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Vei Wang

Publications and source records attributed to Vei Wang.

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H3Se in the Im-3m Phase: A High-Pressure Superconductor with Tc Reaching 200 K at 64 GPa Mediated by Anharmonic Phonons

Hydrogen-based compounds have attracted significant attention in recent years due to the discovery of conventional superconductivity with high critical temperature under high pressure, rekindling hopes for searching room temperature superconductor. In this work, we investigated systematically the vibrational and superconducting properties of H3Se in Im-3m phase under pressures ranging from 50 to 200 GPa. Our approach combines the stochastic self-consistent harmonic approximation with first-principles calculations to address effects from the quantum and anharmonic vibrations of ions. It turns out that these effects significantly modify the crystal structure, increasing the inner pressure by about 8 GPa compared to situations where they are ignored. The phonon spectra suggest that with these effects included, the crystal can be stabilized at pressures as low as about 61 GPa, much lower than the previously predicted value of over 100 GPa. Our calculations also highlight the critical role of quantum and anharmonic effects on the electron-phonon coupling properties. Neglecting these factors could result in a substantial overestimation of the superconducting critical temperature Tc, by approximately 25 K at 125 GPa, for example. With anharmonic phonons, the Tc derived from the Migdal-Eliashberg equations, reaches 200 K ($\mu^\star$= 0.1, $\lambda$=4.1) as the pressure decreases to 64 GPa, making the crystal a rare high-Tc superconductor at moderate pressures.

cond-mat.supr-con

Computational Search for Two-Dimensional Photocatalysts

To overcome current serious energy and environmental issues, photocatalytic water splitting holds great promise because it requires only solar energy as an energy input to produce hydrogen. Two-dimensional (2D) semiconductors and heterostructures possess several inherent advantages which are more suitable for boosting solar energy than their bulk counterparts. In this work, by performing high-throughput first-principles calculations combined with a semiempirical van der Waals dispersion correction, we first provided the periodic table of band alignment type for van der Waals heterostructures when packing any two of the 260 semiconductor monolayers obtained from our 2D semiconductor database (2DSdb) (https://materialsdb.cn/2dsdb/index.html). Based on the rules of thumb for photocatalytic water splitting, we have further screened dozens of potential semiconductors and thousands of heterostructures which are promising for photocatalytic water splitting. The resulting database would provide a useful guidance for experimentalists to design suitable 2D vdWHs and photocatalysts according to desired applications.

cond-mat.mtrl-sci

Orbital-Energy Splitting in Anion Ordered Ruddlesden-Popper Halide Perovskites for Tunable Optoelectronic Applications

The electronic orbital characteristics at the band edges plays an important role in determining the electrical, optical and defect properties of perovskite photovoltaic materials. It is highly desirable to establish the relationship between the underlying atomic orbitals and the optoelectronic properties as a guide to maximize the photovoltaic performance. Here, using first-principles calculations and taking anion ordered Ruddlesden-Popper (RP) phase halide perovskites Cs$_{n+1}$Ge$_n$I$_{n+1}$Cl$_{2n}$ as an example, we demonstrate how to rationally optimize the optoelectronic properties (e.g., band gap, transition dipole matrix elements, carrier effective masses, band width) through a simple band structure parameter. Our results show that reducing the splitting energy $|\Delta c|$ of p orbitals of B-site atom can effectively reduce the band gap and carrier effective masses while greatly improving the optical absorption in the visible region. Thereby, the orbital-property relationship with $\Delta c$ is well established through biaxial compressive strain. Finally, it is shown that this approach can be reasonably extended to several other non-cubic halide perovskites with similar p orbitals characteristics at the conduction band edges. Therefore, we believe that our proposed orbital engineering approach provides atomic-level guidance for understanding and optimizing the device performance of layered perovskite solar cells.

cond-mat.mtrl-sci

Modulation of Nearly Free Electron States in Hydroxyl-Functionalized MXenes: A First-Principles Study

The transition metal carbides (namely MXenes) and their functionalized derivatives exhibit various physical and chemical characteristics and offer many potential applications in electronic devices and sensors. Using density functional theory (DFT), it is revealed that the nearly free electron (NFE) states are near the Fermi levels in hydroxyl (OH) functionalized MXenes. Most of the OH-terminated MXene are metallic, but some of them, e.g. Sc2C(OH)2, are semiconductors and the NFE states are conduction bands. In this paper, to investigate the NFE states in MXenes, an attractive image-potential well model is adopted. Compared the solutions of this model with the DFT calculations, it is found that due to the overlap of spatially extensive wave functions of NFE states and their hybridization between the artificial neighboring layers imposed by the periodical boundary conditions (PBCs), the DFT results represent the properties of multiple layers, intrinsically. Based on the DFT calculations, it is found that the energy gap widths are affected by the interlayer distances. We address that the energetics of the NFE states can be modulated by the external electric fields and it is possible to convert semiconducting MXenes into metals. This band-gap manipulation makes the OH-terminated semiconducting MXenes an excellent candidate for electronic switch applications. Finally, using a set of electron transport calculations, I-V characteristics of Sc2C(OH)2 devices are investigated with the gate voltages.

cond-mat.mes-hall

VASPKIT: A User-friendly Interface Facilitating High-throughput Computing and Analysis Using VASP Code

We present the VASPKIT, a command-line program that aims at providing a powerful and user-friendly interface to perform high-throughput analysis of a variety of material properties from the raw data produced by the VASP code. It consists of mainly the pre- and post-processing modules. The former module is designed to prepare and manipulate input files such as the necessary input files generation, symmetry analysis, supercell transformation, k-path generation for a given crystal structure. The latter module is designed to extract and analyze the raw data about elastic mechanics, electronic structure, charge density, electrostatic potential, linear optical coefficients, wave function plots in real space, and etc. This program can run conveniently in either interactive user interface or command line mode. The command-line options allow the user to perform high-throughput calculations together with bash scripts. This article gives an overview of the program structure and presents illustrative examples for some of its usages. The program can run on Linux, MacOS, and Windows platforms. The executable versions of VASPKIT and the related examples, together with the tutorials, are available in its official website vaspkit.com.

cond-mat.mtrl-sci

Electronic structures of iMAX phases and their two-dimensional derivatives: A family of piezoelectric materials

Recently, a group of MAX phases, (Mo$_{2/3}$Y$_{1/3}$)$_2$AlC, (Mo$_{2/3}$Sc$_{1/3}$)$_2$AlC, (W$_{2/3}$Sc$_{1/3}$)$_2$AlC, (W$_{2/3}$Y$_{1/3}$)$_2$AlC, and (V$_{2/3}$Zr$_{1/3}$)$_2$AlC, with in-plane ordered double transition metals, named iMAX phases, have been synthesized. Experimentally, some of these MAX phases can be chemically exfoliated into two-dimensional (2D) single- or multilayered transition metal carbides, so-called MXenes. Accordingly, the 2D nanostructures derived from iMAX phases are named iMXenes. Here, we investigate the structural stabilities and electronic structures of the experimentally discovered iMAX phases and their possible iMXene derivatives. We show that the iMAX phases and their pristine, F, or OH-terminated iMXenes are metallic. However, upon O termination, (Mo$_{2/3}$Y$_{1/3}$)$_2$C, (Mo$_{2/3}$Sc$_{1/3}$)$_2$C, (W$_{2/3}$Y$_{1/3}$)$_2$C, and (W$_{2/3}$Sc$_{1/3}$)$_2$C iMXenes turn into semiconductors. Owing to the absence of centrosymmetry, the semiconducting iMXenes may find applications in piezoelectricity. Our calculations reveal that the semiconducting iMXenes possess giant piezoelectric coefficients as large as 45$\times10^{-10}$~C/m.

cond-mat.mtrl-sci

High-Throughput Computational Screening of Two-Dimensional Semiconductors

By performing high-throughput first-principles calculations combined with a semiempirical van der Waals dispersion correction, we have screened 74 direct- and 185 indirect-gap two dimensional (2D) nonmagnetic semiconductors from near 1000 monolayers according to the criteria for energetic, thermodynamic, mechanical, dynamic and thermal stabilities, and conductivity type. We present the calculated lattice constants, simulated scanning tunnel microscopy, formation energy, Young's modulus, Poisson's ratio, shear modulus, anisotropic effective mass, band structure, band gap, ionization energy, and electron affinity for each candidate meeting our criteria. The resulting 2D semiconductor database (2DSdb) can be accessed via the website https://materialsdb.cn/2dsdb/index.html. The 2DSdb provides an ideal platform for computational modeling and design of new 2D semiconductors and heterostructures in photocatalysis, nanoscale devices, and other applications. Further, a linear fitting model was proposed to evaluate band gap, ionization energy and electron affinity of semiconductor from the density functional theory (DFT) calculated data as initial input. This model can be as precise as hybrid DFT but with much lower computational cost.

cond-mat.mes-hall

Electron spin-orbit interaction in helically coiled carbon nanotube

Recent theoretical and experimental works on carbon nanotubes (CNTs) have revealed that spin-orbit interaction (SOI) is more robust than it was thought. Motivated by this, we investigate the SOI in helically coiled CNTs. Calculations are performed within the tight-binding model with the inclusion of a four-orbital basis set; thereby the full symmetry of the helical lattice and the hybridization of $π$\ and $σ$ bands are considered. By virtue of unitary transformation and perturbation approach, we obtain the analytic solution for the torsion-dependent SOI in helically coiled CNTs. Due to the enhancement of curvature and torsion, the calculated SOI values reach the order of meV which has been confirmed by \textit{ab initio} electronic structure calculation.

cond-mat.mes-hall