High-Performance Atomically-Thin Room-Temperature NO2 Sensor.

The development of room-temperature sensing devices for detecting small concentrations of molecular species is imperative for a wide range of low-power sensor applications. We demonstrate a room-temperature, highly sensitive, selective, stable, and reversible chemical sensor based on a monolayer of the transition-metal dichalcogenide Re0.5Nb0.5S2. The sensing device exhibits a thickness-dependent carrier type, and upon exposure to NO2 molecules, its electrical resistance considerably increases or decreases depending on the layer number. The sensor is selective to NO2 with only minimal response to other gases such as NH3, CH2O, and CO2. In the presence of humidity, not only are the sensing properties not deteriorated but also the monolayer sensor shows complete reversibility with fast recovery at room temperature. We present a theoretical analysis of the sensing platform and identify the atomically sensitive transduction mechanism.

Frustration and Atomic Ordering in a Monolayer Semiconductor Alloy.

Frustrated interactions can lead to short-range ordering arising from incompatible interactions of fundamental physical quantities with the underlying lattice. The simplest example is the triangular lattice of spins with antiferromagnetic interactions, where the nearest-neighbor spin-spin interactions cannot simultaneously be energy minimized. Here we show that engineering frustrated interactions is a possible route for controlling structural and electronic phenomena in semiconductor alloys. Using aberration-corrected scanning transmission electron microscopy in conjunction with density functional theory calculations, we demonstrate atomic ordering in a two-dimensional semiconductor alloy as a result of the competition between geometrical constraints and nearest-neighbor interactions. Statistical analyses uncover the presence of short-range ordering in the lattice. In addition, we show how the induced ordering can be used as another degree of freedom to considerably modify the band gap of monolayer semiconductor alloys.

Experimental and Theoretical Study of Possible Collective Electronic States in Exfoliable Re-Doped NbS2.

Metallic transition-metal dichalcogenides (TMDs) are rich material systems in which the interplay between strong electron-electron and electron-phonon interactions often results in a variety of collective electronic states, such as charge density waves (CDWs) and superconductivity. While most metallic group V TMDs exhibit coexisting superconducting and CDW phases, 2H-NbS2 stands out with no charge ordering. Further, due to strong interlayer interaction, the preparation of ultrathin samples of 2H-NbS2 has been challenging, limiting the exploration of presumably rich quantum phenomena in reduced dimensionality. Here, we demonstrate experimentally and theoretically that light substitutional doping of NbS2 with heavy atoms is an effective approach to modify both interlayer interaction and collective electronic states in NbS2. Very low concentrations of Re dopants (<1%) make NbS2 exfoliable (down to monolayer) while maintaining its 2H crystal structure and superconducting behavior. In addition, first-principles calculations suggest that Re dopants can stabilize some native CDW patterns that are not stable in pristine NbS2.

Sculpting Liquids with Two-Dimensional Materials: The Assembly of Ti3C2Tx MXene Sheets at Liquid-Liquid Interfaces.

The self-assembly of nanoscale materials at the liquid-liquid interface allows for fabrication of three-dimensionally structured liquids with nearly arbitrary geometries and tailored electronic, optical, and magnetic properties. Two-dimensional (2D) materials are highly anisotropic, with thicknesses on the order of a nanometer and lateral dimensions upward of hundreds of nanometers to micrometers. Controlling the assembly of these materials has direct implications for their properties and performance. We here describe the interfacial assembly and jamming of Ti3C2Tx MXene nanosheets at the oil-water interface. Planar, as well as complex, programmed three-dimensional all-liquid objects are realized. Our approach presents potential for the creation of all-liquid 3D-printed devices for possible applications in all-liquid electrochemical and energy storage devices and electrically active, all-liquid fluidics that exploits the versatile structure, functionality, and reconfigurability of liquids.