Fabrication of Multilayer Borophene on Insulator Structure.

The X-ray photoelectron spectroscopy spectra indicate the peak of BB bonds, implying that the elemental boron structure might be formed after the process. The multilayer ß-borophene is directly observed by transmission electron microscopy (TEM) and the lattice parameters are valid. The middle SiNx layer also can be identified in TEM image. Furthermore, the 1.61 eV bandgap of the multilayer ß-borophene is announced in this study.

Remarkably enhanced photovoltaic effects and first-principles calculations in neodymium doped BiFeO3.

Remarkably enhanced photovoltaic effects have been observed in the heterostructures of p-type A-site Nd3+-doped BiFeO3 (Bi0.9375Nd0.0625)FeO3 (or BFONd) polycrystalline ceramics and the n-type ITO thin film. The maximum power conversion is ~0.82%, which is larger than 0.015% in BiFeO3 (BFO) under blue-ultraviolet irradiation of wavelength λ = 405 nm. The current-voltage (I-V) characteristic curve suggests a p-n junction interface between the ITO thin film and BFO (or BFONd) ceramics. The band gaps calculated from first-principles for BFO and BFONd are respectively 2.25 eV and 2.23 eV, which are consistent with the experimental direct band gaps of 2.24 eV and 2.20 eV measured by optical transmission spectra. The reduction of the band gap in BFONd can be explained by the lower electronic Fermi level due to acceptor states revealed by first-principles calculations. The optical calculations show a larger absorption coefficient in BFONd than in BFO.

Synthesis of nonepitaxial multilayer silicene assisted by ion implantation.

Nonepitaxial multilayer silicene with a lonsdaleite structure was synthesized from a 4H-SiC substrate using an implantation-assisted process. An sp(3)-like bonding signal was fitted in a lonsdaleite Si XPS spectrum. The multilayer silicene was directly observed and the derived interplanar distances were found to be nearly consistent with the theoretical values.

The advent of multilayer antimonene nanoribbons with room temperature orange light emission.

Multilayer antimonene nanoribbons with room temperature orange light emission uniformly distributed on InSb were synthesized by the plasma-assisted process. The bandgap opening was caused by the quantum confinement effect of the nanoribbon structure and the turbostratic stacking of antimonene layers. This attractive two-dimensional material, whose band structure is proper for applications of transistors and light-emitting diodes, was first synthesized.

Plasma-Assisted Synthesis of High-Mobility Atomically Layered Violet Phosphorus.

Two-dimensional layered materials such as graphene, transition metal dichalcogenides, and black phosphorus have demonstrated outstanding properties due to electron confinement as the thickness is reduced to atomic scale. Among the phosphorus allotropes, black phosphorus, and violet phosphorus possess layer structure with the potential to be scaled down to atomically thin film. For the first time, the plasma-assisted synthesis of atomically layered violet phosphorus has been achieved. Material characterization supports the formation of violet phosphorus/InN over InP substrate where the layer structure of violet phosphorus is clearly observed. The identification of the crystal structure and lattice constant ratifies the formation of violet phosphorus indeed. The critical concept of this synthesis method is the selective reaction induced by different variations of Gibbs free energy (ΔG) of reactions. Besides, the Hall mobility of the violet phosphorus on the InP substrate greatly increases over the theoretical values of InP bulk material without much reduction in the carrier concentration, suggesting that the mobility enhancement results from the violet phosphorus layers. Furthermore, this study demonstrates a low-cost technique with high compatibility to synthesize the high-mobility atomically layered violet phosphorus and open the space for the study of the fundamental properties of this intriguing material as a new member of the fast growing family of 2D crystals.

Sequential cation exchange generated superlattice nanowires forming multiple p-n heterojunctions.

Fabrication of superlattice nanowires (NWs) with precisely controlled segments normally requires sequential introduction of reagents to the growing wires at elevated temperatures and low pressure. Here we demonstrate the fabrication of superlattice NWs possessing multiple p-n heterojunctions by converting the initially formed CdS to Cu2S NWs first and then to segmented Cu2S-Ag2S NWs through sequential cation exchange at low temperatures. In the formation of Cu2S NWs, twin boundaries generated along the NWs act as the preferred sites to initiate the nucleation and growth of Ag2S segments. Varying the immersion time of Cu2S NWs in a AgNO3 solution controls the Ag2S segment length. Adjacent Cu2S and Ag2S segments in a NW were found to display the typical electrical behavior of a p-n junction.