Crystalline thermoelectric materials, especially SnSe crystals, have emerged as promising candidates for power generation and electronic cooling. In this study, significant enhancement in ZT is achieved through the combined effects of lattice distortions and band convergence in multiple electronic valence bands. Density functional theory (DFT) calculations demonstrate that cation vacancies together with Pb substitutional doping promote the band convergence and increase the density of states (DOS) near the Fermi surface of SnSe, leading to a notable increase in the Seebeck coefficient (S). The complex defects formed by Sn vacancies and Pb doping not only boost the Seebeck coefficient but also optimize carrier concentration (nH) and enhance electrical conductivity (σ), resulting in a higher power factor (PF). Furthermore, the localized lattice distortions induced by these defects increase phonon scattering, significantly reducing lattice thermal conductivity (κlat) to as low as 0.29 W m−1 K−1at 773 K in Sn0.92Pb0.03Se. Consequently, these synergistic effects on phonon and electron transport contribute to a high ZT of 1.8. This study provides a framework for rational design of high-performance thermoelectric materials based on first-principles insights and experimental validation.

Heterostructures offer superior photocatalytic characteristics over their constituent counterparts due to their charge separation abilities. Here, we conduct a systematic study of a recently synthesized novel family of palladium-based pentagonal air-stable 2D monolayers, PdSe₂, PdPSe, and PdPS, and their heterostructures using first-principles calculations for photocatalytic applications. Electronic band structure calculations reveal moderate bandgaps of 2.27 eV for PdSe2, 2.01 eV for PdPSe, and 2.25 eV for PdPS, indicating their suitability for photocatalytic water splitting. Moreover, to spatially separate and reduce the recombination possibility of photoinduced electron-hole pairs, we propose three van der Waals heterostructures: PdPSe/PdSe₂, PdPS/PdSe₂, PdPS/PdPS, with the corresponding bandgaps of 1.84 eV, 1.64 eV, and 1.65 eV, respectively. Based on work functions and the staggered band alignment of constituting monolayers, all three heterostructures are identified as type-II photocatalysts, which makes them notable photocatalyst. Additionally, band-edge potentials of PdPSe/PdSe₂ and PdPS/PdSe₂ confirm their suitability for overall water splitting via photocatalysis, whereas PdPS/PdPSe is suitable for oxygen evolution reactions only. The optical absorption spectra show the ability of each system to operate under a wide range of the spectrum, from visible light to high-energy (UV) regions. These characteristics make these systems valuable and attractive for photocatalytic applications.

Recently, triboelectric nanogenerators (TENGs) have been widely used for energy harvesting and self-powered sensing due to their significant and unique advantages. However, the intrinsic mechanisms that contribute to tribo-electricification (TE) between two materials remain as a subject of rigorous debate. In addition to predicting the qualitative charge transfer in solid-solid contacts based on the difference in the work functions of the two moieties constituting the interface, we argue that it is essential to obtain atomic-level, first principles, insights into the bonding properties, quantitative charge transfer, and the possible presence of a electrostatic potential barrier at the interface to fully understand the TE mechanism of a system. We have utilized dispersion-corrected density functional theory (DFT) calculations in this study to systematically investigate the TE potential of bare surface Ti3C2 and Ti3N2 2D MXene monolayers and their surface functionalized modifications Ti3C2R2 and Ti3N2R2 (where R = -O, -OH, or -F) in contact with Al(111). For these heterostructures, we have analyzed the adhesive energy of the interfaces, the nature of interaction through the electron localization function (ELF), and the charge distribution, which have revealed distinct characteristics of MXene/Al contacts for these monolayer/metal interfaces at their equilibrium distance and the changes in their properties under uniaxial pressure. Among all the metallic 2D MXene variants investigated in this study, we have determined that Ti3C2F2/Al and Ti3N2F2/Al interfaces show exceptional potential for TE.

The adsorption of organic molecules to surfaces is a central issue to achieve fully-functional molecular devices, for which porphyrins are well-studied due to their chemical stability and functional diversity. Herein, we investigate both the physical and the chemical adsorption of the free-base tetraphenylporphyrin 2H-TPP on the Cu(111) surface within the framework of density functional theory and find that the most stable physisorbed configuration is more weakly bound by -0.36 eV than the chemisorbed configuration. We use the electron localization function to investigate the difference in binding mechanisms between strong physisorption and weak chemisorption. We have computed a reaction barrier of 0.12 eV in going from physical binding to chemical bonding to the surface, and a barrier of 50 meV in going between neighboring physical binding sites. Our results support the possibility of realizing free-base porphyrins either physisorbed or chemisorbed on Cu(111) depending on the deposition procedure and experimental conditions.

We have used density functional theory simulations to explore the topological characteristics of a new MXene-like material, V4C3, and its oxide counterpart, assessing their potential as anode materials for Mg-ion batteries. Our research reveals that V4C3 monolayer is a topological type-II nodal line semimetal, protected by time reversal and spatial inversion symmetries. This type-II nodal line is marked by unique drumhead-like edge states that appear either inside or outside the loop circle, contingent upon the edge ending. Intriguingly, even with an increase in metallicity due to oxygen functionalization, the topological features of V4C3 remain intact. Consequently, the monolayer V4C3 has a topologically enhanced electrical conductivity that amplifies further upon oxygen functionalization. During the charging phase, a remarkable storage concentration led to a peak specific capacity of 894.73 mAh g−1 for V4C3, which only decreases to 789.33 mAh g−1 for V4C3O2. When compared to V2C, V4C3 displays a significantly lower specific capacity loss due to functionalization, demonstrating its superior electrochemical properties. Additionally, V4C3 and V4C3O2 exhibit moderate average open-circuit voltages (0.54 V for V4C3 and 0.58 V for V4C3O2) and energy barriers for intercalation migration (ranging between 0.29–0.63 eV), which are desirable for anode materials. Thus, our simulation results support V4C3 potential as an efficient anode material for Mg-ion batteries.

Transition metal phosphorus trichalcogenides retain spin-charge coupling and lattice vibrations in different layers, which are useful for spintronic and optoelectronic devices. The phonon, magnons and excitonic properties of two-dimensional ternary nickel-phosphorus trisulfides (NiPS3) are investigated using Raman spectroscopy and photoluminescence (PL) study. With magnetic exchange interaction, an exotic phonon scattering degenerates the optical phonons into in-plane Ag and Bg modes. We have observed eight Raman modes with two acoustic anisotropic magnon modes (M1, M2) below the critical temperature for co-(XX), while only M1 at cross (XY) polarizations. The M1 mode is coupled with the phonon Bg mode that can survive after transition temperature. The phonon and magnon modes soften with variations in temperature, which is attributed to anharmonic phonon–phonon coupling and interlayer forces. The polarized Raman shows the two-fold and four-fold symmetry orientations of the phonon and magnon modes, respectively, which exhibit strong in-plane anisotropic phonon/magnon. The PL spectra revealed the existence of bound excitonic features and ensemble emitters in NiPS3. The robust interlayer excitation and structural stability further revealed the optothermal properties. Moreover, the fabricated field-effect transistor on NiPS3 reveals p-type semiconducting nature with an ON/OFF ratio of 5 × 106 and mobility of ∼16.34 cm2 V−1 s−1. In contrast, the rectification ratio indicates their diode characteristics. Similarly, the photocurrent is enhanced by changing the wavelength of light, which shows the potential for optoelectronics. The strong spin-charge interaction provides new insights into these materials’ magneto-optical and thermal properties for memory devices.

In the present work, we investigate, for the first time, quasi 3D porous tetragonal silicon–carbon polymorphs t(SiC)₁₂ and t(SiC)₂₀ on the basis of first-principles density functional theory calculations. The structural design of these q3-t(SiC)12 and q3-t(SiC)₂₀ polymorphs follows an intuitive rational approach based on armchair nanotubes of a tetragonal SiC monolayer where C–C and Si–Si bonds are arranged in a paired configuration for retaining a 1:1 ratio of the two elements. Our calculations uncover that q3-t(SiC)₁₂ and q3-t(SiC)₂₀ polymorphs are thermally, dynamically, and mechanically stable with this lattice framework. The results demonstrate that the smaller polymorph q3-t(SiC)₁₂ shows a small band gap (∼0.59 eV), while the larger polymorph of q3-t(SiC)₂₀ displays a Dirac nodal line semimetal. Moreover, the 1D channels are favorable for accommodating Na ions with excellent (>300 mAh g^–1) reversible theoretical capacities. Thus confirming potential suitability of the two porous polymorphs with an appropriate average voltage and vanishingly small volume change (<6%) as anodes for Na-ion batteries.

Anti-perovskites A₃SnO (A = Ca, Sr, and Ba) are an important class of materials due to the emergence of Dirac cones and tiny mass gaps in their band structures originating from an intricate interplay of crystal symmetry, spin-orbit coupling, and band overlap. This provides an exciting playground for modulating their electronic properties in the two-dimensional (2D) limit. Herein, we employ first-principles density functional theory (DFT) calculations by combining dispersion-corrected SCAN + rVV10 and mBJ functionals for a comprehensive side-by-side comparison of the structural, thermodynamic, dynamical, mechanical, electronic, and thermoelectric properties of bulk and monolayer (one unit cell thick) A₃SnO anti-perovskites. Our results show that 2D monolayers derived from bulk A₃SnO anti-perovskites are structurally and energetically stable. Moreover, Rashba-type splitting in the electronic structure of Ca₃SnO and Sr₃SnO monolayers is observed owing to strong spin-orbit coupling and inversion asymmetry. On the other hand, monolayer Ba₃SnO exhibits Dirac cone at the high-symmetry Γ point due to the domination of band overlap. Based on the predicted electronic transport properties, it is shown that inversion asymmetry plays an essential character such that the monolayers Ca₃SnO and Sr₃SnO outperform thermoelectric performance of their bulk counterparts.