Realization of large-area ultraflat chiral blue phosphorene.

Blue phosphorene (BlueP), a theoretically proposed phosphorous allotrope with buckled honeycomb lattice, has attracted considerable interest due to its intriguing properties. Introducing chirality into BlueP can further enrich its physical and chemical properties, expanding its potential for applications. However, the synthesis of chiral BlueP remains elusive. Here, we demonstrate the growth of large-area BlueP films on Cu(111), with lateral size limited by the wafer dimensions. Importantly, we discovered that the BlueP is characterized by an ultraflat honeycomb lattice, rather than the prevailing buckled structure, and develops highly ordered spatial chirality plausibly resulting from the rotational stacking with the substrate and interface strain release, as further confirmed by the geometric phase analysis. Moreover, spectroscopic measurements reveal its intrinsic metallic nature and different characteristic quantum oscillations in the image-potential states, which can be exploited for a range of potential applications including polarization optics, spintronics, and chiral catalysis.

Theoretical prediction and characterization of novel two-dimensional ternary tetradymite compounds La2X2Y (X = I, Br, Cl; Y = Ge, Te) as anode materials for metal-ion batteries.

Tetradymite compounds, such as Bi2Te3, crystallizing in rhombohedral structures have triggered tremendous research interest from the scientific community because of their intriguing properties. Herein, using the state-of-the-art first-principles calculations, we identify that La2X2Y (X = I, Br, Cl; Y = Ge, Te) nanosheets exhibit a ternary tetradymite-type structure with extraordinary electrical and electrochemical properties. It is first demonstrated that the layered La2X2Y compounds exhibit weak interlayer coupling with cleavage energies in the range of ∼0.28-0.38 J m-2, allowing the ready separation of monolayers that can be synthesized by mechanical exfoliation from their bulk counterparts. Next, we predict that La2X2Ge nanosheets exhibit a semiconducting nature, and upon physical realistic strain, a Dirac cone can be realized. These findings can be exploited in the transport properties. Furthermore, we comprehensively investigated the electrochemical properties of the predicted systems to evaluate their potential use in metal-ion (Li/Na) batteries. Our detailed analyses reveal that the Li (Na) adatoms are sufficiently mobile on the surface of the studied systems. For instance, the binding energy for the Li (Na) adatom on La2I2Ge is -2.24(-1.79) eV with a diffusion barrier of as small as ∼0.31(0.20) eV. Subsequently, the maximum theoretical specific capacity for Li (Na) reaches as high as 887(1064) mA h g-1, which can be attributed to a much higher storage capacity compared to previously identified 2D anode materials. These findings substantiate that the predicted nanosheets could be synthesized to explore their potential applications in future metal-ion batteries.

Black phosphorene/blue phosphorene van der Waals heterostructure: a potential anode material for lithium-ion batteries.

Van der Waals (vdW) heterostructure-based electrodes have invoked tremendous research interest due to their intriguing properties and their capability to break the limitations of the restricted properties of single-material systems. Herein, based on first-principles approaches, we propose that the black phosphorene/blue phosphorene (BLK-P/BLE-P) vdW heterostructure can be a capable anode material for power-driving lithium-ion batteries (LIBs), as it exhibits a large theoretical capacity, together with a relatively strong binding strength compared with the individual BLK-P and BLE-P monolayers. Our calculation results show that the Li adatom prefers to intercalate into the interlayer of the BLK-P/BLE-P vdW heterostructure due to the synergistic interfacial effect, resulting in a high binding strength and a diffusivity comparable to the BLK-P and BLE-P monolayers. Subsequently, the theoretical specific capacity is found to be as high as 552.8 mA h g-1, which can be attributed to the much higher storage capacity of Li adatoms in the BLK-P/BLE-P vdW heterostructure. Furthermore, electronic structure calculations reveal that a large amount of charge transfer assists in semiconductor to metallic transition upon lithiation, which would ensure good electrical conductivity. These simulations prove that the BLK-P/BLE-P heterostructure has great potential in LIBs and is essential for future battery design.