Search Results (632)

Exhaled breath analysis has emerged as a promising non-invasive approach for disease diagnosis, leveraging gas sensors for their high sensitivity, portability, and real-time monitoring capabilities. Two-dimensional nanomaterials, such as graphene, transition metal dichalcogenides (TMDs), MXenes, black phosphorus, and metal–organic frameworks (MOFs), exhibit exceptional gas-sensing properties due to their atomic-scale thickness, ultra-large specific surface area, and tunable electronic structures. These characteristics enable enhanced gas adsorption and room-temperature operation, making them ideal for detecting ppb-level biomarkers like acetone, ammonia, and nitric oxide in breath. However, sensors based on pristine 2D materials face challenges including slow response/recovery kinetics, poor stability, weak humidity resistance, and limited selectivity in complex breath environments. To address these limitations, functionalization strategies have been developed to engineer material properties. Key approaches include heteroatom doping to modulate electronic band structures, heterojunction construction to facilitate charge transfer and improve selectivity, and noble metal decoration for catalytic enhancement of gas adsorption. Additionally, light irradiation has been employed to regulate the carrier concentration on the surface of sensitive materials. These strategies significantly boost sensor performance, achieving ppb-level detection limits, robust humidity resistance, and rapid response. Future directions involve integrating functionalized 2D materials into wearable, multiplexed sensor arrays for simultaneous biomarker detection, coupled with machine learning for real-time diagnostic platforms. Full article

Two-dimensional transient electroluminescent devices have attracted considerable attention owing to their simple device architecture and reduced contact-barrier dependence. However, the influence of semiconductor transport polarity on transient electroluminescence (EL) remains unclear. Here, we compare four representative transition metal dichalcogenide (TMDC) semiconductors with different transport polarities and find that ambipolar WSe₂ exhibits a stronger transient EL signal under identical driving conditions, a trend that cannot be explained by relative photoluminescence quantum yield (PLQY) alone. Transfer characteristics and gate-modulated photoluminescence (PL) measurements were further used to analyze the gate-dependent carrier doping states and the local spectral response associated with interfacial carrier modulation near the metal/TMDC interface during abrupt gate-voltage switching. Based on these results, we propose a possible physical picture in which ambipolar WSe₂ is more likely to form a transient interfacial electron–hole distribution favorable for electron–hole radiative recombination, whereas predominantly n-type materials tend to form electron-rich interfacial carrier states. These findings suggest that semiconductor transport polarity is an important material factor for designing low-dimensional transient electroluminescent devices. Full article

Two-dimensional black phosphorus (2D BP) has emerged as one of the most promising two-dimensional semiconductors for next-generation micro and nanoelectronics beyond Moore’s Law. It is distinguished by its unique combination of a layer dependent direct bandgap, broadband photoresponse, and pronounced in-plane anisotropy, addressing key intrinsic limitations that have hindered the widespread application of graphene and conventional transition metal dichalcogenides (TMDCs). This review provides a systematic and comprehensive overview of recent advances in the controllable fabrication of 2D BP and its applications in transistors and photodetectors. We first elucidate its crystal lattice structure and fundamental physical properties, then categorize and summarize synthesis strategies based on production scale ranging from small scale methods (e.g., mechanical exfoliation and solution based exfoliation) to large scale methods (e.g., Chemical Vapor Deposition (CVD) and Pulsed Laser Deposition (PLD)), with a particular focus on recent advances in high-speed field-effect transistors and broadband photodetectors. In summary, the key to achieving large-scale controllable synthesis lies in addressing the challenges of high-temperature oxidation of black phosphorus and the uncontrollable diffusion of phosphorus sources. In the future, industrial applications are expected to be realized through CVD based regulation of phosphorus sources, low-temperature growth by PLD, and deep integration with silicon-based processes. Full article

Two-dimensional heterostructures have attracted considerable attention in electrocatalytic hydrogen evolution due to their pronounced interfacial effects, tunable electronic properties, and large specific surface areas. In this work, two representative oxygen-terminated transition metal carbides (MXenes) and three typical transition metal dichalcogenides (TMDs) were selected to construct six heterostructures. Using first-principles density functional theory (DFT) calculations, their binding energies, structural stability, electronic structures, and HER catalytic performance were systematically investigated. The results showed that all heterostructures possessed good thermodynamic stability and favorable electronic properties. In particular, SnS₂/Ti₂CO₂, SnSe₂/Ti₂CO₂, SnTe₂/Ti₂CO₂, and SnTe₂/Zr₂CO₂ exhibited near-optimal hydrogen adsorption Gibbs free energy, indicating excellent HER activity. Moreover, the variation in Gibbs free energy of hydrogen adsorption from isolated monolayers to heterostructures could be effectively correlated with the work function difference. The predicted trends provided a useful descriptor for catalytic performance. Overall, this study provides theoretical insights into the rational design of efficient, advanced HER catalysts and contributes to the advancement of sustainable energy conversion technologies. As this work is based solely on first-principles calculations, the predicted catalytic activity of the heterostructure should be regarded as a theoretical prediction and awaits experimental confirmation. Full article

Active control of multi-mode light–matter interactions is crucial for advancing quantum photonic technologies. Although triple-mode plasmon–exciton systems involving two distinct excitonic transitions offer a pathway to multi-level polaritonic states, achieving reversible electrical tuning at room temperature remains challenging. Here, we numerically investigate an electrically tunable triple-mode strong-coupling system comprising a J-aggregate-coated Au@Ag nanorod coupled with monolayer WS₂. The simulated spectra show a UPB–LPB energy separation of approximately 239 meV near the zero-detuning condition. A modest gate voltage (2.0 V to 3.8 V) selectively modulates the middle and lower polariton branches over ∼46 meV, while the upper branch remains largely unaffected. This selective control is elucidated via a triple-mode coupled-oscillator model and Hopfield coefficient analysis, linking the polariton response to the excitonic composition. These results establish a framework for electrically reconfigurable multi-level polaritonic devices, offering potential for ultracompact optical modulators, high-sensitivity multiplexed sensors, and programmable quantum photonic circuits. Full article

The integration density of photonic integrated circuits is fundamentally limited by evanescent field overlap and subsequent inter-channel crosstalk. Layered transition metal dichalcogenides (TMDCs) bypass these confinement constraints through intrinsic optical birefringence and high refractive indices. Here, we report the near-infrared optical constants and waveguide dispersion of molybdenum diselenide (MoSe₂). Ellipsometry performed on centimeter-scale crystals yields an in-plane refractive index of 4.1–4.7 over 1000–2000 nm, with an extinction coefficient close to the sensitivity limit of the fit away from strong excitonic resonances. To validate the anisotropic dielectric tensor at the device scale, scattering-type scanning near-field optical microscopy (s-SNOM) was utilized to map the propagation of transverse-magnetic modes in 235 nm thick exfoliated flakes. Spatial Fourier analysis of the edge-scattered near-field interference yields effective mode indices that precisely match the modeled dispersion. Using the verified dielectric tensor, finite-element simulations demonstrate that single-mode MoSe₂ waveguides optically outperform equivalent tungsten disulfide (WS₂) benchmarks. The enhanced evanescent field suppression in the claddings of MoSe₂ waveguide increases the coupling length by a factor of 3.5, reducing the required routing pitch and enabling a 12.5% direct increase in on-chip integration density. The results identify MoSe₂ as a high-index anisotropic platform for compact waveguiding in the near-infrared. Full article

Platinum ditelluride (PtTe₂) is an emerging topological semimetal with intriguing optoelectronic properties. Scalable and controllable growth techniques are fundamental for its technological exploitation. Here, we synthesize large-area PtTe₂ films by tellurization of pre-deposited platinum layers. By selectively modifying the tellurization parameters, we demonstrate the possibility of controlling the layer orientation of tellurized films and of introducing microscopic corrugation in the PtTe₂ film. The first result is obtained by increasing the thermal budget of the process, which changes PtTe₂ preferential crystalline orientation from (001) to (1−13)/(103) growth directions. The latter result is achieved by modifying the heating rate of the process at a fixed growth temperature equal to 550 °C. From the Raman analysis of a wrinkled sample, we find the coexistence of tensile and compressive strains depending on the corrugation site. The demonstrated control over grain orientation and microscopic corrugation provides a powerful strategy to tailor the structural and strain landscape of topological semimetals, providing a robust platform for strain engineering. Full article

To address contact-limited transport commonly encountered in two-dimensional semiconductors, this study fabricated few-layer two-dimensional molybdenum disulfide (MoS₂) films on sapphire substrates via controllable oxide-to-sulfide conversion. Combined sputtering deposition of molybdenum trioxide and precise chemical-vapor sulfidation afforded high-quality, high-uniformity, and thickness-tunable MoS₂. The resulting films exhibit distinct differences in the frequencies of the Raman modes, consistent elemental ratios, and uniform interlayer spacing of ~0.65 nm. The MoS₂-based devices exhibit robust photodetection with microampere-scale photocurrents. Bilayer MoS₂ exhibited negative photoconductivity under ambient atmosphere, which is hypothesized to be linked to environment-induced surface doping and molecular adsorption rather than permanent structural traps. Contact engineering via mild thermal annealing of Ni electrodes significantly enhanced the photocurrent by improving effective interfacial carrier injection. These findings underscore the oxide sulfidation strategy as a scalable approach for engineering the layer-dependent behavior of transition metal dichalcogenides for optoelectronic applications. Full article

Two-dimensional (2D) transition metal dichalcogenide (TMDC) nanoscrolls have attracted significant attention in recent years owing to their fascinating properties, including high specific surface area, unique electronic structure, and excellent optoelectronic performance. These properties arise from their intrinsic one-dimensional (1D) spiral scroll geometry. In this review, we systematically present the preparation methods, properties, and applications of TMDC nanoscrolls. For fabrication, we detail a variety of preparation strategies, both on substrates and in solution. Next, we discuss the characterization and physical properties of TMDC nanoscrolls. Finally, we summarize their applications in photodetection, the hydrogen evolution reaction (HER), optoelectronic synapses, and other related fields. Full article

Ultrathin ferrimagnetic heterostructures have emerged as promising platforms for next-generation spintronic devices, yet the role of two-dimensional substrates in modulating their magnetic properties remains underexplored. Here, we report a comprehensive study of the thickness- and temperature-dependent magnetic behavior of amorphous Fe₇₃Co₈Gd₁₉ films (4–32 nm) deposited on Si, WSe₂ bilayer, and WSe₂ monolayer substrates. Structural integrity and stoichiometry were confirmed via X-Ray Diffraction (XRD), X-Ray Reflectivity (XRR), Raman spectroscopy, and Energy-Dispersive Spectroscopy (EDS) analysis. In-plane magnetometry from 10–300 K reveals that monolayer WSe₂ promotes stronger interfacial spin alignment, with the 4 nm film exhibiting a sharp increase in coercivity below 50 K, where $H_c$ exceeds 23 mT and even surpasses thicker counterparts, alongside enhanced saturation magnetization (∼790 kA/m at 100 K). This dramatic enhancement of coercivity is the most significant result of this work, underscoring the dominant role of interfacial coupling in governing low-temperature magnetic hardness. Conversely, films on bilayer exhibit suppressed magnetization and soft magnetic behavior ($H_c$ < 10 mT) across all temperatures, making them attractive for ultralow-power and high-speed spintronic applications. These findings demonstrate that atomically thin WSe₂ interfaces can modulate coercivity, magnetization, and squareness through proximity effects, establishing a tunable and thermally stable platform for spintronic device applications. Full article

The twist angle serves as a geometric tuning parameter in two-dimensional layered materials, enabling modulation of interlayer coupling and band structures without altering the chemical composition. In this work, six commensurate twisted bilayer WSe₂ configurations with rotation angles of 0°, 9.4°, 13.14°, 21.9°, 27.8°, and 60° were systematically investigated using first-principles density functional theory. Structural optimization, together with calculations of electronic structures, density of states, charge redistribution, effective masses, and optical properties, was performed. The results show that AA (0°) and 2H (60°) stackings exhibit the largest and smallest interlayer separations, respectively, whereas intermediate twist angles yield similar average spacings but distinct local stacking registries. All configurations remain indirect-gap semiconductors, with the valence band maximum located at K and the conduction band minimum near the Q point along the K–Γ path. The band gap increases from 1.450 eV at 0° to 1.579 eV at 27.8°, before decreasing to 1.333 eV at 60°, indicating strong twist-angle modulation of interlayer coupling. Density-of-states analysis shows that the valence-band edge mainly originates from Se-p and W-d hybridized states, whereas the conduction-band edge is dominated by W-d states, with intermediate angles exhibiting enhanced band folding and localization features. Charge-density analyses further reveal notable interfacial charge redistribution, which is most pronounced at 9.4°. Optical responses in the in-plane directions are nearly identical and significantly stronger than those along the out-of-plane direction. Optical absorption mainly occurs in the ultraviolet region, with band-edge features appearing in the near-infrared range. Intermediate twist angles exhibit broader dielectric responses in the visible region and extended long-wavelength tails, indicating enhanced interband transition channels. These results demonstrate that twist-angle engineering enables effective tuning of electronic and optical properties in bilayer WSe₂, providing theoretical guidance for the design of tunable optoelectronic devices. Full article

In the post-Moore era, large-area manufacturing of high-quality two-dimensional (2D) materials remains a central bottleneck for the industrialization of next-generation microelectronic and optoelectronic devices. Conventional mechanical exfoliation is limited by randomness and small lateral size, whereas chemical vapor deposition inevitably introduces grain boundaries, stress, and interfacial contamination, making it difficult to achieve both high quality and scalability. Metal-assisted exfoliation (MAE) enables controllable exfoliation and nondestructive transfer of large-area, high-quality monolayer 2D materials via precise modulation of metal-2D interfacial interactions dominated by strain-induced decoupling and atomic intercalation. This article systematically outlines the interfacial physical mechanisms and technological evolution of MAE, and highlights its state-of-the-art applications in patterned transfer, high-performance field-effect transistors, and complementary logic circuits, aiming to provide a firm theoretical and technical basis for advancing 2D materials from fundamental research toward practical applications. Full article

Innovations in nanomaterial science, engineering and printing technologies have increasingly driven advances in electrochemical sensing. Screen-printed electrodes (SPEs) have become a versatile, low-cost, and scalable solution for developing portable electrochemical detection platforms. However, their analytical performance remains intrinsically limited by surface area, electron transfer efficiency, and the immobilization of biomolecules. Recent developments in nanostructured materials, ranging from two-dimensional (2D) materials such as graphene, MXenes, and transition metal dichalcogenides, to one-dimensional nanostructures and hybrid nanocomposites, have transformed the signal transduction landscape of SPE-based electrochemical sensors. Integration of nanomaterials into SPEs has successfully transformed their analytical capabilities, but the diversity of materials and modification strategies has made it difficult to consolidate current knowledge in the field. Strategies that integrate nanomaterials via ink formulation, surface modification, or in situ growth have yielded sensors with unprecedented sensitivity, reproducibility, and selectivity across various chemical and biological targets. This review offers a cross-material synthesis of how nanomaterial engineering transforms the electrochemical performance of SPEs. By integrating insights across morphology, interfacial chemistry, and device-level behavior, it establishes a unified perspective that has been missing from the current literature and clarifies the design principles driving next-generation SPE-based sensing platforms. Full article

The development of reproducible and stable plasmon-free substrates for surface-enhanced Raman scattering (SERS) is critical for practical applications in analytical chemistry. Transition metal dichalcogenides (TMDCs) have emerged as promising candidates due to their unique electronic properties, yet their performance is often constrained by the chemical inertness of their pristine basal planes. This work presents a systematic comparison of crystalline flakes and nanoparticles of tungsten diselenide (WSe₂) and tungsten ditelluride (WTe₂), prepared via liquid-phase ultrasonic exfoliation and non-equilibrium femtosecond pulsed laser ablation in liquid (PLAL), respectively. The results demonstrate that nanoparticle-based substrates consistently outperform their flake-based counterparts, achieving enhancement factors in the range of ${10}^4$. The superior performance of the nanoparticles is hypothesized to originate from the synthesis-induced defects and high-curvature regions in the nanoparticles shell which facilitates efficient, defect-mediated charge transfer between the substrate and the analyte. At the same time, the inner polycrystalline volume conserves the important characteristics of the bulk counterparts like excitons in semiconducting WSe₂ and broadband absorption in semimetallic WTe₂, which unblocks the tunable photothermal colloidal response. The study establishes morphology engineering through non-equilibrium synthesis as a powerful and generalizable strategy for designing high-performance, dual-function colloidal platforms, offering a pathway toward robust and reproducible analytical systems. Full article

The global energy transition and the implementation of carbon capture, utilization, and storage (CCUS) strategies require energy-efficient and scalable CO₂ separation technologies. Mixed-matrix membranes (MMMs), combining polymer matrices with functional inorganic or hybrid nanofillers, have emerged as advanced separation platforms capable of surpassing the conventional permeability–selectivity trade-off observed in neat polymer membranes. This review critically evaluates recent developments in modern hybrid membranes for CO₂ separation from synthetic and industrial gas mixtures, including CO₂/N₂ (flue gas), CO₂/CH₄ (natural gas and biogas upgrading), and syngas systems. Particular emphasis is placed on MMMs incorporating covalent organic frameworks (COFs), metal–organic frameworks (MOFs), graphene oxide (GO), MXenes, transition metal dichalcogenides (TMDs), carbon nanotubes (CNTs), g-C₃N₄, layered double hydroxides (LDH), zeolites, metal oxides, and magnetic nanoparticles. Reported performance ranges include CO₂ permeability (P_CO2) typically between 100 and 800 Barrer, CO₂/N₂ selectivity up to 319, and CO₂/CH₄ selectivity up to 249, depending on filler chemistry, loading, and interfacial compatibility. The mechanisms governing gas transport—molecular sieving, selective adsorption, facilitated transport, and diffusion-pathway engineering—are systematically discussed. Key challenges addressed include filler dispersion, polymer–filler interfacial defects, physical aging, moisture sensitivity, oxidation (particularly in MXenes), and scalability toward industrial membrane modules. Future perspectives focus on sub-nanometer pore engineering, surface functionalization to enhance CO₂ affinity, controlled alignment of 2D nanosheets to promote directional transport, multifunctional core–shell and hollow structures, and the integration of computational modeling and machine learning for accelerated material design. Modern hybrid MMMs are identified as strategically important materials enabling high-efficiency CO₂ separation processes aligned with decarbonization and energy transition objectives. Full article