Node Distortion as a Tunable Mechanism for Negative Thermal Expansion in Metal-Organic Frameworks

Chemically functionalized series of metal-organic frameworks (MOFs), with subtle differences in local structure but divergent properties, provide a valuable opportunity to explore how local chemistry can be coupled to long-range structure and functionality. Using in situ synchrotron X-ray total scattering, with powder diffraction and pair distribution function (PDF) analysis, we investigate the temperature dependence of the local-and longrange structure of MOFs based on NU-1000, in which Zr6O8 nodes are coordinated by different capping ligands (H2O/OH, Cl- ions, formate, acetylacetonate, and hexafluoroacetylacetonate). We show that the local distortion of the Zr6 nodes depends on the lability of the ligand and contributes to a negative thermal expansion (NTE) of the extended framework. Using multivariate data analyses, involving non-negative matrix factorization (NMF), we demonstrate a new mechanism for NTE: progressive increase in the population of a smaller, distorted node state with increasing temperature leads to global contraction of the framework. The transformation between discrete node states is noncooperative and not ordered within the lattice, i.e., a solid solution of regular and distorted nodes. Density functional theory calculations show that removal of ligands from the node can lead to distortions consistent with the Zr center dot center dot center dot Zr distances observed in the experiment PDF data. Control of the node distortion imparted by the nonlinker ligand in turn controls the NTE behavior. These results reveal a mechanism to control the dynamic structure of MOFs based on local chemistry.

Automated summary

In this study, the temperature dependence of the local and long-range structure of metal-organic frameworks (MOFs) based on NU-1000 was investigated using synchrotron X-ray total scattering. It was found that the local distortion of Zr6 nodes was dependent on the stability of the ligands, leading to a negative thermal expansion of the extended framework. A new mechanism for this negative thermal expansion was revealed, which involved an increase in the population of a smaller, distorted node state with increasing temperature. Control of the node distortion allowed for control of the dynamic structure of MOFs.