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Yeong-Ah Soh

Publications and source records attributed to Yeong-Ah Soh.

3 recordsLinked to original sources

Quantum phase transition in a common metal.

The classical theory of solids, based on the quantum mechanics of single electrons moving in periodic potentials, provides an excellent description of substances ranging from semiconducting silicon to superconducting aluminium. Over the last fifteen years, it has become increasingly clear that there are substances for which the conventional approach fails. Among these are certain rare earth compounds and transition metal oxides, including high-temperature superconductors. A common feature of these materials is complexity, in the sense that they have relatively large unit cells containing heterogeneous mixtures of atoms. Although many explanations have been put forward for their anomalous properties, it is still possible that the classical theory might suffice. Here we show that a very common chromium alloy has some of the same peculiarities as the more exotic materials, including a quantum critical point, a strongly temperature-dependent Hall resistance and evidence for a 'pseudogap'. This implies that complexity is not a prerequisite for unconventional behaviour. Moreover, it should simplify the general task of explaining anomalous properties because chromium is a relatively simple system in which to work out in quantitative detail the consequences of the conventional theory of solids.

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Atomic-scale images of charge ordering in a mixed-valence manganite.

Transition-metal perovskite oxides exhibit a wide range of extraordinary but imperfectly understood phenomena. The best known examples are high-temperature superconductivity in copper oxides, and colossal magnetoresistance in manganese oxides ('manganites'). All of these materials undergo a range of order-disorder transitions associated with changes in charge, spin, orbital and lattice degrees of freedom. Measurements of such order are usually made by diffraction techniques, which detect the ionic cores and the spins of the conduction electrons. Unfortunately, because such techniques are only weakly sensitive to valence electrons and yield superpositions of signals from distinct submicrometre-scale phases, they cannot directly image phase coexistence and charge ordering, two key features of the manganites. Here we present scanning tunnelling microscope measurements of the manganite Bi1-xCaxMnO3. We show that charge ordering and phase separation can be resolved in real space with atomic-scale resolution. By taking together images and current-voltage spectroscopy data we find that charge order correlates with both structural order and the local conductive state (either metallic or insulating). These experiments provide an atomic-scale basis for descriptions of manganites as mixtures of electronically and structurally distinct phases.

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