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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.

Metal foams are highly sought-after porous structures for heterogeneous catalysis, which are fabricated by templating, injecting gas, or admixing blowing agents into a metallic melt at high temperatures. They also require additional catalytic material coating. Here, a low-melting-point liquid metal is devised for the single-step formation of catalytic foams in mild aqueous environments. A hybrid catalytic foam fabrication process is presented via simultaneous chemical foaming, melting, and sintering reaction of liquid metal nanoparticles. As a model, nanoparticles of tertiary low-melting-point eutectic alloy of indium, bismuth, and tin (Field's metal) are processed with sodium hydrogen carbonate, an environmentally benign blowing agent. The competing endothermic foaming and exothermic sintering reactions are triggered by an aqueous acidic bath. The overall foaming process occurs at a localized temperature above 200 °C, producing submicron- to micron-sized open-cell pore foams with conductive cores and semiconducting surface decorations. The catalytic properties of the metal foams are explored for a range of applications including photo-electrocatalysis, bacteria electrofiltration, and CO2 electroconversion. In particular, the Field's metal-based foams show exceptional CO2 electrochemical conversion performance at low applied voltages. The facile process presented here can be extended to other low-temperature post transition and transition metal alloys.

The intriguing properties of two-dimensional transition metal dichalcogenides (2D TMDCs) have led to a significant body of fundamental research and rapid uptake of these materials in many applications. Specifically, 2D TMDCs have shown great potential in biological systems due to their tunable electronic characteristics, unique optical properties, stability in aqueous environments, large surface area that can be manipulated and functionalized as well as an intercalatable layered structure, and low levels of toxicity. Here, the characteristics and use of 2D TMDCs for biological applications are reviewed and future possibilities for these materials in biological systems are outlined.

Chaotic advection plays an important role in microplatforms for a variety of applications. Currently used mechanisms for inducing chaotic advection in small scale, however, are limited by their complicated fabrication processes and relatively high power consumption. Here, a soft actuator is reported which utilizes a droplet of Galinstan liquid metal to induce harmonic Marangoni fl ow at the surface of liquid metal when activated by a sinusoidal signal. This liquid metal actuator has no rigid parts and employs continuous electrowetting effect to induce chaotic advection with exceptionally low power consumption. The theory behind the operation of this actuator is developed and validated via a series of experiments. The presented actuator can be readily integrated into other microfl uidic components for a wide range of applications.

A new platform described as the liquid metal/metal oxide (LM/MO) framework is introduced. The constituent spherical structures of these frameworks are made of micro- to nanosized liquid metal spheres and nanosized metal oxides, combining the advantages of both materials. It is shown that the diameters of the spheres and the stoichiometry of the structures can be actively controlled. Additionally, the liquid suspension of these spheres demonstrates tuneable plasmon resonances. These spherical structures are assembled to form LM/MO frameworks which are capable of demonstrating high sensitivity towards low concentrations of heavy metal ions, and enhanced solar light driven photocalalytic activities. These demonstrations imply that the LM/MO frameworks are a suitable candidate for the development of future high performance electronic and optical devices.

Liquid metals offer unprecedented chemistry. Here it is shown that they can facilitate self-limiting oxidation processes on their surfaces, which enables the growth of metal oxides that are atomically thin. This claim is exemplified by creating atomically thin hydrated MnO2 using a Galvanic replacement reaction between permanganate ions and a liquid gallium–indium alloy (EGaIn). The “liquid solution”–“liquid metal” process leads to the reduction of the permanganate ions, resulting in the formation of the oxide monolayer at the interface. It is presented that under mechanical agitation liquid metal droplets are established, and simultaneously, hydrated gallium oxides and manganese oxide sheets delaminate themselves from the interfacial boundaries. The produced nanosheets encapsulate a metallic core, which is found to consist of solid indium only, with the full migration of gallium out of the droplets. This process produces core/shell structures, where the shells are made of stacked atomically thin nanosheets. The obtained core/shell structures are found to be an efficient photocatalyst for the degradation of an organic dye under simulated solar irradiation. This study presents a new research direction toward the modification and functionalization of liquid metals through spontaneous interfacial redox reactions, which has implications for many applications beyond photocatalysis.

In the quest to discover the properties of planar semiconductors, two-dimensional molybdenum trioxide and dichalcogenides have recently attracted a large amount of interest. This family, which includes molybdenum trioxide (MoO 3 ), disulphide (MoS 2 ), diselenide (MoSe 2 ) and ditelluride (MoTe 2 ), possesses many unique properties that make its compounds appealing for a wide range of applications. These properties can be thickness dependent and may be manipulated via a large number of physical and chemical processes. In this Feature Article, a comprehensive review is delivered of the fundamental properties, synthesis techniques and applications of layered and planar MoO 3 , MoS 2 , MoSe 2 , and MoTe 2 along with their future prospects.

Liquid metal marbles that are droplets of liquid metal encapsulated by micro- or nanoparticles are introduced. Droplets of galinstan liquid metal are coated with insulators (including Teflon and silica) and semiconductors (including WO3, TiO2, MoO3, In2O3 and carbon nanotubes) by rolling over a powder bed and also by submerging in colloidal suspensions. It is shown that these marbles can be split and merged, can be suspended on water, and are even stable when moving under the force of gravity and impacting a flat solid surface. Furthermore, the marble coating can operate as an active electronic junction and the nanomaterial coated liquid metal marble can act as a highly sensitive electrochemical based heavy metal ion sensor. This new element thus represents a significant platform for the advancement of research into soft electronics.

Metal oxides are the key ingredients for the development of many advanced functional materials and smart devices. Nanostructuring has emerged as one of the best tools to unlock their full potential. Tungsten oxides (WOx) are unique materials that have been rigorously studied for their chromism, photocatalysis, and sensing capabilities. However, they exhibit further important properties and functionalities that have received relatively little attention in the past. This Feature Article presents a general review of nanostructured WOx, their properties, methods of synthesis, and a description of how they can be used in unique ways for different applications. Tungsten oxides (WOx) are unique functional materials that can be obtained in a vast variety of nanostructured forms. This Feature Article presents a comprehensive review on the properties of WOx that goes beyond chromism and photocatalysis, for which they are usually investigated for. This is followed by a survey of their synthesis methods and implementations for different applications.

Exothermic chemical reactions that are coupled to Bi2Te3 porous layers, which are deposited onto terracotta or alumina (Al2O3) substrates, are used to produce self-propagating thermal waves that are guided along the surface. Nitrocellulose is used as the highly reactive chemical. Bi2Te3 is employed because of its large Seebeck coefficient and high electrical conductivity. For the Al2O3 based structures, the thermal conduction of the substrate results in strong oscillations of the output signals. Such thermopower waves produce a power as large as 10 mW and voltages as high as 150 mV. The power per mass ratio of the developed system is quite remarkable, namely, on the order of 1 kW kg(-1). Depending on the thermal conductivity of the substrate used, the wave front average propagation velocity is either slow (ca. 0.009 m s(-1) for terracotta) or much faster (on the order of 0.4 m s(-1) for Al2O3). We have used a mathematical model based on two coupled heat transport equations, in conjunction with the chemical reaction equation, to predict the behavior of the system, which describes the average propagation velocity and the time between oscillation peaks.

Plasmonic biosensors based on noble metals generally suffer from low sensitivities if the perturbation of refractive-index in the ambient is not significant. By contrast, the features of degenerately doped semiconductors offer new dimensions for plasmonic biosensing, by allowing charge-based detection. Here, this concept is demonstrated in plasmonic hydrogen doped molybdenum oxides (H x MoO 3 ), with the morphology of 2D nanodisks, using a representative enzymatic glucose sensing model. Based on the ultrahigh capacity of the molybdenum oxide nanodisks for accommodating H + , the plasmon resonance wavelengths of H x MoO 3 are shifted into visible-near-infrared wavelengths. These plasmonic features alter significantly as a function of the intercalated H + concentration. The facile H + deintercalation out of H x MoO 3 provides an exceptional sensitivity and fast kinetics to charge perturbations during enzymatic oxidation. The optimum sensing response is found at H 1.55 MoO 3 , achieving a detection limit of 2 × 10 -9 m at 410 nm, even when the biosensing platform is adapted into a light-emitting diode-photodetector setup. The performance is superior in comparison to all previously reported plasmonic enzymatic glucose sensors, providing a great opportunity in developing high performance biosensors.

Gallium is a near room temperature liquid metal with extraordinary properties that partly originate from the self-limiting oxide layer formed on its surface. Taking advantage of the surface gallium oxide (Ga2O3), this work introduces a novel technique to synthesize gallium oxide nanoflakes at high yield by harvesting the self-limiting native surface oxide of gallium. The synthesis process follows a facile two-step method comprising liquid gallium metal sonication in DI water and subsequent annealing. In order to explore the functionalities of the product, the obtained hexagonal α-Ga2O3 nanoflakes are used as a photocatalytic material to decompose organic model dyes. Excellent photocatalytic activity is observed under solar light irradiation. To elucidate the origin of these enhanced catalytic properties, the electronic band structure of the synthesized α-Ga2O3 is carefully assessed. Consequently, this excellent photocatalytic performance is associated with an energy bandgap reduction, due to the presence of trap states, which are located at ≈1.65 eV under the conduction band minimum. This work presents a novel route for synthesizing oxide nanostructures that can be extended to other low melting temperature metals and their alloys, with great prospects for scaling up and high yield synthesis.