Electronic Control of Chemistry and Catalysis at the Surface of an Individual Tin Oxide Nanowire

Tin oxide single nanowires configured as field effect transistors were shown to be operable and tunable alternately as gas sensors or as catalysts under a gaseous atmosphere that simulated realistic ambient conditions. The unusually large surface-to-volume ratio available with nanowires causes adsorption or desorption of donor or acceptor molecules on the nanowire's surface to greatly alter its bulk electron density at relatively small values of the gate voltage. This process can be sensitively monitored as changes in the nanowire's conductivity. The potentially radical change in carrier density can lead to significant changes in the nanowire's sensitivity as a sensor or reciprocally as a catalyst in reactions that involve charge exchange across the nanowire's surface. This leads to the prospect of tuning catalysis or other surface reactions entirely through electronic means

Symmetry Relationship and Strain-Induced Transitions between Insulating M1 and M2 and Metallic R phases of Vanadium Dioxide

The ability to synthesize VO2 in the form of single-crystalline nanobeams and nano- and microcrystals uncovered a number of previously unknown aspects of the metal−insulator transition (MIT) in this oxide. In particular, several reports demonstrated that the MIT can proceed through competition between two monoclinic (insulating) phases M1 and M2 and the tetragonal (metallic) R phase under influence of strain. The nature of such phase behavior has been not identified. Here we show that the competition between M1 and M2 phases is purely lattice-symmetry-driven. Within the framework of the Ginzburg−Landau formalism, both M phases correspond to different directions of the same four-component structural order parameter, and as a consequence, the M2 phase can appear under a small perturbation of the M1 structure such as doping or stress. We analyze the strain-controlled phase diagram of VO2 in the vicinity of the R−M2−M1 triple point using the Ginzburg−Landau formalism and identify and experimentally verify the pathways for strain-control of the transition. These insights open the door toward more systematic approaches to synthesis of VO2 nanostructures in desired phase states and to use of external fields in the control of the VO2 phase states. Additionally, we report observation of the triclinic T phase at the heterophase domain boundaries in strained quasi-two-dimensional VO2 nanoplatelets, and theoretically predict phases that have not been previously observed