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Douxing Pan

Publications and source records attributed to Douxing Pan.

3 recordsLinked to original sources

Strain-Engineered Widely-Tunable Perfect Absorption Angle in Black Phosphorus from First-Principles

Using the density functional theory of electronic structure, we compute the anisotropic dielectric response of bulk black phosphorus subject to strain. Employing the obtained permittivity tensor, we solve Maxwell's equations and study the electromagnetic response of a layered structure comprising a film of black phosphorus stacked on a metallic substrate. Our results reveal that a small compressive or tensile strain, $\sim 4\%$, exerted either perpendicular or in the plane to the black phosphorus growth direction, efficiently controls the epsilon-near-zero response, and allows a perfect absorption tuning from low-angle of the incident beam $\theta=0^\circ$ to high values $\theta\approx 90^\circ$ while switching the energy flow direction. Incorporating a spatially inhomogeneous strain model, we also find that for certain thicknesses of the black phosphorus, near-perfect absorption can be achieved through controlled variations of the in-plane strain. These findings can serve as guidelines for designing largely tunable perfect electromagnetic wave absorber devices.

cond-mat.mtrl-sci

Bending-induced extension in two-dimensional crystals

According to the classical theory of elasticity, a plate subjected to a bending moment always deflects with symmetric tensile and compressive strains in its two sides, without overall deformation perpendicular to the bending moment. Here, we find by ab initio simulations that significant overall tensile strain can be induced by pure bending in a wide range of two-dimensional crystals perpendicular to the bending moment, just like an accordion being bent to open. This accordion effect is raised by asymmetric response of chemical bonds and electron density to the bending curvature, with the tensile strain being a power function of the curvature.

cond-mat.mtrl-sci

Self-assembled chiral phosphorus nanotubes from phosphorene: a molecular dynamics study

Controlled syntheses in nanoscale structures should be expected and phosphorous nanotubes with predefined chiralities are important in electronic devices with tunable bandgap. Here, incorporating molecular dynamics simulations with theoretical analyses, we show that a zigzag phosphorene nanoribbon can self-assemble and form a corresponding chiral phosphorous nanotube surrounding a template armchair phosphorous nanotube. The van der Waals potential between the nanoribbon and the nanotube is transformed to the intrinsic deformed and chemical bonding energies of the synthesized tube together with partial kinetic energy. The self-assembly process has an apparent temperature dependence and size effect and the formed chiral tube is thermodynamically stable. Also, the chirality and measurement can be tuned by the radius of template tube and the aspect ratio of raw ribbon. The study suggests a novel and feasible approach for controlled synthesis of phosphorous nanotubes and thus is of great interest for semiconductor device applications.

cond-mat.mtrl-sci