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Metal-organic framework (MOF) UiO-66 nanocrystals were previously believed to be piezo/ferro-electrically inactive because of their centrosymmetric lattice symmetries (Fm-3m (225)) revealed by Powder X-ray diffraction. However, via delicate dual AC resonance tracking piezoresponse force microscopy and piezoresponse force spectroscopy characterizations, our nanoscale probing for the first time demonstrate that UiO-66 nanocrystals show piezo/ferro-electric response. Our compelling experimental and theoretically analyses disclose that the structure of UiO-66 should not be the highly centrosymmetric Fm-3m (225) but a reduced symmetry form instead. UiO-66(Hf)-type MOFs possess stronger piezoresponse and better ferroelectric switching behaviours than their counterparts UiO-66 (Zr)-type MOFs. Our study not only enriches the structural understanding of UiO-66 MOF, but also suggests possible modification of electronic property of the MOFs by judicious selection of metal ions and functional ligands.
Molecular dynamics simulations combined with periodic electronic structure calculations are performed to decipher structural, thermodynamical and dynamical properties of the interfaced vs. confined water adsorbed in hexagonal 1D channels of the 2D la
It is textbookly regarded that phonons, i.e., an energy quantum of propagating lattice waves, are the main heat carriers in perfect crystals. As a result, in many crystals, e.g., bulk silicon, the temperature-dependent thermal conductivity shows the
We present a three-dimensional Ising model where lines of equal spins are frozen in such that they form an ordered framework structure. The frame spins impose an external field on the rest of the spins (active spins). We demonstrate that this porous
The ability of metal-organic frameworks (MOFs) to gelate under specific synthetic conditions opens up new opportunities in the preparation and shaping of hierarchically porous MOF monoliths, which could be directly implemented for catalytic and adsor
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