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Elaheh Akbarnejad

Publications and source records attributed to Elaheh Akbarnejad.

2 recordsLinked to original sources

A thermally grown SiO2 diffusion barrier enabling high-temperature investigation of Ag-Au-Pd-Pt thin films

Combinatorial processing platforms (CPPs), integrating Si microtip arrays with combinatorial thin film synthesis and atom probe tomography (APT), enable near-atomic-scale characterization of compositionally complex solid solutions (CCSSs) under diverse processing and reaction conditions, including oxidation, thermal phase stability and electrocatalytic reactions. Their application at elevated temperatures, however, can be limited when CCSS constituents such as Pd and Pt react with the Si support to form silicides. Although thermally grown SiO2 has proven effective as a diffusion barrier between pure Pt and Si, its performance for multicomponent CCSS thin films is unclear. Here, using Ag-Au-Pd-Pt as a model system, we compare a 25 nm thermally grown SiO2 barrier with native Si oxide during annealing using APT and transmission electron microscopy. Native Si oxide prevents detectable interfacial reactions up to 300°C, but at 400°C Pd and Pt react with Si, causing silicide formation and substantial redistribution of the film constituents. At 600°C, extensive substrate reactions disrupt the CCSS film and produce a pronounced needle-shaped silicide morphology. In contrast, thermally grown SiO2 suppresses CCSS thin film-substrate reactions up to 600°C and retains the CCSS composition. The thermally grown SiO2 thus extends the applicable temperature range of Si-based CPPs to at least 600°C for near-atomic-scale characterization of CCSS thin films.

cond-mat.mtrl-sci

A hidden low-temperature transformation pathway in compositionally complex materials

Most compositionally complex materials (CCMs, frequently referred to as high entropy alloys) are metastable and their attractive properties often belong to kinetically trapped states. However, pathways towards lower-free-energy phase states governing long-term stability, can remain hidden because diffusion-controlled atomic redistribution is too slow to be revealed at experimentally accessible timescales. This blind spot is acute in CCM design: enormous compositional spaces are screened for performance, yet the low-temperature kinetics and the associated transformation pathways determining whether that performance persists are rarely considered in material selection. Here we use defect-rich nanoscale volumes coupled with atom-probe tomography to access and reconstruct the hidden phase-evolution pathway in a metastable Ag24Au20Pd50Pt6 electrocatalyst, without relying on elevated temperatures to accelerate the transformation. By varying microstructural starting state, annealing temperature and time, we reveal precipitation of a Pt-rich phase within the fcc matrix, its coarsening and re-homogenization. The Pt-rich phase recurs after homogenization with delayed kinetic accessibility, while prolonged annealing extends the pathway to 300°C. Atomistic simulations independently predict the same Pt-rich phase selection. The transformation is accompanied by a 3.7-fold loss of catalytic activity for hydrogen evolution. These results establish hidden phase-evolution pathways as a materials-design variable: resolving them can guide the selection of metastable CCMs not only for their as-synthesized properties, but also for the phase states and associated functionalities they may access over time.

cond-mat.mtrl-sci