Chemical Engineering of Altermagnetism in Two-Dimensional Metal-Organic Frameworks

TL;DR

This paper demonstrates how chemical engineering of 2D metal-organic frameworks can induce altermagnetism, enabling tunable spin splitting for potential spintronic applications.

Contribution

It introduces a coordination-driven strategy to realize and control altermagnetic spin splitting in 2D MOFs through ligand modification and symmetry engineering.

Findings

g-wave spin splitting up to 65 meV achieved

d-wave spin splitting up to 83.9 meV demonstrated

AM spin splitting observed in spin wave spectrum with chiral magnon splitting

Abstract

Altermagnetism represents a novel class of collinear antiferromagnetism exhibiting non-relativistic spin splitting without net magnetization, driven by lattice symmetry rather than spin-orbit coupling (SOC). Here, we introduce a coordination-driven chemical strategy to realize altermagnetic (AM) spin splitting in two-dimensional (2D) planar tetracoordinated Cr-based metal-organic frameworks (MOFs). Using density functional theory (DFT) calculations, we demonstrate that replacing centrosymmetric pyrazine (pyz) ligands with non-centrosymmetric imidazole (imz) linkers in Cr-based MOFs reduces lattice symmetry, enabling g-wave AM spin splitting up to 65 meV. Furthermore, frontier molecular orbital engineering (FMOE) allows selective ligand spin polarization, inducing a shift to d-wave AM anisotropy in polycyclic ligand-based 2D MOFs with spin splitting up to 83.9 meV. Microscopic magnetic exchange interactions (J) analysis reveals that ligand-mediated interactions dominate over metal-metal coupling, stabilizing AM order in systems with radical ligands. Interestingly, we further confirm AM spin splitting in spin wave spectrum, where chiral magnon splitting is observed. Finally, we show that AM spin splitting gives rise to experimentally accessible charge to spin conversion, emerging as a linear response in d-wave and as a symmetry-allowed nonlinear effect in g-wave 2D AM MOFs. This work establishes coordination chemistry as a powerful and versatile route to symmetry control in 2D MOFs, enabling rational design of 2D molecular materials with tunable electronic and AM properties for next-generation spintronic devices.