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Martina Ruffino

Publications and source records attributed to Martina Ruffino.

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The role of disconnections in redox-induced phase transformation of metal oxides

Detailed atomic-level understanding of the phase transformation between magnetite (${\rm Fe_3 O_4}$) and haematite (${\rm Fe_2 O_3}$) is lacking, despite widespread interest in redox reactions of metal oxide systems. While the magnetite-to-haematite transformation entails the addition of oxygen to the system and thus a net diffusive flux, haematite formations have been reported to grow along well-defined habits on the close-packed $\{0001\}_{\rm Fe_2 O_3}//\{111\}_{\rm Fe_3 O_4}$ planes. The propagation of the phase interface in the bulk is thus thought to maintain the oxygen sublattice fixed up to a shear, and to require long-range diffusion of iron ions. In this letter we propose interfacial steps with dislocation character, i.e. disconnections, as the elementary defects propagating the transformation. We use the topological model of interfacial defects to predict three disconnection modes for the system, and we employ scanning transmission electron microscopy to ascertain their presence in a haematite/magnetite interface of a partially oxidised magnetite powder. Using atomistic simulations, we determine the equilibrium structures of the disconnections, and study their motion and how they accomplish the transformation, obtaining excellent agreement with atomic-resolution experimental observations.

cond-mat.mtrl-sci

Domain Boundaries in a Metallic Distortive Polar Metal

Polar metals are an underexplored material class combining two properties that are typically incompatible, namely a polar crystal structure and reasonable electrical conductivity. These intriguing materials offer a unique combination of properties, potentially relevant to optoelectronics, catalysis, memory devices, among other applications. The distortive polar metal (DPM) subclass forms through a symmetry-lifting phase transformation into a non-centrosymmetric polar crystal structure. In the process, domains with uniform geometric polar directions form, oftentimes separated by domain boundaries with polarity discontinuities arranged in "charged" head-to-head (H-H) or tail-to-tail (T-T) morphologies. To date, only metallic oxide DPM microstructures have been studied. Here we reveal, in the intermetallic DPM Mn$_{5}$Al$_{8}$, different surface interactions and electron transfer reactivity at domain boundaries depending on their H-H or T-T character. Variable surface reactivity suggests localized changes in electronic work functions due to an increase (H-H) or decrease (T-T) in the electronic density of states. These findings suggest that metallic DPMs may offer functionalizable domain boundaries and deserve increased attention, given that they allow tunable chemistries and various thermomechanical processing or transformation protocols. Ultimately, this study proposes unconventional metal physics, propelling the discovery and design of advanced electronic materials and devices.

cond-mat.mtrl-sci