arXiv subjects

Weizhen Meng

Publications and source records attributed to Weizhen Meng.

7 recordsLinked to original sources

arXiv2026

Interstitial-Electron Altermagnetism in Two Dimensions

Altermagnetism has so far been associated with compensated magnetic moments carried by atoms. Here we introduce Stoner instability induced interstitial-electron altermagnetism, a distinct mechanism in which altermagnetic order is carried instead by interstitial anionic electrons in electrides. We show that, owing to the quasi-nucleus-free nature of interstitial electrons, the Stoner instability in electrides hosting two interstitial electrons can naturally stabilize an altermagnetic state rather than the conventional ferromagnetic one. This mechanism leads to a practical design principle for two-dimensional materials, from which we identify monolayers Zr2N and Ti2N as representative candidates. The strong sensitivity of interstitial electrons to cavity size enables efficient strain control of the altermagnetic order and a pronounced piezo-altermagnetic effect. Moreover, we investigate the evolution of the magnetism in Zr2N under ultrafast laser excitation, which exhibits dynamics distinct from those in all previously reported magnetic materials where magnetism is carried by real atoms. Our work not only offers a novel pathway to realize altermagnetism but also reveals an efficient non-magnetic route for its control.

cond-mat.str-el↗

arXiv2025

Chiral Altermagnetic Magnetoelectrics

In this work, we introduce a new class of chiral altermagnetic magnetoelectrics in structurally chiral, nonpolar altermagnetic systems and identify the experimentally well-characterized three-dimensional metal-organic framework K[Co(HCOO)$_3$] as a promising material platform. K[Co(HCOO)$_3$] exhibits chirality-locked \emph{g}-wave altermagnetic spin splitting together with dual-mode switchable electric polarization controlled by N\'eel-vector reorientation and structural chirality. Specifically, N\'eel-vector reorientation generates a finite electric polarization and reverses its sign, whereas chirality switching between left- and right-handed enantiomers produces an additional sign reversal. The associated electronic and optical responses provide effective readout channels for these switchable states. Our results establish chiral altermagnetic magnetoelectrics as a promising route to chirality- and N\'eel-vector-controlled nonvolatile multifunctional spintronics.

cond-mat.mtrl-sci↗

arXiv2023

Magnetic Electrides: High-Throughput Material Screening, Intriguing Properties, and Applications

Electrides are a unique class of electron-rich materials where excess electrons are localized in interstitial lattice sites as anions, leading to a range of unique properties and applications. While hundreds of electrides have been discovered in recent years, magnetic electrides have received limited attention, with few investigations into their fundamental physics and practical applications. In this work, 51 magnetic electrides (12 antiferromagnetic, 13 ferromagnetic, and 26 interstitial-magnetic) were identified using high-throughput computational screening methods and the latest Material Project database. Based on their compositions, these magnetic electrides can be classified as magnetic semiconductors, metals, or half-metals, each with unique topological states and excellent catalytic performance for N2 fixation due to their low work functions and excess electrons. The novel properties of magnetic electrides suggest potential applications in spintronics, topological electronics, electron emission, and as high-performance catalysts. This work marks the beginning of a new era in the identification, investigation, and practical applications of magnetic electrides.

cond-mat.mtrl-sci↗

arXiv2021

Topological quantum catalyst: the case of two-dimensional traversing nodal line states associated with high catalytic performance for hydrogen evolution reaction

Topological quantum catalysts (TQCs), where metallic surface states from nontrivial band topology serve as the mechanism to favor heterogeneous catalysis processes, have been well demonstrated in three dimensional (3D) examples but have been rarely discussed in 2D scale. Here, we develop a design scheme to realize 2D TQCs with showing traversing nodal line at the Brillouin zone boundary, large Fermi arc on the edge, and nearly zero Gibbs free energy (ΔGH*) for hydrogen evolution reaction (HER). We demonstrate the 2D Cu2C2N4 sheet is a such example. The material manifests an open nodal line traversing the whole k-path S-Y. It shows a long Fermi arc that spans the entire edge boundary, which is robust against spin-orbit coupling and the H adsorption. As the result, the edge of Cu2C2N4 sheet is relatively active for HER catalysis with possessing a ΔGH* as low as 0.10 eV, which is comparable with that of Pt and superior to other traditional catalysts and 3D TQCs as well. Our work offers an effective route to develop high performance HER catalysis without containing noble metals by utilizing 2D TQCs with traversing nodal line.

cond-mat.mtrl-sci↗

arXiv2021

Theoretical realization of hybrid Weyl state and associated high catalytic performance for hydrogen evolution in NiSi

For electrochemical hydrogen evolution reaction (HER), developing high-performance catalysts without containing precious metals has been a major research focus in the current. Herein, we show the feasibility of HER catalytic enhancement in Ni-based materials based on topological engineering from hybrid Weyl states. Via a high-throughput computational screening from 140 000 materials, we identify a chiral compound NiSi is a hybrid Weyl semimetal (WSM) with showing bulk type-I and type-II Weyl nodes and long surface Fermi arcs near the Fermi level. Sufficient evidences verify that topological charge carriers participate in the HER process, and make the certain surface of NiSi highly active with the Gibbs free energy nearly zero (0.07 eV), which is even lower than Pt and locates on the top of the volcano plots. This work opens up a new routine to develop no-precious-metal-containing HER catalysts via topological engineering, rather than traditional defect engineering, doping engineering, or strain engineering.

cond-mat.mtrl-sci↗

arXiv2021

Multiple-Fold Fermions and Topological Fermi Arcs Induced Catalytic Enhancement in Nanoporous Electride C12A7

Topological materials are recently regarded as the idea catalysts due to the protected surface metallic states and high carrier mobility, however the fundamental mechanism and the underlying relationship between the catalytic performance and topological states are in debate. Here, by means of symmetry analysis and first-principles calculations, we discover that the electride material of C12A7 hosts the multiple-fold fermions due to the interstitial-electrons, with the sixfold- and fourfold- degenerate points locating at high symmetric points near the Fermi energy, which are identified as the underlying reason of the enhanced catalytic ability in C12A7-based catalysts. The multiple-fold fermions exhibit much longer Fermi arcs on the (001) surface than traditional Weyl/Dirac fermions, the surface is thus highly chemical active and possesses a low Gibbs free energy for the hydrogen evolution reaction. The underlying relationship between catalytic performance and the topological surface state is explicitly verified by artificially hole doping, external strain and similar electride without the Fermi arcs, where the Gibbs free energies are significantly increased when the Fermi arcs is shifted to higher energy level. This work offers a guiding principle for understanding catalytic nature of electrides and the topological quantum catalysts.

cond-mat.mtrl-sci↗

arXiv2019

Mn2C monolayer: hydrogenation/oxygenation induced strong room-temperature ferromagnetism and potential applications

Two-dimensional ferromagnetic materials with strong ferromagnetism and high Curie temperature are significantly desired for the applications of nanoscale devices. Here, based on first-principles computations, we report hydrogenated/oxygenated Mn2C monolayer is a such material with strong room-temperature ferromagnetism. The bare Mn2C monolayer is an antiferromagnetic metal with the local magnetic moment of Mn ~ 3μB. However, the antiferromagnetic coupling of Mn atoms can transform into the ferromagnetic order under hydrogenation/oxygenation. Especially, the magnetic moments in hydrogenated/oxygenated Mn2C monolayer can be as large as 6 μB per unit cell, and the Curie temperatures are above 290K. Beside the potential applications in spintronic devices, our work suggests that Mn2C monolayer is also promising to be used in hydrogen/oxygen detection and removal devices.

cond-mat.mtrl-sci↗