Abstract
The crystal structure of NH(2)(CH(3))(2)CuCl(3), an organic-inorganic hybrid perovskite, undergoes a phase transition from triclinic to monoclinic at the phase transition temperature T (C) of 287 K. We investigated the temperature dependencies of NMR chemical shifts and spin-lattice relaxation time T (1ρ) to gain insights into the structural geometry and molecular dynamics during the transition from phase II to phase I at high temperatures. Analysis of the (1)H and (13)C NMR chemical shifts of the cation revealed a continuous change in the surrounding structural geometry with temperature, without any anomalous changes around T (C). The sudden decrease in T (1ρ) values from low to high temperatures indicated a significant variation in proton and carbon dynamics at T (C), arising from the slowing motion of molecular dynamics across the phase transition. The activation energies E (a) obtained from the temperature dependence of T (1ρ) for (1)H and (13)C were larger in phase I than in phase II. This suggests that molecular motions in phase II exhibit a higher degree of freedom compared to those in phase I, where they are more constrained. These findings on NH(2)(CH(3))(2)CuCl(3) are presented to enhance its potential applications by elucidating the crystal configuration and structural molecular dynamics of ABX(3) type compound.