서강대학교

초록/요약 도움말

A fully ordered noncentrosymmetric barium molybdenum oxyfluoride, alpha-BaMoO2F4, has been synthesized by a hydrothermal reaction at 200 degrees C in a concentrated hydrofluoric acid solution. A centrosymmetric polymorph with O/F disorder, beta-BaMoO2F4, has been obtained in several minutes when the reaction mixture was stirred at room temperature in the same medium. Interestingly, we found that the metastable beta-BaMoO2F4 transforms into the thermodynamically stable alpha-BaMoO2F4 in an ambient condition. More detailed kinetic studies using powder X-ray diffraction indicate that the MoO2F4 octahedra in the kinetic phase, beta-BaMoO2F4, rearrange through the constant dissolution/precipitation process to find a more stable orientation and form the fully ordered alpha-BaMoO2F4. Density functional theory (DFT) calculations suggest that the formation of the thermodynamically stable alpha-BaMoO2F4 is driven by the strong Mo-O pi-interactions induced by Ba2+ cations. The new finding on the understanding of the kinetics of solid-state reactions suggests a novel way toward an effective discovery of functional materials with asymmetric structures.