Size-Dependent Spin Crossover and Bond Flexibility in Metal–Organic Framework Nanoparticles

Abstract

Size reduction offers a synthetic route to tunable phase change behavior. Preparing materials as nanoparticles causes drastic modulations to critical temperatures (T c), hysteresis widths, and the “sharpness” of first-order versus second-order phase transitions. A microscopic picture of the chemistry underlying this size dependence in phenomena ranging from melting to superconductivity remains debated. As a case study with broad implications, we report that size-dependent spin crossover (SCO) in nanocrystals of the metal–organic framework (MOF) Fe(1,2,3-triazolate)2 arises from metal-linker bonds becoming more labile in smaller particles. In comparison to the bulk material, differential scanning calorimetry indicates a ∼ 30–40% reduction in T c and ΔH in the smallest particles. Variable-temperature vibrational spectroscopy reveals a diminished long-range structural cooperativity, while X-ray diffraction evidence an over 3-fold increase in the thermal expansion coefficients. This “phonon softening” provides a molecular mechanism for designing size-dependent behavior in framework materials and for understanding phase changes in general.