Realising square and diamond lattice Heisenberg antiferromagnet models in the and phases of the coordination framework, KTi(CO)\textit{x}HO
arXiv:2009.03214 · doi:10.1103/PhysRevMaterials.4.104414
Abstract
We report the crystal structures and magnetic properties of two psuedo-polymorphs of the Ti coordination framework, KTi(CO)xHO. Single-crystal X-ray and powder neutron diffraction measurements on -KTi(CO)xHO confirm its structure in the tetragonal space group with a square planar arrangement of Ti ions. Magnetometry and specific heat measurements reveal weak antiferromagnetic interactions, with K and indicating a slight frustration of nearest- and next-nearest-neighbor interactions. Below K, undergoes a transition to G-type antiferromagnetic order with magnetic moments aligned along the axis of the tetragonal structure. The estimated ordered moment of Ti in is suppressed from its spin-only value to , thus verifying the two-dimensional nature of the magnetic interactions within the system. -KTi(CO)2HO, on the other hand, realises a three-dimensional diamond-like magnetic network of Ti moments within a hexagonal structure. An antiferromagnetic exchange coupling of K -- an order of magnitude larger than in -- is extracted from magnetometry and specific heat data. undergoes Néel ordering at K, with the magnetic moments aligned within the plane and a slightly reduced ordered moment of per Ti. Through density-functional theory calculations, we address the origin of the large difference in the exchange parameters between the and psuedo-polymorphs. Given their observed magnetic behaviors, we propose -KTi(CO)xHO and -KTi(CO)2HO as close to ideal model Heisenberg square and diamond lattice antiferromagnets, respectively.
12 pages, 7 figures