Designing Chiral Organometallic Nanosheets with Room-Temperature Multiferroicity and Topological Nodes

Two-dimensional (2D) room-temperature chiral multiferroic and magnetic topological materials are essential for constructing functional spintronic devices, yet their number is extremely limited. Here, by using the chiral and polar HPP (HPP = 4-(3-hydroxypyridin-4-yl)pyridin-3-ol) as an organic linker and transition metals (TM = Cr, Mo, W) as nodes, we predict a class of 2D TM(HPP)₂ organometallic nanosheets that incorporate homochirality, room-temperature magnetism, ferroelectricity, and topological nodes. The homochirality is introduced by chiral HPP linkers, and the change in structural chirality induces a topological phase transition of Weyl phonons. The room-temperature magnetism arises from the strong d-p spin coupling between TM cations and HPP doublet anions. The ferroelectricity is attributed to the breaking of spatial inversion symmetry in the lattice structure. Additionally, by adjusting the type of TMs, these nanosheets show rich and tunable band structures. Notably, all predicted materials are topologically nontrivial, featuring a quadratic nodal point around the Fermi level.