Demonstration of a tunable conductivity of the LaAlO(3)/SrTiO(3) interfaces drew significant attention to the development of oxide electronic structures where electronic confinement can be reduced to the nanometer range. While the mechanisms for the conductivity modulation are quite different and include metal-insulator phase transition and surface charge writing, generally it is implied that this effect is a result of electrical modification of the LaAlO(3) surface (either due to electrochemical dissociation of surface adsorbates or free charge deposition) leading to the change in the two-dimensional electron gas (2DEG) density at the LaAlO(3)/SrTiO(3) (LAO/STO) interface. In this paper, using piezoresponse force microscopy we demonstrate a switchable electromechanical response of the LAO overlayer, which we attribute to the motion of oxygen vacancies through the LAO layer thickness. These electrically induced reversible changes in bulk stoichiometry of the LAO layer are a signature of a possible additional mechanism for nanoscale oxide 2DEG control on LAO/STO interfaces.

The power conversion efficiency of most thin film solar cells is compromised by competing optical and electronic constraints, wherein a cell must be thick enough to collect light yet thin enough to efficiently extract current. Here, we introduce a nanoscale solar architecture inspired by a well‐known radio technology concept, the coaxial cable, that naturally resolves this “thick–thin” conundrum. Optically thick and elec‐ tronically thin amorphous silicon “nanocoax” cells are in the range of 8% efficiency, higher than any nanostructured thin film solar cell to date. Moreover, the thin nature of the cells reduces the Staebler–Wronski light‐induced degradation effect, a major problem with conventional solar cells of this type. This nanocoax represents a new platform for low cost, high efficiency solar power. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)