According to the third law of thermodynamics, the entropy of crystals tends to zero as T → 0. In many molecular crystals, the configurational entropy Sc is zero and the remaining vibrational entropy Sv decreases with decreasing temperature, which vanishes as T → 0. However, in some crystals, molecules can move around even in the crystalline states, where Sc remains non-zero. In this study, we focused on two types of such compounds, one with partially deuterated methyl groups and endohedral fullerenes, and have investigated how the Sc in those crystals approach to zero as T → 0. In the first system, the locations of H and D atoms in a partially deuterated methyl group are exchangeable even in the crystalline phase, which remains Sc = Rln3. The Sc is released at around 10 K where Schottky type anomalies are observed in heat capacity. This is caused by the splitting of the triply degenerated ground states due to the symmetry breaking by the partial deuteration. In the second system, a Li+ ion circulates quantum mechanically in a C60 fullerene at 300 K, which localizes into two pockets below 100 K, and into one pocket below 24 K due to the Coulombic interactions with the neighboring ions. A H2O encapsulated in a C60, on the other hand, rotates quantum mechanically even at 1 K.
Keywords:quantum rotation, orientational ordering, heat capacity, configurational entropy, partially deuterated methyl groups, endohedral fullerenes
Publication Date: 2021-04-25