Low-temperature ferromagnetic order in a two-Level layered Co2+ material

The magnetic properties of a 2D layered material consisting of high-spin Co2+ complexes, [Co(NH3NH2)2(H2O)2Cl2]Cl2 (CoHyd2Cl4), have been extensively characterized using electron paramagnetic resonance, magnetic susceptibility, and low-temperature heat capacity measurements. Electron paramagnetic resonance spectroscopy studies suggest that below 50 K, the J = 3/2 orbital triplet state of Co is gradually depopulated in favor of the J = 1/2 spin state, which is dominant below 20 K. In light of this, the magnetic susceptibility has been fitted with a two-level model, indicating that the interactions in this material are much weaker than previously thought. This two-level model is unable to fit the data at low temperatures and, combined with electron paramagnetic resonance spectroscopy, suggests that ferromagnetic interactions between Co2+ cations in the J = 1/2 state become significant approaching 2 K. Heat capacity measurements suggest the emergence of a long-range ordered state below 246 mK, which neutron diffraction confirms to be ferromagnetic.