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Gareth Tainton

Publications and source records attributed to Gareth Tainton.

2 recordsLinked to original sources

Moir\'e-induced lattice reconstruction at buried atomic interfaces

Atomic reconstruction at twisted two-dimensional interfaces governs many of their emergent optical, electronic, and mechanical properties, including sliding ferroelectricity. Despite recent progress in understanding lattice reconstruction in suspended twisted bilayers, structural changes at van der Waals heterointerfaces between multilayer crystals remain largely unexplored. Here we use multi-slice electron ptychography to non-invasively recover the three-dimensional atomic structure at marginally twisted rhombohedral interfaces between thick transition-metal dichalcogenide crystals. With a position precision of ~3 pm and a depth resolution ~1 nm, we resolve the twist-induced lattice reconstruction field per layer, and the resulting dislocation network at the buried interface. Despite the bulk nature, we observe markedly strong in-plane interfacial reconstruction due to suppression of the out-of-plane bending by outer layers, exceeding predictions from our three-dimensional modelling. Furthermore, we extract the strain tensor evolution during the decay of the reconstruction into the bulk, providing a structural foundation for understanding multi-layer moir\'e systems.

cond-mat.mes-hall

Atomic-resolution imaging of gold species at organic liquid-solid interfaces

Understanding solid-liquid interfaces at the atomic-scale is key to improved performance of heterogeneous catalysts, electrodes and membranes. Here we combine unique specimen design, record atomic resolution in situ electron microscopy, and artificial intelligence-enabled analysis to achieve a step change in quantitative understanding of interfacial atomic behaviour. We create the first graphene liquid cells with organic solvents and employ them to track over 106 gold adatoms and clusters at a graphene surface immersed in acetone and cyclohexanone. We reveal dynamic correlated behaviour of gold adatom monomers, dimers, trimers and clusters, strongly influenced by each other, the solvent properties, and the atomic lattice of the substrate, in good agreement with theoretical calculations. We use the results to interpret differences in catalytic activity towards the industrially important acetylene hydrochlorination reaction. This new capability for exploration of atomic scale chemistry could enable rational design of future catalysts, membranes and electrodes with improved functionality.

cond-mat.mtrl-sci