The ability to control the size and morphology is crucial in optimizing nanoceria catalytic activity as this is governed by the atomistic arrangement of species and structural features at the surfaces. Here, we show that cuboidal cerium oxide nanoparticles can be obtained via microwave-assisted hydrothermal synthesis in highly alkaline media. High-resolution transmission electron microscopy (HRTEM) revealed that the cube edges were truncated by CeO 2 {110} surfaces and the cube corners were truncated by CeO 2 {111} surfaces. When adjusting synthesis conditions by increasing NaOH concentration, the average particle size increased. Although this was accompanied by an increase of the cube faces, CeO 2 {100}, the cube edges, CeO 2 {110}, and cube corners, CeO 2 {111}, remained of constant size. Molecular dynamics (MD) was used to rationalize this behavior and revealed that energetically, the corners and edges cannot be atomically sharp, rather they are truncated by {111} and {110} surfaces, respectively, to stabilize the nanocube; both the experiment and simulation showed agreement regarding the minimum size of ∼1.6 nm associated with this truncation. Moreover, HRTEM and MD revealed {111}/{110} faceting of the {110} edges, which balances the surface energy associated with the exposed surfaces, which follows {111} > {110} > {100}, although only the {110} surface facets because of the ease of extracting oxygen from its surface and follows {111} > {100} > {110}. Finally, MD revealed that the {100} surfaces are "liquid-like" with a surface oxygen mobility 5 orders of magnitude higher than that on the {111} surfaces; this arises from the flexibility of the surface species network that can access many different surface arrangements because of very small energy differences. This finding has implications for understanding the surface chemistry of nanoceria and provides avenues to rationalize the design of catalytically active materials at the nanoscale.

The control over the size and shape of nanoMOFs is essential for their exploitation in integrated devices such as sensors, membranes for gas separation, photoelectrodes, etc. Here, we demonstrate the synthesis of nanowires and three-dimensionally interconnected nanowire networks of Cu-based metal−organic frameworks (MOFs) by a combination of ion-track technology and electrochemical methods. In particular, Cu nanowires and nanowire networks were electrodeposited inside polymeric etched ion-track membranes and subsequently converted by electrochemical oxidation into different Cu-based MOFs such as the wellknown Cu 3 (BTC) 2 (also known as HKUST-1) and the lesserknown MOF Cu(INA) 2 . The MOFs are formed inside the template, therefore adopting the shape of the host nanochannels. The synthesized MOF nanowires exhibit tunable diameters between 80 and 260 nm. Characterization by X-ray diffraction, thermogravimetric analysis/differential scanning calorimetry, scanning electron microscopy, and transmission electron microscopy indicates that the employed electrochemical conversion includes the formation of Cu 2 O as an intermediate, as well as the initial formation of an amorphous MOF phase, which crystallizes upon longer reaction times.

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Copper ferrite, belonging to the wide and technologically relevant class of spinel ferrites, was grown in the form of t-CuFe2O4 nanocrystals within a porous matrix of silica in the form of either an aerogel or a xerogel, and compared to a bulk sample. Extended X-ray absorption fine structure (EXAFS) spectroscopy revealed the presence of two different sub-lattices within the crystal structure of t-CuFe2O4, one tetragonal and one cubic, defined by the Cu2+ and Fe3+ ions respectively. Our investigation provides evidence that the Jahn-Teller distortion, which occurs on the Cu2+ ions located in octahedral sites, does not affect the coordination geometry of the Fe3+ ions, regardless of their location in octahedral or tetrahedral sites.