Increase in the Magnetic Ordering Temperature (T_c) as a Function of the Applied Pressure for A₂Mn[Mn(CN)₆] (A = K,...

Magnetization measurements under pressure reveal that the external hydrostatic pressure significantly increases in the ferrimagnetic transition temperature, T_c, for A₂Mn[Mn(CN)₆] (A = K, Rb, Cs). In the case of monoclinic A = K and Rb, dT_c/dp values are 21.2 and 14.6 K GPa^-1, respectively, and T_c increases by 53 and 39%, respectively, from ambient pressure to 1.0 GPa. The cubic A = Cs compound also shows a monotonous increase with an initial rate of 4.22 K GPa^-1 and about 11.4 K GPa^-1 above 0.6 GPa, and an overall T_c increase by 26% at 1.0 GPa. The increase in T_c is attributed to deformation of the structure such that the Mn^II-N≡C angle decreases with increasing pressure. The smaller the alkali cation, the greater the decrease in the Mn^II-N≡C angle induced by pressure and the larger the increase of dT_c/dp. This is in accordance with the ambient-pressure structures for A₂Mn[Mn(CN)₆] (A = K, Rb, Cs), which have decreasing Mn^II-N≡C angles that correlate to the observed increasing T_cs as K > Rb > Cs. The large increase in T_c for the A = K compound is the highest class among several cyano-bridged metal complexes. The tuning of the transition temperature by such a weak pressure may lead to additional applications such as switching devices.