Inelastic neutron scattering experiments are performed on a nanoporous metal complex Cu-Trans-1,4-Cyclohexanedicarboxylic Acid (Cu-CHD) adsorbing O2 molecules to identify the spin model of the O2-based magnet realized in the host complex. It is found
that the magnetic excitations of Cu-CHDs adsorbing low- and high-concentration O2 molecules are explained by different spin models, the former by spin dimers and the latter by spin trimers. By using the obtained parameters and also by assuming that the levels of the higher energy states are reduced because of the non-negligible spin dependence of the molecular potential of oxygen, the magnetization curves are explained in quantitative level.
Spin dynamics of the square lattice Heisenberg antiferromagnet, BaMnGeO, is studied by a combination of bulk measurements, neutron diffraction, and inelastic neutron scattering techniques. Easy plane type antiferromagnetic order is identified at $T l
e 4.0$ K. The exchange interactions are estimated as $J_1$ = 27.8(3)${mu}$eV and $J_2$ = 1.0(1) ${mu}$eV, and the saturation field $H_{rm C}$ is 9.75 T. Magnetic excitation measurements with high experimental resolution setup by triple axis neutron spectrometer reveals the instability of one magnon excitation in the field range of $0.7H_{rm C} lesssim H lesssim 0.85H_{rm C}$.
We performed inelastic neutron scattering experiment to study magnetic excitation of O$_2$ molecules adsorbed in microporous compound. The dispersionless excitation with characteristic intensity modulation is observed at $hbar omega = 7.8$ meV at low
temperature. The neutron cross section is explained by spin dimer model with intradimer distance of 3.1 AA . Anomalous behaviour in the temperature dependence is discussed in the context of enhanced magnetoelasticity in the soft framework of O$_2$ molecule.
