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The library of true two-dimensional materials is limited since many transition metal compounds are not stratified and can thus not be easily isolated as nanosheets. Here, micron-sized ultrathin rutile TiO2 nanosheets featuring uniform thickness (2 ± 0.5 nm) with dielectric constant (e⊥ = 24) have been synthesized via a liquid metal synthesis strategy.

Intriguing physical and chemical properties of atomically thin semiconductors provide avenues for the development of the next-generation electronics, optoelectronics, and sensing applications. Howe...

The library of true two-dimensional materials is limited since many transition metal compounds are not stratified and can thus not be easily isolated as nanosheets. Here, micron-sized ultrathin rutile TiO2 nanosheets featuring uniform thickness (2 ± 0.5 nm) with dielectric constant (ε⊥ = 24) have been synthesized via a liquid metal synthesis strategy.

Planar 2D materials are possibly the ideal channel candidates for future field effect transistors (FETs), due to their unique electronic properties. However, the performance of FETs based on 2D materials is yet to exceed those of conventional silicon based devices. Here, a 2D channel thin film made from liquid phase exfoliated molybdenum oxide nanoflake inks with highly controllable substoichiometric levels is presented. The ability to induce oxygen vacancies by solar light irradiation in an aqueous environment allows the tuning of electronic properties in 2D substoichiometric molybdenum oxides (MoO3−x). The highest mobility is found to be ≈600 cm2 V−1 s−1 with an estimated free electron concentration of ≈1.6 × 1021 cm−3 and an optimal IOn/IOff ratio of >105 for the FETs made of 2D flakes irradiated for 30 min (x = 0.042). These values are significant and represent a real opportunity to realize the next generation of tunable electronic devices using electronic inks.

The use of membranes for gas permeation and phase separation offers many distinct advantages over other more energy-dependent processes. The operational efficiencies of these membranes rely heavily on high gas permeability. Here, we report membranes with significantly increased permeability without a considerable decrease in mechanical strength or selectivity, synthesized from a polymer nanocomposite that incorporates graphene and polydimethylsiloxane (PDMS). These graphene–PDMS nanocomposite membranes were able to enhance the gas permeation of N2, CO2, Ar, and CH4 in reference to pristine PDMS membranes. This is achieved by creating interfacial voids between the graphene flakes and polymer chains, which increases the fractional free volume within the nanocomposites, giving rise to an increase in permeation. An optimal loading of graphene was found to be 0.25 wt%, while greater loading created agglomeration of the graphene flakes, hence reducing the effective surface area. We present the enhancements that...

The exhibition of plasmon resonances in two-dimensional (2D) semiconductor compounds is desirable for many applications. Here, by electrochemically intercalating lithium into 2D molybdenum disulfide (MoS2) nanoflakes, plasmon resonances in the visible and near UV wavelength ranges are achieved. These plasmon resonances are controlled by the high doping level of the nanoflakes after the intercalation, producing two distinct resonance peak areas based on the crystal arrangements. The system is also benchmarked for biosensing using bovine serum albumin. This work provides a foundation for developing future 2D MoS2 based biological and optical units.

A liquid-based organic solvent-assisted grinding and sonication method was adopted for the formation of two dimensional (2D) moderately hydrated α -MoO 3 nanoflake suspensions, with a flake thickness in the order of ∼1.4 nm. This thickness is equal to the largest unit cell parameter of α -MoO 3 . The implemented method had the advantage of simplicity and resulted in a high yield of nanoflakes that were highly crystalline across the planes. This method can be incorporated into 2D semiconducting material-enabled devices. Conductometric transduction templates based on drop-casted thin films of these 2D α -MoO 3 flakes were developed for H 2 gas sensing. The sensors showed large responses to H 2 gas with response and recovery time in the order of seconds. The impressive operation of these devices was attributed to the 2D flake-like structure of the thin films.

Heterostructures assembled from atomically thin materials have led to a new paradigm in the development of the next-generation high-performing functional devices. However, the construction of the ultrathin van der Waals (vdW) heterostructures is challenging and/or limited to materials with layered crystal structures. Herein, liquid metal vdW transfer method is used to construct large area heterostructures of atomically thin metal oxides of p-SnO/n-In2O3 with ease. The heterostructure exhibits both outstanding photodetectivity of 5 x 10(9) Jones and photoresponsivity of 1047 A W-1 with fast response time of 1 ms under illumination of the 280 nm light. Such excellent performances are due to the formation of the narrow bandgap of the staggered gap at the p-n junction produced by the high-quality SnO/In2O3 heterostructure. The facile production of high-quality vdW heterostructures using the liquid metal-based method therefore provides a promising pathway for realizing future optoelectronic devices.

Few-layer two-dimensional (2D) molybdenum oxide nanoflakes are exfoliated using a grinding assisted liquid phase sonication exfoliation method. The sonication process is carried out in five different mixtures of water with both aprotic and protic solvents. We found that surface energy and solubility of mixtures play important roles in changing the thickness, lateral dimension, and synthetic yield of the nanoflakes. We demonstrate an increase in proton intercalation in 2D nanoflakes upon simulated solar light exposure. This results in substoichiometric flakes and a subsequent enhancement in free electron concentrations, producing plasmon resonances. Two plasmon resonance peaks associated with the thickness and the lateral dimension axes are observable in the samples, in which the plasmonic peak positions could be tuned by the choice of the solvent in exfoliating 2D molybdenum oxide. The extinction coefficients of the plasmonic absorption bands of 2D molybdenum oxide nanoflakes in all samples are found to be high (ε10(9) L mol(-1) cm(-1)). It is expected that the tunable plasmon resonances of 2D molybdenum oxide nanoflakes presented in this work can be used in future electronic, optical, and sensing devices.

Nanoporous Nb2O5 has been previously demonstrated to be a viable electrochromic material with strong intercalation characteristics. Despite showing such promising properties, its potential for optical gas sensing applications, which involves the production of ionic species such as H(+), has yet to be explored. Nanoporous Nb2O5 can accommodate a large amount of H(+) ions in a process that results in an energy bandgap change of the material which induces an optical response. Here, we demonstrate the optical hydrogen gas (H2) sensing capability of nanoporous anodic Nb2O5 with a large surface-to-volume ratio prepared via a high temperature anodization method. The large active surface area of the film provides enhanced pathways for efficient hydrogen adsorption and dissociation, which are facilitated by a thin layer of Pt catalyst. We show that the process of H2 sensing causes optical modulations that are investigated in terms of response magnitudes and dynamics. The optical modulations induced by the intercalation process and sensing properties of nanoporous anodic Nb2O5 shown in this work can potentially be used for future optical gas sensing systems.

The exhibition of plasmon resonances in two-dimensional (2D) semiconductor compounds is desirable for many applications. Here, by electrochemically intercalating lithium into 2D molybdenum disulfide (MoS2) nanoflakes, plasmon resonances in the visible and near UV wavelength ranges are achieved. These plasmon resonances are controlled by the high doping level of the nanoflakes after the intercalation, producing two distinct resonance peak areas based on the crystal arrangements. The system is also benchmarked for biosensing using bovine serum albumin. This work provides a foundation for developing future 2D MoS2 based biological and optical units.

Two-dimensional (2D) molybdenum oxides at their various stoichiometries are promising candidates for generating plasmon resonances in visible light range. Herein, we demonstrate plasmonic 2D molybdenum oxide flakes for gas sensing applications, in which hydrogen (H2) is selected as a model gas. The 2D molybdenum oxide flakes are obtained using a grinding-assisted liquid exfoliation method and exposed to simulated sunlight to acquire its substoichiometric quasi-metallic form. After the exposure to H2 gas molecules, the quasi-metallic molybdenum oxide flakes are partially transformed into semiconducting states, thus gradually losing their plasmonic properties. The novel 2D plasmonic sensing platform is tested using different concentrations of H2 gas at various operating temperatures to comprehensively assess its sensing performance. The presented 2D plasmonic system offers great opportunities for future sensing and optical applications.

Tunable plasmon resonances in suspended 2D molybdenum oxide flakes are demonstrated. The 2D configuration generates a large depolarization factor and the presence of ultra-doping produces visible-light plasmon resonances. The ultra-doping process is conducted by reducing the semiconducting 2D MoO 3 flakes using simulated solar irradiation. The generated plasmon resonances can be controlled by the doping levels and the flakes' lateral dimensions, as well as by exposure to a model protein.