Regulating the thermal expansion of a [FePt(CN)4] layer by axial coordination and dimensional reduction.

Abstract

Thermal expansion regulation by chemical decoration at a molecular level is of great technological value for materials science. Herein, we show that the spin crossover active compound Fe(pyz)Pt(CN)4 (pyz = pyrazine) shows a rare 2D negative thermal expansion (NTE) in the ab-plane. By introducing axial coordination iodine ions or reducing the framework dimension from 3D to 2D, the NTE behavior can be effectively switched to positive thermal expansion (PTE) or even zero thermal expansion (ZTE). Moreover, it is found that different spin states of Fe2+ also influence the magnitude of NTE. Compared with the low-spin (LS) sate, the high-spin (HS) state tends to enhance the magnitude of NTE. Combined in situ structural and Raman spectral analyses revealed that the NTE mainly originates from the transverse vibration of a bridging cyano group and the tailorable thermal expansion is closely related to the state of the Fe-CN-Pt linkage. The present study shows how the rational regulation of the building unit and framework dimensions can effectively control thermal expansion behaviors. This insight can serve as guidance for designing and synthesizing novel NTE materials.