Search Results (7)

The morphology modulation of target crystals is important for understanding their growth mechanisms and potential applications. Herein, we report a convenient method for modulating the morphology of MoO₂ by controlling different growth temperatures. With an increase in growth temperature, the morphology of MoO₂ changes from a nanoribbon to a nanoflake. Various characterization methods, including optical microscopy, atomic force microscopy, (vertical and tilted) scanning electron microscopy, Raman spectroscopy, high-resolution transmission electron microscopy, and selected area electron diffraction, were performed to unveil the morphology modulation and lattice structure of MoO₂. Both MoO₂ nanoribbons and nanoflakes display a standing-up growth mode on c-sapphire substrates, and their basal planes are MoO₂(100). Further investigations into devices based on MoS₂ with Au/Ti/MoO₂ electrodes show the potential applications of MoO₂ in two-dimensional electrodes. These findings are helpful for the synthesis of MoO₂ with different morphologies and applications in the field of optoelectronic nanodevices. Full article

An ethylenediamine (EDA) gas sensor based on a composite of MoO₃ nanoribbon and reduced graphene oxide (rGO) was fabricated in this work. MoO₃ nanoribbon/rGO composites were synthesized using a hydrothermal process. The crystal structure, morphology, and elemental composition of MoO₃/rGO were analyzed via XRD, FT-IR, Raman, TEM, SEM, XPS, and EPR characterization. The response value of MoO₃/rGO to 100 ppm ethylenediamine was 843.7 at room temperature, 1.9 times higher than that of MoO₃ nanoribbons. The MoO₃/rGO sensor has a low detection limit (LOD) of 0.235 ppm, short response time (8 s), good selectivity, and long-term stability. The improved gas-sensitive performance of MoO₃/rGO composites is mainly due to the excellent electron transport properties of graphene, the generation of heterojunctions, the higher content of oxygen vacancies, and the large specific surface area in the composites. This study presents a new approach to efficiently and selectively detect ethylenediamine vapor with low power. Full article

Terahertz frequency has promising applications in communication, security scanning, medical imaging, and industry. THz absorbers are one of the required components for future THz applications. However, nowadays, obtaining a high absorption, simple structure, and ultrathin absorber is a challenge. In this work, we present a thin THz absorber that can be easily tuned through the whole THz range (0.1–10 THz) by applying a low gate voltage (<1 V). The structure is based on cheap and abundant materials (MoS₂/graphene). Nanoribbons of MoS₂/graphene heterostructure are laid over a SiO₂ substrate with an applied vertical gate voltage. The computational model shows that we can achieve an absorptance of approximately 50% of the incident light. The absorptance frequency can be tuned through varying the structure and the substrate dimensions, where the nanoribbon width can be varied approximately from 90 nm to 300 nm, while still covering the whole THz range. The structure performance is not affected by high temperatures (500 K and above), so it is thermally stable. The proposed structure represents a low-voltage, easily tunable, low-cost, and small-size THz absorber that can be used in imaging and detection. It is an alternative to expensive THz metamaterial-based absorbers. Full article

We report on the facile and scalable catalytic conversion of natural graphite and MoS₂ minerals into α-MoO₃ nanoribbons incorporated into hexagonal MoS₂ and graphene nanosheets, and evaluate the structural, morphological and electrochemical performances of the hybrid nanostructured material obtained. Mechanochemical treatment of raw materials, followed by catalytic molten salt treatment leads to the formation of nanostructures with promising electrochemical performances. We examined the effect of processing temperature on the electrochemical performance of the products. At 1100 °C, an excellent Li-ion storage capacity of 773.5 mAh g⁻¹ is obtained after 180 cycles, considerably greater than that of MoS₂ (176.8 mAh g⁻¹). The enhanced capacity and the rate performance of this electrode are attributed to the well-integrated components, characterized by the formation of interfacial molybdenum oxycarbide layer during the synthesis process, contributing to the reduced electrical/electrochemical resistance of the sample. This unique morphology promotes the charge and ions transfer through the reduction of the Li-ion diffusion coefficient (1.2 × 10⁻¹⁸ cm² s⁻¹), enhancing the pseudocapacitive performance of the electrode; 59.3% at the scan rate of 0.5 mV s⁻¹. This article provides a green and low-cost route to convert highly available natural graphite and MoS₂ minerals into nanostructured hybrid materials with promising Li-ion storage performance. Full article

Recently, two-dimensional (2D) materials and their heterostructures have attracted considerable attention in gas sensing applications. In this work, we synthesized 2D MoS₂@MoO₃ heterostructures through post-sulfurization of α-MoO₃ nanoribbons grown via vapor phase transport (VPT) and demonstrated highly sensitive NO₂ gas sensors based on the hybrid heterostructures. The morphological, structural, and compositional properties of the MoS₂@MoO₃ hybrids were studied by a combination of advanced characterization techniques revealing a core-shell structure with the coexistence of 2H-MoS₂ multilayers and intermediate molybdenum oxysulfides on the surface of α-MoO₃. The MoS₂@MoO₃ hybrids also exhibit room-temperature ferromagnetism, revealed by vibrating sample magnetometry (VSM), as a result of the sulfurization process. The MoS₂@MoO₃ gas sensors display a p-type-like response towards NO₂ with a detection limit of 0.15 ppm at a working temperature of 125 °C, as well as superb selectivity and reversibility. This p-type-like sensing behavior is attributed to the heterointerface of MoS₂-MoO₃ where interfacial charge transfer leads to a p-type inversion layer in MoS₂, and is enhanced by magnetic dipole interactions between the paramagnetic NO₂ and the ferromagnetic sensing layer. Our study demonstrates the promising application of 2D molybdenum hybrid compounds in gas sensing applications with a unique combination of electronic and magnetic properties. Full article

Anisotropic materials provide a new platform for building diverse polarization-dependent optical devices. Two-dimensional α-phase molybdenum trioxides (α-MoO₃), as newly emerging natural van der Waals materials, have attracted significant attention due to their unique anisotropy. In this work, we theoretically propose an anisotropic perfect metamaterial absorber in visible frequencies, the unit cell of which consists of a multi-layered α-MoO₃ nanoribbon/dielectric structure stacked on a silver substrate. Additionally, the number of perfect absorption bands is closely related to the α-MoO₃ nanoribbon/dielectric layers. When the proposed absorber is composed of three α-MoO₃ nanoribbon/dielectric layers, electromagnetic simulations show that triple-band perfect absorption can be achieved for polarization along [100], and [001] in the direction of, α-MoO₃, respectively. Moreover, the calculation results obtained by the finite-difference time-domain (FDTD) method are consistent with the effective impedance of the designed absorber. The physical mechanism of multi-band perfect absorption can be attributed to resonant grating modes and the interference effect of Fabry–Pérot cavity modes. In addition, the absorption spectra of the proposed structure, as a function of wavelength and the related geometrical parameters, have been calculated and analyzed in detail. Our proposed absorber may have potential applications in spectral imaging, photo-detectors, sensors, etc. Full article

The structural stability and structural and electronic properties of lateral monolayer transition metal chalcogenide superlattice zigzag and armchair nanoribbons have been studied by employing a first-principles method based on the density functional theory. The main focus is to study the effects of varying the width and periodicity of nanoribbon, varying cationic and anionic elements of superlattice parent compounds, biaxial strain, and nanoribbon edge passivation with different elements. The band gap opens up when the (MoS₂)₃/(WS₂)₃ and (MoS₂)₃/(MoTe₂)₃ armchair nanoribbons are passivated by H, S and O atoms. The H and O co-passivated (MoS₂)₃/(WS₂)₃ armchair nanoribbon exhibits higher energy band gap. The band gap with the edge S vacancy connecting to the W atom is much smaller than the S vacancy connecting to the Mo atom. Small band gaps are obtained for both edge and inside Mo vacancies. There is a clear difference in the band gap states between inside and edge Mo vacancies for symmetric nanoribbon structure, while there is only a slight difference for asymmetric structure. The electronic orbitals of atoms around Mo vacancy play an important role in determining the valence band maximum, conduction band minimum, and impurity level in the band gap. Full article