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Yutian Bao

Publications and source records attributed to Yutian Bao.

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Mechanochemical Nano-Writing of an Atomically Thin Metal

Mechanical energy accelerates many physicochemical processes, including materials syntheses that are hard to produce with thermal energy alone. However, physical understanding connecting applied mechanical forces with internal stresses and ensuing reaction mechanisms is lacking. Here we demonstrate mechanical force-enabled synthesis and nanoscale patterning to metallize a two-dimensional (2D) material, producing an atomically-thin superconducting material. Localized force applied by atomic force microscope tips to van der Waals (vdW) encapsulated stacks of 2D bilayer MoTe2 and adjacent source Pd guides 2D Pd7MoTe2 growth with 50 nm lateral resolution. Force accelerates reaction kinetics exponentially per Eyring's stress-assisted thermal activation model, reducing synthesis temperatures from ~200 °C to near-room temperature. Finite element simulations, density functional theory, and ab-initio grand canonical Monte Carlo calculations show that tip-induced compression facilitates Pd chemisorption to tensile-strained MoTe2 that converts to uniform Pd7MoTe2. This demonstrates a new, generalizable paradigm for nanoscale synthesis of quantum materials, and high-precision engineering of superconductivity.

cond-mat.mes-hall

Periodic Trends in Adsorption Energies Around Single-Atom Alloy Active Sites

Single-Atom Alloys (SAAs) are a special class of alloy surface catalysts that offer well defined, isolated active sites in a more inert metal host. The dopant sites are generally assumed to have little or no influence on the properties of the host metal, and transport of chemical reactants and products to and from the dopant sites is generally assumed to be facile. Here, by performing density functional theory calculations and surface science experiments, we identify a new physical effect on SAA surfaces, whereby adsorption is destabilised by up to 300 meV on host sites within the perimeter of the reactive dopant site. We identify periodic trends for this behaviour, and demonstrate a zone of exclusion around the reactive sites for a range of adsorbates and combinations of host and dopant metals. Experiments confirm an increased barrier for CO diffusion towards the dopant on a RhCu SAA. This effect offers new possibilities for understanding and designing active sites with tunable energetic landscapes surrounding them.

cond-mat.mtrl-sci