds the shortest one- or two-ring chain. Furthermore, the threshold voltage (at which the maximum conductance appears) gradually decreases with the length of the chain and eventually remains at 0.7 V. The valuable negative differential resistance (NDR) effect could be found in such a molecular chain, which becomes more obvious as the length rises until the seven-ring chain reaches the peak. Our findings shed light on the relations between electronic properties and the length of a new-type molybdenum disulfide-ring chain, and provide support for such new-type chains in applications of innovative low-power and controllable electronics. Full article

Monolayer (ML) molybdenum disulfide (MoS₂) is a typical valleytronic material which has important applications in, for example, polarization optics and information technology. In this study, we examine the effect of continuous wave (CW) laser pumping on the basic optoelectronic properties of ML MoS₂ placed on a sapphire substrate, where the pump photon energy is larger than the bandgap of ML MoS₂. The pump laser source is provided by a compact semiconductor laser with a 445 nm wavelength. Through the measurement of THz time-domain spectroscopy, we obtain the complex optical conductivity for ML MoS₂, which are found to be fitted exceptionally well with the Drude–Smith formula. Therefore, we expect that the reduction in conductivity in ML MoS₂ is mainly due to the effect of electronic backscattering or localization in the presence of the substrate. Meanwhile, one can optically determine the key electronic parameters of ML MoS₂, such as the electron density n_e, the intra-band electronic relaxation time τ, and the photon-induced electronic localization factor c. The dependence of these parameters upon CW laser pump intensity is examined here at room temperature. We find that 445 nm CW laser pumping results in the larger n_e, shorter τ, and stronger c in ML MoS₂ indicating that laser excitation has a significant impact on the optoelectronic properties of ML MoS₂. The origin of the effects obtained is analyzed on the basis of solid-state optics. This study provides a unique and tractable technique for investigating photo-excited carriers in ML MoS₂. Full article

One of the key challenges in commercializing proton exchange membrane (PEM) electrolyzer technology is reducing the production costs while maintaining high efficiency and operational stability. Significant contributors to the overall cost of the device are the electrode catalysts with IrO₂ and Pt/C. Due to the high cost and limited availability of noble metals, there is growing interest in developing alternative, low-cost catalytic materials. In recent years, two-dimensional transition metal dichalcogenides (2D TMDCs), such as molybdenum disulfide (MoS₂) and rhenium disulfide (ReS₂), have attracted considerable attention due to their promising electrochemical properties for hydrogen evolution reactions (HERs). These materials exhibit unique properties, such as a high surface area or catalytic activity localized at the edges of the layered structure, which can be further enhanced through defect engineering or phase modulation. To increase the catalytically active surface area, the investigated materials were deposited on a carbon-based support—Vulcan XC-72R—selected for its high electrical conductivity and large specific surface area. This study investigated the physicochemical and electrochemical properties of six catalyst samples with varying MoS₂ and ReS₂ to carbon support ratios. Among the composites analyzed, the best sample on MoS₂ (containing the most carbon soot) and the best sample on ReS₂ (containing the least carbon soot) were selected. These were then used as cathode catalysts in an experimental PEM electrolyzer setup. The results confirmed satisfactory catalytic activity of the tested materials, indicating their potential as alternatives to conventional noble metal-based catalysts and providing a foundation for further research in this area. Full article

Due to the increase in energy demand, photocatalytic hydrogen (H₂) production has received enormous interest from the scientific community due to its simplicity and cost-effectiveness. The photocatalyst (PC) plays a vital role in H₂ evolution, and it is well understood that an efficient PC should have a larger surface area and better charge separation and transport properties. Previously, extensive efforts were made to prepare the efficient PC for photocatalytic H₂ production. In some cases, pristine catalyst could not catalyze the catalytic reactions due to a fast recombination rate or poor catalytic behavior. Thus, cocatalysts can be explored to boost the photocatalytic H₂ production. In this regard, a promising cocatalyst should have a large surface area, more active sites, decent conductivity, and improved catalytic properties. Molybdenum disulfide (MoS₂) is one of the two-dimensional (2D) layered materials that have excellent optical, electrical, and physicochemical properties. MoS₂ has been widely utilized as a cocatalyst for the photocatalytic H₂ evolution under visible light. Herein, we have reviewed the progress in the fabrication of MoS₂ and its composites with metal oxides, perovskite, graphene, carbon nanotubes, graphitic carbon nitrides, polymers, MXenes, metal-organic frameworks, layered double hydroxides, metal sulfides, etc. for photocatalytic H₂ evolution. The reports showed that MoS₂ is one of the desirable cocatalysts for photocatalytic H₂ production applications. The challenges and future perspectives are also mentioned. This study may be beneficial for the researchers working on the design and fabrication of MoS₂-based PCs for photocatalytic H₂ evolution applications. Full article

Layered transition metal dichalcogenides (TMDs) have gained considerable attention as promising cathodes for aqueous zinc-ion batteries (AZIBs) because of their tunable interlayer architecture and rich active sites for Zn²⁺ storage. However, unmodified TMDs face significant challenges, including limited redox activity, sluggish kinetics, and insufficient structural stability during cycling. These limitations are primarily attributed to their narrow interlayer spacing, strong electrostatic interactions, the large ionic hydration radius, and their high binding energy of Zn²⁺ ions. To address these restrictions, an in situ organic polyaniline (PANI) intercalation strategy is proposed to construct molybdenum disulfide (MoS₂)-based cathodes with extended layer spacing, thereby improving the zinc storage capabilities. The intercalation of PANI effectively enhances interplanar spacing of MoS₂ from 0.63 nm to 0.98 nm, significantly facilitating rapid Zn²⁺ diffusion. Additionally, the π-conjugated electron structure introduced by PANI effectively shields the electrostatic interaction between Zn²⁺ ions and the MoS₂ host, thereby promoting Zn²⁺ diffusion kinetics. Furthermore, PANI also serves as a structural stabilizer, maintaining the integrity of the MoS₂ layers during Zn-ion insertion/extraction processes. Furthermore, the conductive conjugated PANI boosts the ionic and electronic conductivity of the electrodes. As expected, the PANI–MoS₂ electrodes exhibit exceptional electrochemical performance, delivering a high specific capacity of 150.1 mA h g⁻¹ at 0.1 A g⁻¹ and retaining 113.3 mA h g⁻¹ at 1 A g⁻¹, with high capacity retention of 81.2% after 500 cycles. Ex situ characterization techniques confirm the efficient and reversible intercalation/deintercalation of Zn²⁺ ions within the PANI–MoS₂ layers. This work supplies a rational interlayer engineering strategy to optimize the electrochemical performance of MoS₂-based electrodes. By addressing the structural and kinetic limitations of TMDs, this approach offers new insights into the development of high-performance AZIBs for energy storage applications. Full article

Molybdenum disulfide (MoS₂) is a promising earth-abundant electrocatalyst for the hydrogen evolution reaction (HER), attributed to its favorable electronic structure and chemical stability. Nevertheless, its application is limited by poor electrical conductivity and low exposure of active sites. This review highlights recent progress in the synthesis and structural engineering of MoS₂-based catalysts to improve HER performance. Strategies such as morphology tuning, phase modulation, defect engineering, and heterostructure construction are systematically evaluated for their roles in enhancing charge transport, increasing active site density, and improving intrinsic catalytic activity. Additionally, the relationship between atomic structure, electronic properties, and HER kinetics is discussed to elucidate fundamental structure–activity correlations. These insights advance the development of MoS₂ as a cost-effective and scalable catalyst for hydrogen production and inform the rational design of future HER materials. Full article

The growing demand for low-cost biosensors has stimulated the study of new technologies and materials like molybdenum disulfide (MoS₂). Due to its electroconductive nature and high surface-to-volume ratio, it allows for the ultra-sensitive detection of biomarkers. The crystal structure of MoS₂ provides it with a unique micrometer thickness, making it appropriate for biosensing in healthcare, environmental monitoring, and food safety. As compared to traditional materials, MoS₂ can work without labels (through field-effect transduction or plasmonic shifts) while maintaining biocompatibility and low-cost fabrication, which fill significant voids in the early diagnosis of diseases. This paper provides an overview of the recent advancements in MoS₂-based biosensors, which are primarily focused on the field-effect transistors and surface plasmon resonance techniques and fabrication methods for MoS₂-based biosensors like mechanical exfoliation, liquid-phase exfoliation, physical vapor deposition, chemical vapor deposition, and chemical exfoliation, applications in various industries, and their characterization techniques to evaluate the quality and functionality of MoS₂ nanosheets in biosensors. While certain challenges remain like improving conductivity and scalability, MoS₂-based biosensors serve as a powerful tool for the precise and reliable detection of biomarkers in environmental, food, and healthcare industries. Full article

Transition metal dichalcogenides, especially molybdenum disulfide (MoS₂), exhibit exceptional properties that make them suitable for a wide range of applications. However, the interaction between MoS₂ and technologically relevant substrates, such as platinum (Pt) electrodes, can significantly influence its properties. This study investigates the growth and properties of MoS₂ thin films on Pt substrates using ionized jet deposition, a versatile, low-cost vacuum deposition technique. We explore the effects of the roughness of Pt substrates and self-heating during deposition on the chemical composition, structure, and strain of MoS₂ films. By optimizing the deposition system to achieve crystalline MoS₂ at room temperature, we compare as-deposited and annealed films. The results reveal that as-deposited MoS₂ films are initially amorphous and conform to the Pt substrate roughness, but crystalline growth is reached when the sample holder is sufficiently heated by the plasma. Further post-annealing at 270 °C enhances crystallinity and reduces sulfur-related defects. We also identify a change in the MoS₂–Pt interface properties, with a reduction in Pt–S interactions after annealing. Our findings contribute to the understanding of MoS₂ growth on Pt and provide insights for optimizing MoS₂-based devices in catalysis and electronics. Full article

The early and accurate detection of cancer remains a critical challenge in biomedical diagnostics. In this work, we propose and investigate a novel surface plasmon resonance (SPR) biosensor platform based on a multilayer configuration incorporating copper (Cu), silicon nitride (Si₃N₄), and molybdenum disulfide (MoS₂) for the optical detection of various cancer types. Four distinct sensor architectures (Sys₁–Sys₄) were optimized through the systematic tuning of Cu thickness, Si₃N₄ dielectric layer thickness, and the number of MoS₂ monolayers to enhance sensitivity, angular shift, and spectral sharpness. The optimized systems were evaluated using refractive index data corresponding to six cancer types (skin, cervical, blood, adrenal, breast T1, and breast T2), with performance metrics including sensitivity, detection accuracy, quality factor, figure of merit, limit of detection, and comprehensive sensitivity factor. Among the configurations, Sys₃ (BK7–Cu–Si₃N₄–MoS₂) demonstrated the highest sensitivity, reaching 254.64 °/RIU for adrenal cancer, while maintaining a low detection limit and competitive figures of merit. Comparative analysis revealed that the MoS₂-based designs, particularly Sys₃, outperform conventional noble-metal architectures in terms of sensitivity while using earth-abundant, scalable materials. These results confirm the potential of Cu/Si₃N₄/MoS₂-based SPR biosensors as practical and effective tools for label-free cancer diagnosis across multiple malignancy types. Full article

The widespread presence of pesticides—especially malathion—in aquatic environments presents a major obstacle to conventional remediation strategies, while the ongoing global energy crisis underscores the urgency of developing renewable energy sources such as hydrogen. In this context, photocatalytic water splitting emerges as a promising approach, though its practical application remains limited by poor charge carrier dynamics and insufficient visible-light utilization. Herein, we report the design and evaluation of a series of TiO₂-based ternary nanocomposites comprising commercial P25 TiO₂, reduced graphene oxide (rGO), and molybdenum disulfide (MoS₂), with MoS₂ loadings ranging from 1% to 10% by weight. The photocatalysts were fabricated via a two-step method: hydrothermal integration of rGO into P25 followed by solution-phase self-assembly of exfoliated MoS₂ nanosheets. The composites were systematically characterized using X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. Photocatalytic activity was assessed through two key applications: the degradation of malathion (20 mg/L) under simulated solar irradiation and hydrogen evolution from water in the presence of sacrificial agents. Quantification was performed using UV-Vis spectroscopy, gas chromatography–mass spectrometry (GC-MS), and thermal conductivity detection (GC-TCD). Results showed that the integration of rGO significantly enhanced surface area and charge mobility, while MoS₂ served as an effective co-catalyst, promoting interfacial charge separation and acting as an active site for hydrogen evolution. Nearly complete malathion degradation (~100%) was achieved within two hours, and hydrogen production reached up to 6000 µmol g⁻¹ h⁻¹ under optimal MoS₂ loading. Notably, photocatalytic performance declined with higher MoS₂ content due to recombination effects. Overall, this work demonstrates the synergistic enhancement provided by rGO and MoS₂ in a stable P25-based system and underscores the viability of such ternary nanocomposites for addressing both environmental remediation and sustainable energy conversion challenges. Full article

Extensive research has been conducted on the catalytic properties of molybdenum disulfide (MoS₂) materials in the context of the hydrogen evolution reaction (HER). This study focuses on exploring hybrid MoS₂/Au structures as a catalyst for HER, utilizing linear sweep voltammetry as the experimental methodology. Firstly, 2D-MoS₂ flakes were synthesized by the chemical vapor deposition (CVD) approach and directly added to gold nanoparticles during or after their preparation process. The prepared nanocomposites were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy with energy-dispersive X-ray analysis (SEM/EDX). The HER performance was tested for the two resulting samples to show that the preparation of gold nanoparticles with the coexistence of CVD-MoS₂ flakes produces a superior electrocatalytic performance of the sample in a neutral medium. Notably, the onset potential was measured as −0.152 V (versus reversible hydrogen electrode (RHE)) with an exchange current density (j₀) of 0.22 mA/cm². Chronoamperometric data show that all composites retained initial current densities for 15 hours, confirming stable, efficient HER performance post-decay. Full article

Molybdenum disulfide (MoS₂) has gained attention for its promising gas-sensing capabilities due to its high surface area and tunable electronic properties. In this study, we investigate the time-dependent growth (under constant conditions) of sputtered MoS₂ films on ZnO nanorods and their impact on NO₂ sensing performance. ZnO nanorods, synthesized via a hydrothermal method, provide a high-surface-area template to enhance charge transport and gas adsorption. Gas-sensing experiments revealed a strong correlation between MoS₂ thickness and NO₂ response, with the 25-min-sputtered MoS₂ film exhibiting the highest response of 20.9%. The synergistic interaction between MoS₂ and ZnO nanorods facilitated charge transfer and enhanced adsorption sites for NO₂ molecules. These findings emphasize the critical role of time-dependent growth of MoS₂ film in modulating gas-sensing performance and provide insights into designing high-sensitivity NO₂ sensors at room temperature. This study contributes to the development of hybrid MoS₂/ZnO nanostructures for next-generation environmental monitoring applications. Full article

The exacerbation of the global energy crisis has brought the development of efficient and sustainable hydrogen energy to the forefront of contemporary research endeavors. Molybdenum disulfide (MoS₂), recognized for its outstanding electrocatalytic performance as a two-dimensional material, has attracted significant interest for its potential in the hydrogen evolution reaction (HER). This review delves into the heteroatom-doped modification strategy centered on MoS₂ and its effectiveness in enhancing electrocatalytic hydrogen evolution. The influence of various doping elements (including noble metals, transition metals, and non-metals) on the electronic structure and catalytic efficiency of MoS₂ is also analyzed, elucidating the mechanism by which heteroatom doping enhances the catalytic performance and stability of MoS₂. Looking ahead, the integration of multiple doping elements, utilization of advanced computational techniques, and advancement of novel synthetic methods position MoS₂ for practical applications in the field of hydrogen energy, driving the progress and improvement of sustainable energy initiatives. Full article