Chemical design of monolayer altermagnets
Fuente:
arXiv
Guardado en:
| Autores principales: | , , |
|---|---|
| Formato: | Preprint |
| Publicado: |
2025
|
| Materias: | |
| Acceso en línea: | |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
| _version_ | 1866914167786569728 |
|---|---|
| author | Xu, Runzhang Gao, Yifan Liu, Junwei |
| author_facet | Xu, Runzhang Gao, Yifan Liu, Junwei |
| contents | The crystal-symmetry-paired spin-momentum locking (CSML) arisen from the intrinsic crystal symmetry connecting different magnetic sublattices in altermagnets enables many exotic spintronics properties such as unconventional piezomagnetism and noncollinear spin current. However, the shortage of monolayer altermagnets restricts further exploration of dimensionally confined phenomena and applications of nanostructured devices. Here, we propose general chemical design principles inspired by sublattice symmetry of layered altermagnet V$_2$(Se,Te)$_2$O through symmetry-preserving structural modification and valence-adaptive chemical substitutions. In total, we construct 2600 candidates across four structural frameworks, M$_2$A$_2$B$_{1,0}$ and their Janus derivatives. High-throughput calculations identify 670 potential altermagnets with Néel-ordered ground states, among which 91 ones exhibiting CSML Dirac cones that enable spin-polarized ultra-fast transport. These materials also feature different ground-state magnetic orderings and demonstrate diverse electronic behaviors, ranging from semiconductors, metals, half-metals, to Dirac semimetals. This work not only reveals abundant monolayer altermagnets, but also establishes a rational principle for their design, opening gates for exploration of confined magnetism and spintronics in atomically thin systems. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2505_15484 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Chemical design of monolayer altermagnets Xu, Runzhang Gao, Yifan Liu, Junwei Materials Science Mesoscale and Nanoscale Physics The crystal-symmetry-paired spin-momentum locking (CSML) arisen from the intrinsic crystal symmetry connecting different magnetic sublattices in altermagnets enables many exotic spintronics properties such as unconventional piezomagnetism and noncollinear spin current. However, the shortage of monolayer altermagnets restricts further exploration of dimensionally confined phenomena and applications of nanostructured devices. Here, we propose general chemical design principles inspired by sublattice symmetry of layered altermagnet V$_2$(Se,Te)$_2$O through symmetry-preserving structural modification and valence-adaptive chemical substitutions. In total, we construct 2600 candidates across four structural frameworks, M$_2$A$_2$B$_{1,0}$ and their Janus derivatives. High-throughput calculations identify 670 potential altermagnets with Néel-ordered ground states, among which 91 ones exhibiting CSML Dirac cones that enable spin-polarized ultra-fast transport. These materials also feature different ground-state magnetic orderings and demonstrate diverse electronic behaviors, ranging from semiconductors, metals, half-metals, to Dirac semimetals. This work not only reveals abundant monolayer altermagnets, but also establishes a rational principle for their design, opening gates for exploration of confined magnetism and spintronics in atomically thin systems. |
| title | Chemical design of monolayer altermagnets |
| topic | Materials Science Mesoscale and Nanoscale Physics |
| url | https://arxiv.org/abs/2505.15484 |